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ESP: PubMed Auto Bibliography 15 Nov 2025 at 01:52 Created:
Microbial Ecology
Wikipedia: Microbial Ecology (or environmental microbiology) is the ecology of microorganisms: their relationship with one another and with their environment. It concerns the three major domains of life — Eukaryota, Archaea, and Bacteria — as well as viruses. Microorganisms, by their omnipresence, impact the entire biosphere. Microbial life plays a primary role in regulating biogeochemical systems in virtually all of our planet's environments, including some of the most extreme, from frozen environments and acidic lakes, to hydrothermal vents at the bottom of deepest oceans, and some of the most familiar, such as the human small intestine. As a consequence of the quantitative magnitude of microbial life (Whitman and coworkers calculated 5.0×1030 cells, eight orders of magnitude greater than the number of stars in the observable universe) microbes, by virtue of their biomass alone, constitute a significant carbon sink. Aside from carbon fixation, microorganisms' key collective metabolic processes (including nitrogen fixation, methane metabolism, and sulfur metabolism) control global biogeochemical cycling. The immensity of microorganisms' production is such that, even in the total absence of eukaryotic life, these processes would likely continue unchanged.
Created with PubMed® Query: ( "microbial ecology" ) NOT pmcbook NOT ispreviousversion
Citations The Papers (from PubMed®)
RevDate: 2025-11-14
Dysbiosis of Bacterial and Fungal Microbiomes Affects the Disease Process and Treatment Outcome in Fungal Keratitis.
Experimental eye research pii:S0014-4835(25)00518-4 [Epub ahead of print].
Fungal keratitis (FK) is a severe eye infection mainly caused by Aspergillus flavus and Fusarium solani. We examined the changes in bacterial and fungal microbiome profiles over a week of disease progression, treatment, and clinical status using targeted next-generation sequencing (NGS). Samples were collected from infected and healthy contralateral eyes of 25 FK patients and one eye of 10 healthy, non-infected cataract controls. QIIME (Quantitative Insights into Microbial Ecology) and MicrobiomeAnalyst were utilised for the data analysis. There was a reduction in beneficial bacteria like Prevotella, Lactobacillus, and Leuconostoc in FK patients compared to the control samples. On the other hand, opportunistic bacteria including Clostridium, Bifidobacterium, and Pseudomonas increased in FK patients. Aspergillus, Colletotrichum, and Basidiobolus were more abundant in keratitis patients, whereas Malassezia and Trichoderma were less abundant. This dysbiosis was also evident in the uninfected contralateral eyes of FK patients. Treatment resulted in significant changes in bacterial genera like Dolosigranulum, Sutterella, and Akkermansia, and fungal genera such as Myrothecium, Corynespora, and Penicillium. Further, treatment returned them to the control group levels, except for Akkermansia and Corynespora. Among the treated patients, a large subset remains nonresponsive to treatment. This treatment outcome, responder versus non-responder, was reflected in the abundance of bacterial genera such as Tannerella, Sutterella, Odoribacter, and fungal genera such as Coprinellus and Volutella. This study highlights the clinical relevance of microbiome signatures in FK, demonstrating bilateral dysbiosis, integrated bacterial-fungal profiling, and correlations with treatment outcomes. These findings suggest potential for microbiome-informed diagnostics, prognostic biomarkers, and risk stratification.
Additional Links: PMID-41237939
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@article {pmid41237939,
year = {2025},
author = {Devarajan, B and Sharma, S and Mills, B and Prajna, L and Venkatesh, PN and Dharmalingam, K},
title = {Dysbiosis of Bacterial and Fungal Microbiomes Affects the Disease Process and Treatment Outcome in Fungal Keratitis.},
journal = {Experimental eye research},
volume = {},
number = {},
pages = {110745},
doi = {10.1016/j.exer.2025.110745},
pmid = {41237939},
issn = {1096-0007},
abstract = {Fungal keratitis (FK) is a severe eye infection mainly caused by Aspergillus flavus and Fusarium solani. We examined the changes in bacterial and fungal microbiome profiles over a week of disease progression, treatment, and clinical status using targeted next-generation sequencing (NGS). Samples were collected from infected and healthy contralateral eyes of 25 FK patients and one eye of 10 healthy, non-infected cataract controls. QIIME (Quantitative Insights into Microbial Ecology) and MicrobiomeAnalyst were utilised for the data analysis. There was a reduction in beneficial bacteria like Prevotella, Lactobacillus, and Leuconostoc in FK patients compared to the control samples. On the other hand, opportunistic bacteria including Clostridium, Bifidobacterium, and Pseudomonas increased in FK patients. Aspergillus, Colletotrichum, and Basidiobolus were more abundant in keratitis patients, whereas Malassezia and Trichoderma were less abundant. This dysbiosis was also evident in the uninfected contralateral eyes of FK patients. Treatment resulted in significant changes in bacterial genera like Dolosigranulum, Sutterella, and Akkermansia, and fungal genera such as Myrothecium, Corynespora, and Penicillium. Further, treatment returned them to the control group levels, except for Akkermansia and Corynespora. Among the treated patients, a large subset remains nonresponsive to treatment. This treatment outcome, responder versus non-responder, was reflected in the abundance of bacterial genera such as Tannerella, Sutterella, Odoribacter, and fungal genera such as Coprinellus and Volutella. This study highlights the clinical relevance of microbiome signatures in FK, demonstrating bilateral dysbiosis, integrated bacterial-fungal profiling, and correlations with treatment outcomes. These findings suggest potential for microbiome-informed diagnostics, prognostic biomarkers, and risk stratification.},
}
RevDate: 2025-11-14
CmpDate: 2025-11-14
Differential Assembly of Core and Non-Core Host-Microbe Network Structures Along a Land-Use Change Gradient.
Ecology letters, 28(11):e70255.
Microbial communities are fundamental to host health, yet their assembly dynamics under environmental change remain poorly understood. We analysed individual-level host-microbe networks in the non-native wild black rats (Rattus rattus) across a land-use gradient in Madagascar. By applying a moving prevalence threshold, we distinguished between core and non-core microbes and compared the assembly drivers shaping their network structures. Non-core microbes formed fragmented, modular networks shaped mainly by heterogeneous selection, reflecting environmental filtering. In contrast, core microbes exhibited stable, less modular networks driven primarily by stochastic ecological drift. These distinct assembly processes persisted across thresholds, highlighting fundamental differences in microbial structuring. Land-use change significantly influenced the modular structure of non-core microbes but had minimal effects on core microbes, demonstrating the differential sensitivity of microbial groups to environmental variation. This study advances our understanding of host-microbe interactions and provides a framework for assessing microbiome assembly under anthropogenic change.
Additional Links: PMID-41236361
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@article {pmid41236361,
year = {2025},
author = {Markfeld, M and Titcomb, G and Randriamoria, TM and Sehgal, G and Baksh, N and Kerrigan, A and Soarimalala, V and Nunn, CL and Pilosof, S},
title = {Differential Assembly of Core and Non-Core Host-Microbe Network Structures Along a Land-Use Change Gradient.},
journal = {Ecology letters},
volume = {28},
number = {11},
pages = {e70255},
doi = {10.1111/ele.70255},
pmid = {41236361},
issn = {1461-0248},
support = {1281/20//Israel Science Foundation/ ; 2308460//National Science Foundation/ ; R01-TW011493//NIH-NSF-NIFA Ecology and Evolution of Infectious Diseases program/ ; 2022721//United States-Israel Binational Science Foundation/ ; Provost's Collaboratory Award//Duke University/ ; RGY0064/2022//Human Frontier Science Program/ ; //Duke Lemur Center/ ; },
mesh = {Animals ; Rats/microbiology ; Madagascar ; *Microbiota ; *Host Microbial Interactions ; },
abstract = {Microbial communities are fundamental to host health, yet their assembly dynamics under environmental change remain poorly understood. We analysed individual-level host-microbe networks in the non-native wild black rats (Rattus rattus) across a land-use gradient in Madagascar. By applying a moving prevalence threshold, we distinguished between core and non-core microbes and compared the assembly drivers shaping their network structures. Non-core microbes formed fragmented, modular networks shaped mainly by heterogeneous selection, reflecting environmental filtering. In contrast, core microbes exhibited stable, less modular networks driven primarily by stochastic ecological drift. These distinct assembly processes persisted across thresholds, highlighting fundamental differences in microbial structuring. Land-use change significantly influenced the modular structure of non-core microbes but had minimal effects on core microbes, demonstrating the differential sensitivity of microbial groups to environmental variation. This study advances our understanding of host-microbe interactions and provides a framework for assessing microbiome assembly under anthropogenic change.},
}
MeSH Terms:
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Animals
Rats/microbiology
Madagascar
*Microbiota
*Host Microbial Interactions
RevDate: 2025-11-14
Keystone protist suppression triggers mesopredator release and biotic homogenization in complex soil microbial communities.
The ISME journal pii:8323206 [Epub ahead of print].
The keystone species concept holds that certain members of an ecological community, despite their low abundance, exert disproportionately large effects on species diversity and composition. In microbial ecology, experimental validation of this concept has been limited because targeted removal of individual species remains technically challenging. Here, we developed a procedure to test the keystone species concept within a soil microbial food web by selectively suppressing a protist predator at the microscale via UV-induced phototoxicity in a microfluidic soil chip system. We targeted a hypotrich ciliate (subclass Hypotrichia), and combined microscopy with high-throughput amplicon sequencing of microbial taxonomic markers to assess, across multiple trophic levels, how its suppression affected microbial community abundance, diversity, and composition. Over the 20-day incubation, the chip system supported complex communities of bacteria, fungi, and protists. Following Hypotrichia suppression, two distinct ecological responses were observed: first, an increase in the relative abundance of flagellates, consistent with mesopredator release, accompanied by a significant rise in overall protist diversity; second, a convergence in protist community composition, indicative of biotic homogenization. Bacterial community abundance, richness, and composition remained unchanged, likely due to compensatory predation from a relative increase in bacterivorous flagellates. In contrast, fungal diversity decreased, presumably because the altered protist community favored facultative fungal consumers. Collectively, these findings provide direct experimental evidence that low abundance microbial predators can function as keystone species, modulating predator community composition and diversity, and exerting cascading effects on lower trophic levels within microbial brown food webs.
Additional Links: PMID-41236145
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@article {pmid41236145,
year = {2025},
author = {Maillard, F and Klinghammer, F and Beatty, BH and Zou, H and Lara, E and Hammer, EC and Tunlid, A and Kennedy, PG},
title = {Keystone protist suppression triggers mesopredator release and biotic homogenization in complex soil microbial communities.},
journal = {The ISME journal},
volume = {},
number = {},
pages = {},
doi = {10.1093/ismejo/wraf253},
pmid = {41236145},
issn = {1751-7370},
abstract = {The keystone species concept holds that certain members of an ecological community, despite their low abundance, exert disproportionately large effects on species diversity and composition. In microbial ecology, experimental validation of this concept has been limited because targeted removal of individual species remains technically challenging. Here, we developed a procedure to test the keystone species concept within a soil microbial food web by selectively suppressing a protist predator at the microscale via UV-induced phototoxicity in a microfluidic soil chip system. We targeted a hypotrich ciliate (subclass Hypotrichia), and combined microscopy with high-throughput amplicon sequencing of microbial taxonomic markers to assess, across multiple trophic levels, how its suppression affected microbial community abundance, diversity, and composition. Over the 20-day incubation, the chip system supported complex communities of bacteria, fungi, and protists. Following Hypotrichia suppression, two distinct ecological responses were observed: first, an increase in the relative abundance of flagellates, consistent with mesopredator release, accompanied by a significant rise in overall protist diversity; second, a convergence in protist community composition, indicative of biotic homogenization. Bacterial community abundance, richness, and composition remained unchanged, likely due to compensatory predation from a relative increase in bacterivorous flagellates. In contrast, fungal diversity decreased, presumably because the altered protist community favored facultative fungal consumers. Collectively, these findings provide direct experimental evidence that low abundance microbial predators can function as keystone species, modulating predator community composition and diversity, and exerting cascading effects on lower trophic levels within microbial brown food webs.},
}
RevDate: 2025-11-14
CmpDate: 2025-11-14
Alteration of gut microbial ecology by the direct activation of the brain: Inverse gut-microbiome-brain dynamics.
iScience, 28(11):113709.
The gut-microbiome-brain axis is a bidirectional communication system influencing host physiology and overall fitness. While "bottom-up" effects-where gut microbes influence brain function and behavior-are well established, direct evidence for "top-down" modulation-where the brain shapes the gut microbial ecology-remains elusive. Here, we show that the selective expression of the bacterial ion channel mNaChBac in glutamatergic lateral habenula (LHb) neurons increases their bursting activity and leads to endophentypes associated with depression. Importantly, this chronic activation leads to changes in the gut microbiome composition over time, as reflected by shifts in alpha-diversity and alterations in specific microbial taxa. These findings provide direct evidence that the persistent activation of the brain acts as a selective pressure that affects the stability and diversity of the gut microbiome, providing a new dimension by which gut-microbiome-brain interactions may cooperate to modulate host physiology and health.
Additional Links: PMID-41234770
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@article {pmid41234770,
year = {2025},
author = {Wang, IC and Swanson, JL and Waters, JL and Kochukov, MY and Buffington, SA and Dooling, SW and Arenkiel, BR and Costa-Mattioli, M},
title = {Alteration of gut microbial ecology by the direct activation of the brain: Inverse gut-microbiome-brain dynamics.},
journal = {iScience},
volume = {28},
number = {11},
pages = {113709},
pmid = {41234770},
issn = {2589-0042},
abstract = {The gut-microbiome-brain axis is a bidirectional communication system influencing host physiology and overall fitness. While "bottom-up" effects-where gut microbes influence brain function and behavior-are well established, direct evidence for "top-down" modulation-where the brain shapes the gut microbial ecology-remains elusive. Here, we show that the selective expression of the bacterial ion channel mNaChBac in glutamatergic lateral habenula (LHb) neurons increases their bursting activity and leads to endophentypes associated with depression. Importantly, this chronic activation leads to changes in the gut microbiome composition over time, as reflected by shifts in alpha-diversity and alterations in specific microbial taxa. These findings provide direct evidence that the persistent activation of the brain acts as a selective pressure that affects the stability and diversity of the gut microbiome, providing a new dimension by which gut-microbiome-brain interactions may cooperate to modulate host physiology and health.},
}
RevDate: 2025-11-13
CmpDate: 2025-11-14
Red seaweed supplementation suppresses methanogenesis in the rumen, revealing potentially advantageous traits among hydrogenotrophic bacteria.
Microbiome, 13(1):231.
BACKGROUND: Macroalgae belonging to the genus Asparagopsis have shown to reduce methane (CH4) production during rumen fermentation, while increasing feed efficiency when added to the feed of cattle. However, little is known about how the rumen microbiome responds to Asparagopsis supplementation, and how changes in the microbiome may contribute to changes in rumen function and host phenotype. Here, we generated and analyzed metagenomic and metatranscriptomic data from the rumen microbiome from cows receiving (treatment) and not receiving (control) an Asparagopsis armata supplemented diet.
RESULTS: Using a combination of metatranscriptome and metagenome analysis, we found that reduction of CH4 emission from animals receiving A. armata was coupled to a significant reduction in the transcription of methanogenesis pathways. Additionally, a significant decrease in the transcription of genes for carbon catabolism and a reorganization of carbon catabolic gene expression occurred at the species level within the rumen microbiome of animals that received red seaweed with their diet. Increased H2 production, a consequence of methanogenesis suppression, was coupled to a significant increase in the transcription of hydrogenases that mediate hydrogenotrophic metabolism in the treatment group. Metatranscriptome analysis identified a single metagenome assembled genome (MAG) of a Duodenibacillus sp., a hitherto uncultured hydrogenotrophic bacterial species, as the dominant driver of this transcriptional change.
CONCLUSIONS: Comparative genomic analysis between the Duodenibacillus sp. and other hydrogenotrophic rumen organisms revealed metabolic traits that may provide Duodenibacillus sp. with a competitive advantage in H2 scavenging. Our findings provide an initial understanding of how the rumen microbiome responds to a promising CH4 reducing feed additive and serve as a model for alternative stable rumen microbiome states that produce less methane and increase animal productivity. Ultimately, insights from the work presented here might enable the development of advanced microbiome-based strategies to reduce enteric methane production.
Additional Links: PMID-41233937
PubMed:
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@article {pmid41233937,
year = {2025},
author = {Zhang, P and Roque, B and Romero, P and Shapiro, N and Eloe-Fadrosh, E and Kebreab, E and Diamond, S and Hess, M},
title = {Red seaweed supplementation suppresses methanogenesis in the rumen, revealing potentially advantageous traits among hydrogenotrophic bacteria.},
journal = {Microbiome},
volume = {13},
number = {1},
pages = {231},
pmid = {41233937},
issn = {2049-2618},
mesh = {Animals ; *Rumen/microbiology/metabolism ; *Methane/metabolism/biosynthesis ; Cattle ; *Seaweed ; *Dietary Supplements ; *Bacteria/genetics/metabolism/classification/isolation & purification ; Animal Feed/analysis ; *Gastrointestinal Microbiome ; Fermentation ; Metagenome ; Metagenomics ; Hydrogen/metabolism ; },
abstract = {BACKGROUND: Macroalgae belonging to the genus Asparagopsis have shown to reduce methane (CH4) production during rumen fermentation, while increasing feed efficiency when added to the feed of cattle. However, little is known about how the rumen microbiome responds to Asparagopsis supplementation, and how changes in the microbiome may contribute to changes in rumen function and host phenotype. Here, we generated and analyzed metagenomic and metatranscriptomic data from the rumen microbiome from cows receiving (treatment) and not receiving (control) an Asparagopsis armata supplemented diet.
RESULTS: Using a combination of metatranscriptome and metagenome analysis, we found that reduction of CH4 emission from animals receiving A. armata was coupled to a significant reduction in the transcription of methanogenesis pathways. Additionally, a significant decrease in the transcription of genes for carbon catabolism and a reorganization of carbon catabolic gene expression occurred at the species level within the rumen microbiome of animals that received red seaweed with their diet. Increased H2 production, a consequence of methanogenesis suppression, was coupled to a significant increase in the transcription of hydrogenases that mediate hydrogenotrophic metabolism in the treatment group. Metatranscriptome analysis identified a single metagenome assembled genome (MAG) of a Duodenibacillus sp., a hitherto uncultured hydrogenotrophic bacterial species, as the dominant driver of this transcriptional change.
CONCLUSIONS: Comparative genomic analysis between the Duodenibacillus sp. and other hydrogenotrophic rumen organisms revealed metabolic traits that may provide Duodenibacillus sp. with a competitive advantage in H2 scavenging. Our findings provide an initial understanding of how the rumen microbiome responds to a promising CH4 reducing feed additive and serve as a model for alternative stable rumen microbiome states that produce less methane and increase animal productivity. Ultimately, insights from the work presented here might enable the development of advanced microbiome-based strategies to reduce enteric methane production.},
}
MeSH Terms:
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hide MeSH Terms
Animals
*Rumen/microbiology/metabolism
*Methane/metabolism/biosynthesis
Cattle
*Seaweed
*Dietary Supplements
*Bacteria/genetics/metabolism/classification/isolation & purification
Animal Feed/analysis
*Gastrointestinal Microbiome
Fermentation
Metagenome
Metagenomics
Hydrogen/metabolism
RevDate: 2025-11-13
CmpDate: 2025-11-14
Putative promiscuous symbionts in deep-sea corals and crinoids may contribute to nitrogen cycling.
Microbiome, 13(1):234.
BACKGROUND: Crinoids (feather stars) are frequently found in association with corals, yet the physiological and microbial interactions between these organisms remain poorly understood. Both corals and crinoids host symbiotic microorganisms, but the functional roles of these symbionts, particularly in deep-sea environments, are largely unexplored. This study characterizes the microbiomes of the deep-sea corals Desmophyllum pertusum and Solenosmilia variabilis and their associated crinoid Koehlermetra sp. (Thalassometridae) from the Campos Basin, Brazil, to investigate potential cross-host microbial interactions and their ecological implications. We used multiple approaches for this investigation, including amplicon sequencing surveys, genome-resolved metagenomics, and fluorescence in situ hybridization.
RESULTS: We found that the same endosymbiotic members of the families Endozoicomonadaceae and Nitrosopumilaceae inhabit both corals and the crinoids, suggesting promiscuity in host-symbiont relationships. Metagenomic analysis revealed a novel and dominant Endozoicomonas species (E. promiscua sp. nov.), whose genome encodes pathways for dissimilatory nitrate reduction to ammonia (DNRA). This metabolic capability could provide a substrate for ammonia-oxidizing archaea (Nitrosopumilaceae), indicating a potential cross-host nitrogen-cycling network. Shared microbial taxa between corals and crinoids further support the hypothesis of symbiont promiscuity, where metabolic redundancy may facilitate colonization across species.
CONCLUSIONS: Our findings suggest that nitrogen cycling plays a key role in structuring microbial symbioses in deep-sea coral-crinoid holobionts. The promiscuous distribution of symbionts across hosts implies that metabolic interactions, such as DNRA-driven ammonia provisioning, could underpin resilience in nutrient-limited environments. This study highlights the importance of microbial versatility in deep-sea ecosystems and provides new insights into how cross-host symbiosis may contribute to biogeochemical cycling in the ocean. Video Abstract.
Additional Links: PMID-41233936
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@article {pmid41233936,
year = {2025},
author = {Modolon, F and N Garritano, A and J Hill, L and Duarte, G and Bendia, A and de Moura, R and Pellizari, V and Thomas, T and Peixoto, RS},
title = {Putative promiscuous symbionts in deep-sea corals and crinoids may contribute to nitrogen cycling.},
journal = {Microbiome},
volume = {13},
number = {1},
pages = {234},
pmid = {41233936},
issn = {2049-2618},
support = {141954/2019-1//Conselho Nacional de Desenvolvimento Científico e Tecnológico/ ; ANP 21005-4//Shell, Brazil/ ; BAS/1/1095-01-01 and FCC/1/1976-40-01//KAUST/ ; },
mesh = {*Anthozoa/microbiology ; Animals ; *Symbiosis ; *Nitrogen Cycle ; Metagenomics/methods ; Microbiota ; Brazil ; *Bacteria/classification/genetics/metabolism/isolation & purification ; Phylogeny ; RNA, Ribosomal, 16S/genetics ; In Situ Hybridization, Fluorescence ; },
abstract = {BACKGROUND: Crinoids (feather stars) are frequently found in association with corals, yet the physiological and microbial interactions between these organisms remain poorly understood. Both corals and crinoids host symbiotic microorganisms, but the functional roles of these symbionts, particularly in deep-sea environments, are largely unexplored. This study characterizes the microbiomes of the deep-sea corals Desmophyllum pertusum and Solenosmilia variabilis and their associated crinoid Koehlermetra sp. (Thalassometridae) from the Campos Basin, Brazil, to investigate potential cross-host microbial interactions and their ecological implications. We used multiple approaches for this investigation, including amplicon sequencing surveys, genome-resolved metagenomics, and fluorescence in situ hybridization.
RESULTS: We found that the same endosymbiotic members of the families Endozoicomonadaceae and Nitrosopumilaceae inhabit both corals and the crinoids, suggesting promiscuity in host-symbiont relationships. Metagenomic analysis revealed a novel and dominant Endozoicomonas species (E. promiscua sp. nov.), whose genome encodes pathways for dissimilatory nitrate reduction to ammonia (DNRA). This metabolic capability could provide a substrate for ammonia-oxidizing archaea (Nitrosopumilaceae), indicating a potential cross-host nitrogen-cycling network. Shared microbial taxa between corals and crinoids further support the hypothesis of symbiont promiscuity, where metabolic redundancy may facilitate colonization across species.
CONCLUSIONS: Our findings suggest that nitrogen cycling plays a key role in structuring microbial symbioses in deep-sea coral-crinoid holobionts. The promiscuous distribution of symbionts across hosts implies that metabolic interactions, such as DNRA-driven ammonia provisioning, could underpin resilience in nutrient-limited environments. This study highlights the importance of microbial versatility in deep-sea ecosystems and provides new insights into how cross-host symbiosis may contribute to biogeochemical cycling in the ocean. Video Abstract.},
}
MeSH Terms:
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*Anthozoa/microbiology
Animals
*Symbiosis
*Nitrogen Cycle
Metagenomics/methods
Microbiota
Brazil
*Bacteria/classification/genetics/metabolism/isolation & purification
Phylogeny
RNA, Ribosomal, 16S/genetics
In Situ Hybridization, Fluorescence
RevDate: 2025-11-13
Hydrogel-based experimental models of the gastrointestinal tract.
Microbiome, 13(1):233.
The gut microbiome plays a pivotal role in human health, yet its complexity has long eluded detailed study under physiologically relevant conditions. Hydrogel-based models are revolutionizing microbiome research by bridging the gap between traditional in vitro systems and the complexity of in vivo environments. These advanced systems replicate key physical and biochemical features of the gastrointestinal tract, offering unprecedented opportunities to study microbial behavior, adaptation, and interactions within three-dimensional, tunable architectures. Unlike suspension cultures, hydrogels provide porous, mucosa-like environments that enable the cultivation of mucosa-associated microbes, co-culturing with human cells, and mimicking healthy and disease-related states. This review explores the transformative potential of hydrogel matrices in unveiling the spatial organization, nutrient gradients, and community communication that define microbial ecosystems. By integrating the benefits of in vitro and in vivo models, hydrogel-based platforms promise to accelerate discoveries in microbiome science, with far-reaching implications for understanding human health and developing targeted therapeutics. Video Abstract.
Additional Links: PMID-41233829
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@article {pmid41233829,
year = {2025},
author = {Sieders, M and Candry, P and El Aidy, S},
title = {Hydrogel-based experimental models of the gastrointestinal tract.},
journal = {Microbiome},
volume = {13},
number = {1},
pages = {233},
pmid = {41233829},
issn = {2049-2618},
abstract = {The gut microbiome plays a pivotal role in human health, yet its complexity has long eluded detailed study under physiologically relevant conditions. Hydrogel-based models are revolutionizing microbiome research by bridging the gap between traditional in vitro systems and the complexity of in vivo environments. These advanced systems replicate key physical and biochemical features of the gastrointestinal tract, offering unprecedented opportunities to study microbial behavior, adaptation, and interactions within three-dimensional, tunable architectures. Unlike suspension cultures, hydrogels provide porous, mucosa-like environments that enable the cultivation of mucosa-associated microbes, co-culturing with human cells, and mimicking healthy and disease-related states. This review explores the transformative potential of hydrogel matrices in unveiling the spatial organization, nutrient gradients, and community communication that define microbial ecosystems. By integrating the benefits of in vitro and in vivo models, hydrogel-based platforms promise to accelerate discoveries in microbiome science, with far-reaching implications for understanding human health and developing targeted therapeutics. Video Abstract.},
}
RevDate: 2025-11-13
CmpDate: 2025-11-13
Exploring gut microbiota and its predicted functions in pulmonary tuberculosis: A multi-regional study using public 16S datasets.
PloS one, 20(11):e0336337 pii:PONE-D-25-41202.
BACKGROUND: Pulmonary tuberculosis, caused by the bacillus Mycobacterium tuberculosis, remains a major global health challenge, particularly in developing countries. In this study, we analyzed publicly available 16S amplicon sequencing datasets from four geographical locations using a single workflow.
METHODS: We employed Quantitative Insights Into Microbial Ecology v.2 for microbial diversity analysis and Phylogenetic Investigation of Communities by Reconstruction of Unobserved States v.2 for functional pathway predictions of the gut microbiota in patients with PTB and antitubercular therapy.
RESULTS: Our analysis revealed statistically significant alpha diversity differences in West Africa with decreased microbial diversity in pulmonary tuberculosis patients after two months of antitubercular therapy. Additionally, there were no statistically significant differences observed in pairwise comparisons within the same location or in the aggregate beta diversity of the datasets. The predicted microbial metabolic pathways related to vitamin biosynthesis, amino acid synthesis, and energy production were depleted in pulmonary tuberculosis patients following antitubercular therapy.
CONCLUSIONS: The observed alterations of gut microbial diversity and predicted functional profile underscores the influence of antitubercular therapy on gut health, suggesting that longer treatment durations may aggravate these alterations in gut microbial function. Moreover, geographical location exerts a more significant impact on microbial diversity than the disease state in a specific location, highlighting the potential for precision medicine to tailor interventions based on individual or regional microbiome characteristics.
Additional Links: PMID-41231796
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PubMed:
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@article {pmid41231796,
year = {2025},
author = {Baral, T and Maile, A and Adimurthy, NH and Saravu, K and Kudru, CU and Singh, J and Mukhopadhyay, C and Rao, M and Manu, MK and Sekhar Miraj, S},
title = {Exploring gut microbiota and its predicted functions in pulmonary tuberculosis: A multi-regional study using public 16S datasets.},
journal = {PloS one},
volume = {20},
number = {11},
pages = {e0336337},
doi = {10.1371/journal.pone.0336337},
pmid = {41231796},
issn = {1932-6203},
mesh = {Humans ; *Gastrointestinal Microbiome/genetics/drug effects ; *Tuberculosis, Pulmonary/microbiology/drug therapy ; Phylogeny ; *RNA, Ribosomal, 16S/genetics ; Antitubercular Agents/therapeutic use ; Male ; Female ; Mycobacterium tuberculosis/genetics ; Middle Aged ; Adult ; },
abstract = {BACKGROUND: Pulmonary tuberculosis, caused by the bacillus Mycobacterium tuberculosis, remains a major global health challenge, particularly in developing countries. In this study, we analyzed publicly available 16S amplicon sequencing datasets from four geographical locations using a single workflow.
METHODS: We employed Quantitative Insights Into Microbial Ecology v.2 for microbial diversity analysis and Phylogenetic Investigation of Communities by Reconstruction of Unobserved States v.2 for functional pathway predictions of the gut microbiota in patients with PTB and antitubercular therapy.
RESULTS: Our analysis revealed statistically significant alpha diversity differences in West Africa with decreased microbial diversity in pulmonary tuberculosis patients after two months of antitubercular therapy. Additionally, there were no statistically significant differences observed in pairwise comparisons within the same location or in the aggregate beta diversity of the datasets. The predicted microbial metabolic pathways related to vitamin biosynthesis, amino acid synthesis, and energy production were depleted in pulmonary tuberculosis patients following antitubercular therapy.
CONCLUSIONS: The observed alterations of gut microbial diversity and predicted functional profile underscores the influence of antitubercular therapy on gut health, suggesting that longer treatment durations may aggravate these alterations in gut microbial function. Moreover, geographical location exerts a more significant impact on microbial diversity than the disease state in a specific location, highlighting the potential for precision medicine to tailor interventions based on individual or regional microbiome characteristics.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Humans
*Gastrointestinal Microbiome/genetics/drug effects
*Tuberculosis, Pulmonary/microbiology/drug therapy
Phylogeny
*RNA, Ribosomal, 16S/genetics
Antitubercular Agents/therapeutic use
Male
Female
Mycobacterium tuberculosis/genetics
Middle Aged
Adult
RevDate: 2025-11-13
CmpDate: 2025-11-13
In Silico Prediction and In Vitro Validation of Bacterial Interactions in the Plant Rhizosphere Using a Synthetic Bacterial Community.
Bio-protocol, 15(21):e5496.
The rhizosphere, a 2-10 mm region surrounding the root surface, is colonized by numerous microorganisms, known as the rhizosphere microbiome. These microorganisms interact with each other, leading to emergent properties that affect plant fitness. Mapping these interactions is crucial to understanding microbial ecology in the rhizosphere and predicting and manipulating plant health. However, current methods do not capture the chemistry of the rhizosphere environment, and common plant-microbe interaction study setups do not map bacterial interactions in this niche. Additionally, studying bacterial interactions may require the creation of transgenic bacterial lines with markers for antibiotic resistance/fluorescent probes and even isotope labeling. Here, we describe a protocol for both in silico prediction and in vitro validation of bacterial interactions that closely recapitulate the major chemical constituents of the rhizosphere environment using a widely used Murashige & Skoog (MS)-based gnotobiotic plant growth system. We use the auto-fluorescent Pseudomonas, abundantly found in the rhizosphere, to estimate their interactions with other strains, thereby avoiding the need for the creation of transgenic bacterial strains. By combining artificial root exudate medium, plant cultivation medium, and a synthetic bacterial community (SynCom), we first simulate their interactions using genome-scale metabolic models (GSMMs) and then validate these interactions in vitro, using growth assays. We show that the GSMM-predicted interaction scores correlate moderately, yet significantly, with their in vitro validation. Given the complexity of interactions among rhizosphere microbiome members, this reproducible and efficient protocol will allow confident mapping of interactions of fluorescent Pseudomonas with other bacterial strains within the rhizosphere microbiome. Key features • This method builds upon the widely used MS-based gnotobiotic system for growing plants and a synthetic bacterial community (SynCom) for plant-microbe interaction studies. • It considers the chemical composition of plant growth media (MS) and root exudates to map bacterial interactions. • It provides a method to both predict and validate interactions of fluorescent Pseudomonas with other strains within a SynCom. • This method is scalable for any bacterial pair with distinguishing markers (e.g., fluorescence, antibiotic resistance).
Additional Links: PMID-41230548
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@article {pmid41230548,
year = {2025},
author = {Mukherjee, A and Tan, BH and Swarup, S},
title = {In Silico Prediction and In Vitro Validation of Bacterial Interactions in the Plant Rhizosphere Using a Synthetic Bacterial Community.},
journal = {Bio-protocol},
volume = {15},
number = {21},
pages = {e5496},
pmid = {41230548},
issn = {2331-8325},
abstract = {The rhizosphere, a 2-10 mm region surrounding the root surface, is colonized by numerous microorganisms, known as the rhizosphere microbiome. These microorganisms interact with each other, leading to emergent properties that affect plant fitness. Mapping these interactions is crucial to understanding microbial ecology in the rhizosphere and predicting and manipulating plant health. However, current methods do not capture the chemistry of the rhizosphere environment, and common plant-microbe interaction study setups do not map bacterial interactions in this niche. Additionally, studying bacterial interactions may require the creation of transgenic bacterial lines with markers for antibiotic resistance/fluorescent probes and even isotope labeling. Here, we describe a protocol for both in silico prediction and in vitro validation of bacterial interactions that closely recapitulate the major chemical constituents of the rhizosphere environment using a widely used Murashige & Skoog (MS)-based gnotobiotic plant growth system. We use the auto-fluorescent Pseudomonas, abundantly found in the rhizosphere, to estimate their interactions with other strains, thereby avoiding the need for the creation of transgenic bacterial strains. By combining artificial root exudate medium, plant cultivation medium, and a synthetic bacterial community (SynCom), we first simulate their interactions using genome-scale metabolic models (GSMMs) and then validate these interactions in vitro, using growth assays. We show that the GSMM-predicted interaction scores correlate moderately, yet significantly, with their in vitro validation. Given the complexity of interactions among rhizosphere microbiome members, this reproducible and efficient protocol will allow confident mapping of interactions of fluorescent Pseudomonas with other bacterial strains within the rhizosphere microbiome. Key features • This method builds upon the widely used MS-based gnotobiotic system for growing plants and a synthetic bacterial community (SynCom) for plant-microbe interaction studies. • It considers the chemical composition of plant growth media (MS) and root exudates to map bacterial interactions. • It provides a method to both predict and validate interactions of fluorescent Pseudomonas with other strains within a SynCom. • This method is scalable for any bacterial pair with distinguishing markers (e.g., fluorescence, antibiotic resistance).},
}
RevDate: 2025-11-13
CmpDate: 2025-11-13
Impact of Artificial Diet Versus Mulberry Leaves on Silkworm Growth, Nutrient Composition, and Gut Microbiota.
Archives of insect biochemistry and physiology, 120(3):e70113.
Silkworms (Bombyx Mori) are traditionally reared on mulberry leaves; however, artificial diets have been developed to enable year-round rearing and automation. The physiological performance and cocoon yield of silkworms fed artificial diets remain inferior to those reared on mulberry leaves. We compared growth and nutrient composition in larvae reared on mulberry leaves (ML) and antibiotic-free artificial diet (ADS), and profiled gut microbiota in ML, ADS, and antibiotic-supplemented artificial diet (ADSA) to assess dietary effects on host physiology and microbial ecology. Proximate analysis revealed that protein accumulation was greater in ML-fed larvae, while ADS-fed larvae showed relatively higher fat content at the late fifth instar. Amino acid profiling showed consistently higher silk-related residues (Gly, Ala, Ser) and the derived Silk Amino Acid Index in ML-fed larvae, indicating enhanced fibroin synthesis potential. Microbiome analysis using 16S rRNA amplicon sequencing demonstrated dominance of Enterococcus mundtii in ADS groups, resulting in reduced alpha diversity and uneven community structure. In contrast, ML-fed larvae harbored diverse taxa, including Methylorubrum and Methylobacterium, while ADSA groups exhibited intermediate profiles with occasional dominance of Bacillus cereus. These findings highlight that artificial diet alters host nutrient metabolism and drives dysbiosis of gut microbiota, underscoring the need for optimized formulations and microbiome-stabilizing strategies, such as probiotics or prebiotics.
Additional Links: PMID-41229186
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PubMed:
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@article {pmid41229186,
year = {2025},
author = {Park, JW and Park, JS and Kook, PR and Cho, YH and Park, SK and Lee, JH and Kang, SK and Kim, SW and Kim, SR},
title = {Impact of Artificial Diet Versus Mulberry Leaves on Silkworm Growth, Nutrient Composition, and Gut Microbiota.},
journal = {Archives of insect biochemistry and physiology},
volume = {120},
number = {3},
pages = {e70113},
doi = {10.1002/arch.70113},
pmid = {41229186},
issn = {1520-6327},
support = {PJ01721401.//This study was supported by the 2025 RDA Fellowship Program of the National Institute of Agricultural Science./ ; },
mesh = {Animals ; *Gastrointestinal Microbiome ; *Morus/chemistry ; *Bombyx/growth & development/microbiology/metabolism ; Plant Leaves/chemistry ; Larva/growth & development/microbiology ; *Diet ; *Animal Feed/analysis ; Nutrients/analysis ; RNA, Ribosomal, 16S ; },
abstract = {Silkworms (Bombyx Mori) are traditionally reared on mulberry leaves; however, artificial diets have been developed to enable year-round rearing and automation. The physiological performance and cocoon yield of silkworms fed artificial diets remain inferior to those reared on mulberry leaves. We compared growth and nutrient composition in larvae reared on mulberry leaves (ML) and antibiotic-free artificial diet (ADS), and profiled gut microbiota in ML, ADS, and antibiotic-supplemented artificial diet (ADSA) to assess dietary effects on host physiology and microbial ecology. Proximate analysis revealed that protein accumulation was greater in ML-fed larvae, while ADS-fed larvae showed relatively higher fat content at the late fifth instar. Amino acid profiling showed consistently higher silk-related residues (Gly, Ala, Ser) and the derived Silk Amino Acid Index in ML-fed larvae, indicating enhanced fibroin synthesis potential. Microbiome analysis using 16S rRNA amplicon sequencing demonstrated dominance of Enterococcus mundtii in ADS groups, resulting in reduced alpha diversity and uneven community structure. In contrast, ML-fed larvae harbored diverse taxa, including Methylorubrum and Methylobacterium, while ADSA groups exhibited intermediate profiles with occasional dominance of Bacillus cereus. These findings highlight that artificial diet alters host nutrient metabolism and drives dysbiosis of gut microbiota, underscoring the need for optimized formulations and microbiome-stabilizing strategies, such as probiotics or prebiotics.},
}
MeSH Terms:
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Animals
*Gastrointestinal Microbiome
*Morus/chemistry
*Bombyx/growth & development/microbiology/metabolism
Plant Leaves/chemistry
Larva/growth & development/microbiology
*Diet
*Animal Feed/analysis
Nutrients/analysis
RNA, Ribosomal, 16S
RevDate: 2025-11-13
CmpDate: 2025-11-13
Hyocholic Acid Species as the Key Modulator for Cecal Epithelial Homeostasis in Low-Birth-Weight Piglets.
Nutrients, 17(21): pii:nu17213415.
Background: Low birth weight (LBW) is correlated with gut microbiota dysbiosis and intestinal barrier function disruption, increasing susceptibility to enteric diseases. These alterations underscore the critical need to identify key regulators of gut homeostasis, among which bile acids are increasingly recognized as pivotal for barrier integrity, microbial ecology, and host metabolism. Methods: Eight pairs of LBW (the initial BW was 0.850 ± 0.053 kg) and normal-birth-weight (NBW; 1.488 ± 0.083 kg) piglets were compared to evaluate cecal morphology and bile acid profiles. Subsequently, sixteen LBW piglets and eight NBW piglets were allocated into three groups: NBW (1.563 ± 0.052 kg), LBW control (LBW-CON; 0.950 ± 0.120 kg), and LBW with bile acid supplementation (LBW-bile powder; 0.925 ± 0.116 kg). Piglets in the LBW-bile powder group received 25 mg/kg BW of bile powder (hyodeoxycholic acid-enriched) by daily oral gavage for 14 days. Results: LBW piglets exhibited retarded cecal development and lower abundance of hyocholic acid species (p = 0.006). Importantly, bile powder supplementation significantly improved cecal length (p = 0.009) and mucosal thickness (p = 0.020) compared with LBW-CON piglets. Microbial analysis showed that the microbial dysbiosis index was restored to near-normal levels. Transcriptomic analysis revealed impaired extracellular matrix structure and mucus secretion in LBW piglets. Notably, bile powder supplementation markedly upregulated the protein expression of WNT8B (p < 0.001) and the bile acid receptors (i.e., GPBAR1 and FXR), alongside enhanced tight junctions and the goblet cell marker mucin-2 expression (p < 0.05). Conclusions: These findings suggest that specific bile acid supplementation improves gut barrier function and partially supports cecal development in LBW piglets.
Additional Links: PMID-41228488
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PubMed:
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@article {pmid41228488,
year = {2025},
author = {Yin, C and Liu, X and Fang, W and Meng, Q and Feng, X and Zhang, W and Dang, G and Zhong, R and Chen, L and Wang, Z and Zhang, H},
title = {Hyocholic Acid Species as the Key Modulator for Cecal Epithelial Homeostasis in Low-Birth-Weight Piglets.},
journal = {Nutrients},
volume = {17},
number = {21},
pages = {},
doi = {10.3390/nu17213415},
pmid = {41228488},
issn = {2072-6643},
support = {32202709//National Natural Science Foundation of China/ ; U22A20515//National Natural Science Foundation of China/ ; Y2023QC09//Youth Innovation of Chinese Academy of Agricultural Sciences/ ; },
mesh = {Animals ; *Cecum/microbiology/drug effects/metabolism ; Swine ; *Homeostasis/drug effects ; Gastrointestinal Microbiome/drug effects ; *Intestinal Mucosa/metabolism/drug effects ; Bile Acids and Salts ; Animals, Newborn ; Birth Weight ; Dietary Supplements ; *Cholic Acids/pharmacology ; Dysbiosis ; },
abstract = {Background: Low birth weight (LBW) is correlated with gut microbiota dysbiosis and intestinal barrier function disruption, increasing susceptibility to enteric diseases. These alterations underscore the critical need to identify key regulators of gut homeostasis, among which bile acids are increasingly recognized as pivotal for barrier integrity, microbial ecology, and host metabolism. Methods: Eight pairs of LBW (the initial BW was 0.850 ± 0.053 kg) and normal-birth-weight (NBW; 1.488 ± 0.083 kg) piglets were compared to evaluate cecal morphology and bile acid profiles. Subsequently, sixteen LBW piglets and eight NBW piglets were allocated into three groups: NBW (1.563 ± 0.052 kg), LBW control (LBW-CON; 0.950 ± 0.120 kg), and LBW with bile acid supplementation (LBW-bile powder; 0.925 ± 0.116 kg). Piglets in the LBW-bile powder group received 25 mg/kg BW of bile powder (hyodeoxycholic acid-enriched) by daily oral gavage for 14 days. Results: LBW piglets exhibited retarded cecal development and lower abundance of hyocholic acid species (p = 0.006). Importantly, bile powder supplementation significantly improved cecal length (p = 0.009) and mucosal thickness (p = 0.020) compared with LBW-CON piglets. Microbial analysis showed that the microbial dysbiosis index was restored to near-normal levels. Transcriptomic analysis revealed impaired extracellular matrix structure and mucus secretion in LBW piglets. Notably, bile powder supplementation markedly upregulated the protein expression of WNT8B (p < 0.001) and the bile acid receptors (i.e., GPBAR1 and FXR), alongside enhanced tight junctions and the goblet cell marker mucin-2 expression (p < 0.05). Conclusions: These findings suggest that specific bile acid supplementation improves gut barrier function and partially supports cecal development in LBW piglets.},
}
MeSH Terms:
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Animals
*Cecum/microbiology/drug effects/metabolism
Swine
*Homeostasis/drug effects
Gastrointestinal Microbiome/drug effects
*Intestinal Mucosa/metabolism/drug effects
Bile Acids and Salts
Animals, Newborn
Birth Weight
Dietary Supplements
*Cholic Acids/pharmacology
Dysbiosis
RevDate: 2025-11-13
CmpDate: 2025-11-13
Prebiotic Structural Diversity Shapes Gut Microbial Diversity, Community Composition, and Metabolic Activity In Vitro.
Foods (Basel, Switzerland), 14(21):.
Prebiotics are selectively utilized substrates that modulate gut microbiota and host health, yet different prebiotic structures may elicit distinct ecological and metabolic responses. In this study, we investigated the effects of five structurally diverse prebiotics-isomaltooligosaccharides (IMO), arabinogalactans (AG), pectin, inulin, and stachyose-on human gut microbiota via a 24 h in vitro anaerobic culture with healthy donors' gut microbiota. Microbial community dynamics were profiled by 16S rRNA gene sequencing, and short-chain fatty acids (SCFAs) production was analyzed. All treatments resulted in decreased α-diversity compared with baseline, with pectin most effectively preserving microbial richness and evenness, whereas stachyose led to the greatest reduction. Community composition and functional profiles shifted in a substrate-specific manner, with AG promoting Bacteroidaceae, IMO stimulating Lachnospiraceae and Faecalibacterium, and pectin supporting balanced microbial structures and SCFA production. Pectin, IMO, and inulin enhanced butyrate levels, whereas AG and pectin promoted propionate formation. These findings demonstrate that prebiotic structural differences strongly shape gut microbial ecology and metabolism, providing a mechanistic basis for rationally selecting and combining prebiotics to beneficially modulate the gut microbiota.
Additional Links: PMID-41227744
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@article {pmid41227744,
year = {2025},
author = {Fu, Y and Wang, Y and Zhang, J and Ren, J and Fang, B},
title = {Prebiotic Structural Diversity Shapes Gut Microbial Diversity, Community Composition, and Metabolic Activity In Vitro.},
journal = {Foods (Basel, Switzerland)},
volume = {14},
number = {21},
pages = {},
pmid = {41227744},
issn = {2304-8158},
support = {81770558//National Natural Science Foundation of China/ ; 3502Z20149031//Xiamen Joint Projects for Major Diseases/ ; 22278343//National Natural Science Foundation of China/ ; },
abstract = {Prebiotics are selectively utilized substrates that modulate gut microbiota and host health, yet different prebiotic structures may elicit distinct ecological and metabolic responses. In this study, we investigated the effects of five structurally diverse prebiotics-isomaltooligosaccharides (IMO), arabinogalactans (AG), pectin, inulin, and stachyose-on human gut microbiota via a 24 h in vitro anaerobic culture with healthy donors' gut microbiota. Microbial community dynamics were profiled by 16S rRNA gene sequencing, and short-chain fatty acids (SCFAs) production was analyzed. All treatments resulted in decreased α-diversity compared with baseline, with pectin most effectively preserving microbial richness and evenness, whereas stachyose led to the greatest reduction. Community composition and functional profiles shifted in a substrate-specific manner, with AG promoting Bacteroidaceae, IMO stimulating Lachnospiraceae and Faecalibacterium, and pectin supporting balanced microbial structures and SCFA production. Pectin, IMO, and inulin enhanced butyrate levels, whereas AG and pectin promoted propionate formation. These findings demonstrate that prebiotic structural differences strongly shape gut microbial ecology and metabolism, providing a mechanistic basis for rationally selecting and combining prebiotics to beneficially modulate the gut microbiota.},
}
RevDate: 2025-11-13
CmpDate: 2025-11-13
Polyphasic Characterisation of Microbiota Associated with Sant'Agostino Table Olives Flavoured with Foeniculum vulgare.
Foods (Basel, Switzerland), 14(21):.
Sant'Agostino green table olives, traditionally processed in Apulia and flavoured with Foeniculum vulgare, represent a niche product whose microbial ecology remains largely unexplored. This study aimed to characterise the microbiota of the final product (both brine and fruit) after six months of storage with wild fennel. Four production batches were analysed using a combined culture-dependent and culture-independent approach. Microbiological counts revealed variable levels of aerobic mesophilic microorganisms, yeasts, lactic acid bacteria (LAB), and staphylococci, with yeasts and LAB being predominant. Ten LAB strains were identified, including Enterococcus faecium, Leuconostoc mesenteroides subsp. jonggajibkimchii, Leuconostoc mesenteroides subsp. cremoris, Leuconostoc pseudomesenteroides, Lactiplantibacillus plantarum, and Lactiplantibacillus pentosus. Yeast isolates belonged to Candida tropicalis, Torulaspora delbrueckii, and Saccharomyces cerevisiae. Amplicon sequencing (MiSeq Illumina) revealed distinct bacterial profiles between fruit and brine samples, with taxa from Actinobacteria, Bacteroidetes, Enterococcus, Lactobacillus, Leuconostoc, Alphaproteobacteria, Enterobacteriaceae, and other Gammaproteobacteria. Enterococcus and Leuconostoc were consistently detected, while Lactobacillus sensu lato appeared only in one fruit and one brine sample. These findings provide new insights into the microbial diversity of Sant'Agostino olives and contribute to the understanding of their fermentation ecology and potential for quality and safety enhancement.
Additional Links: PMID-41227660
PubMed:
Citation:
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@article {pmid41227660,
year = {2025},
author = {Alfonzo, A and Gaglio, R and Alongi, D and Franciosi, E and Perricone, G and Garofalo, G and Prestianni, R and Naselli, V and Pirrone, A and Francesca, N and Moschetti, G and Settanni, L},
title = {Polyphasic Characterisation of Microbiota Associated with Sant'Agostino Table Olives Flavoured with Foeniculum vulgare.},
journal = {Foods (Basel, Switzerland)},
volume = {14},
number = {21},
pages = {},
pmid = {41227660},
issn = {2304-8158},
support = {B7521002300001//Ministry of University and Research in Italy/ ; B73C23000060001//European Union/ ; },
abstract = {Sant'Agostino green table olives, traditionally processed in Apulia and flavoured with Foeniculum vulgare, represent a niche product whose microbial ecology remains largely unexplored. This study aimed to characterise the microbiota of the final product (both brine and fruit) after six months of storage with wild fennel. Four production batches were analysed using a combined culture-dependent and culture-independent approach. Microbiological counts revealed variable levels of aerobic mesophilic microorganisms, yeasts, lactic acid bacteria (LAB), and staphylococci, with yeasts and LAB being predominant. Ten LAB strains were identified, including Enterococcus faecium, Leuconostoc mesenteroides subsp. jonggajibkimchii, Leuconostoc mesenteroides subsp. cremoris, Leuconostoc pseudomesenteroides, Lactiplantibacillus plantarum, and Lactiplantibacillus pentosus. Yeast isolates belonged to Candida tropicalis, Torulaspora delbrueckii, and Saccharomyces cerevisiae. Amplicon sequencing (MiSeq Illumina) revealed distinct bacterial profiles between fruit and brine samples, with taxa from Actinobacteria, Bacteroidetes, Enterococcus, Lactobacillus, Leuconostoc, Alphaproteobacteria, Enterobacteriaceae, and other Gammaproteobacteria. Enterococcus and Leuconostoc were consistently detected, while Lactobacillus sensu lato appeared only in one fruit and one brine sample. These findings provide new insights into the microbial diversity of Sant'Agostino olives and contribute to the understanding of their fermentation ecology and potential for quality and safety enhancement.},
}
RevDate: 2025-11-13
CmpDate: 2025-11-13
Girgentana's Goat Milk Microbiota Investigated in an Organic Farm During Dry Season.
Animals : an open access journal from MDPI, 15(21):.
Milk microbiota is a complex microbial ecosystem with implications for product quality, safety, and animal health. However, limited data exist on goat milk microbiota, particularly in local breeds. This study provides the first detailed characterization of the milk microbiota of Girgentana goats, a resilient Sicilian breed valued for high-quality dairy products. Illumina NovaSeq sequencing was used to analyze the 16S rRNA V3-V4 regions of 44 individual and 3 bulk milk samples. Briefly, 16S rRNA-gene sequencing produced a total of 8,135,944 high-quality reads, identifying 1134 operational taxonomic units (OTUs) across all individual samples. On average, each sample showed 864 OTUs with counts > 0. Alpha diversity metrics, based on richness estimators (Chao1: 948.1; ACE: 936.3) and diversity indices (Shannon: 4.06; Simpson: 0.95; Fisher: 118.5), indicated a heterogeneous community with both common and low-abundance taxa. Firmicutes (51%) and Proteobacteria (27%) were the predominant phyla, with Lactobacillaceae (54%) and Bifidobacteriaceae (22%) dominating at the family level. Notably, farm bulk milk profiles closely mirrored individual samples. These results establish a milk microbiota baseline for the Girgentana breed and offer valuable insights into microbial ecology in traditional dairy systems, supporting future comparisons across breeds and farming practices.
Additional Links: PMID-41227479
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@article {pmid41227479,
year = {2025},
author = {Chessari, G and Tumino, S and Castiglioni, B and Biscarini, F and Bordonaro, S and Avondo, M and Marletta, D and Cremonesi, P},
title = {Girgentana's Goat Milk Microbiota Investigated in an Organic Farm During Dry Season.},
journal = {Animals : an open access journal from MDPI},
volume = {15},
number = {21},
pages = {},
pmid = {41227479},
issn = {2076-2615},
support = {Agritech National Research Center and received funding from the European Union Next-GenerationEU (National Recovery and Resilience Plan (NRRP), Mission 4, Component 2, Investment 1.4-D.D. 1032 17/06/2022, CN00000022//Agritech National Research/ ; },
abstract = {Milk microbiota is a complex microbial ecosystem with implications for product quality, safety, and animal health. However, limited data exist on goat milk microbiota, particularly in local breeds. This study provides the first detailed characterization of the milk microbiota of Girgentana goats, a resilient Sicilian breed valued for high-quality dairy products. Illumina NovaSeq sequencing was used to analyze the 16S rRNA V3-V4 regions of 44 individual and 3 bulk milk samples. Briefly, 16S rRNA-gene sequencing produced a total of 8,135,944 high-quality reads, identifying 1134 operational taxonomic units (OTUs) across all individual samples. On average, each sample showed 864 OTUs with counts > 0. Alpha diversity metrics, based on richness estimators (Chao1: 948.1; ACE: 936.3) and diversity indices (Shannon: 4.06; Simpson: 0.95; Fisher: 118.5), indicated a heterogeneous community with both common and low-abundance taxa. Firmicutes (51%) and Proteobacteria (27%) were the predominant phyla, with Lactobacillaceae (54%) and Bifidobacteriaceae (22%) dominating at the family level. Notably, farm bulk milk profiles closely mirrored individual samples. These results establish a milk microbiota baseline for the Girgentana breed and offer valuable insights into microbial ecology in traditional dairy systems, supporting future comparisons across breeds and farming practices.},
}
RevDate: 2025-11-12
A hitchhiker's guide to modern, practical cyanobacterial taxonomy.
Journal of phycology [Epub ahead of print].
There has been an explosion of new Cyanobacterial taxa described within the last two decades. Cyanobacteria exhibit incredible ecological versatility and morphological variability, and thousands of species have already been described using "traditional" approaches (e.g., morphological features). However, DNA sequencing and other molecular tools have provided extensive evidence that the diversity of cyanobacteria is not necessarily congruent with morphology, as many morphological genera (e.g., Phormidium, Leptolyngbya, and Nostoc) are polyphyletic, and species within the genera are often morphologically indistinguishable, thus cryptic. Further confounding systematic assessments, newly erected taxa are often based on a single strain with one or two 16S rRNA gene sequences, may have incomplete formal descriptions, and lack indication of the employed species concepts. Here we have proposed a set of guidelines for cyanobacterial taxonomists. We have focused on the whole process of erecting new taxa: sampling, sequencing (including genomes), phylogenetic inference, phenotype characterization, species concepts, formal descriptions, and codes of nomenclature. Our hope is that these guidelines will help with the laborious but ever-rewarding task of identifying and describing the taxa within the world of cyanobacteria.
Additional Links: PMID-41222858
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PubMed:
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@article {pmid41222858,
year = {2025},
author = {Dvořák, P and Skoupý, S and Stanojković, A and Johansen, JR and Villanueva, C and Jung, P and Briegel-Williams, L and Laughinghouse, HD and Lefler, FW and Berthold, DE and Kaštovský, J and Hurley, AC and Casamatta, DA},
title = {A hitchhiker's guide to modern, practical cyanobacterial taxonomy.},
journal = {Journal of phycology},
volume = {},
number = {},
pages = {},
doi = {10.1111/jpy.70102},
pmid = {41222858},
issn = {1529-8817},
support = {23-06507S//Grant Agency of the Czech Republic/ ; },
abstract = {There has been an explosion of new Cyanobacterial taxa described within the last two decades. Cyanobacteria exhibit incredible ecological versatility and morphological variability, and thousands of species have already been described using "traditional" approaches (e.g., morphological features). However, DNA sequencing and other molecular tools have provided extensive evidence that the diversity of cyanobacteria is not necessarily congruent with morphology, as many morphological genera (e.g., Phormidium, Leptolyngbya, and Nostoc) are polyphyletic, and species within the genera are often morphologically indistinguishable, thus cryptic. Further confounding systematic assessments, newly erected taxa are often based on a single strain with one or two 16S rRNA gene sequences, may have incomplete formal descriptions, and lack indication of the employed species concepts. Here we have proposed a set of guidelines for cyanobacterial taxonomists. We have focused on the whole process of erecting new taxa: sampling, sequencing (including genomes), phylogenetic inference, phenotype characterization, species concepts, formal descriptions, and codes of nomenclature. Our hope is that these guidelines will help with the laborious but ever-rewarding task of identifying and describing the taxa within the world of cyanobacteria.},
}
RevDate: 2025-11-12
CmpDate: 2025-11-12
Persistent human-associated microbial signatures in burial soils from the 17th and 18th century New York African burial ground.
ISME communications, 5(1):ycaf181.
Understanding the long-term persistence of human-associated microbial signatures in burial soils offers a untapped insights into historical human health, decomposition, and ecological transformation. This study investigates whether centuries-old burial soils retain distinguishable microbial evidence of human decomposition using 16S rRNA gene sequencing on 81 samples from the New York African Burial Ground (NYABG), a 17th and 18th century cemetery for free and enslaved Africans. Comparative analyses against six control soils from nearby urban parks were conducted using QIIME2, ALDEx2, and ANCOM. Burial soils exhibited significantly greater alpha diversity (Faith's PD, Shannon, observed ASVs; P < .01) and distinct beta diversity patterns (Bray-Curtis, UniFrac; PERMANOVA P = .001). Enrichment of Firmicutes, Actinobacteriota, and gut-associated genera such as Bacillus and Ruminococcus characterized burial soils, whereas oligotrophic taxa dominated controls. Tentative identifications of human-associated pathogenic genera (e.g. Fusobacterium periodonticum, Prevotella pleuritidis) were observed exclusively in burial soils, suggesting their origin from the interred individuals but requiring further validation. These findings demonstrate that soil microbiomes reflect host-associated microbial communities long after decomposition, providing a scalable, nondestructive approach for reconstructing ancient microbial communities and host-associated health signatures. This work establishes the NYABG burial soil microbiome as a valuable model for microbial archaeology and introduces a replicable framework for integrating environmental microbiology, bioarchaeology, and historical epidemiology through the lens of postmortem microbial ecology.
Additional Links: PMID-41221507
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@article {pmid41221507,
year = {2025},
author = {Clinton, CK and Jackson, FLC},
title = {Persistent human-associated microbial signatures in burial soils from the 17th and 18th century New York African burial ground.},
journal = {ISME communications},
volume = {5},
number = {1},
pages = {ycaf181},
pmid = {41221507},
issn = {2730-6151},
abstract = {Understanding the long-term persistence of human-associated microbial signatures in burial soils offers a untapped insights into historical human health, decomposition, and ecological transformation. This study investigates whether centuries-old burial soils retain distinguishable microbial evidence of human decomposition using 16S rRNA gene sequencing on 81 samples from the New York African Burial Ground (NYABG), a 17th and 18th century cemetery for free and enslaved Africans. Comparative analyses against six control soils from nearby urban parks were conducted using QIIME2, ALDEx2, and ANCOM. Burial soils exhibited significantly greater alpha diversity (Faith's PD, Shannon, observed ASVs; P < .01) and distinct beta diversity patterns (Bray-Curtis, UniFrac; PERMANOVA P = .001). Enrichment of Firmicutes, Actinobacteriota, and gut-associated genera such as Bacillus and Ruminococcus characterized burial soils, whereas oligotrophic taxa dominated controls. Tentative identifications of human-associated pathogenic genera (e.g. Fusobacterium periodonticum, Prevotella pleuritidis) were observed exclusively in burial soils, suggesting their origin from the interred individuals but requiring further validation. These findings demonstrate that soil microbiomes reflect host-associated microbial communities long after decomposition, providing a scalable, nondestructive approach for reconstructing ancient microbial communities and host-associated health signatures. This work establishes the NYABG burial soil microbiome as a valuable model for microbial archaeology and introduces a replicable framework for integrating environmental microbiology, bioarchaeology, and historical epidemiology through the lens of postmortem microbial ecology.},
}
RevDate: 2025-11-12
CmpDate: 2025-11-12
From obesity to cancer: Gut microbiome mechanisms, biomarkers, and U.S. public health strategies.
Oncoscience, 12:175-188.
BACKGROUND: Obesity, metabolic syndrome, and colorectal cancer (CRC) remain major public health challenges in the United States, collectively driving substantial morbidity, mortality, and economic burden. Beyond diet and genetics, the gut microbiome has emerged as a pivotal determinant of host metabolism, immunity, and carcinogenesis, influenced by both environmental and behavioral factors.
OBJECTIVE: This review synthesizes current evidence linking gut microbial dysbiosis to obesity, metabolic syndrome, and CRC, emphasizing mechanistic pathways, environmental modifiers, and translational opportunities relevant to U.S. public health and precision medicine.
METHODS: Comprehensive searches of PubMed and Scopus (2000-2025) identified large epidemiologic studies, mechanistic experiments, and clinical trials, prioritizing research from U.S. populations and nationally representative databases including NHANES, SEER, and the Nurses' Health Study.
RESULTS: Microbial alterations such as enrichment of Fusobacterium nucleatum, enterotoxigenic Bacteroides fragilis, and colibactin-producing Escherichia coli contribute to CRC initiation and progression. In obesity and metabolic syndrome, shifts in Firmicutes-to-Bacteroidetes ratios, altered short-chain fatty acid metabolism, and endotoxin-mediated inflammation disrupt metabolic homeostasis. Environmental and lifestyle exposures, including air pollutants, smoking, and Westernized diets, modulate microbial ecology across the aerodigestive tract, affecting disease susceptibility. The emerging discipline of Molecular Pathological Epidemiology (MPE) integrates lifestyle, microbiome, and biomarker data to elucidate exposure-outcome relationships, enabling personalized prevention and therapeutic strategies.
CONCLUSIONS: The gut microbiome functions as both a biomarker and therapeutic target across metabolic and neoplastic diseases. Integrating microbiome science with environmental epidemiology and MPE frameworks offers transformative potential for precision prevention and equitable public health strategies in the U.S.
Additional Links: PMID-41220415
PubMed:
Citation:
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@article {pmid41220415,
year = {2025},
author = {Moseeb, HM and Aizaz, MM and Aiza, K and Hafsa, TH and Sania, M and Kamran, Z and Shamama, ZT and Usama, AM and Maroof, QP and Feroze, F and Ahmed, R and Ammara, N and Mahima, G},
title = {From obesity to cancer: Gut microbiome mechanisms, biomarkers, and U.S. public health strategies.},
journal = {Oncoscience},
volume = {12},
number = {},
pages = {175-188},
pmid = {41220415},
issn = {2331-4737},
abstract = {BACKGROUND: Obesity, metabolic syndrome, and colorectal cancer (CRC) remain major public health challenges in the United States, collectively driving substantial morbidity, mortality, and economic burden. Beyond diet and genetics, the gut microbiome has emerged as a pivotal determinant of host metabolism, immunity, and carcinogenesis, influenced by both environmental and behavioral factors.
OBJECTIVE: This review synthesizes current evidence linking gut microbial dysbiosis to obesity, metabolic syndrome, and CRC, emphasizing mechanistic pathways, environmental modifiers, and translational opportunities relevant to U.S. public health and precision medicine.
METHODS: Comprehensive searches of PubMed and Scopus (2000-2025) identified large epidemiologic studies, mechanistic experiments, and clinical trials, prioritizing research from U.S. populations and nationally representative databases including NHANES, SEER, and the Nurses' Health Study.
RESULTS: Microbial alterations such as enrichment of Fusobacterium nucleatum, enterotoxigenic Bacteroides fragilis, and colibactin-producing Escherichia coli contribute to CRC initiation and progression. In obesity and metabolic syndrome, shifts in Firmicutes-to-Bacteroidetes ratios, altered short-chain fatty acid metabolism, and endotoxin-mediated inflammation disrupt metabolic homeostasis. Environmental and lifestyle exposures, including air pollutants, smoking, and Westernized diets, modulate microbial ecology across the aerodigestive tract, affecting disease susceptibility. The emerging discipline of Molecular Pathological Epidemiology (MPE) integrates lifestyle, microbiome, and biomarker data to elucidate exposure-outcome relationships, enabling personalized prevention and therapeutic strategies.
CONCLUSIONS: The gut microbiome functions as both a biomarker and therapeutic target across metabolic and neoplastic diseases. Integrating microbiome science with environmental epidemiology and MPE frameworks offers transformative potential for precision prevention and equitable public health strategies in the U.S.},
}
RevDate: 2025-11-11
Diversity of Yeast and Drosophila Species Associated with Grape Sour Rot in China.
Microbial ecology, 88(1):121.
Sour rot is a complex disease of grapes, primarily caused by the synergistic effects of yeast and Drosophila species, leading to fruit decay, poor quality, and significant economic losses. The lack of information on species distribution and diversity of these organisms in China limits the efficacy of control strategies. In this study, we sequenced the 26S rRNA D1/D2 region in yeasts and the COI region in Drosophila. Nine yeast genera were identified. Hanseniaspora spp. (45.76% of total) were the most abundant, followed by Starmerella spp. (23.62%) and Saccharomyces spp. (17.34%). At the species level, 14 yeast species were identified. Starmerella bacillaris (23.62%), Saccharomyces cerevisiae (17.34%), H. opuntiae (17.34%), and H. uvarum (15.13%) predominated. Of the five species of Drosophila present, Drosophila melanogaster (63.16%) was the dominant species. This study is the first to characterize the diversity of yeasts and Drosophila across major grape-producing regions in China. The findings provide a scientific foundation for elucidating the key drivers of sour rot and designing targeted control strategies.
Additional Links: PMID-41219483
PubMed:
Citation:
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@article {pmid41219483,
year = {2025},
author = {Han, J and Fang, Q and Hao, Y and Huang, X and Kong, F and Chen, H and Liu, Y},
title = {Diversity of Yeast and Drosophila Species Associated with Grape Sour Rot in China.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {121},
pmid = {41219483},
issn = {1432-184X},
support = {2022E02073//Special Regional Collaborative Innovation Project of Xinjiang Uygur Autonomous Region (Science and Technology Aid Xinjiang Program)/ ; 32272550//National Natural Science Foundation of China/ ; CARS-29-bc-5//Agriculture Research System of China/ ; 202305AF150129//Expert Workstation Project in Yunnan Province/ ; },
abstract = {Sour rot is a complex disease of grapes, primarily caused by the synergistic effects of yeast and Drosophila species, leading to fruit decay, poor quality, and significant economic losses. The lack of information on species distribution and diversity of these organisms in China limits the efficacy of control strategies. In this study, we sequenced the 26S rRNA D1/D2 region in yeasts and the COI region in Drosophila. Nine yeast genera were identified. Hanseniaspora spp. (45.76% of total) were the most abundant, followed by Starmerella spp. (23.62%) and Saccharomyces spp. (17.34%). At the species level, 14 yeast species were identified. Starmerella bacillaris (23.62%), Saccharomyces cerevisiae (17.34%), H. opuntiae (17.34%), and H. uvarum (15.13%) predominated. Of the five species of Drosophila present, Drosophila melanogaster (63.16%) was the dominant species. This study is the first to characterize the diversity of yeasts and Drosophila across major grape-producing regions in China. The findings provide a scientific foundation for elucidating the key drivers of sour rot and designing targeted control strategies.},
}
RevDate: 2025-11-12
CmpDate: 2025-11-12
Integrated Multi-Omics Analysis Reveals Microbial Community Restructuring and its Role in Key Carbohydrate Metabolic Pathways During Tobacco Leaf Curing.
Microbial ecology, 88(1):122.
Microorganisms play a significant role in improving the flavor and quality of plant products. Analyzing how tobacco processing affects the microbial community structure is essential. Understanding the synergistic mechanisms of microorganisms during this process can help optimize the flavor and quality of plant products. In this study, samples were collected from four processing stages (T1: fresh leaves, T2: 42 °C, T3: 54 °C, T4: 68 °C), and metabolite and Phylloplane microbial data of tobacco leaves were generated. A comprehensive multi-omics analysis was conducted. The study shows that the increase in temperature and the decrease in humidity during the processing lead to the reorganization of the microbial community. Brevibacterium, Staphylococcus, Aspergillus, and Ganoderma were identified as core biomarkers. Bacteria dominate in the initial degradation of starch, while fungi promote the accumulation of soluble sugars through the transformation of intermediate products. This study deepens our understanding of the role of microorganisms and their carbohydrate metabolism in the tobacco leaf processing process and proposes a new strategy for constructing regulatory models by integrating multi-omics.
Additional Links: PMID-41219454
PubMed:
Citation:
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@article {pmid41219454,
year = {2025},
author = {Zhang, C and Zhang, X and Wang, F and Li, G and Ding, J and Cao, Y and Wang, H and Wu, S and Shang, X and Wei, K and Yang, L},
title = {Integrated Multi-Omics Analysis Reveals Microbial Community Restructuring and its Role in Key Carbohydrate Metabolic Pathways During Tobacco Leaf Curing.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {122},
pmid = {41219454},
issn = {1432-184X},
support = {1102022202016 / 110202201019 (LS-03)//Science and Technology Project of China Tobacco General Corporation/ ; QKHJC-ZK [2022] YB288//Science and Technology Project of Guizhou Provincial Department of Science and Technology/ ; 2022XM17//Science and Technology Project of Guizhou Tobacco Industry Technology Center/ ; 202111/WT_/Wellcome Trust/United Kingdom ; },
mesh = {*Plant Leaves/microbiology/metabolism/chemistry ; *Nicotiana/microbiology/metabolism/chemistry ; *Microbiota ; *Fungi/metabolism/genetics/classification/isolation & purification ; *Carbohydrate Metabolism ; *Bacteria/metabolism/classification/genetics/isolation & purification ; Metabolic Networks and Pathways ; Temperature ; Metabolomics ; Multiomics ; },
abstract = {Microorganisms play a significant role in improving the flavor and quality of plant products. Analyzing how tobacco processing affects the microbial community structure is essential. Understanding the synergistic mechanisms of microorganisms during this process can help optimize the flavor and quality of plant products. In this study, samples were collected from four processing stages (T1: fresh leaves, T2: 42 °C, T3: 54 °C, T4: 68 °C), and metabolite and Phylloplane microbial data of tobacco leaves were generated. A comprehensive multi-omics analysis was conducted. The study shows that the increase in temperature and the decrease in humidity during the processing lead to the reorganization of the microbial community. Brevibacterium, Staphylococcus, Aspergillus, and Ganoderma were identified as core biomarkers. Bacteria dominate in the initial degradation of starch, while fungi promote the accumulation of soluble sugars through the transformation of intermediate products. This study deepens our understanding of the role of microorganisms and their carbohydrate metabolism in the tobacco leaf processing process and proposes a new strategy for constructing regulatory models by integrating multi-omics.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Plant Leaves/microbiology/metabolism/chemistry
*Nicotiana/microbiology/metabolism/chemistry
*Microbiota
*Fungi/metabolism/genetics/classification/isolation & purification
*Carbohydrate Metabolism
*Bacteria/metabolism/classification/genetics/isolation & purification
Metabolic Networks and Pathways
Temperature
Metabolomics
Multiomics
RevDate: 2025-11-11
Microbial community dynamics and its relationship with biogeochemical processes under geochemical perturbations.
Water research, 289(Pt B):124889 pii:S0043-1354(25)01792-0 [Epub ahead of print].
Environmental microbial communities are crucial in regulating ecosystem functions and are increasingly affected by human-induced geochemical perturbations. While microbial communities are known to shift under such perturbations, the explicit link between these shifts and corresponding biogeochemical processes remains unclear. Here, we conducted time-series sediment incubation experiments under elevated nitrate conditions, combining 16S rRNA gene sequencing, qPCR, and metagenomics to track microbial taxonomic and functional dynamics. We further developed a gene-centric, process-based biogeochemical model to quantitatively connect microbial community structure to geochemical reaction kinetics. Our results revealed that functional metagenomics provided a broader view of functional diversity than qPCR and enabled detailed analysis of gene co-occurrence. Through modeling, we uncover a quantitative coupling between functional gene abundance and reaction rates under geochemical perturbations. However, this relationship can be obscured by redox-driven abiotic processes affected by perturbations and the nonlinear nature of enzyme-mediated reactions, making it difficult to resolve using standard statistical approaches. Together, these findings improve our understanding of the linkage between microbial function and biogeochemical processes, and underscore the value of gene-centric, process-based models for predicting ecosystem behavior under geochemical stress.
Additional Links: PMID-41218435
Publisher:
PubMed:
Citation:
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@article {pmid41218435,
year = {2025},
author = {Ren, J and Wang, J and Dong, Y and Xiao, L and Wang, L and Ji, J and Liu, Y},
title = {Microbial community dynamics and its relationship with biogeochemical processes under geochemical perturbations.},
journal = {Water research},
volume = {289},
number = {Pt B},
pages = {124889},
doi = {10.1016/j.watres.2025.124889},
pmid = {41218435},
issn = {1879-2448},
abstract = {Environmental microbial communities are crucial in regulating ecosystem functions and are increasingly affected by human-induced geochemical perturbations. While microbial communities are known to shift under such perturbations, the explicit link between these shifts and corresponding biogeochemical processes remains unclear. Here, we conducted time-series sediment incubation experiments under elevated nitrate conditions, combining 16S rRNA gene sequencing, qPCR, and metagenomics to track microbial taxonomic and functional dynamics. We further developed a gene-centric, process-based biogeochemical model to quantitatively connect microbial community structure to geochemical reaction kinetics. Our results revealed that functional metagenomics provided a broader view of functional diversity than qPCR and enabled detailed analysis of gene co-occurrence. Through modeling, we uncover a quantitative coupling between functional gene abundance and reaction rates under geochemical perturbations. However, this relationship can be obscured by redox-driven abiotic processes affected by perturbations and the nonlinear nature of enzyme-mediated reactions, making it difficult to resolve using standard statistical approaches. Together, these findings improve our understanding of the linkage between microbial function and biogeochemical processes, and underscore the value of gene-centric, process-based models for predicting ecosystem behavior under geochemical stress.},
}
RevDate: 2025-11-11
The Saccharomyces killer toxin K62 is a protein of the aerolysin family.
mBio [Epub ahead of print].
UNLABELLED: K62 is an antifungal killer toxin produced by Saccharomyces paradoxus, encoded by a double-stranded RNA satellite. The toxin exhibits a unique antifungal activity but lacks sequence homology to other killer toxins, and its antifungal mechanism of action remains unknown. To understand the function of K62, its tertiary structure was predicted using AlphaFold, followed by molecular dynamics simulations to create high-confidence molecular models. These analyses revealed that K62 monomers closely resemble the five-beta-strand domain found in pore-forming aerolysin toxins. Models of K62 oligomers yielded a circular complex and beta-barrel with structural and biochemical similarities to aerolysin-family pre-pores and pores. Consistent with the formation of aerolysin-like pores, recombinant K62 assembled into membrane-associated high molecular weight oligomers (>250 kDa) that were heat- and detergent-resistant. K62 has more than 1,000 uncharacterized sequence homologs, which were mostly found in fungi of the Ascomycota, as well as in the Chytridiomycota, Basidiomycota, plants, and bacteria, with evidence of extensive horizontal gene transfer. Homologs were also identified in pathogenic fungal species, including human and plant pathogens from the Candida and Fusarium genera, but unlike aerolysins, K62 appeared to be non-toxic to higher eukaryotes. K62 is the first aerolysin family protein discovered in yeasts, revealing a likely role in fungal niche competition and establishing an entirely new, expansive family of aerolysin-like proteins.
IMPORTANCE: Pore-forming toxins are potent biological weapons used across nature, from virulence factors to immune defense proteins. This study identifies K62, a little-known antifungal toxin produced by a wild yeast, as a structural and functional relative of the aerolysin family, which is well-known for forming damaging pores in cell membranes. Using structure prediction, molecular simulations, and biochemical analysis, we show that K62 assembles into large, stable pore-like complexes. Remarkably, K62 is just one member of a large and previously unrecognized family of similar toxin-like proteins found in fungi, plants, and bacteria, including pathogens that affect humans and crops. These findings uncover an unexpected evolutionary link across kingdoms, suggesting that pore-forming toxins may play a widespread role in fungal pathogenesis and microbial warfare. This work lays the foundation for understanding a new group of antifungal molecules and their potential impacts on health, agriculture, and microbial ecology.
Additional Links: PMID-41217184
Publisher:
PubMed:
Citation:
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@article {pmid41217184,
year = {2025},
author = {Creagh, JW and Rolfsmeier, M and Evans, KJ and Bizarria, R and Reetz, DC and Badigian, TJ and Fredericks, LR and Hasenoehrl, AM and Brown, AP and Graves, BM and Alexander, CK and Rodrigues, A and Stoffregen, EP and Patel, JS and Ytreberg, FM and Rowley, PA},
title = {The Saccharomyces killer toxin K62 is a protein of the aerolysin family.},
journal = {mBio},
volume = {},
number = {},
pages = {e0142525},
doi = {10.1128/mbio.01425-25},
pmid = {41217184},
issn = {2150-7511},
abstract = {UNLABELLED: K62 is an antifungal killer toxin produced by Saccharomyces paradoxus, encoded by a double-stranded RNA satellite. The toxin exhibits a unique antifungal activity but lacks sequence homology to other killer toxins, and its antifungal mechanism of action remains unknown. To understand the function of K62, its tertiary structure was predicted using AlphaFold, followed by molecular dynamics simulations to create high-confidence molecular models. These analyses revealed that K62 monomers closely resemble the five-beta-strand domain found in pore-forming aerolysin toxins. Models of K62 oligomers yielded a circular complex and beta-barrel with structural and biochemical similarities to aerolysin-family pre-pores and pores. Consistent with the formation of aerolysin-like pores, recombinant K62 assembled into membrane-associated high molecular weight oligomers (>250 kDa) that were heat- and detergent-resistant. K62 has more than 1,000 uncharacterized sequence homologs, which were mostly found in fungi of the Ascomycota, as well as in the Chytridiomycota, Basidiomycota, plants, and bacteria, with evidence of extensive horizontal gene transfer. Homologs were also identified in pathogenic fungal species, including human and plant pathogens from the Candida and Fusarium genera, but unlike aerolysins, K62 appeared to be non-toxic to higher eukaryotes. K62 is the first aerolysin family protein discovered in yeasts, revealing a likely role in fungal niche competition and establishing an entirely new, expansive family of aerolysin-like proteins.
IMPORTANCE: Pore-forming toxins are potent biological weapons used across nature, from virulence factors to immune defense proteins. This study identifies K62, a little-known antifungal toxin produced by a wild yeast, as a structural and functional relative of the aerolysin family, which is well-known for forming damaging pores in cell membranes. Using structure prediction, molecular simulations, and biochemical analysis, we show that K62 assembles into large, stable pore-like complexes. Remarkably, K62 is just one member of a large and previously unrecognized family of similar toxin-like proteins found in fungi, plants, and bacteria, including pathogens that affect humans and crops. These findings uncover an unexpected evolutionary link across kingdoms, suggesting that pore-forming toxins may play a widespread role in fungal pathogenesis and microbial warfare. This work lays the foundation for understanding a new group of antifungal molecules and their potential impacts on health, agriculture, and microbial ecology.},
}
RevDate: 2025-11-11
A global deep terrestrial biosphere core microbiome.
ISME communications, 5(1):ycaf176.
The deep biosphere encompasses life beneath the Earth's surface and constitutes a substantial portion of the planet's microbial biomass. This study analyzed nucleic acid datasets from low-carbon and low-energy deep terrestrial subsurface groundwaters across four continents and revealed four core global populations. These populations exhibited metabolic strategies and adaptations reflecting depth and environmental constraints. Erythrobacter featured heterotrophic metabolism; Thiobacillus demonstrated sulfur oxidation coupled to denitrification along with carbon and nitrogen fixation; Methanobacteriaceae were methanogenic autotrophs using the Wood-Ljungdahl pathway (WL); and Candidatus Desulforudis audaxviator functioned as a sulfate-reducer also encoding the WL pathway. Depth-related adaptations suggested heterotrophic dominance at shallower depths with increasing contributions from autotrophy with depth. Finally, comparative genomics revealed minimal evolutionary changes among these populations, suggesting functional conservation since diverging from their ancestral lineages. These findings underscore a global deep biosphere core community.
Additional Links: PMID-41216320
PubMed:
Citation:
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@article {pmid41216320,
year = {2025},
author = {González-Rosales, C and Rezaei Somee, M and Buck, M and Bertilsson, S and Mehrshad, M and Dopson, M},
title = {A global deep terrestrial biosphere core microbiome.},
journal = {ISME communications},
volume = {5},
number = {1},
pages = {ycaf176},
pmid = {41216320},
issn = {2730-6151},
abstract = {The deep biosphere encompasses life beneath the Earth's surface and constitutes a substantial portion of the planet's microbial biomass. This study analyzed nucleic acid datasets from low-carbon and low-energy deep terrestrial subsurface groundwaters across four continents and revealed four core global populations. These populations exhibited metabolic strategies and adaptations reflecting depth and environmental constraints. Erythrobacter featured heterotrophic metabolism; Thiobacillus demonstrated sulfur oxidation coupled to denitrification along with carbon and nitrogen fixation; Methanobacteriaceae were methanogenic autotrophs using the Wood-Ljungdahl pathway (WL); and Candidatus Desulforudis audaxviator functioned as a sulfate-reducer also encoding the WL pathway. Depth-related adaptations suggested heterotrophic dominance at shallower depths with increasing contributions from autotrophy with depth. Finally, comparative genomics revealed minimal evolutionary changes among these populations, suggesting functional conservation since diverging from their ancestral lineages. These findings underscore a global deep biosphere core community.},
}
RevDate: 2025-11-11
Marine Bacterioplankton Composition Predicts Oxygen Consumption During Dissolved Organic Matter Degradation Experiments.
Environmental microbiology, 27(11):e70197.
Microbial communities play pivotal roles in ocean biogeochemistry, yet linking their composition to ecosystem functions remains a significant challenge. In this study, we demonstrate the predictive power of bacterioplankton taxonomic composition in explaining oxygen consumption during dissolved organic matter (DOM) degradation. Using 4 years of experimental data, we integrated 'omics with statistical modeling, applying feature selection and dimensionality reduction to develop high-performance linear regression models with strong predictive accuracy. Our framework also identifies key microbial groups driving oxygen consumption, including taxa known for their differential capabilities in DOM processing and recently shown to exhibit distinct respiration rates. Flavobacteriales emerge as central contributors to oxygen consumption, underscoring their ecological importance in nutrient-rich, highly productive coastal systems often referred to as 'green seas'. Their consistent dominance across varying oxygen consumption categories highlights their pivotal role in sustaining ecosystem functions in these environments. Beyond oxygen consumption, this framework provides a versatile tool for investigating microbially driven biogeochemical processes. By linking community composition with ecosystem functions, our study advances predictive microbial ecology. These findings deepen our understanding of microbial contributions to the ocean's carbon and oxygen cycles, improving our ability to anticipate their responses to environmental change.
Additional Links: PMID-41215682
Publisher:
PubMed:
Citation:
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@article {pmid41215682,
year = {2025},
author = {Alonso, C and Zanetti, J and Griffero, L and Pereira-Flores, E and González, B and Lescano, C and Pérez-Parada, A and Crisci, C and Amann, R},
title = {Marine Bacterioplankton Composition Predicts Oxygen Consumption During Dissolved Organic Matter Degradation Experiments.},
journal = {Environmental microbiology},
volume = {27},
number = {11},
pages = {e70197},
doi = {10.1111/1462-2920.70197},
pmid = {41215682},
issn = {1462-2920},
support = {ANII_MPI_ID_2017_1_1007663//Agencia Nacional de Investigación e Innovación/ ; Grupos I+D 2022//Comisión Sectorial de Investigación Científica/ ; },
abstract = {Microbial communities play pivotal roles in ocean biogeochemistry, yet linking their composition to ecosystem functions remains a significant challenge. In this study, we demonstrate the predictive power of bacterioplankton taxonomic composition in explaining oxygen consumption during dissolved organic matter (DOM) degradation. Using 4 years of experimental data, we integrated 'omics with statistical modeling, applying feature selection and dimensionality reduction to develop high-performance linear regression models with strong predictive accuracy. Our framework also identifies key microbial groups driving oxygen consumption, including taxa known for their differential capabilities in DOM processing and recently shown to exhibit distinct respiration rates. Flavobacteriales emerge as central contributors to oxygen consumption, underscoring their ecological importance in nutrient-rich, highly productive coastal systems often referred to as 'green seas'. Their consistent dominance across varying oxygen consumption categories highlights their pivotal role in sustaining ecosystem functions in these environments. Beyond oxygen consumption, this framework provides a versatile tool for investigating microbially driven biogeochemical processes. By linking community composition with ecosystem functions, our study advances predictive microbial ecology. These findings deepen our understanding of microbial contributions to the ocean's carbon and oxygen cycles, improving our ability to anticipate their responses to environmental change.},
}
RevDate: 2025-11-11
Fermented probiotic dairy products with buriti and orange byproducts enhance gut and bone health.
Food research international (Ottawa, Ont.), 221(Pt 3):117364.
The integration of functional ingredients and probiotics in dairy matrices is a promising strategy to nehance bone and intestinal health and preventing the onset of diseases. This study aimed to evaluate the impact of fortification of fermented dairy products (yogurt and fermented milk) with buriti pulp or orange bagasse added, added or not of a probiotic strain L. acidophilus DSM 13241 (Nu-trish® LA-5®) (Chr. Hansen, Hoersholm, Denmark) (yogurt and fermented milk) on bone and intestinal health of Wistar rats. The experimental design consisted of male Wistar rats (n = 6/group) that received supplementation daily for 60 days. The parameters assessed included the quantification of minerals (Ca, P, and Mg) in the products and femurs, the biomechanical and densitometric parameters, the fecal microbiota composition through the sequencing analysis of the 16S rRNA gene, the short-chain fatty acid (SCFA) content, and the permeability of the intestinal barrier. It was observed that the consumption of buriti pulp was responsible for the bone strength and stiffness of the femurs. The consumption of buriti pulp increased the bone strength and stiffness of the femurs and the relative abundance of the Lachnospiraceae NK4A136 group. The fortification of probiotic yogurt with buriti pulp led to an increase in the production of SCFA (acetic acid) and the daily intake of Ca, Mg, and P. The consumption of orange bagasse increased the magnesium mineral content in the femur and serum calcium values. The consumption of orange bagasse increased the Mg content in the femur and serum values of Ca, improved the permeability of the intestinal barrier (reducing serum levels of lipopolysaccharide), and positively impacted the fecal composition (increases in the relative abundance of Lactobacillus and Muribaculaceae). The concentration of acetic and propionic acid increased after consumption of the two fermented milk formulations containing orange bagasse (LA OB and LA OX OB). The groups that consumed yogurt containing buriti pulp (Y BP) and yogurt containing L. acidophilus DSM 13241 (Nu-trish® LA-5®) and buriti pulp (Y LA BP) presented higher concentrations of acetic acid in the feces compared to the group that consumed only yogurt (Y). The consumption of all fermented products containing the probiotic L. acidophilus DSM 13241 (Nu-trish® LA-5®) (fermented milk or natural yogurts and yogurts fortified with buriti pulp and orange pulp: LA, LA OB, LA OX OB, Y LA, and Y LA BP) increased the abundance of the Lachnospiraceae family NK4A136 group. The findings of this study indicate that fruit byproducts and probiotic fermented dairy products exert synergistic effects on bone and gut microbial ecology health in growing rats. These results support the use of sustainable functional ingredients in food innovation to promote systemic health benefits.
Additional Links: PMID-41215000
Publisher:
PubMed:
Citation:
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@article {pmid41215000,
year = {2025},
author = {Graça, JS and Sachinelli, LDS and Tobar, N and Guadagnini, D and Cabral, L and Noronha, MF and Coutinho, LL and Cazarin, CBB and Bogusz-Junior, S and Belangero, WD and Brunetto, SQ and Pimentel, TC and Saad, MJA and Sant'Ana, AS},
title = {Fermented probiotic dairy products with buriti and orange byproducts enhance gut and bone health.},
journal = {Food research international (Ottawa, Ont.)},
volume = {221},
number = {Pt 3},
pages = {117364},
doi = {10.1016/j.foodres.2025.117364},
pmid = {41215000},
issn = {1873-7145},
abstract = {The integration of functional ingredients and probiotics in dairy matrices is a promising strategy to nehance bone and intestinal health and preventing the onset of diseases. This study aimed to evaluate the impact of fortification of fermented dairy products (yogurt and fermented milk) with buriti pulp or orange bagasse added, added or not of a probiotic strain L. acidophilus DSM 13241 (Nu-trish® LA-5®) (Chr. Hansen, Hoersholm, Denmark) (yogurt and fermented milk) on bone and intestinal health of Wistar rats. The experimental design consisted of male Wistar rats (n = 6/group) that received supplementation daily for 60 days. The parameters assessed included the quantification of minerals (Ca, P, and Mg) in the products and femurs, the biomechanical and densitometric parameters, the fecal microbiota composition through the sequencing analysis of the 16S rRNA gene, the short-chain fatty acid (SCFA) content, and the permeability of the intestinal barrier. It was observed that the consumption of buriti pulp was responsible for the bone strength and stiffness of the femurs. The consumption of buriti pulp increased the bone strength and stiffness of the femurs and the relative abundance of the Lachnospiraceae NK4A136 group. The fortification of probiotic yogurt with buriti pulp led to an increase in the production of SCFA (acetic acid) and the daily intake of Ca, Mg, and P. The consumption of orange bagasse increased the magnesium mineral content in the femur and serum calcium values. The consumption of orange bagasse increased the Mg content in the femur and serum values of Ca, improved the permeability of the intestinal barrier (reducing serum levels of lipopolysaccharide), and positively impacted the fecal composition (increases in the relative abundance of Lactobacillus and Muribaculaceae). The concentration of acetic and propionic acid increased after consumption of the two fermented milk formulations containing orange bagasse (LA OB and LA OX OB). The groups that consumed yogurt containing buriti pulp (Y BP) and yogurt containing L. acidophilus DSM 13241 (Nu-trish® LA-5®) and buriti pulp (Y LA BP) presented higher concentrations of acetic acid in the feces compared to the group that consumed only yogurt (Y). The consumption of all fermented products containing the probiotic L. acidophilus DSM 13241 (Nu-trish® LA-5®) (fermented milk or natural yogurts and yogurts fortified with buriti pulp and orange pulp: LA, LA OB, LA OX OB, Y LA, and Y LA BP) increased the abundance of the Lachnospiraceae family NK4A136 group. The findings of this study indicate that fruit byproducts and probiotic fermented dairy products exert synergistic effects on bone and gut microbial ecology health in growing rats. These results support the use of sustainable functional ingredients in food innovation to promote systemic health benefits.},
}
RevDate: 2025-11-10
A molecular toolbox to modulate gene expression and protein secretion in the bacterial predator Bdellovibrio bacteriovorus.
PLoS genetics, 21(11):e1011935 pii:PGENETICS-D-25-00685 [Epub ahead of print].
The predatory bacterium Bdellovibrio bacteriovorus kills and consumes other bacteria, thrives in diverse environments and holds great potential to address major challenges in medicine, agriculture, and biotechnology. As a bacterial predator it represents an alternative to traditional antimicrobial strategies to combat multidrug-resistant bacterial pathogens and prevent food waste, while the multitude of predatory enzymes it produces have potential for biotechnological applications. However, while a limited set of genetic tools exist, the lack of secretion assays and fine-tuning of secretion constrain both fundamental studies and bioengineering of B. bacteriovorus. Here, we present a molecular toolbox for B. bacteriovorus by systematically tuning gene expression and secretion of a reporter protein. Building on functional native and synthetic promoters from the Anderson library with varying expression levels of fluorescent reporter protein mScarletI3, we evaluated different ribosomal binding sites (RBS) to fine-tune gene expression. To examine secretion, we established a novel protocol to quantify extracellular release of a Nanoluc luciferase reporter protein in B. bacteriovorus using different native Sec-dependent signal sequences. We anticipate that the newly developed genetic toolkit and techniques will advance research on this fundamental predator-prey system, laying the foundation for its broader application and future bioengineering efforts. This work will pave the way for tailored applications of B. bacteriovorus in microbial ecology, agriculture, biotechnology, and medicine.
Additional Links: PMID-41212898
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@article {pmid41212898,
year = {2025},
author = {Mihajlovic, L and Hofacker, LM and Lindner, F and Jayakumar, P and Diepold, A and Huwiler, SG},
title = {A molecular toolbox to modulate gene expression and protein secretion in the bacterial predator Bdellovibrio bacteriovorus.},
journal = {PLoS genetics},
volume = {21},
number = {11},
pages = {e1011935},
doi = {10.1371/journal.pgen.1011935},
pmid = {41212898},
issn = {1553-7404},
abstract = {The predatory bacterium Bdellovibrio bacteriovorus kills and consumes other bacteria, thrives in diverse environments and holds great potential to address major challenges in medicine, agriculture, and biotechnology. As a bacterial predator it represents an alternative to traditional antimicrobial strategies to combat multidrug-resistant bacterial pathogens and prevent food waste, while the multitude of predatory enzymes it produces have potential for biotechnological applications. However, while a limited set of genetic tools exist, the lack of secretion assays and fine-tuning of secretion constrain both fundamental studies and bioengineering of B. bacteriovorus. Here, we present a molecular toolbox for B. bacteriovorus by systematically tuning gene expression and secretion of a reporter protein. Building on functional native and synthetic promoters from the Anderson library with varying expression levels of fluorescent reporter protein mScarletI3, we evaluated different ribosomal binding sites (RBS) to fine-tune gene expression. To examine secretion, we established a novel protocol to quantify extracellular release of a Nanoluc luciferase reporter protein in B. bacteriovorus using different native Sec-dependent signal sequences. We anticipate that the newly developed genetic toolkit and techniques will advance research on this fundamental predator-prey system, laying the foundation for its broader application and future bioengineering efforts. This work will pave the way for tailored applications of B. bacteriovorus in microbial ecology, agriculture, biotechnology, and medicine.},
}
RevDate: 2025-11-10
Microbial Volatiles from Human Skin and Floral Nectar: Insufficiently Understood Adult Feeding Cues To Improve Odor-Based Traps for Aedes Vector Control.
Journal of chemical ecology, 51(6):108.
Mosquitoes of the genus Aedes, including the invasive Aedes albopictus, are responsible for the transmission of arboviruses such as dengue, chikungunya, and Zika. Their global expansion has intensified public health concerns, while the efficacy of insecticide-based control is declining due to resistance and environmental risks. These limitations have increased interest in odor-baited traps as complementary tools for surveillance and population reduction. Yet, their performance in the field remains inconsistent, largely because lures rely on a restricted set of human skin microbial volatiles and capture mainly host-seeking females. This review highlights the contribution of microorganisms inhabiting human skin and floral nectar to mosquito feeding ecology. Skin microbiota shape odor profiles by producing volatile organic compounds that mediate host attractiveness and species-specific mosquito responses. Likewise, nectar-dwelling yeasts and bacteria alter nectar chemistry and floral scent, generating volatiles that influence insect foraging, although their role in Aedes attraction remains poorly studied. By integrating data from Aedes and other insect models, we highlight microbial semiochemicals with demonstrated or potential roles in guiding blood- and sugar-feeding behaviors. We further discuss how microbial ecology, compound concentration, and chemical interactions drive variability in mosquito responses, raising both opportunities and challenges for trap design. Expanding research to nectar-associated microbial cues, while considering ecological specificity and possible non-target effects, could help create more versatile lures that attract both sexes and multiple feeding stages. This review advances our understanding of microbial-associated cues as critical drivers of mosquito behavior and outlines future directions to improve odor-based surveillance and control of Aedes vectors.
Additional Links: PMID-41212266
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@article {pmid41212266,
year = {2025},
author = {Malassigné, S and Valiente Moro, C and Luis, P},
title = {Microbial Volatiles from Human Skin and Floral Nectar: Insufficiently Understood Adult Feeding Cues To Improve Odor-Based Traps for Aedes Vector Control.},
journal = {Journal of chemical ecology},
volume = {51},
number = {6},
pages = {108},
pmid = {41212266},
issn = {1573-1561},
abstract = {Mosquitoes of the genus Aedes, including the invasive Aedes albopictus, are responsible for the transmission of arboviruses such as dengue, chikungunya, and Zika. Their global expansion has intensified public health concerns, while the efficacy of insecticide-based control is declining due to resistance and environmental risks. These limitations have increased interest in odor-baited traps as complementary tools for surveillance and population reduction. Yet, their performance in the field remains inconsistent, largely because lures rely on a restricted set of human skin microbial volatiles and capture mainly host-seeking females. This review highlights the contribution of microorganisms inhabiting human skin and floral nectar to mosquito feeding ecology. Skin microbiota shape odor profiles by producing volatile organic compounds that mediate host attractiveness and species-specific mosquito responses. Likewise, nectar-dwelling yeasts and bacteria alter nectar chemistry and floral scent, generating volatiles that influence insect foraging, although their role in Aedes attraction remains poorly studied. By integrating data from Aedes and other insect models, we highlight microbial semiochemicals with demonstrated or potential roles in guiding blood- and sugar-feeding behaviors. We further discuss how microbial ecology, compound concentration, and chemical interactions drive variability in mosquito responses, raising both opportunities and challenges for trap design. Expanding research to nectar-associated microbial cues, while considering ecological specificity and possible non-target effects, could help create more versatile lures that attract both sexes and multiple feeding stages. This review advances our understanding of microbial-associated cues as critical drivers of mosquito behavior and outlines future directions to improve odor-based surveillance and control of Aedes vectors.},
}
RevDate: 2025-11-10
Contrasted impacts of commercial diets and rearing water on Aedes aegypti fitness and microbiota.
mSphere [Epub ahead of print].
Mosquito rearing optimization in laboratory conditions is crucial for both vector research and control. Although the addition of nutrients is important for Aedes aegypti development from immature stages to adult mosquitoes, little is known about the nutrient composition of commercial diets used for mosquito rearing and their influence on Ae. aegypti life traits. Here, we evaluated the influence of four commercial diets commonly used to rear Ae. aegypti in the laboratory on its fitness, lifespan, and microbiota. We also compared the effect of these diets on this mosquito when combined with two different rearing waters (laboratory versus field-collected waters). Our investigations demonstrated that higher levels of protein and lipid in commercial diets promote better Ae. aegypti development, lifespan, and size in both water. Metagenomic analysis revealed specific modulations of adult microbiota composition according to both diet and rearing water. Chryseobacterium dominated the microbiota of female mosquitoes reared in laboratory water, except for yeast condition, where a more diverse microbiota was observed. When reared in larval site water, the microbiota diversity was overall higher despite diet addition, except for fish food, which promoted Sphingobacterium dominance. Given the pivotal influence of diet addition during the larval stage on Ae. aegypti microbiota and life traits, rearing conditions should be carefully chosen according to the goals of the research (i.e., vectorial capacity estimations) or vector control intervention.IMPORTANCEAedes aegypti is the main vector of arbovirus, such as dengue, yellow fever, and chikungunya viruses. Vector research and control are primarily carried out in laboratories, with larval stage rearing conducted using commercial diet. If many nutrients are essential for Ae. aegypti development, gaining insight into the influence of these diets and their nutrient levels is important to promote optimized rearing worldwide. In this study, our results indicated a significant impact of commercial diet on Ae. aegypti development, lifespan, size, and microbiota related to contrasted protein, lipid, and carbohydrate levels in these diets. This study will help people working with Ae. aegypti raise awareness in staff working with Ae. aegypti to select optimized diets for their specific purpose.
Additional Links: PMID-41211947
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PubMed:
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@article {pmid41211947,
year = {2025},
author = {Calvez, E and Quétel, I and Saint-Alban, L and Gutiérrez-Bugallo, G and Dollin, C and Ramdini, C and Vega-Rúa, A},
title = {Contrasted impacts of commercial diets and rearing water on Aedes aegypti fitness and microbiota.},
journal = {mSphere},
volume = {},
number = {},
pages = {e0054325},
doi = {10.1128/msphere.00543-25},
pmid = {41211947},
issn = {2379-5042},
abstract = {Mosquito rearing optimization in laboratory conditions is crucial for both vector research and control. Although the addition of nutrients is important for Aedes aegypti development from immature stages to adult mosquitoes, little is known about the nutrient composition of commercial diets used for mosquito rearing and their influence on Ae. aegypti life traits. Here, we evaluated the influence of four commercial diets commonly used to rear Ae. aegypti in the laboratory on its fitness, lifespan, and microbiota. We also compared the effect of these diets on this mosquito when combined with two different rearing waters (laboratory versus field-collected waters). Our investigations demonstrated that higher levels of protein and lipid in commercial diets promote better Ae. aegypti development, lifespan, and size in both water. Metagenomic analysis revealed specific modulations of adult microbiota composition according to both diet and rearing water. Chryseobacterium dominated the microbiota of female mosquitoes reared in laboratory water, except for yeast condition, where a more diverse microbiota was observed. When reared in larval site water, the microbiota diversity was overall higher despite diet addition, except for fish food, which promoted Sphingobacterium dominance. Given the pivotal influence of diet addition during the larval stage on Ae. aegypti microbiota and life traits, rearing conditions should be carefully chosen according to the goals of the research (i.e., vectorial capacity estimations) or vector control intervention.IMPORTANCEAedes aegypti is the main vector of arbovirus, such as dengue, yellow fever, and chikungunya viruses. Vector research and control are primarily carried out in laboratories, with larval stage rearing conducted using commercial diet. If many nutrients are essential for Ae. aegypti development, gaining insight into the influence of these diets and their nutrient levels is important to promote optimized rearing worldwide. In this study, our results indicated a significant impact of commercial diet on Ae. aegypti development, lifespan, size, and microbiota related to contrasted protein, lipid, and carbohydrate levels in these diets. This study will help people working with Ae. aegypti raise awareness in staff working with Ae. aegypti to select optimized diets for their specific purpose.},
}
RevDate: 2025-11-10
Minor contribution of ammonia oxidizers to inorganic carbon fixation in the ocean.
Nature geoscience, 18(11):1144-1151.
Ammonia-oxidizing archaea are the most abundant chemolithoautotrophs in the ocean and are assumed to dominate carbon fixation below the sunlit surface layer. However, the supply of reduced nitrogen delivered from the surface in sinking particulate organic matter is insufficient to support the amount of nitrification required to sustain measured carbon fixation rates in the dark ocean. Here we attempt to reconcile this observed discrepancy by quantifying the contribution of ammonia oxidizers to dark carbon fixation in the eastern tropical and subtropical Pacific Ocean. We used phenylacetylene-a specific inhibitor of the ammonia monooxygenase enzyme-to selectively inhibit ammonia oxidizers in samples collected throughout the water column (60-600 m depth). We show that, despite their high abundances, ammonia oxidizers contribute only a small fraction to dark carbon fixation, accounting for 4-25% of the total depth-integrated rates in the eastern tropical Pacific. The highest contributions were observed within the upper mesopelagic zone (120-175 m depth), where ammonia oxidation could account for ~50% of dark carbon fixation at some stations. Our results challenge the current view that carbon fixation in the dark ocean is primarily sustained by nitrification and suggest that other microbial metabolisms, including heterotrophy, might play a larger role than previously assumed.
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@article {pmid41210076,
year = {2025},
author = {Bayer, B and Kitzinger, K and Paul, NL and Albers, JB and Saito, MA and Wagner, M and Carlson, CA and Santoro, AE},
title = {Minor contribution of ammonia oxidizers to inorganic carbon fixation in the ocean.},
journal = {Nature geoscience},
volume = {18},
number = {11},
pages = {1144-1151},
pmid = {41210076},
issn = {1752-0894},
abstract = {Ammonia-oxidizing archaea are the most abundant chemolithoautotrophs in the ocean and are assumed to dominate carbon fixation below the sunlit surface layer. However, the supply of reduced nitrogen delivered from the surface in sinking particulate organic matter is insufficient to support the amount of nitrification required to sustain measured carbon fixation rates in the dark ocean. Here we attempt to reconcile this observed discrepancy by quantifying the contribution of ammonia oxidizers to dark carbon fixation in the eastern tropical and subtropical Pacific Ocean. We used phenylacetylene-a specific inhibitor of the ammonia monooxygenase enzyme-to selectively inhibit ammonia oxidizers in samples collected throughout the water column (60-600 m depth). We show that, despite their high abundances, ammonia oxidizers contribute only a small fraction to dark carbon fixation, accounting for 4-25% of the total depth-integrated rates in the eastern tropical Pacific. The highest contributions were observed within the upper mesopelagic zone (120-175 m depth), where ammonia oxidation could account for ~50% of dark carbon fixation at some stations. Our results challenge the current view that carbon fixation in the dark ocean is primarily sustained by nitrification and suggest that other microbial metabolisms, including heterotrophy, might play a larger role than previously assumed.},
}
RevDate: 2025-11-10
The assembly processes and network characteristics of bacterial, fungal and archaeal communities in the middle Yangtze River and river-connected lakes.
Frontiers in microbiology, 16:1701799.
Despite the crucial ecological roles of bacterial, fungal and archaeal communities in rivers and lakes, their interactions and dynamic changes in large, hydrologically-connected river-lake systems remain poorly understood. This study investigated the biogeographic patterns, assembly processes and co-occurrence network characteristics of bacterial, fungal and archaeal communities in the middle reaches of Yangtze River (MYR) and its two largest connected lakes, Dongting Lake (DTL) and Poyang Lake (PYL). Our results revealed significant spatial heterogeneity in microbial diversity and composition, with higher sedimentary microbial diversity in lakes than in the river. Stochastic processes, particularly dispersal limitation, dominated community assembly across all habitats. β-NRI analysis showed that deterministic processes were more influential for planktonic bacterial and archaeal communities in the lakes. Co-occurrence network analysis demonstrated that inter-domain cooperation was prevalent in PYL, whereas intra-domain interactions were more common in MYR and DTL, reflecting distinct hydrological connectivity. Keystone taxa differed between rivers and lakes, with rare taxa prevailing in MYR and both rare and abundant taxa contributing in lakes. Our findings highlight how connectivity and flow dynamics fundamentally shape microbial ecology, providing insights into for the management and conservation of large river-lake ecosystems.
Additional Links: PMID-41209725
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Citation:
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@article {pmid41209725,
year = {2025},
author = {Wang, F and Li, S and Li, P and Feng, C and Zhao, Z and Yang, Y and Han, F and Xue, A and Li, Z and Han, P},
title = {The assembly processes and network characteristics of bacterial, fungal and archaeal communities in the middle Yangtze River and river-connected lakes.},
journal = {Frontiers in microbiology},
volume = {16},
number = {},
pages = {1701799},
pmid = {41209725},
issn = {1664-302X},
abstract = {Despite the crucial ecological roles of bacterial, fungal and archaeal communities in rivers and lakes, their interactions and dynamic changes in large, hydrologically-connected river-lake systems remain poorly understood. This study investigated the biogeographic patterns, assembly processes and co-occurrence network characteristics of bacterial, fungal and archaeal communities in the middle reaches of Yangtze River (MYR) and its two largest connected lakes, Dongting Lake (DTL) and Poyang Lake (PYL). Our results revealed significant spatial heterogeneity in microbial diversity and composition, with higher sedimentary microbial diversity in lakes than in the river. Stochastic processes, particularly dispersal limitation, dominated community assembly across all habitats. β-NRI analysis showed that deterministic processes were more influential for planktonic bacterial and archaeal communities in the lakes. Co-occurrence network analysis demonstrated that inter-domain cooperation was prevalent in PYL, whereas intra-domain interactions were more common in MYR and DTL, reflecting distinct hydrological connectivity. Keystone taxa differed between rivers and lakes, with rare taxa prevailing in MYR and both rare and abundant taxa contributing in lakes. Our findings highlight how connectivity and flow dynamics fundamentally shape microbial ecology, providing insights into for the management and conservation of large river-lake ecosystems.},
}
RevDate: 2025-11-09
Unraveling the Ecological Mechanisms Influencing the Structure and Composition of Lung Cancer Microbiomes.
Microbial ecology, 88(1):119.
This study investigates the ecological mechanisms governing the structure and composition of lung microbiome communities within tumor tissue from lung cancer patients. While this field has attracted increasing research attention, the ecological and etiological mechanisms driving microbial community assembly in this environment remain poorly characterized. To address this gap, we applied Sloan's near neutral model, Ning et al.'s normalized stochasticity ratio framework and Harris et al.'s multi-site neutral model to evaluate the influences of stochastic and deterministic factors at species, community and metacommunity levels, respectively. Our findings include: (i) Stochastic drift exhibited predominant influence at both species and community levels in normal adjacent tissue (NT), exceeding its effects in LUAD (lung adenocarcinoma) and LUSC (lung squamous cell carcinoma). (ii) At the metacommunity level, neutrality was not rejected at the metacommunity or local community levels, which is consistent with the previous finding (i). (iii) Elevated metacommunity biodiversity (θ) and immigration rates (m) in LUAD/LUSC compared to NT (observed in ∼50% of cases) suggest that tumor occurrence/progression may actively promote microbial recruitment to tumor microenvironments. We propose three non-exclusive mechanistic interpretations: (i) Tumor-mediated immune modulation creates permissive ecological niches; (ii) structural remodeling of tissue enhances microbial colonization potential; (iii) selective enrichment of opportunistic taxa (e.g., Streptococcus) through tumor-specific microenvironmental changes. Our results demonstrate that LUAD and LUSC microbiomes are shaped by deterministic tumor-driven selection, in contrast to the predominantly stochastic assembly observed in NT microbiomes. These findings reveal substantial reorganization of tumor-associated microbial communities, warranting further biomedical investigation and clinical validation.
Additional Links: PMID-41207985
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Citation:
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@article {pmid41207985,
year = {2025},
author = {Mei, J and Li, L and Ma, ZS},
title = {Unraveling the Ecological Mechanisms Influencing the Structure and Composition of Lung Cancer Microbiomes.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {119},
pmid = {41207985},
issn = {1432-184X},
abstract = {This study investigates the ecological mechanisms governing the structure and composition of lung microbiome communities within tumor tissue from lung cancer patients. While this field has attracted increasing research attention, the ecological and etiological mechanisms driving microbial community assembly in this environment remain poorly characterized. To address this gap, we applied Sloan's near neutral model, Ning et al.'s normalized stochasticity ratio framework and Harris et al.'s multi-site neutral model to evaluate the influences of stochastic and deterministic factors at species, community and metacommunity levels, respectively. Our findings include: (i) Stochastic drift exhibited predominant influence at both species and community levels in normal adjacent tissue (NT), exceeding its effects in LUAD (lung adenocarcinoma) and LUSC (lung squamous cell carcinoma). (ii) At the metacommunity level, neutrality was not rejected at the metacommunity or local community levels, which is consistent with the previous finding (i). (iii) Elevated metacommunity biodiversity (θ) and immigration rates (m) in LUAD/LUSC compared to NT (observed in ∼50% of cases) suggest that tumor occurrence/progression may actively promote microbial recruitment to tumor microenvironments. We propose three non-exclusive mechanistic interpretations: (i) Tumor-mediated immune modulation creates permissive ecological niches; (ii) structural remodeling of tissue enhances microbial colonization potential; (iii) selective enrichment of opportunistic taxa (e.g., Streptococcus) through tumor-specific microenvironmental changes. Our results demonstrate that LUAD and LUSC microbiomes are shaped by deterministic tumor-driven selection, in contrast to the predominantly stochastic assembly observed in NT microbiomes. These findings reveal substantial reorganization of tumor-associated microbial communities, warranting further biomedical investigation and clinical validation.},
}
RevDate: 2025-11-09
Metabarcoding Profiling Reveals Microbiome Structure and Predicts Functional Shifts in Grapevines Challenged by Phyllosticta ampelicida.
Microbial ecology, 88(1):120.
Black rot disease (BRD), caused by the still understudied Phyllosticta ampelicida, is spreading across several grape producing countries, posing a growing threat to the agroindustry. The role of the grapevine microbiome in defending against this pathogen, particularly in terms of microbiota structure and community homeostasis, remains unclear. In this study, we aimed to characterize the epiphytic phyllosphere microbiota of grapevines and identify shifts in microbial genetic structure associated with BRD symptoms. We sampled three vineyards of the cultivar "Touriga Nacional" in the Douro region (Portugal), collecting 20 leaves from (a) five healthy and (b) five BRD-symptomatic grapevines. The presence of P. ampelicida was confirmed in all symptomatic samples. Epiphytic bacterial DNA was extracted and sequenced using next-generation sequencing (NGS). Results indicate that although overall the diversity and richness indexes were not different in diseased plants compared to healthy ones, there was a reduction in OTU richness in black rot-affected grapevines. Diseased plants exhibited significant shifts in microbial network assemblages and showed an increased relative abundance of certain taxa, such as Acinetobacter, suggesting a possible recruitment of beneficial bacteria in response to biotic stress. Additionally, we observed a higher abundance of antibiotic resistance-related KEGG Orthologues (KOS) in symptomatic plants, raising potential concerns for human health. This study presents the first characterization of the grapevine phyllosphere epiphytic bacterial microbiota and its structural shifts in response to BRD.
Additional Links: PMID-41207977
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@article {pmid41207977,
year = {2025},
author = {Oliveira-Pinto, PR and Oliveira-Fernandes, J and Gramaje, D and Santos, C},
title = {Metabarcoding Profiling Reveals Microbiome Structure and Predicts Functional Shifts in Grapevines Challenged by Phyllosticta ampelicida.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {120},
pmid = {41207977},
issn = {1432-184X},
abstract = {Black rot disease (BRD), caused by the still understudied Phyllosticta ampelicida, is spreading across several grape producing countries, posing a growing threat to the agroindustry. The role of the grapevine microbiome in defending against this pathogen, particularly in terms of microbiota structure and community homeostasis, remains unclear. In this study, we aimed to characterize the epiphytic phyllosphere microbiota of grapevines and identify shifts in microbial genetic structure associated with BRD symptoms. We sampled three vineyards of the cultivar "Touriga Nacional" in the Douro region (Portugal), collecting 20 leaves from (a) five healthy and (b) five BRD-symptomatic grapevines. The presence of P. ampelicida was confirmed in all symptomatic samples. Epiphytic bacterial DNA was extracted and sequenced using next-generation sequencing (NGS). Results indicate that although overall the diversity and richness indexes were not different in diseased plants compared to healthy ones, there was a reduction in OTU richness in black rot-affected grapevines. Diseased plants exhibited significant shifts in microbial network assemblages and showed an increased relative abundance of certain taxa, such as Acinetobacter, suggesting a possible recruitment of beneficial bacteria in response to biotic stress. Additionally, we observed a higher abundance of antibiotic resistance-related KEGG Orthologues (KOS) in symptomatic plants, raising potential concerns for human health. This study presents the first characterization of the grapevine phyllosphere epiphytic bacterial microbiota and its structural shifts in response to BRD.},
}
RevDate: 2025-11-09
A new scenario of pathogen-microbiota interactions involving the oomycete Plasmopara viticola.
FEMS microbiology ecology pii:8316132 [Epub ahead of print].
A key question in microbial ecology is how the microbiota regulates host invasion by pathogens. Several ecological theories link the diversity, abundance and assembly processes of the microbiota with its resistance to invasion, but the specific properties of microbial communities that confer protection to the host are poorly understood. We addressed this question for the oomycete Plasmopara viticola, the causal agent of grapevine downy mildew. Using state-of-the-art microbial ecology methods, we compared microbial communities associated with asymptomatic and symptomatic leaf tissues to elucidate pathogen-microbiota interactions. Despite visible symptoms, P. viticola infection induced only subtle changes in microbial community composition. Symptomatic tissues showed enrichment in basidiomycete yeasts and Bacillus species, both known for their biocontrol activity, and exhibited a higher degree of determinism in community assembly processes. Asymptomatic tissues hosted more diverse microbiota, but lacked consistent associations with known biocontrol agents. Instead, they were often associated with other airborne grapevine pathogens. These findings suggest a novel interaction scenario: upon infection, P. viticola reshapes locally the leaf microbiota, excluding other pathogens and selecting for beneficial microbes. Although further studies are needed to uncover the underlying mechanisms, these findings underscore the relevance of targeting disease lesions in the search for protective microbial consortia.
Additional Links: PMID-41206559
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@article {pmid41206559,
year = {2025},
author = {Fournier, P and Pellan, L and Aubert, J and This, P and Vacher, C},
title = {A new scenario of pathogen-microbiota interactions involving the oomycete Plasmopara viticola.},
journal = {FEMS microbiology ecology},
volume = {},
number = {},
pages = {},
doi = {10.1093/femsec/fiaf111},
pmid = {41206559},
issn = {1574-6941},
abstract = {A key question in microbial ecology is how the microbiota regulates host invasion by pathogens. Several ecological theories link the diversity, abundance and assembly processes of the microbiota with its resistance to invasion, but the specific properties of microbial communities that confer protection to the host are poorly understood. We addressed this question for the oomycete Plasmopara viticola, the causal agent of grapevine downy mildew. Using state-of-the-art microbial ecology methods, we compared microbial communities associated with asymptomatic and symptomatic leaf tissues to elucidate pathogen-microbiota interactions. Despite visible symptoms, P. viticola infection induced only subtle changes in microbial community composition. Symptomatic tissues showed enrichment in basidiomycete yeasts and Bacillus species, both known for their biocontrol activity, and exhibited a higher degree of determinism in community assembly processes. Asymptomatic tissues hosted more diverse microbiota, but lacked consistent associations with known biocontrol agents. Instead, they were often associated with other airborne grapevine pathogens. These findings suggest a novel interaction scenario: upon infection, P. viticola reshapes locally the leaf microbiota, excluding other pathogens and selecting for beneficial microbes. Although further studies are needed to uncover the underlying mechanisms, these findings underscore the relevance of targeting disease lesions in the search for protective microbial consortia.},
}
RevDate: 2025-11-08
CmpDate: 2025-11-08
Phytoplankton Under Pressure: Temperature, Precipitation and Cyanobacterial Blooms as Drivers of Chytrid Infections.
Environmental microbiology reports, 17(6):e70224.
The area of fungal parasitism is attracting growing attention because of its great importance for aquatic organisms and their community dynamics. Despite increasing interest in this area, few studies have addressed baseline data on occurrence and environmental factors associated with chytrid parasite infections in natural ecosystems. This work provides insights into occurrence, prevalence, and dynamics of parasitic infections by studying three freshwater reservoirs over a period of 6 years. Chytrid infections were detected in each of the studied water bodies, infecting species of cyanobacteria, green algae and diatoms. However, recurring and prevalent infections were observed in only one water body, which is classified as a natural aquatic ecosystem. The recorded infection prevalence (IPC) ranged between 0% and 20%, while the mean infection severity remained low. Infection rates were highest in summer and most prominent during cyanobacterial blooms. Yet, the most infected group of phytoplankton consisted of green algae. GLM revealed a significantly positive correlation between IPC and water temperature and precipitation. Overall, these results demonstrate the dynamic nature of chytrid infections, which are shaped by multiple environmental factors across space and time.
Additional Links: PMID-41204663
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PubMed:
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@article {pmid41204663,
year = {2025},
author = {Budziak, M and Ilicic, D and Grossart, HP and Krztoń, W and Walusiak, E and Fyda, J and Wilk-Woźniak, E},
title = {Phytoplankton Under Pressure: Temperature, Precipitation and Cyanobacterial Blooms as Drivers of Chytrid Infections.},
journal = {Environmental microbiology reports},
volume = {17},
number = {6},
pages = {e70224},
doi = {10.1111/1758-2229.70224},
pmid = {41204663},
issn = {1758-2229},
support = {Statutory funds//Institute of Nature Conservation Polish Academy of Sciences/ ; GR 1540/48-1//German Research Foundation (DFG)/ ; COST Action ParAqua CA20125//European Cooperation in Science and Technology/ ; life17 env/lt/000407//European Union (EU) Life programme/ ; },
mesh = {Temperature ; *Cyanobacteria/growth & development ; *Phytoplankton/microbiology/growth & development ; Seasons ; Fresh Water/microbiology ; Ecosystem ; Rain ; Diatoms/microbiology ; *Chytridiomycota/isolation & purification ; Chlorophyta/microbiology ; Eutrophication ; },
abstract = {The area of fungal parasitism is attracting growing attention because of its great importance for aquatic organisms and their community dynamics. Despite increasing interest in this area, few studies have addressed baseline data on occurrence and environmental factors associated with chytrid parasite infections in natural ecosystems. This work provides insights into occurrence, prevalence, and dynamics of parasitic infections by studying three freshwater reservoirs over a period of 6 years. Chytrid infections were detected in each of the studied water bodies, infecting species of cyanobacteria, green algae and diatoms. However, recurring and prevalent infections were observed in only one water body, which is classified as a natural aquatic ecosystem. The recorded infection prevalence (IPC) ranged between 0% and 20%, while the mean infection severity remained low. Infection rates were highest in summer and most prominent during cyanobacterial blooms. Yet, the most infected group of phytoplankton consisted of green algae. GLM revealed a significantly positive correlation between IPC and water temperature and precipitation. Overall, these results demonstrate the dynamic nature of chytrid infections, which are shaped by multiple environmental factors across space and time.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Temperature
*Cyanobacteria/growth & development
*Phytoplankton/microbiology/growth & development
Seasons
Fresh Water/microbiology
Ecosystem
Rain
Diatoms/microbiology
*Chytridiomycota/isolation & purification
Chlorophyta/microbiology
Eutrophication
RevDate: 2025-11-07
CmpDate: 2025-11-08
Bacterial Communities Harboured by Amblyomma Hebraeum Infesting Small Stock in Mahikeng city, South Africa.
Microbial ecology, 88(1):118.
Ticks are important vectors of pathogens affecting livestock productivity and public health, yet their bacterial communities remain poorly characterized in many parts of South Africa. This study investigated the bacterial diversity and potential pathogenic bacterial etiology associated with Amblyomma hebraeum ticks collected from sheep and goats in Mahikeng, North West province. A total of 168 adult ticks were sampled across four villages. Microbiome profiling was performed using high-throughput sequencing of the V3-V4 hypervariable regions of the 16S rRNA gene on the Illumina MiSeq platform. High-throughput 16S rRNA sequencing revealed 16,193 ASVs in goat-derived ticks and 16,510 ASVs in those from sheep. Proteobacteria emerged as the dominant phylum across all samples, with ticks collected from goats showing a particularly high dominance of Rickettsia spp. (51.64% relative abundance), suggesting potential zoonotic risks. In contrast, ticks from sheep harboured significantly more diverse and evenly distributed bacterial communities, as indicated by Shannon (p = 0.0138) and Simpson (p = 0.0233) diversity indices, despite comparable species richness. A core microbiome comprising 1,374 ASVs (32.3%) was shared across all ticks, alongside 1,504 and 1,372 unique ASVs in goat- and sheep-derived ticks, respectively. Notably, several medically and veterinary-relevant genera, including Coxiella, Ehrlichia, Staphylococcus, Bacillus, Acinetobacter, Corynebacterium, and Streptococcus, were detected across both host groups. While total species richness was comparable between hosts, alpha diversity indices that account for evenness revealed host-based differences, and beta diversity patterns further showed clear separation of bacterial communities by host species. This study indicates that the host plays a crucial role as an ecological driver affecting the diversity of microbial communities associated with ticks. This study improves our understanding of the diversity, composition, and abundance of tick-associated microbiomes and pathogens in South African small ruminants. These insights support the development of microbiome-targeted strategies for detecting and controlling tick-borne diseases.
Additional Links: PMID-41204024
PubMed:
Citation:
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@article {pmid41204024,
year = {2025},
author = {Mileng, K and Mani, S and Bezuidenhout, JJ and Mokgokong, PS and Ramatla, TA and Thekisoe, OMM and Lekota, KE},
title = {Bacterial Communities Harboured by Amblyomma Hebraeum Infesting Small Stock in Mahikeng city, South Africa.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {118},
pmid = {41204024},
issn = {1432-184X},
support = {GUN: CSUR23030681021//National Research Foundation/ ; },
mesh = {Animals ; South Africa ; *Bacteria/classification/genetics/isolation & purification ; Goats/parasitology/microbiology ; *Microbiota ; RNA, Ribosomal, 16S/genetics ; Sheep/parasitology ; *Amblyomma/microbiology ; *Tick Infestations/veterinary/parasitology/epidemiology ; *Goat Diseases/parasitology/microbiology/epidemiology ; Phylogeny ; *Sheep Diseases/parasitology/microbiology/epidemiology ; DNA, Bacterial/genetics ; High-Throughput Nucleotide Sequencing ; },
abstract = {Ticks are important vectors of pathogens affecting livestock productivity and public health, yet their bacterial communities remain poorly characterized in many parts of South Africa. This study investigated the bacterial diversity and potential pathogenic bacterial etiology associated with Amblyomma hebraeum ticks collected from sheep and goats in Mahikeng, North West province. A total of 168 adult ticks were sampled across four villages. Microbiome profiling was performed using high-throughput sequencing of the V3-V4 hypervariable regions of the 16S rRNA gene on the Illumina MiSeq platform. High-throughput 16S rRNA sequencing revealed 16,193 ASVs in goat-derived ticks and 16,510 ASVs in those from sheep. Proteobacteria emerged as the dominant phylum across all samples, with ticks collected from goats showing a particularly high dominance of Rickettsia spp. (51.64% relative abundance), suggesting potential zoonotic risks. In contrast, ticks from sheep harboured significantly more diverse and evenly distributed bacterial communities, as indicated by Shannon (p = 0.0138) and Simpson (p = 0.0233) diversity indices, despite comparable species richness. A core microbiome comprising 1,374 ASVs (32.3%) was shared across all ticks, alongside 1,504 and 1,372 unique ASVs in goat- and sheep-derived ticks, respectively. Notably, several medically and veterinary-relevant genera, including Coxiella, Ehrlichia, Staphylococcus, Bacillus, Acinetobacter, Corynebacterium, and Streptococcus, were detected across both host groups. While total species richness was comparable between hosts, alpha diversity indices that account for evenness revealed host-based differences, and beta diversity patterns further showed clear separation of bacterial communities by host species. This study indicates that the host plays a crucial role as an ecological driver affecting the diversity of microbial communities associated with ticks. This study improves our understanding of the diversity, composition, and abundance of tick-associated microbiomes and pathogens in South African small ruminants. These insights support the development of microbiome-targeted strategies for detecting and controlling tick-borne diseases.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Animals
South Africa
*Bacteria/classification/genetics/isolation & purification
Goats/parasitology/microbiology
*Microbiota
RNA, Ribosomal, 16S/genetics
Sheep/parasitology
*Amblyomma/microbiology
*Tick Infestations/veterinary/parasitology/epidemiology
*Goat Diseases/parasitology/microbiology/epidemiology
Phylogeny
*Sheep Diseases/parasitology/microbiology/epidemiology
DNA, Bacterial/genetics
High-Throughput Nucleotide Sequencing
RevDate: 2025-11-07
CmpDate: 2025-11-08
Microbial communities and tight junction protein expression in the gastrointestinal tract of feedlot cattle.
Scientific reports, 15(1):39055.
The gastrointestinal tract (GIT) of cattle plays a vital role in nutrient absorption, immune function, and microbial homeostasis. While the importance of the GIT microbiome and epithelial barrier integrity has been increasingly recognized, the typical composition of microbial communities and the expression of tight junction proteins (TJPs) in feedlot cattle remains poorly characterized. We investigated microbial community structure and TJP expression at three GIT sites: the rumen (RU), small intestine (SI), and large intestine (LI) in 21 finish-fed feedlot steers sourced from 21 commercial feedyards in the Texas Panhandle. Samples of luminal contents and GIT tissue were collected from each region, as well as feces and liver abscess material. Microbial communities were characterized using 16S rRNA gene sequencing. TJP gene expression was quantified by RT-qPCR using synthetic standards, and protein expression was evaluated by immunohistochemistry (IHC) with both computer-generated and pathologist-generated scoring. Microbial community structures varied primarily by GIT region rather than by individual animals raised at different locations. Nine bacterial families were identified as core microbiome members, with Lachnospiraceae being the most abundant across the GIT. TJP gene expression varied considerably by site, with RU having significantly lower Claudin 1, Claudin 2, and E-Cadherin expression than the SI and LI. IHC results paralleled qPCR findings, with region-specific patterns of protein localization and intensity. Computerized and pathologist-generated H-scores showed moderate agreement but differed notably between epithelial and lamina propria regions. This study provides a comprehensive baseline of microbial and host factors associated with gut health in a uniquely diverse population of feedlot cattle. The identification of regional microbial communities and distinct TJP expression patterns offers foundational insights into gastrointestinal physiology and barrier function. This work establishes baseline data to support future investigations into the relationships among microbial ecology, epithelial barrier function, and cattle health and productivity.
Additional Links: PMID-41203821
PubMed:
Citation:
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@article {pmid41203821,
year = {2025},
author = {Young, JD and Pinnell, LJ and Wolfe, CA and Scott, MA and Lawrence, TE and Cavasin, JP and Ellis, JA and Langsten, KL and Richeson, JT and Morley, PS},
title = {Microbial communities and tight junction protein expression in the gastrointestinal tract of feedlot cattle.},
journal = {Scientific reports},
volume = {15},
number = {1},
pages = {39055},
pmid = {41203821},
issn = {2045-2322},
mesh = {Animals ; Cattle ; *Tight Junction Proteins/metabolism/genetics ; *Gastrointestinal Microbiome ; *Gastrointestinal Tract/microbiology/metabolism ; RNA, Ribosomal, 16S/genetics ; Rumen/microbiology/metabolism ; Male ; Tight Junctions/metabolism ; Bacteria/genetics/classification ; },
abstract = {The gastrointestinal tract (GIT) of cattle plays a vital role in nutrient absorption, immune function, and microbial homeostasis. While the importance of the GIT microbiome and epithelial barrier integrity has been increasingly recognized, the typical composition of microbial communities and the expression of tight junction proteins (TJPs) in feedlot cattle remains poorly characterized. We investigated microbial community structure and TJP expression at three GIT sites: the rumen (RU), small intestine (SI), and large intestine (LI) in 21 finish-fed feedlot steers sourced from 21 commercial feedyards in the Texas Panhandle. Samples of luminal contents and GIT tissue were collected from each region, as well as feces and liver abscess material. Microbial communities were characterized using 16S rRNA gene sequencing. TJP gene expression was quantified by RT-qPCR using synthetic standards, and protein expression was evaluated by immunohistochemistry (IHC) with both computer-generated and pathologist-generated scoring. Microbial community structures varied primarily by GIT region rather than by individual animals raised at different locations. Nine bacterial families were identified as core microbiome members, with Lachnospiraceae being the most abundant across the GIT. TJP gene expression varied considerably by site, with RU having significantly lower Claudin 1, Claudin 2, and E-Cadherin expression than the SI and LI. IHC results paralleled qPCR findings, with region-specific patterns of protein localization and intensity. Computerized and pathologist-generated H-scores showed moderate agreement but differed notably between epithelial and lamina propria regions. This study provides a comprehensive baseline of microbial and host factors associated with gut health in a uniquely diverse population of feedlot cattle. The identification of regional microbial communities and distinct TJP expression patterns offers foundational insights into gastrointestinal physiology and barrier function. This work establishes baseline data to support future investigations into the relationships among microbial ecology, epithelial barrier function, and cattle health and productivity.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Animals
Cattle
*Tight Junction Proteins/metabolism/genetics
*Gastrointestinal Microbiome
*Gastrointestinal Tract/microbiology/metabolism
RNA, Ribosomal, 16S/genetics
Rumen/microbiology/metabolism
Male
Tight Junctions/metabolism
Bacteria/genetics/classification
RevDate: 2025-11-07
Long-Term Oral Administration of Inactivated Vibrio harveyi Vaccine Triggers Immunosuppression in Penaeus vannamei.
Fish & shellfish immunology pii:S1050-4648(25)00872-1 [Epub ahead of print].
This study investigated optimal oral vaccination strategies to enhance Vibrio resistance in Penaeus vannamei by comparing two feeding regimens: continuous administration of inactivated Vibrio harveyi (IVH) (CF group) and intermittent IVH feeding (7-day IVH followed by 7-day commercial feed, IF group). Results demonstrated that 7-day IVH feeding effectively induced anti-Vibrio immunity. The IF group maintained >60% relative percent survival (RPS) during challenge tests at 14, 21 and 28 days post-immunization, whereas the CF group exhibited a sharp RPS decline to -22.73% at day 14, with persistently low values thereafter. Specific growth rates were significantly reduced in the CF group compared to controls. Immune enzymatic activity analysis at day 14 revealed sustained high levels in the IF group but marked declines in the CF group. Histopathological examination confirmed severe cellular necrosis in intestinal and hepatopancreatic tissues of the CF group at day 14. Gut microbiota analysis indicated comparable dominant taxa between groups at day 14, while the IF group exhibited higher proportions of Ruegeria genera. Proteomic profiling identified distinct expression patterns between groups, with the CF group displaying significant downregulation of proteins associated with energy metabolism, immune responses, metabolic pathways, and cell/tissue maintenance. These data demonstrated that continuous IVH feeding elicited substantial physiological stress, leading to cellular and tissue damage and consequent immunosuppression in P. vannamei, whereas intermittent feeding mitigated immune impairment and conferred V. harveyi resistance. This study highlights the critical need for temporally optimized vaccination protocols in shrimp aquaculture.
Additional Links: PMID-41202998
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PubMed:
Citation:
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@article {pmid41202998,
year = {2025},
author = {Kuang, B and Yang, W and Li, C and Lee, CW and Liu, BY and Bong, CW and Wang, W and Chen, S},
title = {Long-Term Oral Administration of Inactivated Vibrio harveyi Vaccine Triggers Immunosuppression in Penaeus vannamei.},
journal = {Fish & shellfish immunology},
volume = {},
number = {},
pages = {110983},
doi = {10.1016/j.fsi.2025.110983},
pmid = {41202998},
issn = {1095-9947},
abstract = {This study investigated optimal oral vaccination strategies to enhance Vibrio resistance in Penaeus vannamei by comparing two feeding regimens: continuous administration of inactivated Vibrio harveyi (IVH) (CF group) and intermittent IVH feeding (7-day IVH followed by 7-day commercial feed, IF group). Results demonstrated that 7-day IVH feeding effectively induced anti-Vibrio immunity. The IF group maintained >60% relative percent survival (RPS) during challenge tests at 14, 21 and 28 days post-immunization, whereas the CF group exhibited a sharp RPS decline to -22.73% at day 14, with persistently low values thereafter. Specific growth rates were significantly reduced in the CF group compared to controls. Immune enzymatic activity analysis at day 14 revealed sustained high levels in the IF group but marked declines in the CF group. Histopathological examination confirmed severe cellular necrosis in intestinal and hepatopancreatic tissues of the CF group at day 14. Gut microbiota analysis indicated comparable dominant taxa between groups at day 14, while the IF group exhibited higher proportions of Ruegeria genera. Proteomic profiling identified distinct expression patterns between groups, with the CF group displaying significant downregulation of proteins associated with energy metabolism, immune responses, metabolic pathways, and cell/tissue maintenance. These data demonstrated that continuous IVH feeding elicited substantial physiological stress, leading to cellular and tissue damage and consequent immunosuppression in P. vannamei, whereas intermittent feeding mitigated immune impairment and conferred V. harveyi resistance. This study highlights the critical need for temporally optimized vaccination protocols in shrimp aquaculture.},
}
RevDate: 2025-11-07
The dawn of a new air pollutant: inhalable microplastics as emerging vectors of hazardous contaminants and their implications for human health.
Environment international, 205:109897 pii:S0160-4120(25)00648-8 [Epub ahead of print].
This study presents the first comprehensive research on inhalable microplastics (iMPs, <10 μm), a notorious subset of airborne microplastics (AMPs). To identify human health risk, ambient iMPs concentrations were assessed at human breathing height across the markets of four major Indian cities. With winter evening being the highest iMPs concentration, in Kolkata (14.23 µg/m[3]), followed by Delhi (14.18 µg/m[3]), linked to the highest footfalls, use of synthetic clothing, and poor waste management. Coastal cities (Chennai: 4 µg/m[3], and Mumbai: 2.65 µg/m[3]) showed lower levels, likely due to improved air circulation, less winter, and reduced apparel, confirmed by Principal Component Analysis. Py-GC-MS quantified 11 polymers, with PET (Polyester) from textiles as the most abundant, followed by PE and SBR from single-use plastics, packaging, vehicles, and footwear. Urban areas in India show an average iMPs concentration of 8.8 µg/m[3], translating to a lifetime lung load of ∼2.9 g/person. Furthermore, this investigation highlights the risks of iMPs-associated tracers such as diethyl phthalates and lead. This pioneering research is the first-ever study to explore AMPs carrier capabilities for ultrafine particulate matter, PTEs, POPs, PPCPs, and microbes. During peak exposure periods like autumn festivals, AMPs harbored diverse microbial communities, including pathogenic (Aspergillus fumigatus) and new strains of bacteria/fungi with antibiotic resistance and virulence factor genes. This suggests that microbes carried by iMPs possess enhanced pathogenicity and resistance against broad-spectrum drugs like tetracycline and are more likely to be multidrug-resistant. Cross-referencing toxicological databases revealed that exposure to AMPs-linked modern-day contaminants elevates the risk of cancer, gastrointestinal, endocrine, breast, and respiratory diseases.
Additional Links: PMID-41202458
Publisher:
PubMed:
Citation:
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@article {pmid41202458,
year = {2025},
author = {Biswas, A and Saini, N and Chivukula, N and Samal, A and Jansari, MR and Bhadury, P and Darbha, GK},
title = {The dawn of a new air pollutant: inhalable microplastics as emerging vectors of hazardous contaminants and their implications for human health.},
journal = {Environment international},
volume = {205},
number = {},
pages = {109897},
doi = {10.1016/j.envint.2025.109897},
pmid = {41202458},
issn = {1873-6750},
abstract = {This study presents the first comprehensive research on inhalable microplastics (iMPs, <10 μm), a notorious subset of airborne microplastics (AMPs). To identify human health risk, ambient iMPs concentrations were assessed at human breathing height across the markets of four major Indian cities. With winter evening being the highest iMPs concentration, in Kolkata (14.23 µg/m[3]), followed by Delhi (14.18 µg/m[3]), linked to the highest footfalls, use of synthetic clothing, and poor waste management. Coastal cities (Chennai: 4 µg/m[3], and Mumbai: 2.65 µg/m[3]) showed lower levels, likely due to improved air circulation, less winter, and reduced apparel, confirmed by Principal Component Analysis. Py-GC-MS quantified 11 polymers, with PET (Polyester) from textiles as the most abundant, followed by PE and SBR from single-use plastics, packaging, vehicles, and footwear. Urban areas in India show an average iMPs concentration of 8.8 µg/m[3], translating to a lifetime lung load of ∼2.9 g/person. Furthermore, this investigation highlights the risks of iMPs-associated tracers such as diethyl phthalates and lead. This pioneering research is the first-ever study to explore AMPs carrier capabilities for ultrafine particulate matter, PTEs, POPs, PPCPs, and microbes. During peak exposure periods like autumn festivals, AMPs harbored diverse microbial communities, including pathogenic (Aspergillus fumigatus) and new strains of bacteria/fungi with antibiotic resistance and virulence factor genes. This suggests that microbes carried by iMPs possess enhanced pathogenicity and resistance against broad-spectrum drugs like tetracycline and are more likely to be multidrug-resistant. Cross-referencing toxicological databases revealed that exposure to AMPs-linked modern-day contaminants elevates the risk of cancer, gastrointestinal, endocrine, breast, and respiratory diseases.},
}
RevDate: 2025-11-07
CmpDate: 2025-11-07
Warming Accelerates Phytoplankton Bloom Dynamics and Differentially Affects the Fluxes of Carbon, Nitrogen, and Oxygen Through a Coastal Microbial Community.
Microbial ecology, 88(1):117.
Marine heatwaves affect the abundance and community structure of microbial plankton, with implications for food web and ecosystem processes, but their impact on microbially mediated elemental cycling remains poorly constrained. To determine the biogeochemical effects of increased temperature, we conducted an experiment in September 2023 in which a plankton community from a coastal, productive ecosystem (RÃa de Vigo, NW Iberia) was exposed to a warming of + 2 °C and + 4 °C under unamended and nutrient-enriched conditions. The response of microbial plankton was characterized in terms of organic matter production, carbon fixation, nitrogen uptake, and oxygen net production. We found that warming caused increased nutrient consumption and biomass production, as well as faster bloom dynamics, both in unamended and nutrient-enriched treatments, indicating that the community was robust to thermal perturbation. Accelerated nutrient depletion under warming gave way to an earlier decrease in carbon fixation and nitrate uptake rates, together with a shift towards a negative or less positive metabolic balance. Carbon fixation was less sensitive than nitrate uptake to the different temperature and nutrient scenarios, leading to wide changes in the carbon-to-nitrogen uptake ratio, while respiration increased non-linearly with temperature. Overall, the investigated microbial fluxes were more responsive to nutrient availability than to temperature. Our results show that microbially driven ecosystem services in coastal waters have the potential to be enhanced during short-term warming events.
Additional Links: PMID-41201519
PubMed:
Citation:
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@article {pmid41201519,
year = {2025},
author = {López-Sandoval, DC and Fernández-González, C and González-GarcÃa, C and Marañón, E},
title = {Warming Accelerates Phytoplankton Bloom Dynamics and Differentially Affects the Fluxes of Carbon, Nitrogen, and Oxygen Through a Coastal Microbial Community.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {117},
pmid = {41201519},
issn = {1432-184X},
support = {Project POLARIS (PGC2018-094553-B-I00)//Spanish Ministry of Science and Innovation/ ; },
mesh = {*Nitrogen/metabolism ; *Carbon/metabolism ; *Phytoplankton/growth & development/metabolism ; *Oxygen/metabolism ; *Microbiota/physiology ; Seawater/microbiology/chemistry ; Biomass ; *Eutrophication ; Carbon Cycle ; Ecosystem ; Global Warming ; Hot Temperature ; },
abstract = {Marine heatwaves affect the abundance and community structure of microbial plankton, with implications for food web and ecosystem processes, but their impact on microbially mediated elemental cycling remains poorly constrained. To determine the biogeochemical effects of increased temperature, we conducted an experiment in September 2023 in which a plankton community from a coastal, productive ecosystem (RÃa de Vigo, NW Iberia) was exposed to a warming of + 2 °C and + 4 °C under unamended and nutrient-enriched conditions. The response of microbial plankton was characterized in terms of organic matter production, carbon fixation, nitrogen uptake, and oxygen net production. We found that warming caused increased nutrient consumption and biomass production, as well as faster bloom dynamics, both in unamended and nutrient-enriched treatments, indicating that the community was robust to thermal perturbation. Accelerated nutrient depletion under warming gave way to an earlier decrease in carbon fixation and nitrate uptake rates, together with a shift towards a negative or less positive metabolic balance. Carbon fixation was less sensitive than nitrate uptake to the different temperature and nutrient scenarios, leading to wide changes in the carbon-to-nitrogen uptake ratio, while respiration increased non-linearly with temperature. Overall, the investigated microbial fluxes were more responsive to nutrient availability than to temperature. Our results show that microbially driven ecosystem services in coastal waters have the potential to be enhanced during short-term warming events.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Nitrogen/metabolism
*Carbon/metabolism
*Phytoplankton/growth & development/metabolism
*Oxygen/metabolism
*Microbiota/physiology
Seawater/microbiology/chemistry
Biomass
*Eutrophication
Carbon Cycle
Ecosystem
Global Warming
Hot Temperature
RevDate: 2025-11-07
CmpDate: 2025-11-07
Modulating Surfactin Biosynthesis in Bacillus subtilis R31 Enhances Behavioural Traits and Biocontrol Efficacy Against Banana Fusarium Wilt.
Microbial biotechnology, 18(11):e70261.
Surfactin, a lipopeptide antibiotic and quorum-sensing (QS) mediator from Bacillus subtilis, has dual functions in microbial ecology and plant disease suppression. This study engineered B. subtilis R31 to overproduce comK and phrC, key regulators of surfactin biosynthesis, increasing surfactin yield by 45% compared to the WT strain. While elevated surfactin enhanced antimicrobial potential, comK-mediated overproduction impaired biofilm formation and swarming motility, but rhizosphere colonisation was mostly unaffected. 16S rRNA sequencing of banana rhizospheres showed that surfactin selectively shaped the microbial community by enriching beneficial Bacillus species. Mechanistic studies confirmed surfactin's dual role as an antimicrobial and an intercellular signalling molecule for coordinated development in Bacillus populations. These results reveal the molecular mechanisms of R31-mediated suppression of banana Fusarium wilt and offer a strategy for engineering synthetic microbial consortia by manipulating metabolic signalling pathways.
Additional Links: PMID-41199522
Publisher:
PubMed:
Citation:
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@article {pmid41199522,
year = {2025},
author = {Chen, HJ and Liu, Y and Zhong, YS and Li, MZ and Lai, JJ and Luo, YY and Huang, SL and Liu, SQ and Yu, GH and Sun, YH and Shao, MW},
title = {Modulating Surfactin Biosynthesis in Bacillus subtilis R31 Enhances Behavioural Traits and Biocontrol Efficacy Against Banana Fusarium Wilt.},
journal = {Microbial biotechnology},
volume = {18},
number = {11},
pages = {e70261},
doi = {10.1111/1751-7915.70261},
pmid = {41199522},
issn = {1751-7915},
support = {202206010083//Guangzhou Municipal Science and Technology Project/ ; 2021ZDJS002//Guangdong Province Key Discipline Research Capacity Enhancement Project/ ; 32302450//National Natural Science Foundation of China/ ; 22-035-31-23KF03//Guangxi Key Laboratory of Crop Pest Biology Foundation/ ; 2023B0202010012//Guangdong Province Key Area Research and Development Program/ ; },
mesh = {*Fusarium/growth & development/drug effects/physiology ; *Bacillus subtilis/genetics/metabolism/physiology ; *Plant Diseases/microbiology/prevention & control ; *Musa/microbiology ; *Lipopeptides/biosynthesis/pharmacology ; *Peptides, Cyclic/biosynthesis ; RNA, Ribosomal, 16S/genetics ; Metabolic Engineering ; Quorum Sensing ; Rhizosphere ; Biofilms/growth & development ; Bacterial Proteins/genetics/metabolism ; DNA, Ribosomal/chemistry/genetics ; },
abstract = {Surfactin, a lipopeptide antibiotic and quorum-sensing (QS) mediator from Bacillus subtilis, has dual functions in microbial ecology and plant disease suppression. This study engineered B. subtilis R31 to overproduce comK and phrC, key regulators of surfactin biosynthesis, increasing surfactin yield by 45% compared to the WT strain. While elevated surfactin enhanced antimicrobial potential, comK-mediated overproduction impaired biofilm formation and swarming motility, but rhizosphere colonisation was mostly unaffected. 16S rRNA sequencing of banana rhizospheres showed that surfactin selectively shaped the microbial community by enriching beneficial Bacillus species. Mechanistic studies confirmed surfactin's dual role as an antimicrobial and an intercellular signalling molecule for coordinated development in Bacillus populations. These results reveal the molecular mechanisms of R31-mediated suppression of banana Fusarium wilt and offer a strategy for engineering synthetic microbial consortia by manipulating metabolic signalling pathways.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Fusarium/growth & development/drug effects/physiology
*Bacillus subtilis/genetics/metabolism/physiology
*Plant Diseases/microbiology/prevention & control
*Musa/microbiology
*Lipopeptides/biosynthesis/pharmacology
*Peptides, Cyclic/biosynthesis
RNA, Ribosomal, 16S/genetics
Metabolic Engineering
Quorum Sensing
Rhizosphere
Biofilms/growth & development
Bacterial Proteins/genetics/metabolism
DNA, Ribosomal/chemistry/genetics
RevDate: 2025-11-06
Immuno-Microbial Crosstalk in Aplastic Anemia: Role of Gut and Viral Triggers.
Microbial pathogenesis pii:S0882-4010(25)00883-6 [Epub ahead of print].
Aplastic anemia (AA) is a rare but life-threatening hematological disorder, manifested in bone marrow failure and pancytopenia, which occurs worldwide due to the preferential immune mediated destruction of hematopoietic stem and progenitor cells. Despite the autoimmune etiology of AA, recent findings emphasize the key role of microbial and viral factors in the pathogenesis of AA by driving the host immune dysregulation. We delve into the immune-microbial crosstalk that is relevant in AA pathogenesis to provide novel insights related to gut microbial ecology, microbial metabolites, viral infections mediated inflammation and cytotoxicity against bone marrow components. Additionally, providing the roadmap of current knowledge for immune-mediated bone marrow failure focusing on activated cytotoxic T cells, altered regulatory T cells and proinflammatory cytokines. Imbalanced immune activation via defects in gut barrier function which promotes pathogen-associated molecular patterns (PAMPs) signaling through Toll-like receptors (TLRs) and other innate sensors. Considering the role of viral trigger such as Parvovirus B19, Epstein-Barr and Hepatitis as inducers of dysregulated immunity and their ability to affect antigen presentation, T cell receptor repertoires, and interferon pathways. We also delineate the potential of targeting the gut-immune axis for personalized AA therapy, including potential microbiome-directed interventions, antiviral and anti-cytokine approaches, as promising complement lines for standard immunosuppression therapy in AA. This cited approach will provide the advanced and novel clinical paradigm for the interconnected immune-microbial signals in pathogenesis of AA which promotes the host immune surveillance and also lead to precision medicine in AA treatment.
Additional Links: PMID-41197919
Publisher:
PubMed:
Citation:
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@article {pmid41197919,
year = {2025},
author = {Mohit, and Verma, S and Venkatesh, V and Nityanand, S},
title = {Immuno-Microbial Crosstalk in Aplastic Anemia: Role of Gut and Viral Triggers.},
journal = {Microbial pathogenesis},
volume = {},
number = {},
pages = {108158},
doi = {10.1016/j.micpath.2025.108158},
pmid = {41197919},
issn = {1096-1208},
abstract = {Aplastic anemia (AA) is a rare but life-threatening hematological disorder, manifested in bone marrow failure and pancytopenia, which occurs worldwide due to the preferential immune mediated destruction of hematopoietic stem and progenitor cells. Despite the autoimmune etiology of AA, recent findings emphasize the key role of microbial and viral factors in the pathogenesis of AA by driving the host immune dysregulation. We delve into the immune-microbial crosstalk that is relevant in AA pathogenesis to provide novel insights related to gut microbial ecology, microbial metabolites, viral infections mediated inflammation and cytotoxicity against bone marrow components. Additionally, providing the roadmap of current knowledge for immune-mediated bone marrow failure focusing on activated cytotoxic T cells, altered regulatory T cells and proinflammatory cytokines. Imbalanced immune activation via defects in gut barrier function which promotes pathogen-associated molecular patterns (PAMPs) signaling through Toll-like receptors (TLRs) and other innate sensors. Considering the role of viral trigger such as Parvovirus B19, Epstein-Barr and Hepatitis as inducers of dysregulated immunity and their ability to affect antigen presentation, T cell receptor repertoires, and interferon pathways. We also delineate the potential of targeting the gut-immune axis for personalized AA therapy, including potential microbiome-directed interventions, antiviral and anti-cytokine approaches, as promising complement lines for standard immunosuppression therapy in AA. This cited approach will provide the advanced and novel clinical paradigm for the interconnected immune-microbial signals in pathogenesis of AA which promotes the host immune surveillance and also lead to precision medicine in AA treatment.},
}
RevDate: 2025-11-06
Simultaneous control of disinfection by-products, opportunistic pathogens, and antibiotic resistance genes in drinking water based on a novel advanced treatment process consisting of Fenton-like reaction and biological activated carbon.
Bioresource technology pii:S0960-8524(25)01569-X [Epub ahead of print].
Disinfection by-products (DBPs), opportunistic pathogens (OPs), and antibiotic resistance genes (ARGs) are typical drinking water quality risks today, and the synchronous control of these factors has always been an important challenge. Herein, a novel drinking water treatment process (Fe3C-NC/PMS-BAC) consisting of Fe3C-NC Fenton-like reaction and biological activated carbon (BAC) was established in this study. Fe3C-NC/PMS caused the decomposition of high molecular weight organic matter into low molecular weight organic matter, which was efficiently biodegraded in the subsequent BAC biofilter (PBAC). In addition, the suspended extracellular polymeric substances (EPS) in the effluent of PBAC contained only a small amount of polysaccharides, markedly weakening the biofilm stability and its protective effect against OPs. The changes in organic matter and EPS ultimately led to the reduction of DBPs precursors. More importantly, the Fe3C-NC/PMS treatment remarkably changed the microbial ecology in subsequent PBAC, including shaping the microbial community, regulating EPS characteristics, weakening quorum sensing, and even inhibiting microbial activities, contributing to the inhibition of horizontal gene transfer of ARGs. Therefore, the Fe3C-NC/PMS-BAC is a promising alternative to BAC treatment for future applications, providing new ideas for the collaborative removal of chemical and microbial water quality risks in drinking water.
Additional Links: PMID-41197741
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@article {pmid41197741,
year = {2025},
author = {Chen, Y and Chen, Y and Hu, C and Xing, X and Zhang, S and Zeng, K and Yin, Z and Meng, C and Situ, F and Li, J and Chen, C and Ma, K and Chen, J and Li, F},
title = {Simultaneous control of disinfection by-products, opportunistic pathogens, and antibiotic resistance genes in drinking water based on a novel advanced treatment process consisting of Fenton-like reaction and biological activated carbon.},
journal = {Bioresource technology},
volume = {},
number = {},
pages = {133602},
doi = {10.1016/j.biortech.2025.133602},
pmid = {41197741},
issn = {1873-2976},
abstract = {Disinfection by-products (DBPs), opportunistic pathogens (OPs), and antibiotic resistance genes (ARGs) are typical drinking water quality risks today, and the synchronous control of these factors has always been an important challenge. Herein, a novel drinking water treatment process (Fe3C-NC/PMS-BAC) consisting of Fe3C-NC Fenton-like reaction and biological activated carbon (BAC) was established in this study. Fe3C-NC/PMS caused the decomposition of high molecular weight organic matter into low molecular weight organic matter, which was efficiently biodegraded in the subsequent BAC biofilter (PBAC). In addition, the suspended extracellular polymeric substances (EPS) in the effluent of PBAC contained only a small amount of polysaccharides, markedly weakening the biofilm stability and its protective effect against OPs. The changes in organic matter and EPS ultimately led to the reduction of DBPs precursors. More importantly, the Fe3C-NC/PMS treatment remarkably changed the microbial ecology in subsequent PBAC, including shaping the microbial community, regulating EPS characteristics, weakening quorum sensing, and even inhibiting microbial activities, contributing to the inhibition of horizontal gene transfer of ARGs. Therefore, the Fe3C-NC/PMS-BAC is a promising alternative to BAC treatment for future applications, providing new ideas for the collaborative removal of chemical and microbial water quality risks in drinking water.},
}
RevDate: 2025-11-06
CmpDate: 2025-11-06
First Metataxonomic Characterisation of Gut Microbiota of Swordfish (Xiphias gladius).
Environmental microbiology reports, 17(6):e70199.
Swordfish (Xiphias gladius) is a large, migratory apex predator with a carnivorous diet, occupying a top position in the marine food chain. Although it is a valuable teleost pelagic fish with a significant commercial value, its gut microbiota has never been studied. The gut microbiota of 100 individuals was characterised by sequencing the V3-V4 region of the bacterial 16S rRNA gene. Gut microbiota findings were classified with consideration to diversity, taking into account their weight (10-20; 21-30; over 31 kg) and the FAO fishing areas in which they were caught (FAO 27, 34, 37.1.1 areas). Significant differences in the alpha diversity were observed among the weight categories for all metrics examined (except for the evenness index) and only by Shannon's index among the FAO fishing areas. Beta-diversity analysis revealed no significant differences. The phylum Pseudomonadota dominated the swordfish gut microbiota, followed by Fusobacteriota. Photobacterium was the most abundant genus across all weight categories and FAO fishing areas. Smaller fishes showed a less rich and diverse gut microbiota, dominated almost exclusively by Photobacterium. Conversely, Pseudoalteromonas, Psychrobacter, Psychrilyobacter, and Cetobacterium appeared to increase in abundance with fish weight. Although Photobacterium was dominant across the different FAO fishing areas, distinctive microbial community compositions were observed: Cetobacterium was more prevalent in FAO 27, while Pseudoalteromonas was more prevalent in the other areas. Unlike the gut microbiota of other marine fish species, Vibrio and Lactobacillus were largely absent. This study represents the first metataxonomic characterisation of the gut microbiota of swordfish using next-generation sequencing.
Additional Links: PMID-41194431
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@article {pmid41194431,
year = {2025},
author = {Truant, A and Giacometti, F and Losasso, C and Peruzzo, A and Petrin, S and Zancato, I and Di Leva, V and Giaccone, V},
title = {First Metataxonomic Characterisation of Gut Microbiota of Swordfish (Xiphias gladius).},
journal = {Environmental microbiology reports},
volume = {17},
number = {6},
pages = {e70199},
doi = {10.1111/1758-2229.70199},
pmid = {41194431},
issn = {1758-2229},
mesh = {Animals ; *Gastrointestinal Microbiome ; RNA, Ribosomal, 16S/genetics ; *Bacteria/classification/genetics/isolation & purification ; *Perciformes/microbiology ; Phylogeny ; *Fishes/microbiology ; DNA, Bacterial/genetics ; Sequence Analysis, DNA ; Biodiversity ; },
abstract = {Swordfish (Xiphias gladius) is a large, migratory apex predator with a carnivorous diet, occupying a top position in the marine food chain. Although it is a valuable teleost pelagic fish with a significant commercial value, its gut microbiota has never been studied. The gut microbiota of 100 individuals was characterised by sequencing the V3-V4 region of the bacterial 16S rRNA gene. Gut microbiota findings were classified with consideration to diversity, taking into account their weight (10-20; 21-30; over 31 kg) and the FAO fishing areas in which they were caught (FAO 27, 34, 37.1.1 areas). Significant differences in the alpha diversity were observed among the weight categories for all metrics examined (except for the evenness index) and only by Shannon's index among the FAO fishing areas. Beta-diversity analysis revealed no significant differences. The phylum Pseudomonadota dominated the swordfish gut microbiota, followed by Fusobacteriota. Photobacterium was the most abundant genus across all weight categories and FAO fishing areas. Smaller fishes showed a less rich and diverse gut microbiota, dominated almost exclusively by Photobacterium. Conversely, Pseudoalteromonas, Psychrobacter, Psychrilyobacter, and Cetobacterium appeared to increase in abundance with fish weight. Although Photobacterium was dominant across the different FAO fishing areas, distinctive microbial community compositions were observed: Cetobacterium was more prevalent in FAO 27, while Pseudoalteromonas was more prevalent in the other areas. Unlike the gut microbiota of other marine fish species, Vibrio and Lactobacillus were largely absent. This study represents the first metataxonomic characterisation of the gut microbiota of swordfish using next-generation sequencing.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Animals
*Gastrointestinal Microbiome
RNA, Ribosomal, 16S/genetics
*Bacteria/classification/genetics/isolation & purification
*Perciformes/microbiology
Phylogeny
*Fishes/microbiology
DNA, Bacterial/genetics
Sequence Analysis, DNA
Biodiversity
RevDate: 2025-11-05
Comparative genomics reveals adaptive traits in novel Antarctic lithic cyanobacteria.
BMC genomics, 26(1):994.
Additional Links: PMID-41193960
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@article {pmid41193960,
year = {2025},
author = {Van Goethem, MW and Vikram, S and Cowan, DA and Makhalanyane, TP},
title = {Comparative genomics reveals adaptive traits in novel Antarctic lithic cyanobacteria.},
journal = {BMC genomics},
volume = {26},
number = {1},
pages = {994},
pmid = {41193960},
issn = {1471-2164},
}
RevDate: 2025-11-05
CmpDate: 2025-11-05
Contrasting Diversity and Network Dynamics of Soil Fungal Functional Groups in the Plant Rhizosphere.
Microbial ecology, 88(1):116.
Soil microbiomes, critical for plant productivity and ecosystem functioning, mediate essential functions such as pathogenesis, mutualism, and decomposition through different fungal functional groups. Yet, our understanding of the dynamics of co-existing soil fungal functional groups in the rhizosphere remains limited. By leveraging urban farming-featuring fields of different ages and multiple genotypes-we tracked the relative abundance, richness, and microbial networks of putative plant pathogenic fungi, mycorrhizal fungi, and saprotrophic fungi across fields over two years. We observed an increase in the relative abundance of putative plant pathogenic fungi in the rhizosphere in older fields relative to younger fields, supporting the prediction of pathogen accumulation over time. In contrast, there was a decrease in the relative abundance of mycorrhizal fungi in older fields. The relative abundance of saprotrophic fungi remained similar between younger and older fields. While the richness of putative plant pathogenic fungi and saprotrophic fungi was similar across the examined fields, the community structure of both groups differed between younger and older fields. For mycorrhizal fungi, the richness declined in older fields and over the two years. These dynamics led to distinct microbial networks, with decreased network links for mycorrhizal fungi and increased links for saprotrophic fungi in older fields, whereas the links for plant pathogenic fungi remained similar across fields. Our study reveals contrasting dynamics of essential soil fungal functional groups in the rhizosphere and provides predictive insight into the potential shifts in soil function and their impact on plant productivity.
Additional Links: PMID-41193926
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@article {pmid41193926,
year = {2025},
author = {Wei, N and Nakaji-Conley, M and Tan, J},
title = {Contrasting Diversity and Network Dynamics of Soil Fungal Functional Groups in the Plant Rhizosphere.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {116},
pmid = {41193926},
issn = {1432-184X},
support = {2300058//Directorate for Biological Sciences/ ; 2300057//Directorate for Biological Sciences/ ; E455990101//Wuhan Botanical Garden, Chinese Academy of Sciences/ ; },
mesh = {*Rhizosphere ; *Soil Microbiology ; *Fungi/classification/genetics/isolation & purification/physiology ; Mycorrhizae/genetics/classification/isolation & purification ; *Biodiversity ; *Plants/microbiology ; Microbiota ; Soil/chemistry ; Plant Roots/microbiology ; },
abstract = {Soil microbiomes, critical for plant productivity and ecosystem functioning, mediate essential functions such as pathogenesis, mutualism, and decomposition through different fungal functional groups. Yet, our understanding of the dynamics of co-existing soil fungal functional groups in the rhizosphere remains limited. By leveraging urban farming-featuring fields of different ages and multiple genotypes-we tracked the relative abundance, richness, and microbial networks of putative plant pathogenic fungi, mycorrhizal fungi, and saprotrophic fungi across fields over two years. We observed an increase in the relative abundance of putative plant pathogenic fungi in the rhizosphere in older fields relative to younger fields, supporting the prediction of pathogen accumulation over time. In contrast, there was a decrease in the relative abundance of mycorrhizal fungi in older fields. The relative abundance of saprotrophic fungi remained similar between younger and older fields. While the richness of putative plant pathogenic fungi and saprotrophic fungi was similar across the examined fields, the community structure of both groups differed between younger and older fields. For mycorrhizal fungi, the richness declined in older fields and over the two years. These dynamics led to distinct microbial networks, with decreased network links for mycorrhizal fungi and increased links for saprotrophic fungi in older fields, whereas the links for plant pathogenic fungi remained similar across fields. Our study reveals contrasting dynamics of essential soil fungal functional groups in the rhizosphere and provides predictive insight into the potential shifts in soil function and their impact on plant productivity.},
}
MeSH Terms:
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*Rhizosphere
*Soil Microbiology
*Fungi/classification/genetics/isolation & purification/physiology
Mycorrhizae/genetics/classification/isolation & purification
*Biodiversity
*Plants/microbiology
Microbiota
Soil/chemistry
Plant Roots/microbiology
RevDate: 2025-11-05
Current and projected effects of climate change in cryosphere microbial ecosystems.
Nature reviews. Microbiology [Epub ahead of print].
Cold environments, including glaciers, ice sheets, permafrost soils and sea ice, are common across the surface of the Earth. Despite the challenges of life at subzero temperatures, the global cryosphere hosts diverse microbial communities that support biogeochemical cycling and ecosystem functioning in areas where few other organisms can survive. However, the composition and function of cryosphere microbial communities, and the continued existence of cryosphere habitats, are threatened by ongoing climate change, which has disproportionate impacts in polar regions. In this Review, we survey the breadth of cryosphere habitats and the composition, function and unique adaptations of the microbial communities that inhabit them. We outline how climate change can affect these communities and the ecosystem services they provide through short-term changes in substrate availability, enzyme activity and redox potentials as well as longer-term changes in community composition. We also explore the wide-ranging consequences these changes may have for local ecosystems, human communities and the global climate. Finally, we outline the knowledge gaps in cryosphere microbial ecology that contribute to uncertainties about the future of these ecosystems in a warming world.
Additional Links: PMID-41193719
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@article {pmid41193719,
year = {2025},
author = {Sugden, S and Davis, CL and Quinn, MW and Whyte, LG},
title = {Current and projected effects of climate change in cryosphere microbial ecosystems.},
journal = {Nature reviews. Microbiology},
volume = {},
number = {},
pages = {},
pmid = {41193719},
issn = {1740-1534},
abstract = {Cold environments, including glaciers, ice sheets, permafrost soils and sea ice, are common across the surface of the Earth. Despite the challenges of life at subzero temperatures, the global cryosphere hosts diverse microbial communities that support biogeochemical cycling and ecosystem functioning in areas where few other organisms can survive. However, the composition and function of cryosphere microbial communities, and the continued existence of cryosphere habitats, are threatened by ongoing climate change, which has disproportionate impacts in polar regions. In this Review, we survey the breadth of cryosphere habitats and the composition, function and unique adaptations of the microbial communities that inhabit them. We outline how climate change can affect these communities and the ecosystem services they provide through short-term changes in substrate availability, enzyme activity and redox potentials as well as longer-term changes in community composition. We also explore the wide-ranging consequences these changes may have for local ecosystems, human communities and the global climate. Finally, we outline the knowledge gaps in cryosphere microbial ecology that contribute to uncertainties about the future of these ecosystems in a warming world.},
}
RevDate: 2025-11-05
Complete genome and comparative genomic analysis of cefpodoxime resistant Pantoea septica strain GABEPS69 isolated from saliva of a patient diagnosed with treatment resistant schizophrenia.
International journal of medical microbiology : IJMM, 321:151681 pii:S1438-4221(25)00037-2 [Epub ahead of print].
OBJECTIVES: This study aims to generate the first complete genome of Pantoea septica and provide a thorough genomic characterisation of this under-documented species. The study seeks to enhance understanding of P. septica, clarifying features relevant to opportunistic infection in vulnerable cohorts.
METHODS: P. septica GABEPS69 was an opportunistic coloniser isolated from the saliva of a patient prescribed the antipsychotic clozapine, leading to a dysbiotic oral microbiome. A hybrid sequencing approach yielded a closed genome comprising a 4.1 Mb chromosome and six plasmids. Phenotypic susceptibility was determined by disk-diffusion and minimum inhibitory concentration (MIC) assays. Its chromosomal and plasmidic content was bioinformatically analysed alongside all canonical GenBank available P. septica genomes and the type strains of taxonomic neighbours Pantoea piersonii and "Pantoea latae", with focus on virulence-factors (VFs), antimicrobial-resistance-genes (ARGs), metal-resistance-genes (MRGs) and biosynthetic gene clusters.
RESULTS: GABEPS69 exhibited a narrow resistance spectrum, displaying resistance to the third-generation cephalosporin cefpodoxime. Plasmid pGABEPS69_1 harboured an aerobactin pathogenicity island homologue; a locus implicated in enhanced virulence, that was also identified across most other P. septica genomes and in the closely related human-pathogen Pantoea piersonii. A conserved chromosomal class-A β-lactamase homologue was also identified. Additionally, a universal presence of bioactive thiopeptide biosynthetic-gene-clusters was observed in P. septica genomes, suggesting a potential role in microbiome modulation.
CONCLUSION: This study presents a first complete genome of P. septica, revealing its genomic architecture, resistance, and virulence potential. Detailed plasmid analysis and comparative genomics enhance our understanding of the species clinical relevance and microbiome-modulating capacity. These findings motivate surveillance of transient oral microbiota in at-risk populations, including patients receiving clozapine.
Additional Links: PMID-41192073
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@article {pmid41192073,
year = {2025},
author = {McDonagh, F and Kovarova, A and Tumeo, A and O'Connor, A and McEvoy, N and Lonappan, AM and Venkateswaran, K and Murray, EK and Hallahan, B and Miliotis, G},
title = {Complete genome and comparative genomic analysis of cefpodoxime resistant Pantoea septica strain GABEPS69 isolated from saliva of a patient diagnosed with treatment resistant schizophrenia.},
journal = {International journal of medical microbiology : IJMM},
volume = {321},
number = {},
pages = {151681},
doi = {10.1016/j.ijmm.2025.151681},
pmid = {41192073},
issn = {1618-0607},
abstract = {OBJECTIVES: This study aims to generate the first complete genome of Pantoea septica and provide a thorough genomic characterisation of this under-documented species. The study seeks to enhance understanding of P. septica, clarifying features relevant to opportunistic infection in vulnerable cohorts.
METHODS: P. septica GABEPS69 was an opportunistic coloniser isolated from the saliva of a patient prescribed the antipsychotic clozapine, leading to a dysbiotic oral microbiome. A hybrid sequencing approach yielded a closed genome comprising a 4.1 Mb chromosome and six plasmids. Phenotypic susceptibility was determined by disk-diffusion and minimum inhibitory concentration (MIC) assays. Its chromosomal and plasmidic content was bioinformatically analysed alongside all canonical GenBank available P. septica genomes and the type strains of taxonomic neighbours Pantoea piersonii and "Pantoea latae", with focus on virulence-factors (VFs), antimicrobial-resistance-genes (ARGs), metal-resistance-genes (MRGs) and biosynthetic gene clusters.
RESULTS: GABEPS69 exhibited a narrow resistance spectrum, displaying resistance to the third-generation cephalosporin cefpodoxime. Plasmid pGABEPS69_1 harboured an aerobactin pathogenicity island homologue; a locus implicated in enhanced virulence, that was also identified across most other P. septica genomes and in the closely related human-pathogen Pantoea piersonii. A conserved chromosomal class-A β-lactamase homologue was also identified. Additionally, a universal presence of bioactive thiopeptide biosynthetic-gene-clusters was observed in P. septica genomes, suggesting a potential role in microbiome modulation.
CONCLUSION: This study presents a first complete genome of P. septica, revealing its genomic architecture, resistance, and virulence potential. Detailed plasmid analysis and comparative genomics enhance our understanding of the species clinical relevance and microbiome-modulating capacity. These findings motivate surveillance of transient oral microbiota in at-risk populations, including patients receiving clozapine.},
}
RevDate: 2025-11-05
CmpDate: 2025-11-05
Picoplankton nitrogen guilds in the tropical and subtropical oceans: From the surface to the deep.
PloS one, 20(11):e0335222 pii:PONE-D-25-08884.
Ecological guilds quantify the incidence and extent of resource transformation functions, irrespective of the species involved. Therefore, tackling the microbial nitrogen guilds is key to our understanding of the oceanic nitrogen cycle, but quantitative estimates of guild contribution across varying depths and under specific environmental conditions have yet to be accomplished. In this study, we examine the main picoplankton guilds participating in nitrogen cycling within the low and mid-latitude ocean ecosystems, from the surface down to 4000 m, using data obtained from 75 samples belonging to 11 stations in the Malaspina dataset. In particular, we used a quantitative approach to investigate the stability of nitrogen acquisition and nitrogen-redox guilds separately. Our results showed that nitrogen acquisition guilds are more stable and redundant than nitrogen-redox guilds across depths and site specific conditions. For example, differential conditions such as nitrogen depletion and oxygen availability affected the two groups of guilds in different ways. These findings have implications for the understanding of global nitrogen fluxes and the biosphere's functional diversification.
Additional Links: PMID-41191617
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@article {pmid41191617,
year = {2025},
author = {Rivas-Santisteban, J and Fernández-González, N and Laso-Pérez, R and Tamames, J and Pedrós-Alió, C},
title = {Picoplankton nitrogen guilds in the tropical and subtropical oceans: From the surface to the deep.},
journal = {PloS one},
volume = {20},
number = {11},
pages = {e0335222},
doi = {10.1371/journal.pone.0335222},
pmid = {41191617},
issn = {1932-6203},
mesh = {*Nitrogen/metabolism ; Oceans and Seas ; Ecosystem ; *Nitrogen Cycle ; Tropical Climate ; *Plankton/metabolism ; Seawater/microbiology ; *Phytoplankton/metabolism ; },
abstract = {Ecological guilds quantify the incidence and extent of resource transformation functions, irrespective of the species involved. Therefore, tackling the microbial nitrogen guilds is key to our understanding of the oceanic nitrogen cycle, but quantitative estimates of guild contribution across varying depths and under specific environmental conditions have yet to be accomplished. In this study, we examine the main picoplankton guilds participating in nitrogen cycling within the low and mid-latitude ocean ecosystems, from the surface down to 4000 m, using data obtained from 75 samples belonging to 11 stations in the Malaspina dataset. In particular, we used a quantitative approach to investigate the stability of nitrogen acquisition and nitrogen-redox guilds separately. Our results showed that nitrogen acquisition guilds are more stable and redundant than nitrogen-redox guilds across depths and site specific conditions. For example, differential conditions such as nitrogen depletion and oxygen availability affected the two groups of guilds in different ways. These findings have implications for the understanding of global nitrogen fluxes and the biosphere's functional diversification.},
}
MeSH Terms:
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*Nitrogen/metabolism
Oceans and Seas
Ecosystem
*Nitrogen Cycle
Tropical Climate
*Plankton/metabolism
Seawater/microbiology
*Phytoplankton/metabolism
RevDate: 2025-11-04
CmpDate: 2025-11-05
Exploring Multifaceted Roles of Bambusicolous Apiospora in Phyllostachys bambusoides.
Microbial ecology, 88(1):115.
Bamboo plays a crucial role in mitigating climate change. Among various microorganisms inhabiting bamboo, Apiospora is a common bambusicolous fungus that induces black spots, functioning either as a saprobe or as a plant pathogen. However, the diversity and ecological roles of Apiospora as an endophyte in bamboo remain poorly understood. This study explored the diversity and ecological functions of bambusicolous Apiospora in Phyllostachys bambusoides forests. Bamboo samples representing different stages-young (1-year-old, without black spots), mature (aged 3 years, few black spots), and dead (with many black spots)-were collected. Mycobiome analyses across different tissues (culm, leaf, root) and environmental samples (forest soil) revealed diverse Apiospora species throughout the bamboo lifecycle. Notably, Apiospora hysterina emerged as a prevalent endophyte, inhabiting not only mature but also younger, healthier bamboo stages. Biological activity assays, including antioxidant, antifungal, and plant hormone tests, indicated that A. hysterina exhibits potential mutualistic interactions beneficial to bamboo. Conversely, genomic analyses of carbohydrate-active enzyme profiles, effector/virulence factors, and putative biosynthetic gene clusters suggested potential pathogenic capabilities that may involve secondary metabolites, though functional validation is required. These findings reveal the widespread presence of Apiospora species as endophytes from the early to senescent bamboo stages, highlighting A. hysterina's dual capacity as a symbiont and pathogen. Our study underscores the complexity of bambusicolous Apiospora's ecological roles, emphasizing the need for further investigation into its interactions with bamboo ecosystems.
Additional Links: PMID-41188621
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@article {pmid41188621,
year = {2025},
author = {Kwon, SL and Seo, CW and Kwon, H and Cho, M and Yoo, Y and Lee, SH and Kwon, DY and Lee, YM and Heo, YM and Kim, GH and Lim, YW and Lee, D and Choi, YS and Lee, H and Kim, JJ},
title = {Exploring Multifaceted Roles of Bambusicolous Apiospora in Phyllostachys bambusoides.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {115},
pmid = {41188621},
issn = {1432-184X},
support = {2021R1A2C1011894//National Research Foundation of Korea/ ; PN24120//Korea Polar Research Institute/ ; },
mesh = {*Endophytes/genetics/physiology/classification/isolation & purification ; Symbiosis ; *Ascomycota/genetics/physiology/classification/isolation & purification ; Plant Diseases/microbiology ; Mycobiome ; Soil Microbiology ; Phylogeny ; *Cyperaceae/microbiology ; Plant Roots/microbiology ; },
abstract = {Bamboo plays a crucial role in mitigating climate change. Among various microorganisms inhabiting bamboo, Apiospora is a common bambusicolous fungus that induces black spots, functioning either as a saprobe or as a plant pathogen. However, the diversity and ecological roles of Apiospora as an endophyte in bamboo remain poorly understood. This study explored the diversity and ecological functions of bambusicolous Apiospora in Phyllostachys bambusoides forests. Bamboo samples representing different stages-young (1-year-old, without black spots), mature (aged 3 years, few black spots), and dead (with many black spots)-were collected. Mycobiome analyses across different tissues (culm, leaf, root) and environmental samples (forest soil) revealed diverse Apiospora species throughout the bamboo lifecycle. Notably, Apiospora hysterina emerged as a prevalent endophyte, inhabiting not only mature but also younger, healthier bamboo stages. Biological activity assays, including antioxidant, antifungal, and plant hormone tests, indicated that A. hysterina exhibits potential mutualistic interactions beneficial to bamboo. Conversely, genomic analyses of carbohydrate-active enzyme profiles, effector/virulence factors, and putative biosynthetic gene clusters suggested potential pathogenic capabilities that may involve secondary metabolites, though functional validation is required. These findings reveal the widespread presence of Apiospora species as endophytes from the early to senescent bamboo stages, highlighting A. hysterina's dual capacity as a symbiont and pathogen. Our study underscores the complexity of bambusicolous Apiospora's ecological roles, emphasizing the need for further investigation into its interactions with bamboo ecosystems.},
}
MeSH Terms:
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*Endophytes/genetics/physiology/classification/isolation & purification
Symbiosis
*Ascomycota/genetics/physiology/classification/isolation & purification
Plant Diseases/microbiology
Mycobiome
Soil Microbiology
Phylogeny
*Cyperaceae/microbiology
Plant Roots/microbiology
RevDate: 2025-11-04
CmpDate: 2025-11-04
The Gut Microbial Community of Solitary Bees is Acquired through Host and Location Filtering.
Microbial ecology, 88(1):114.
Species traits and environmental conditions are among the many factors that shape bee communities. Their effective conservation is currently challenged due to global changes. The gut microbiome likely contributes to bee plasticity and resilience but is largely understudied in solitary bees. A stable core microbiome in social bees has been identified to be important for health and survival in changing environmental conditions, but knowledge on a host-specific core microbiome in solitary bees is very scarce. In the present study, we analyzed the gut bacterial and fungal communities of eight solitary bee species commonly found in apple orchards along a latitudinal gradient throughout Europe. We aimed to understand the intra- and interspecific variations in the gut microbial communities and the extent to which host species and local environment shape the solitary bee gut microbiota. The bacterial community showed strong host effects, with each bee species having a distinct core bacterial community that was mostly stable across locations. The fungal community was most strongly influenced by the local environment, while different environmental variables were responsible for the variation in bacterial and fungal communities. Our study demonstrated that the examined solitary bee species harbor a distinct microbial diversity and composition, which undergoes host- and location-specific filtering.
Additional Links: PMID-41188517
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@article {pmid41188517,
year = {2025},
author = {Hettiarachchi, A and Tuerlings, T and Weekers, T and Marshall, L and Leclercq, N and Wood, TJ and Cejas, D and Gerard, M and Vereecken, NJ and Michez, D and Smagghe, G and Joossens, M and Vandamme, P},
title = {The Gut Microbial Community of Solitary Bees is Acquired through Host and Location Filtering.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {114},
pmid = {41188517},
issn = {1432-184X},
support = {3094785//Fonds Wetenschappelijk Onderzoek/ ; 3094785//Fonds De La Recherche Scientifique - FNRS/ ; },
mesh = {Animals ; Bees/microbiology/physiology ; *Gastrointestinal Microbiome ; *Fungi/classification/isolation & purification/genetics ; *Bacteria/classification/genetics/isolation & purification ; Europe ; Biodiversity ; },
abstract = {Species traits and environmental conditions are among the many factors that shape bee communities. Their effective conservation is currently challenged due to global changes. The gut microbiome likely contributes to bee plasticity and resilience but is largely understudied in solitary bees. A stable core microbiome in social bees has been identified to be important for health and survival in changing environmental conditions, but knowledge on a host-specific core microbiome in solitary bees is very scarce. In the present study, we analyzed the gut bacterial and fungal communities of eight solitary bee species commonly found in apple orchards along a latitudinal gradient throughout Europe. We aimed to understand the intra- and interspecific variations in the gut microbial communities and the extent to which host species and local environment shape the solitary bee gut microbiota. The bacterial community showed strong host effects, with each bee species having a distinct core bacterial community that was mostly stable across locations. The fungal community was most strongly influenced by the local environment, while different environmental variables were responsible for the variation in bacterial and fungal communities. Our study demonstrated that the examined solitary bee species harbor a distinct microbial diversity and composition, which undergoes host- and location-specific filtering.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
Animals
Bees/microbiology/physiology
*Gastrointestinal Microbiome
*Fungi/classification/isolation & purification/genetics
*Bacteria/classification/genetics/isolation & purification
Europe
Biodiversity
RevDate: 2025-11-05
CmpDate: 2025-11-05
Genomic diversity and global distribution of four new prasinoviruses from the tropical north Pacific.
Microbiology spectrum, 13(11):e0258324.
Viruses that infect phytoplankton are an integral part of marine ecosystems, but the vast majority of viral diversity remains uncultivated. Here, we introduce four near-complete genomic assemblies of viruses that infect the widespread marine picoeukaryote Micromonas commoda, doubling the number of reported genomes of Micromonas dsDNA viruses. All host and virus isolates were obtained from tropical waters of the North Pacific, a first for viruses infecting green algae in the order Mamiellales. Genome length of the new isolates ranges from 205 to 212 kb, and phylogenetic analysis shows that all four are members of the genus Prasinovirus. Three of the viruses form a clade that is adjacent to previously sequenced Micromonas viruses, while the fourth virus is relatively divergent from previously sequenced prasinoviruses. We identified 61 putative genes not previously found in prasinovirus isolates, including a phosphate transporter and a potential apoptosis inhibitor novel to marine viruses. Forty-eight genes in the new viruses are also found in host genome(s) and may have been acquired through horizontal gene transfer. By analyzing the coding sequences of all published prasinoviruses, we found that ~25% of prasinovirus gene content is significantly correlated with host genus identity (i.e., Micromonas, Ostreococcus, or Bathycoccus), and the functions of these genes suggest that much of the viral life cycle is differentially adapted to the three host genera. Mapping of metagenomic reads from global survey data indicates that one of the new isolates, McV-SA1, is relatively common in multiple ocean basins.IMPORTANCEThe genomes analyzed here represent the first viruses from the tropical North Pacific that infect the abundant phytoplankton order Mamiellales. Comparing isolates from the same location demonstrates high genomic diversity among viruses that co-occur and presumably compete for hosts. Comparing all published prasinovirus genomes highlights gene functions that are likely associated with adaptation to different host genera. Metagenomic data indicate these viruses are globally distributed, and one of the novel isolates may be among the most abundant marine viruses.
Additional Links: PMID-41059692
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@article {pmid41059692,
year = {2025},
author = {Bedi de Silva, A and Polson, SW and Schvarcz, CR and Steward, GF and Edwards, KF},
title = {Genomic diversity and global distribution of four new prasinoviruses from the tropical north Pacific.},
journal = {Microbiology spectrum},
volume = {13},
number = {11},
pages = {e0258324},
pmid = {41059692},
issn = {2165-0497},
support = {1559356, 2129697, 1736030//National Science Foundation/ ; Investigator Award in Marine Microbial Ecology and Evolution//Simons Foundation/ ; },
mesh = {*Genome, Viral/genetics ; Phylogeny ; Pacific Ocean ; *Genetic Variation ; Phytoplankton/virology ; Seawater/virology ; *Chlorophyta/virology ; *Phycodnaviridae/genetics/classification/isolation & purification ; *DNA Viruses/genetics/classification/isolation & purification ; },
abstract = {Viruses that infect phytoplankton are an integral part of marine ecosystems, but the vast majority of viral diversity remains uncultivated. Here, we introduce four near-complete genomic assemblies of viruses that infect the widespread marine picoeukaryote Micromonas commoda, doubling the number of reported genomes of Micromonas dsDNA viruses. All host and virus isolates were obtained from tropical waters of the North Pacific, a first for viruses infecting green algae in the order Mamiellales. Genome length of the new isolates ranges from 205 to 212 kb, and phylogenetic analysis shows that all four are members of the genus Prasinovirus. Three of the viruses form a clade that is adjacent to previously sequenced Micromonas viruses, while the fourth virus is relatively divergent from previously sequenced prasinoviruses. We identified 61 putative genes not previously found in prasinovirus isolates, including a phosphate transporter and a potential apoptosis inhibitor novel to marine viruses. Forty-eight genes in the new viruses are also found in host genome(s) and may have been acquired through horizontal gene transfer. By analyzing the coding sequences of all published prasinoviruses, we found that ~25% of prasinovirus gene content is significantly correlated with host genus identity (i.e., Micromonas, Ostreococcus, or Bathycoccus), and the functions of these genes suggest that much of the viral life cycle is differentially adapted to the three host genera. Mapping of metagenomic reads from global survey data indicates that one of the new isolates, McV-SA1, is relatively common in multiple ocean basins.IMPORTANCEThe genomes analyzed here represent the first viruses from the tropical North Pacific that infect the abundant phytoplankton order Mamiellales. Comparing isolates from the same location demonstrates high genomic diversity among viruses that co-occur and presumably compete for hosts. Comparing all published prasinovirus genomes highlights gene functions that are likely associated with adaptation to different host genera. Metagenomic data indicate these viruses are globally distributed, and one of the novel isolates may be among the most abundant marine viruses.},
}
MeSH Terms:
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*Genome, Viral/genetics
Phylogeny
Pacific Ocean
*Genetic Variation
Phytoplankton/virology
Seawater/virology
*Chlorophyta/virology
*Phycodnaviridae/genetics/classification/isolation & purification
*DNA Viruses/genetics/classification/isolation & purification
RevDate: 2025-11-04
CmpDate: 2025-11-04
Drivers of diversity within and between microbial communities during stochastic assembly.
Journal of the Royal Society, Interface, 22(232):20250329.
No two microbial communities share the same species richness and abundance profiles. Experiments have shown that the assembly of new microbial communities from the same environmental pool is sufficient to generate diversity within and between communities: when microbial dispersal is slower than division, communities exhibit low richness but high between-community dissimilarity; when dispersal is faster, richness increases while dissimilarity decreases. Here, we study a minimal stochastic model that recovers these empirically observed assembly regimes. Our mathematical framework yields explicit expressions for the abundance fluctuation distributions across low-, intermediate- and high-dispersal regimes, providing a quantitative lens on microbiome assembly. We derive analytical predictions for the bimodality coefficient that quantifies the transition between assembly regimes, which appears as a robust metric to predict community richness and dissimilarity. Additionally, we highlight the mean relative abundance as a complementary metric sensitive to differences in microbial traits (e.g. dispersal or division rates). Applying these metrics to experimental data indicates their practical value for the rapid identification of assembly regimes and trait asymmetries. Overall, our study provides general predictions about how stochasticity, timescales and microbial traits influence both within-community diversity (richness) and between-community diversity (dissimilarity) during the assembly of new microbial communities. Our work thus contributes to a better understanding of the factors driving variation in microbiome formation.
Additional Links: PMID-41187907
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@article {pmid41187907,
year = {2025},
author = {Marrec, L and Bank, C},
title = {Drivers of diversity within and between microbial communities during stochastic assembly.},
journal = {Journal of the Royal Society, Interface},
volume = {22},
number = {232},
pages = {20250329},
doi = {10.1098/rsif.2025.0329},
pmid = {41187907},
issn = {1742-5662},
support = {//HORIZON EUROPE European Innovation Council/ ; //Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung/ ; },
mesh = {*Microbiota/physiology ; *Models, Biological ; Stochastic Processes ; *Biodiversity ; },
abstract = {No two microbial communities share the same species richness and abundance profiles. Experiments have shown that the assembly of new microbial communities from the same environmental pool is sufficient to generate diversity within and between communities: when microbial dispersal is slower than division, communities exhibit low richness but high between-community dissimilarity; when dispersal is faster, richness increases while dissimilarity decreases. Here, we study a minimal stochastic model that recovers these empirically observed assembly regimes. Our mathematical framework yields explicit expressions for the abundance fluctuation distributions across low-, intermediate- and high-dispersal regimes, providing a quantitative lens on microbiome assembly. We derive analytical predictions for the bimodality coefficient that quantifies the transition between assembly regimes, which appears as a robust metric to predict community richness and dissimilarity. Additionally, we highlight the mean relative abundance as a complementary metric sensitive to differences in microbial traits (e.g. dispersal or division rates). Applying these metrics to experimental data indicates their practical value for the rapid identification of assembly regimes and trait asymmetries. Overall, our study provides general predictions about how stochasticity, timescales and microbial traits influence both within-community diversity (richness) and between-community diversity (dissimilarity) during the assembly of new microbial communities. Our work thus contributes to a better understanding of the factors driving variation in microbiome formation.},
}
MeSH Terms:
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*Microbiota/physiology
*Models, Biological
Stochastic Processes
*Biodiversity
RevDate: 2025-11-04
CmpDate: 2025-11-04
Microbial community reshaping: Calcium chloride-heat treatment synergy in fresh-cut jackfruit preservation via antagonistic yeast enrichment.
Food research international (Ottawa, Ont.), 221(Pt 4):117558.
Fresh-cut jackfruit is highly susceptible to microbial contamination and rapid spoilage due to mechanical damage and its nutrient-rich substrate. We evaluated calcium chloride combined with heat treatment (CH, 2 % CaCl2 - 55 °C) for controlling spoilage and preservation of fresh-cut jackfruit. The results identified Gilbertella hainanensis, Penicillium kongii, and P. citrinum as the dominant spoilage fungi in fresh-cut jackfruit. CH inhibited these fungi with in vitro inhibition rates of 80.14 %, 43.75 %, and 52.94 %, and corresponding in vivo rates of 83.1 %, 77.9 %, and 83.7 %, respectively. In vitro assays indicated CH compromises fungal membrane integrity, causing leakage of cellular contents. Further analysis revealed that CH markedly increased the relative abundance of the antagonistic yeast Meyerozyma guilliermondii (42.82 %, 8.13-fold vs. control) and was associated with reduced relative abundance of plant pathogenic and saprotrophic fungi. Correlation analysis linked dominant yeast genera to higher total phenolic content and reduced weight loss and other quality deterioration. Overall, CH treatment effectively delayed spoilage and preserved fruit physicochemical and nutritional quality, likely via direct antifungal effects and beneficial reshaping of the surface microbiome. These findings advance understanding of jackfruit postharvest microbial ecology and CH as a promising preservation strategy for fresh-cut jackfruit fruit.
Additional Links: PMID-41185310
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PubMed:
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@article {pmid41185310,
year = {2025},
author = {Wu, S and Li, Y and Zhang, H and Pan, Y and Yang, H and Tan, Y},
title = {Microbial community reshaping: Calcium chloride-heat treatment synergy in fresh-cut jackfruit preservation via antagonistic yeast enrichment.},
journal = {Food research international (Ottawa, Ont.)},
volume = {221},
number = {Pt 4},
pages = {117558},
doi = {10.1016/j.foodres.2025.117558},
pmid = {41185310},
issn = {1873-7145},
mesh = {*Calcium Chloride/pharmacology ; *Food Preservation/methods ; *Hot Temperature ; *Food Microbiology/methods ; *Fruit/microbiology ; *Artocarpus/microbiology ; Penicillium/drug effects/growth & development ; *Yeasts/drug effects/growth & development ; Antibiosis ; },
abstract = {Fresh-cut jackfruit is highly susceptible to microbial contamination and rapid spoilage due to mechanical damage and its nutrient-rich substrate. We evaluated calcium chloride combined with heat treatment (CH, 2 % CaCl2 - 55 °C) for controlling spoilage and preservation of fresh-cut jackfruit. The results identified Gilbertella hainanensis, Penicillium kongii, and P. citrinum as the dominant spoilage fungi in fresh-cut jackfruit. CH inhibited these fungi with in vitro inhibition rates of 80.14 %, 43.75 %, and 52.94 %, and corresponding in vivo rates of 83.1 %, 77.9 %, and 83.7 %, respectively. In vitro assays indicated CH compromises fungal membrane integrity, causing leakage of cellular contents. Further analysis revealed that CH markedly increased the relative abundance of the antagonistic yeast Meyerozyma guilliermondii (42.82 %, 8.13-fold vs. control) and was associated with reduced relative abundance of plant pathogenic and saprotrophic fungi. Correlation analysis linked dominant yeast genera to higher total phenolic content and reduced weight loss and other quality deterioration. Overall, CH treatment effectively delayed spoilage and preserved fruit physicochemical and nutritional quality, likely via direct antifungal effects and beneficial reshaping of the surface microbiome. These findings advance understanding of jackfruit postharvest microbial ecology and CH as a promising preservation strategy for fresh-cut jackfruit fruit.},
}
MeSH Terms:
show MeSH Terms
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*Calcium Chloride/pharmacology
*Food Preservation/methods
*Hot Temperature
*Food Microbiology/methods
*Fruit/microbiology
*Artocarpus/microbiology
Penicillium/drug effects/growth & development
*Yeasts/drug effects/growth & development
Antibiosis
RevDate: 2025-11-03
CmpDate: 2025-11-03
Prokaryotic co-occurrence patterns in diverse Indian mangrove ecosystems.
Scientific reports, 15(1):38283.
Mangrove ecosystems are unique coastal zones known to harbour a rich biodiversity of flora and fauna, including microbial communities. These microorganisms play a crucial role in nutrient cycling and sustain the primary productivity driven by plants within this ecosystem. Recent advancements in microbial ecology research emphasise that microbial community structure and composition are critical for an ecosystem to thrive. Studies have focused on the microbial diversity within Indian mangrove forests; however, there is a limited understanding of the co-occurrence patterns and functional roles of microbial communities in these ecosystems. This study explores prokaryotic diversity, primarily focusing on community interactions across three major Indian mangrove forests: the Bhitarkanika mangrove forest in Odisha, the Goan mangroves, and the Sundarbans in West Bengal. By analysing the publicly available 16 S rRNA amplicon datasets of the Indian mangrove microbiomes and performing co-occurrence network analysis on these datasets, we identified positively correlated genera and their predicted functional roles. Furthermore, the findings revealed the co-occurrence of several pathogenic bacteria in two of the mangrove ecosystems. Overall, our study highlights the shared functional roles adopted by co-occurring microbes in three major Indian mangrove ecosystems and suggests the need for large-scale studies in these understudied Indian ecosystems.
Additional Links: PMID-41184333
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@article {pmid41184333,
year = {2025},
author = {Ghosh, A and Maile, A and Nagarajaram, HA},
title = {Prokaryotic co-occurrence patterns in diverse Indian mangrove ecosystems.},
journal = {Scientific reports},
volume = {15},
number = {1},
pages = {38283},
pmid = {41184333},
issn = {2045-2322},
mesh = {India ; *Wetlands ; Biodiversity ; *Bacteria/genetics/classification/isolation & purification ; *Microbiota/genetics ; RNA, Ribosomal, 16S/genetics ; *Ecosystem ; Phylogeny ; Soil Microbiology ; },
abstract = {Mangrove ecosystems are unique coastal zones known to harbour a rich biodiversity of flora and fauna, including microbial communities. These microorganisms play a crucial role in nutrient cycling and sustain the primary productivity driven by plants within this ecosystem. Recent advancements in microbial ecology research emphasise that microbial community structure and composition are critical for an ecosystem to thrive. Studies have focused on the microbial diversity within Indian mangrove forests; however, there is a limited understanding of the co-occurrence patterns and functional roles of microbial communities in these ecosystems. This study explores prokaryotic diversity, primarily focusing on community interactions across three major Indian mangrove forests: the Bhitarkanika mangrove forest in Odisha, the Goan mangroves, and the Sundarbans in West Bengal. By analysing the publicly available 16 S rRNA amplicon datasets of the Indian mangrove microbiomes and performing co-occurrence network analysis on these datasets, we identified positively correlated genera and their predicted functional roles. Furthermore, the findings revealed the co-occurrence of several pathogenic bacteria in two of the mangrove ecosystems. Overall, our study highlights the shared functional roles adopted by co-occurring microbes in three major Indian mangrove ecosystems and suggests the need for large-scale studies in these understudied Indian ecosystems.},
}
MeSH Terms:
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India
*Wetlands
Biodiversity
*Bacteria/genetics/classification/isolation & purification
*Microbiota/genetics
RNA, Ribosomal, 16S/genetics
*Ecosystem
Phylogeny
Soil Microbiology
RevDate: 2025-11-03
A Scoping Review of Disinfection Strategies for Carbapenemase-Producing Enterobacterales (CPE) in Hospital Water Systems.
The Journal of hospital infection pii:S0195-6701(25)00340-8 [Epub ahead of print].
BACKGROUND: Carbapenemase-producing Enterobacterales (CPE) pose a global health crisis. Their resistance to conventional antimicrobials and many disinfectants, increases the healthcare costs of treatment and risk mitigation. Hospital water systems are reservoirs for CPE, necessitating targeted infection prevention and control (IPC) strategies.
OBJECTIVE: To review and consolidate current evidence of disinfection strategies for CPE in hospital water systems, focusing on practical application, challenges and IPC integration.
METHODOLOGY: A scoping review was conducted following PRISMA guidelines, encompassing studies from 1[st] December 2014 to 31[st] December 2024. Of 1,188 records screened, 22 met inclusion criteria. Thematic analysis categorised findings into chemical, physical and integrative strategies.
KEY FINDINGS: Sodium hypochlorite and hydrogen peroxide reduced contamination temporarily but were poorly effective against biofilms, while acetic acid showed consistent efficacy with regular use. Quaternary ammonium compounds proved effective but required standardised protocols. Physical interventions, such as steam cleaning and drain covers, reduced contamination; and plumbing modifications minimised biofilm formation. Resource-intensive measures, like removing contaminated sinks or adopting water-free environments were also effective. Integrative approaches combining chemical disinfection, infrastructural upgrades and enhanced sink protocols demonstrated the most sustained outcomes, with novel technologies like UV light and biofilm-targeting foams showing great promise.
CONCLUSION: Effective CPE control in hospital water systems requires multidisciplinary action addressing biofilm-protected reservoirs. Regular application of proven disinfectants, tailored to specific contexts, coupled with infrastructural upgrades and comprehensively implemented IPC strategies, offers the most promising outcomes. Novel technologies and updated guidelines are essential to standardising practices and mitigating the broader threat of antimicrobial resistance.
Additional Links: PMID-41183683
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PubMed:
Citation:
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@article {pmid41183683,
year = {2025},
author = {Ali, S and Burke, LP and Fitzpatrick, F and Fitzgerald-Hughes, D},
title = {A Scoping Review of Disinfection Strategies for Carbapenemase-Producing Enterobacterales (CPE) in Hospital Water Systems.},
journal = {The Journal of hospital infection},
volume = {},
number = {},
pages = {},
doi = {10.1016/j.jhin.2025.10.021},
pmid = {41183683},
issn = {1532-2939},
abstract = {BACKGROUND: Carbapenemase-producing Enterobacterales (CPE) pose a global health crisis. Their resistance to conventional antimicrobials and many disinfectants, increases the healthcare costs of treatment and risk mitigation. Hospital water systems are reservoirs for CPE, necessitating targeted infection prevention and control (IPC) strategies.
OBJECTIVE: To review and consolidate current evidence of disinfection strategies for CPE in hospital water systems, focusing on practical application, challenges and IPC integration.
METHODOLOGY: A scoping review was conducted following PRISMA guidelines, encompassing studies from 1[st] December 2014 to 31[st] December 2024. Of 1,188 records screened, 22 met inclusion criteria. Thematic analysis categorised findings into chemical, physical and integrative strategies.
KEY FINDINGS: Sodium hypochlorite and hydrogen peroxide reduced contamination temporarily but were poorly effective against biofilms, while acetic acid showed consistent efficacy with regular use. Quaternary ammonium compounds proved effective but required standardised protocols. Physical interventions, such as steam cleaning and drain covers, reduced contamination; and plumbing modifications minimised biofilm formation. Resource-intensive measures, like removing contaminated sinks or adopting water-free environments were also effective. Integrative approaches combining chemical disinfection, infrastructural upgrades and enhanced sink protocols demonstrated the most sustained outcomes, with novel technologies like UV light and biofilm-targeting foams showing great promise.
CONCLUSION: Effective CPE control in hospital water systems requires multidisciplinary action addressing biofilm-protected reservoirs. Regular application of proven disinfectants, tailored to specific contexts, coupled with infrastructural upgrades and comprehensively implemented IPC strategies, offers the most promising outcomes. Novel technologies and updated guidelines are essential to standardising practices and mitigating the broader threat of antimicrobial resistance.},
}
RevDate: 2025-11-03
CmpDate: 2025-11-03
FastST: an efficient tool for inferring decomposition and directionality of microbial communities.
PeerJ, 13:e20161.
Microbiomes play crucial roles in human health, disease development, and global ecosystem functioning. Understanding the origins, movements, and compositions of microbial communities is essential for unraveling the principles governing microbial ecology. Microbial source tracking (MST) approaches have emerged as valuable tools for quantifying the proportions of different microbial sources within target communities, enabling researchers to track transmissions between hosts and environments, identify similarities between microbiome samples, and determine sources of contamination in various settings. Current MST methods like SourceTracker2 and FEAST have advanced the field by employing Bayesian and expectation-maximization approaches, respectively, but are limited by computational inefficiency with high-dimensional data and inability to infer directionality in source-sink relationships. This study presents a novel computational framework for microbial source tracking called FastST. FastST infers the relative contributions of source environments to sink microbiomes while also determining directionality when source-sink relationships are not predefined. Through extensive simulation studies with varying numbers of sources and complexity, FastST demonstrates superior performance in both accuracy and computational efficiency compared to FEAST and SourceTracker2, maintaining consistent execution times even as the number of source environments increases. Furthermore, the proposed method achieved over 90% accuracy in directionality inference across all tested scenarios, even when multiple major sources are present, broadening its applicability in practical microbiome research and environmental monitoring. FastST and data simulation codes are publicly available at https://github.com/joungmin-choi/FastST.
Additional Links: PMID-41180493
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@article {pmid41180493,
year = {2025},
author = {Choi, JM and Wu, X and Zhang, L},
title = {FastST: an efficient tool for inferring decomposition and directionality of microbial communities.},
journal = {PeerJ},
volume = {13},
number = {},
pages = {e20161},
pmid = {41180493},
issn = {2167-8359},
mesh = {*Microbiota ; Humans ; Bayes Theorem ; Computer Simulation ; *Software ; *Computational Biology/methods ; },
abstract = {Microbiomes play crucial roles in human health, disease development, and global ecosystem functioning. Understanding the origins, movements, and compositions of microbial communities is essential for unraveling the principles governing microbial ecology. Microbial source tracking (MST) approaches have emerged as valuable tools for quantifying the proportions of different microbial sources within target communities, enabling researchers to track transmissions between hosts and environments, identify similarities between microbiome samples, and determine sources of contamination in various settings. Current MST methods like SourceTracker2 and FEAST have advanced the field by employing Bayesian and expectation-maximization approaches, respectively, but are limited by computational inefficiency with high-dimensional data and inability to infer directionality in source-sink relationships. This study presents a novel computational framework for microbial source tracking called FastST. FastST infers the relative contributions of source environments to sink microbiomes while also determining directionality when source-sink relationships are not predefined. Through extensive simulation studies with varying numbers of sources and complexity, FastST demonstrates superior performance in both accuracy and computational efficiency compared to FEAST and SourceTracker2, maintaining consistent execution times even as the number of source environments increases. Furthermore, the proposed method achieved over 90% accuracy in directionality inference across all tested scenarios, even when multiple major sources are present, broadening its applicability in practical microbiome research and environmental monitoring. FastST and data simulation codes are publicly available at https://github.com/joungmin-choi/FastST.},
}
MeSH Terms:
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*Microbiota
Humans
Bayes Theorem
Computer Simulation
*Software
*Computational Biology/methods
RevDate: 2025-11-03
CmpDate: 2025-11-03
Microbial cross contamination in household laundering and microbial ecology of household washing machines.
Frontiers in microbiology, 16:1667606.
Household washing machines host diverse microbial communities that may include opportunistic pathogens, potentially impacting laundry hygiene and human health. However, our understanding of these communities and their transfer abilities remains limited. We examined microbial communities from 10 household washing machines (five front-load and five top-load) using surface swabs from specific hotspots and sterile sentinel washcloths. Samples were analyzed using culture-based methods and 16S rRNA/ITS metabarcoding. We tested microbial transfer during washing cycles with and without clothing and evaluated the effects of machine drying on this transfer. Front-load machines had significantly higher microbial loads than top-load machines (average bacterial counts: 6.50 ± 2.46 Log10/swab vs. 3.79 ± 1.73 Log10/swab). The microbial community composition was mainly shaped by the machine user rather than the machine type or sampling location. The dominant bacterial genera included Pseudomonas, Micrococcus, and Sphingomonas, while Aspergillus, Cladosporium, and Penicillium dominated the fungal communities. Opportunistic microorganisms were identified, but no highly pathogenic species (pathogenicity score 3) were found. Machine drying did not significantly decrease microbial loads, whereas the presence of soiled clothing impacted community composition. Household washing machines host user-specific microbial communities, including potential opportunistic pathogens. Current laundry practices may be inadequate for the complete elimination of pathogens, especially in immunocompromised individuals. These results support the need for additional household laundry sanitization strategies.
Additional Links: PMID-41178963
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@article {pmid41178963,
year = {2025},
author = {Whitehead, K and Eppinger, J and Srinivasan, V and Ugalde, JA},
title = {Microbial cross contamination in household laundering and microbial ecology of household washing machines.},
journal = {Frontiers in microbiology},
volume = {16},
number = {},
pages = {1667606},
pmid = {41178963},
issn = {1664-302X},
abstract = {Household washing machines host diverse microbial communities that may include opportunistic pathogens, potentially impacting laundry hygiene and human health. However, our understanding of these communities and their transfer abilities remains limited. We examined microbial communities from 10 household washing machines (five front-load and five top-load) using surface swabs from specific hotspots and sterile sentinel washcloths. Samples were analyzed using culture-based methods and 16S rRNA/ITS metabarcoding. We tested microbial transfer during washing cycles with and without clothing and evaluated the effects of machine drying on this transfer. Front-load machines had significantly higher microbial loads than top-load machines (average bacterial counts: 6.50 ± 2.46 Log10/swab vs. 3.79 ± 1.73 Log10/swab). The microbial community composition was mainly shaped by the machine user rather than the machine type or sampling location. The dominant bacterial genera included Pseudomonas, Micrococcus, and Sphingomonas, while Aspergillus, Cladosporium, and Penicillium dominated the fungal communities. Opportunistic microorganisms were identified, but no highly pathogenic species (pathogenicity score 3) were found. Machine drying did not significantly decrease microbial loads, whereas the presence of soiled clothing impacted community composition. Household washing machines host user-specific microbial communities, including potential opportunistic pathogens. Current laundry practices may be inadequate for the complete elimination of pathogens, especially in immunocompromised individuals. These results support the need for additional household laundry sanitization strategies.},
}
RevDate: 2025-11-02
Impact of freeze-thaw cycle on metagenomics in subsurface wastewater infiltration systems: Ecological implications for greenhouse gas emissions.
Journal of environmental management, 395:127839 pii:S0301-4797(25)03815-0 [Epub ahead of print].
Nitrous oxide (N2O) is a potent greenhouse gas, with a global warming potential 273 times that of carbon dioxide (CO2) and is a significant byproduct of wastewater treatment. Subsurface wastewater infiltration systems (SWIS) effectively treat nitrate-rich wastewater but can also contribute to N2O emissions, particularly during freeze-thaw cycles. This study used metagenomics and [15]N isotope tracing to investigate the impacts of freeze-thaw on microbial ecology and nitrogen transformation in SWIS. Results show that freeze-thaw significantly increased abundances of denitrifying bacteria (Bradyrhizobium, Streptomyces and Nocardioides), on average, by 16-63 %. Denitrification genes (nirK and norB) were also increased by 40 ± 16 % and 22 ± 5 %, while the N2O reductase gene (nosZ) decreased by 19 ± 0.46 %. These impacts collectively increased N2O emissions by more than 20 %. During freezing, about one-third of the added [15]NO3[-]-N was recovered as gas (25 % as N2O and 13 % as N2), increasing to 43 % during thawing (29 % N2O and 15 % N2). This study underscores the need for targeted strategies N2O emission in SWIS, particularly under freeze-thaw conditions, to maximize their sustainability in wastewater treatment.
Additional Links: PMID-41177050
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PubMed:
Citation:
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@article {pmid41177050,
year = {2025},
author = {Su, F and Li, Y and Zhu, C and Gurmesa, GA and Fang, Y},
title = {Impact of freeze-thaw cycle on metagenomics in subsurface wastewater infiltration systems: Ecological implications for greenhouse gas emissions.},
journal = {Journal of environmental management},
volume = {395},
number = {},
pages = {127839},
doi = {10.1016/j.jenvman.2025.127839},
pmid = {41177050},
issn = {1095-8630},
abstract = {Nitrous oxide (N2O) is a potent greenhouse gas, with a global warming potential 273 times that of carbon dioxide (CO2) and is a significant byproduct of wastewater treatment. Subsurface wastewater infiltration systems (SWIS) effectively treat nitrate-rich wastewater but can also contribute to N2O emissions, particularly during freeze-thaw cycles. This study used metagenomics and [15]N isotope tracing to investigate the impacts of freeze-thaw on microbial ecology and nitrogen transformation in SWIS. Results show that freeze-thaw significantly increased abundances of denitrifying bacteria (Bradyrhizobium, Streptomyces and Nocardioides), on average, by 16-63 %. Denitrification genes (nirK and norB) were also increased by 40 ± 16 % and 22 ± 5 %, while the N2O reductase gene (nosZ) decreased by 19 ± 0.46 %. These impacts collectively increased N2O emissions by more than 20 %. During freezing, about one-third of the added [15]NO3[-]-N was recovered as gas (25 % as N2O and 13 % as N2), increasing to 43 % during thawing (29 % N2O and 15 % N2). This study underscores the need for targeted strategies N2O emission in SWIS, particularly under freeze-thaw conditions, to maximize their sustainability in wastewater treatment.},
}
RevDate: 2025-11-01
Fermentation induced changes in physicochemical properties, antioxidant activity, total sugars, and comprehensive polyphenolic profiles of the Rhododendron-infused wine blends.
Food chemistry, 496(Pt 2):146743 pii:S0308-8146(25)03995-0 [Epub ahead of print].
This study evaluated the sensory, physicochemical, and functional attributes of seven experimental wine formulations incorporating apple juice, ginger, honey or sucrose, and varying levels of Rhododendron arboreum flower juice. Sensory scores revealed significant improvements in color, aroma and sweetness in rhododendron-enriched blends, with Treatment T7 (apple + honey + ginger + R. arboreum) achieving the highest overall acceptability. Physicochemical analyses showed variations in titratable acidity (0.19-0.51 %), alcohol (9.50-11.97 %), and ascorbic acid (4.76-8.53 mg/100 mL), influenced by substrate composition and sweetener type. Inclusion of R. arboreum substantially enhanced total phenolic (up to 19.78 mg GAE/mL) and flavonoid levels (25.84 mg QE/mL) alongside targeted compounds such as quercetin and caffeic acid. Antioxidant assays also confirmed superior radical scavenging activity. Multivariate analyses highlighted strong correlations between polyphenolic content and antioxidant performance. Overall, R. arboreum addition improved both sensory appeal and functional properties, supporting its potential in functional wine development.
Additional Links: PMID-41175425
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@article {pmid41175425,
year = {2025},
author = {Awasthi, A and Sandal, A and Mahajan, R and Kaundal, R and Sharma, N and Sharma, S},
title = {Fermentation induced changes in physicochemical properties, antioxidant activity, total sugars, and comprehensive polyphenolic profiles of the Rhododendron-infused wine blends.},
journal = {Food chemistry},
volume = {496},
number = {Pt 2},
pages = {146743},
doi = {10.1016/j.foodchem.2025.146743},
pmid = {41175425},
issn = {1873-7072},
abstract = {This study evaluated the sensory, physicochemical, and functional attributes of seven experimental wine formulations incorporating apple juice, ginger, honey or sucrose, and varying levels of Rhododendron arboreum flower juice. Sensory scores revealed significant improvements in color, aroma and sweetness in rhododendron-enriched blends, with Treatment T7 (apple + honey + ginger + R. arboreum) achieving the highest overall acceptability. Physicochemical analyses showed variations in titratable acidity (0.19-0.51 %), alcohol (9.50-11.97 %), and ascorbic acid (4.76-8.53 mg/100 mL), influenced by substrate composition and sweetener type. Inclusion of R. arboreum substantially enhanced total phenolic (up to 19.78 mg GAE/mL) and flavonoid levels (25.84 mg QE/mL) alongside targeted compounds such as quercetin and caffeic acid. Antioxidant assays also confirmed superior radical scavenging activity. Multivariate analyses highlighted strong correlations between polyphenolic content and antioxidant performance. Overall, R. arboreum addition improved both sensory appeal and functional properties, supporting its potential in functional wine development.},
}
RevDate: 2025-11-01
CmpDate: 2025-11-01
Serotonin modulation of metabolism and stress response in Pseudomonas fluorescens.
BMC biology, 23(1):330.
BACKGROUND: Pseudomonas fluorescens is a Gram-negative bacterium with a remarkable metabolic and physiological versatility that enables it to adapt and colonize diverse ecological niches, including the human small intestine. While serotonin is primarily found in high concentrations in gut tissue, its levels in the lumen can be elevated in conditions such as celiac disease, where P. fluorescens is also found in increased abundance. The potential effects of serotonin on P. fluorescens in such contexts remain unclear.
RESULTS: We demonstrate that P. fluorescens metabolizes serotonin primarily into 5-hydroxyindole-3-acetic acid (5-HIAA) and, to a lesser extent, into 5-hydroxytryptophol and N-acetylserotonin. Gene expression analysis revealed significant changes in oxidative stress-related pathways over time, and proteomic analysis confirmed the shifts seen particularly in amino acid catabolic pathways. Serotonin metabolism also enhanced bacterial resistance to oxidative stress, suggesting a protective role.
CONCLUSIONS: The findings reveal a novel mechanism by which serotonin modulates the metabolism and stress responses of P. fluorescens. This study provides insight into how P. fluorescens adapts to serotonin-rich environments, such as in celiac disease, and may inform future research on microbial interactions with host-derived metabolites in disease contexts.
Additional Links: PMID-41174663
PubMed:
Citation:
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@article {pmid41174663,
year = {2025},
author = {Waclawiková, B and Schwalbe, M and Ilyaskina, D and Toptas, S and Thome, NU and Du, C and Elsayed, SS and de Jong, A and van Wezel, GP and El Aidy, S},
title = {Serotonin modulation of metabolism and stress response in Pseudomonas fluorescens.},
journal = {BMC biology},
volume = {23},
number = {1},
pages = {330},
pmid = {41174663},
issn = {1741-7007},
mesh = {*Pseudomonas fluorescens/metabolism/physiology/genetics ; *Serotonin/metabolism/analogs & derivatives ; Oxidative Stress ; *Stress, Physiological ; },
abstract = {BACKGROUND: Pseudomonas fluorescens is a Gram-negative bacterium with a remarkable metabolic and physiological versatility that enables it to adapt and colonize diverse ecological niches, including the human small intestine. While serotonin is primarily found in high concentrations in gut tissue, its levels in the lumen can be elevated in conditions such as celiac disease, where P. fluorescens is also found in increased abundance. The potential effects of serotonin on P. fluorescens in such contexts remain unclear.
RESULTS: We demonstrate that P. fluorescens metabolizes serotonin primarily into 5-hydroxyindole-3-acetic acid (5-HIAA) and, to a lesser extent, into 5-hydroxytryptophol and N-acetylserotonin. Gene expression analysis revealed significant changes in oxidative stress-related pathways over time, and proteomic analysis confirmed the shifts seen particularly in amino acid catabolic pathways. Serotonin metabolism also enhanced bacterial resistance to oxidative stress, suggesting a protective role.
CONCLUSIONS: The findings reveal a novel mechanism by which serotonin modulates the metabolism and stress responses of P. fluorescens. This study provides insight into how P. fluorescens adapts to serotonin-rich environments, such as in celiac disease, and may inform future research on microbial interactions with host-derived metabolites in disease contexts.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Pseudomonas fluorescens/metabolism/physiology/genetics
*Serotonin/metabolism/analogs & derivatives
Oxidative Stress
*Stress, Physiological
RevDate: 2025-11-01
CmpDate: 2025-11-01
Physicochemical, Structural, and Proteomic Insights into Drinking Water-Isolated Acinetobacter calcoaceticus Aggregation and Biofilm Dynamics.
Microbial ecology, 88(1):113.
Acinetobacter calcoaceticus, a ubiquitous Gram-negative bacterium, exhibits remarkable adaptability across diverse environments, including drinking water distribution systems (DWDS), where its biofilm-forming and coaggregation capabilities pose significant public health challenges. This study integrates physicochemical, structural, and proteomic analyses to elucidate the mechanisms underlying A. calcoaceticus aggregation and biofilm dynamics. Surface characterization through contact angle measurements, zeta potential, and co-adhesion energy assessments revealed a predominantly hydrophilic surface with strong electron donor properties and a highly negative charge, promoting intercellular adhesion. Transmission electron microscopy unveiled dense cellular aggregates with extracellular filamentous structures, indicative of enhanced cell-to-cell interactions and potential extracellular polymeric substance involvement. Proteomic profiling identified 2593 differentially expressed proteins between aggregation stages, highlighting metabolic shifts, stress response activation, and upregulation of biofilm-associated proteins, including chaperones and quorum-sensing regulators. Our multidisciplinary approach emphasizes the importance of surface characterization in understanding bacterial community and underscores the critical role of physicochemical properties and proteomic flexibility in A. calcoaceticus biofilm and aggregation ability.
Additional Links: PMID-41174295
PubMed:
Citation:
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@article {pmid41174295,
year = {2025},
author = {Afonso, AC and Simões, M and Saavedra, MJ and Simões, L and Lema, JM and Trueba-Santiso, A},
title = {Physicochemical, Structural, and Proteomic Insights into Drinking Water-Isolated Acinetobacter calcoaceticus Aggregation and Biofilm Dynamics.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {113},
pmid = {41174295},
issn = {1432-184X},
mesh = {*Biofilms/growth & development ; Proteomics ; Bacterial Proteins/metabolism/genetics ; *Acinetobacter calcoaceticus/physiology/isolation & purification/genetics ; *Drinking Water/microbiology ; *Bacterial Adhesion ; Proteome ; },
abstract = {Acinetobacter calcoaceticus, a ubiquitous Gram-negative bacterium, exhibits remarkable adaptability across diverse environments, including drinking water distribution systems (DWDS), where its biofilm-forming and coaggregation capabilities pose significant public health challenges. This study integrates physicochemical, structural, and proteomic analyses to elucidate the mechanisms underlying A. calcoaceticus aggregation and biofilm dynamics. Surface characterization through contact angle measurements, zeta potential, and co-adhesion energy assessments revealed a predominantly hydrophilic surface with strong electron donor properties and a highly negative charge, promoting intercellular adhesion. Transmission electron microscopy unveiled dense cellular aggregates with extracellular filamentous structures, indicative of enhanced cell-to-cell interactions and potential extracellular polymeric substance involvement. Proteomic profiling identified 2593 differentially expressed proteins between aggregation stages, highlighting metabolic shifts, stress response activation, and upregulation of biofilm-associated proteins, including chaperones and quorum-sensing regulators. Our multidisciplinary approach emphasizes the importance of surface characterization in understanding bacterial community and underscores the critical role of physicochemical properties and proteomic flexibility in A. calcoaceticus biofilm and aggregation ability.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Biofilms/growth & development
Proteomics
Bacterial Proteins/metabolism/genetics
*Acinetobacter calcoaceticus/physiology/isolation & purification/genetics
*Drinking Water/microbiology
*Bacterial Adhesion
Proteome
RevDate: 2025-11-01
Biogenic Amine Degradation by Lactic Acid Bacteria Isolated from Home-Made White Cheese: Molecular and HPLC-Based Assessment.
Probiotics and antimicrobial proteins [Epub ahead of print].
Due to the potential health risks to humans associated with biogenic amines (BAs) accumulation in cheeses and other foods, this study is the first of its kind on Erzurum home-made white cheese to investigate the presence of BA-degrading lactic acid bacteria (LAB). Polymerase chain reaction (PCR) was applied for all putative LAB strains to detect the presence of (hdcA, cadA, tdcA, and odc) genes responsible for BA formation (histamine, cadaverine, tyramine, and putrescine, respectively). Only 72% of all strains showed amplicons for hdcA and tdcA, and no strains were found to have cadA, ldc, and odc genes. High-performance liquid chromatography (HPLC) analysis confirmed these findings. Furthermore, 12% of BA-nonproducing LAB have the sufI gene responsible for Multicopper Oxidases (MCOs) production. HPLC analysis was then applied to these strains to investigate their ability to degrade BAs. Nine strains were found to have degradation abilities with optimal conditions at pH 4.5-5.5 and 32-37 °C. Importantly, analysis of twenty home-made white cheeses revealed that the levels of BAs were within safe limits. This research provides valuable insights into the microbial ecology of these cheeses and highlights the potential of utilizing indigenous LAB for controlling BA formation and improving cheese quality.
Additional Links: PMID-41174268
PubMed:
Citation:
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@article {pmid41174268,
year = {2025},
author = {Almansour, A and Akkaya, SN and Akbulut, S and Adiguzel, G and Yilmaz, B and Adiguzel, A},
title = {Biogenic Amine Degradation by Lactic Acid Bacteria Isolated from Home-Made White Cheese: Molecular and HPLC-Based Assessment.},
journal = {Probiotics and antimicrobial proteins},
volume = {},
number = {},
pages = {},
pmid = {41174268},
issn = {1867-1314},
abstract = {Due to the potential health risks to humans associated with biogenic amines (BAs) accumulation in cheeses and other foods, this study is the first of its kind on Erzurum home-made white cheese to investigate the presence of BA-degrading lactic acid bacteria (LAB). Polymerase chain reaction (PCR) was applied for all putative LAB strains to detect the presence of (hdcA, cadA, tdcA, and odc) genes responsible for BA formation (histamine, cadaverine, tyramine, and putrescine, respectively). Only 72% of all strains showed amplicons for hdcA and tdcA, and no strains were found to have cadA, ldc, and odc genes. High-performance liquid chromatography (HPLC) analysis confirmed these findings. Furthermore, 12% of BA-nonproducing LAB have the sufI gene responsible for Multicopper Oxidases (MCOs) production. HPLC analysis was then applied to these strains to investigate their ability to degrade BAs. Nine strains were found to have degradation abilities with optimal conditions at pH 4.5-5.5 and 32-37 °C. Importantly, analysis of twenty home-made white cheeses revealed that the levels of BAs were within safe limits. This research provides valuable insights into the microbial ecology of these cheeses and highlights the potential of utilizing indigenous LAB for controlling BA formation and improving cheese quality.},
}
RevDate: 2025-10-31
Ocean-M: an integrated global-scale multi-omics database for marine microbial diversity, function and ecological interactions.
Nucleic acids research pii:8307366 [Epub ahead of print].
Multi-omics analyses have significantly advanced the understanding of complex marine microbial communities and their interactions. Despite notable progress from recent large-scale ocean meta-analysis efforts, the effective integration and accessibility of these diverse datasets remain challenging. To address this, we introduce Ocean-M (http://om.qnlm.ac), a comprehensive and publicly accessible platform for marine microbial multi-omics data integration, analysis, and visualization. Ocean-M provides a systematic view of 54 083 high-quality metagenome-assembled genomes, including genome assembly statistics, genome clustering, gene annotation, and interactive tools for global-scale taxonomic profiling. The platform also incorporates microbial community networks, host-microbiome interactions, and environmental DNA datasets to support an integrated ecological framework for studying microbial interactions and ecosystem functions. Additionally, Ocean-M enables large-scale mining of ecologically and biotechnologically important genes, with curated catalogs of 151 798 biosynthetic gene clusters, 52 699 antibiotic resistance genes, and millions of carbohydrate-active enzymes and plastic-active enzymes. By combining multi-omics data with environmental metadata, Ocean-M serves as a valuable resource for advancing marine microbial ecology, global biogeography, and functional gene discovery.
Additional Links: PMID-41171124
Publisher:
PubMed:
Citation:
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@article {pmid41171124,
year = {2025},
author = {Lv, J and Ma, S and Ma, C and Liu, F and Duan, X and Huang, X and Geng, Q and Liu, F and Li, G and Li, Y and Wang, J and Li, C and Zheng, H and Zhang, Y and Sun, Z and Wang, J and Fan, G and Huang, S and Zhang, L and Bao, Z and Wang, S},
title = {Ocean-M: an integrated global-scale multi-omics database for marine microbial diversity, function and ecological interactions.},
journal = {Nucleic acids research},
volume = {},
number = {},
pages = {},
doi = {10.1093/nar/gkaf1098},
pmid = {41171124},
issn = {1362-4962},
support = {2024YFC2816000//National Key Research and Development Program of China/ ; LSKJ202202804//Marine S&T Fund of Shandong Province for Laoshan Laboratory/ ; 2025B1111180001//Guangdong Provincial Key Areas R&D Program Project/ ; SOLZSKY2025013//Hainan Province Science and Technology Special Fund/ ; 32573498//Natural Science Foundation of China/ ; 32222085//Natural Science Foundation of China/ ; QDLYY-2024011//Blue Seed Industry Science and Technology Innovation Project/ ; GZB20250215//Postdoctoral Fellowship Program of CPSF/ ; },
abstract = {Multi-omics analyses have significantly advanced the understanding of complex marine microbial communities and their interactions. Despite notable progress from recent large-scale ocean meta-analysis efforts, the effective integration and accessibility of these diverse datasets remain challenging. To address this, we introduce Ocean-M (http://om.qnlm.ac), a comprehensive and publicly accessible platform for marine microbial multi-omics data integration, analysis, and visualization. Ocean-M provides a systematic view of 54 083 high-quality metagenome-assembled genomes, including genome assembly statistics, genome clustering, gene annotation, and interactive tools for global-scale taxonomic profiling. The platform also incorporates microbial community networks, host-microbiome interactions, and environmental DNA datasets to support an integrated ecological framework for studying microbial interactions and ecosystem functions. Additionally, Ocean-M enables large-scale mining of ecologically and biotechnologically important genes, with curated catalogs of 151 798 biosynthetic gene clusters, 52 699 antibiotic resistance genes, and millions of carbohydrate-active enzymes and plastic-active enzymes. By combining multi-omics data with environmental metadata, Ocean-M serves as a valuable resource for advancing marine microbial ecology, global biogeography, and functional gene discovery.},
}
RevDate: 2025-10-31
Dietary Prebiotics Modulate Omeprazole-Induced Alterations in the Gut Microbial Signature.
Molecular nutrition & food research [Epub ahead of print].
Proton pump inhibitors (PPIs) are commonly used to treat heartburn and acid-related disorders. However, their misuse and prolonged use contribute to gut dysbiosis. This study investigated whether well-known prebiotic dietary sources, blueberries or strawberries, can reverse PPI (omeprazole) induced dysbiosis and gut inflammation by modulating gut microbes. Male C57BL/6J mice (7 weeks old) were fed a diet with or without omeprazole (40 mg/kg diet), blueberry (3.7% in the diet; ∼1.5 human servings) or strawberry (2.35% in the diet; ∼2 human servings) for 12 weeks. Metabolic parameters, gut microbes (in the cecum and colon), and inflammatory markers were assessed. In this study, no changes were observed in metabolic parameters in mice fed a diet supplemented with omeprazole or berries. Second, blueberry or strawberry supplementation at nutritional dosages improved alterations in gut microbial ecology induced by omeprazole, with effects varying between the cecum and colon. Third, strawberry supplementation reduced omeprazole-induced gut inflammation. Fourth, selected genera were either positively or negatively associated with markers of gut inflammation, suggesting that dietary berries can ameliorate inflammatory signaling through modifications in the gut microbiome. Dietary berries represent a potential nutritional strategy for improving PPI-induced gut dysbiosis and inflammation.
Additional Links: PMID-41169038
Publisher:
PubMed:
Citation:
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@article {pmid41169038,
year = {2025},
author = {Buccola, MJ and Satheesh Babu, AK and Paz, HA and Porter, ND and Srinivasan, H and Ricks, RL and Rosquist, K and Torres, JL and Zhong, Y and Jalili, T and Wankhade, UD and Anandh Babu, PV},
title = {Dietary Prebiotics Modulate Omeprazole-Induced Alterations in the Gut Microbial Signature.},
journal = {Molecular nutrition & food research},
volume = {},
number = {},
pages = {e70307},
doi = {10.1002/mnfr.70307},
pmid = {41169038},
issn = {1613-4133},
abstract = {Proton pump inhibitors (PPIs) are commonly used to treat heartburn and acid-related disorders. However, their misuse and prolonged use contribute to gut dysbiosis. This study investigated whether well-known prebiotic dietary sources, blueberries or strawberries, can reverse PPI (omeprazole) induced dysbiosis and gut inflammation by modulating gut microbes. Male C57BL/6J mice (7 weeks old) were fed a diet with or without omeprazole (40 mg/kg diet), blueberry (3.7% in the diet; ∼1.5 human servings) or strawberry (2.35% in the diet; ∼2 human servings) for 12 weeks. Metabolic parameters, gut microbes (in the cecum and colon), and inflammatory markers were assessed. In this study, no changes were observed in metabolic parameters in mice fed a diet supplemented with omeprazole or berries. Second, blueberry or strawberry supplementation at nutritional dosages improved alterations in gut microbial ecology induced by omeprazole, with effects varying between the cecum and colon. Third, strawberry supplementation reduced omeprazole-induced gut inflammation. Fourth, selected genera were either positively or negatively associated with markers of gut inflammation, suggesting that dietary berries can ameliorate inflammatory signaling through modifications in the gut microbiome. Dietary berries represent a potential nutritional strategy for improving PPI-induced gut dysbiosis and inflammation.},
}
RevDate: 2025-10-31
CmpDate: 2025-10-31
Shifts in Microbial Thermal Traits Mitigate Heat-Induced Carbon Losses in Soils.
Global change biology, 31(11):e70579.
Global warming is expected to transfer carbon from soil organic matter to atmospheric CO2, with microbial communities playing a crucial role in regulating this exchange. While the immediate impact of temperature on microbial functions is well understood and causes soil carbon losses, the long-term response remains unclear, with losses stabilising over time, reducing the overall effect of chronic warming on soil organic carbon (SOC) stocks. Here, we examined the temperature dependence of microbial respiration and growth after 9 years of +5°C warming in a temperate forest. Using these temperature dependences and field temperature data, we modelled in situ carbon fluxes and changes in SOC stocks. Results showed that the direct effect of temperature initially increased respiration and growth, projecting a potential 31% SOC stock loss if the trend had persisted. However, the gradual optimisation of microbial traits to warming balanced the direct temperature effects, enhanced carbon use efficiency and offset CO2 emissions. Together, these microbial trait shifts limited the heat-induced SOC loss to 15%, closely aligning with empirical observations. These findings suggest that microbial trait optimisation can moderate carbon emissions, providing a parsimonious mechanistic explanation for observations worldwide and underscoring the need to integrate microbial dynamics into models.
Additional Links: PMID-41168937
Publisher:
PubMed:
Citation:
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@article {pmid41168937,
year = {2025},
author = {BrangarÃ, AC and Knorr, MA and Frey, SD and Rousk, J},
title = {Shifts in Microbial Thermal Traits Mitigate Heat-Induced Carbon Losses in Soils.},
journal = {Global change biology},
volume = {31},
number = {11},
pages = {e70579},
doi = {10.1111/gcb.70579},
pmid = {41168937},
issn = {1365-2486},
support = {2022-01478//Svenska Forskningsrådet Formas/ ; CTS 22: 2131//Carl Tryggers Stiftelse för Vetenskaplig Forskning/ ; KAW 2022.0175//Knut och Alice Wallenbergs Stiftelse/ ; KAW 2023.0384//Knut och Alice Wallenbergs Stiftelse/ ; DEB-1832110//National Science Foundation/ ; DEB-1456610//National Science Foundation/ ; },
mesh = {*Soil Microbiology ; *Soil/chemistry ; *Hot Temperature ; *Carbon/metabolism/analysis ; *Global Warming ; *Carbon Cycle ; Carbon Dioxide/metabolism ; Forests ; },
abstract = {Global warming is expected to transfer carbon from soil organic matter to atmospheric CO2, with microbial communities playing a crucial role in regulating this exchange. While the immediate impact of temperature on microbial functions is well understood and causes soil carbon losses, the long-term response remains unclear, with losses stabilising over time, reducing the overall effect of chronic warming on soil organic carbon (SOC) stocks. Here, we examined the temperature dependence of microbial respiration and growth after 9 years of +5°C warming in a temperate forest. Using these temperature dependences and field temperature data, we modelled in situ carbon fluxes and changes in SOC stocks. Results showed that the direct effect of temperature initially increased respiration and growth, projecting a potential 31% SOC stock loss if the trend had persisted. However, the gradual optimisation of microbial traits to warming balanced the direct temperature effects, enhanced carbon use efficiency and offset CO2 emissions. Together, these microbial trait shifts limited the heat-induced SOC loss to 15%, closely aligning with empirical observations. These findings suggest that microbial trait optimisation can moderate carbon emissions, providing a parsimonious mechanistic explanation for observations worldwide and underscoring the need to integrate microbial dynamics into models.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Soil Microbiology
*Soil/chemistry
*Hot Temperature
*Carbon/metabolism/analysis
*Global Warming
*Carbon Cycle
Carbon Dioxide/metabolism
Forests
RevDate: 2025-10-31
CmpDate: 2025-10-31
Host species and geographic location shape microbial diversity and functional potential in the conifer needle microbiome.
Microbiome, 13(1):222.
BACKGROUND: The aerial surface of plants, known as the phyllosphere, hosts a complex and dynamic microbiome that plays essential roles in plant health and environmental processes. While research has focused on root-associated microbiomes, the phyllosphere remains comparatively understudied, especially in forest ecosystems. Despite the global ecological dominance and importance of conifers, no previous study has applied shotgun metagenomics to their phyllosphere microbiomes.
RESULTS: This study uses metagenomic sequencing to explore the microbial phyllosphere communities of subalpine Western conifer needle surfaces from 67 trees at six sites spanning the Rocky Mountains, including 31 limber pine, 18 Douglas fir, and 18 Engelmann spruce. Sites span ~ 1,075 km and nearly 10° latitude, from Glacier National Park to Rocky Mountain Biological Laboratory, capturing broad environmental variation. Metagenomes were generated for each of the 67 samples, for which we produced individual assemblies, along with three large coassemblies specific to each conifer host. From these datasets, we reconstructed 447 metagenome-assembled genomes (MAGs), 417 of which are non-redundant at the species level. Beyond increasing the total number of extracted MAGs from 153 to 294, the three coassemblies yielded three large MAGs, representing partial sequences of host genomes. Phylogenomics of all microbial MAGs revealed communities predominantly composed of bacteria (n = 327) and fungi (n = 117). We show that both microbial community composition and metabolic potential differ significantly across host tree species and geographic sites, with site exerting a stronger influence than host.
CONCLUSIONS: This dataset offers new insights into the microbial communities inhabiting the conifer needle surface, laying the foundation for future research on needle microbiomes across temporal and spatial scales. Variation in functional capabilities, such as volatile organic compound (VOC) degradation and polysaccharide metabolism, closely tracks shifts in taxonomic composition, indicating that host-specific chemistry, local environmental factors, and regional microbial source pools jointly shape ecological roles. Moreover, the observed patterns of mobile genetic elements and horizontal gene transfer suggest that gene exchange predominantly occurs within microbial lineages, with occasional broader transfers dispersing key functional genes (e.g., those involved in polysaccharide metabolism), which may facilitate microbiome adaptation.
Additional Links: PMID-41168882
PubMed:
Citation:
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@article {pmid41168882,
year = {2025},
author = {Bowers, RM and Bennett, S and Riley, R and Villada, JC and Da Silva, IR and Woyke, T and Frank, AC},
title = {Host species and geographic location shape microbial diversity and functional potential in the conifer needle microbiome.},
journal = {Microbiome},
volume = {13},
number = {1},
pages = {222},
pmid = {41168882},
issn = {2049-2618},
support = {10.46936/10.25585/60000936//U.S. Department of Energy/ ; DEB-1442348//Directorate for Biological Sciences/ ; },
mesh = {*Microbiota/genetics ; *Bacteria/classification/genetics/isolation & purification ; Metagenomics/methods ; *Tracheophyta/microbiology ; Metagenome ; Phylogeny ; *Plant Leaves/microbiology ; Pinus/microbiology ; },
abstract = {BACKGROUND: The aerial surface of plants, known as the phyllosphere, hosts a complex and dynamic microbiome that plays essential roles in plant health and environmental processes. While research has focused on root-associated microbiomes, the phyllosphere remains comparatively understudied, especially in forest ecosystems. Despite the global ecological dominance and importance of conifers, no previous study has applied shotgun metagenomics to their phyllosphere microbiomes.
RESULTS: This study uses metagenomic sequencing to explore the microbial phyllosphere communities of subalpine Western conifer needle surfaces from 67 trees at six sites spanning the Rocky Mountains, including 31 limber pine, 18 Douglas fir, and 18 Engelmann spruce. Sites span ~ 1,075 km and nearly 10° latitude, from Glacier National Park to Rocky Mountain Biological Laboratory, capturing broad environmental variation. Metagenomes were generated for each of the 67 samples, for which we produced individual assemblies, along with three large coassemblies specific to each conifer host. From these datasets, we reconstructed 447 metagenome-assembled genomes (MAGs), 417 of which are non-redundant at the species level. Beyond increasing the total number of extracted MAGs from 153 to 294, the three coassemblies yielded three large MAGs, representing partial sequences of host genomes. Phylogenomics of all microbial MAGs revealed communities predominantly composed of bacteria (n = 327) and fungi (n = 117). We show that both microbial community composition and metabolic potential differ significantly across host tree species and geographic sites, with site exerting a stronger influence than host.
CONCLUSIONS: This dataset offers new insights into the microbial communities inhabiting the conifer needle surface, laying the foundation for future research on needle microbiomes across temporal and spatial scales. Variation in functional capabilities, such as volatile organic compound (VOC) degradation and polysaccharide metabolism, closely tracks shifts in taxonomic composition, indicating that host-specific chemistry, local environmental factors, and regional microbial source pools jointly shape ecological roles. Moreover, the observed patterns of mobile genetic elements and horizontal gene transfer suggest that gene exchange predominantly occurs within microbial lineages, with occasional broader transfers dispersing key functional genes (e.g., those involved in polysaccharide metabolism), which may facilitate microbiome adaptation.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Microbiota/genetics
*Bacteria/classification/genetics/isolation & purification
Metagenomics/methods
*Tracheophyta/microbiology
Metagenome
Phylogeny
*Plant Leaves/microbiology
Pinus/microbiology
RevDate: 2025-10-31
From clonality to complexity: a journey through microbial ecology and evolution.
Nature reviews. Genetics [Epub ahead of print].
Additional Links: PMID-41168506
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Citation:
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@article {pmid41168506,
year = {2025},
author = {Martinez-Urtaza, J},
title = {From clonality to complexity: a journey through microbial ecology and evolution.},
journal = {Nature reviews. Genetics},
volume = {},
number = {},
pages = {},
pmid = {41168506},
issn = {1471-0064},
}
RevDate: 2025-10-30
Differential recovery of chain-elongating bacteria: comparing droplet, plating, and dilution-to-extinction methods.
mSystems [Epub ahead of print].
Microbial chain elongation via reverse β-oxidation offers a more sustainable route to produce medium-chain fatty acids like caproate, commodity chemicals typically produced via (petro)chemical processes. Thermophilic anaerobic microbiomes allow production at a high rate and selectivity but remain poorly understood due to the limited cultivability of their members. To better access functional taxa from a thermophilic chain-elongating reactor community, we applied multiple isolation strategies: conventional anaerobic plating, dilution-to-extinction (DTE), droplet-based microfluidics, and fluorescence-activated cell sorting (FACS). We evaluated the taxonomic range and cultivation success of each method using 16S rRNA gene sequencing. Each method yielded a distinct subset of microbial taxa. While Clostridium acetireducens-related strains were consistently isolated across all strategies, key thermophilic chain elongators (e.g., Thermocaproicibacter melissae-like organisms) only appeared in DTE. Droplet microfluidics enriched the most unique taxa in total, mostly rare taxa, including Caproicibacter and Thermoanaerobacterium spp. Plating yielded the lowest diversity, recovering only dominant taxa. FACS-based approaches failed to yield isolates, likely due to stress during processing. Comparing droplet-based isolation to DTE revealed critical insights: although droplets offer higher throughput, which intrinsically increases the chance of capturing rare taxa, not all DTE-cultivated organisms grew in droplets. This suggests additional contributing factors (apart from an increased throughput), such as encapsulation stress and droplet-specific microenvironments. These findings clarify the advantages and limitations of droplet cultivation strategies, allowing a more informed application of these techniques to access the so-called "microbial dark matter."IMPORTANCEMany environmentally and industrially relevant microbes remain uncultured, limiting our ability to understand and use them. This is especially true in thermophilic anaerobic microbiomes, which are promising systems for producing sustainable chemicals from organic waste streams. In this study, we explored how different cultivation strategies influence which microbes can be isolated from a thermophilic chain-elongating reactor. By comparing traditional and novel methods, including droplet microfluidics, we showed that each method recovers a unique set of microbes. While droplet-based methods enable high sampling depth with minimal effort and excel at isolating rare microbes, we found that they also introduce clear biases, as certain organisms recovered by other methods did not grow in droplets. Our work highlights the importance of the cultivation method in isolation success and helps shine a light on the selective forces at play in droplet-based microbial isolation.
Additional Links: PMID-41165314
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PubMed:
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@article {pmid41165314,
year = {2025},
author = {Nauwynck, W and Sakarika, M and Faust, K and Boon, N},
title = {Differential recovery of chain-elongating bacteria: comparing droplet, plating, and dilution-to-extinction methods.},
journal = {mSystems},
volume = {},
number = {},
pages = {e0135625},
doi = {10.1128/msystems.01356-25},
pmid = {41165314},
issn = {2379-5077},
abstract = {Microbial chain elongation via reverse β-oxidation offers a more sustainable route to produce medium-chain fatty acids like caproate, commodity chemicals typically produced via (petro)chemical processes. Thermophilic anaerobic microbiomes allow production at a high rate and selectivity but remain poorly understood due to the limited cultivability of their members. To better access functional taxa from a thermophilic chain-elongating reactor community, we applied multiple isolation strategies: conventional anaerobic plating, dilution-to-extinction (DTE), droplet-based microfluidics, and fluorescence-activated cell sorting (FACS). We evaluated the taxonomic range and cultivation success of each method using 16S rRNA gene sequencing. Each method yielded a distinct subset of microbial taxa. While Clostridium acetireducens-related strains were consistently isolated across all strategies, key thermophilic chain elongators (e.g., Thermocaproicibacter melissae-like organisms) only appeared in DTE. Droplet microfluidics enriched the most unique taxa in total, mostly rare taxa, including Caproicibacter and Thermoanaerobacterium spp. Plating yielded the lowest diversity, recovering only dominant taxa. FACS-based approaches failed to yield isolates, likely due to stress during processing. Comparing droplet-based isolation to DTE revealed critical insights: although droplets offer higher throughput, which intrinsically increases the chance of capturing rare taxa, not all DTE-cultivated organisms grew in droplets. This suggests additional contributing factors (apart from an increased throughput), such as encapsulation stress and droplet-specific microenvironments. These findings clarify the advantages and limitations of droplet cultivation strategies, allowing a more informed application of these techniques to access the so-called "microbial dark matter."IMPORTANCEMany environmentally and industrially relevant microbes remain uncultured, limiting our ability to understand and use them. This is especially true in thermophilic anaerobic microbiomes, which are promising systems for producing sustainable chemicals from organic waste streams. In this study, we explored how different cultivation strategies influence which microbes can be isolated from a thermophilic chain-elongating reactor. By comparing traditional and novel methods, including droplet microfluidics, we showed that each method recovers a unique set of microbes. While droplet-based methods enable high sampling depth with minimal effort and excel at isolating rare microbes, we found that they also introduce clear biases, as certain organisms recovered by other methods did not grow in droplets. Our work highlights the importance of the cultivation method in isolation success and helps shine a light on the selective forces at play in droplet-based microbial isolation.},
}
RevDate: 2025-10-30
A Novel Protistan Trait Database Reveals Functional Redundancy and Complementarity in Terrestrial Protists (Amoebozoa and Rhizaria).
Molecular ecology resources [Epub ahead of print].
The inclusion of functional traits of protists in environmental sequencing surveys, in addition to the traditional taxonomic framework, is essential for a better understanding of their roles and impacts on ecosystem processes. We provide a database of functional traits for a widespread and important clade of protists-the Amoebozoa-based on extensive literature research in eight trait categories: Habitat, locomotion, nutrition, morphology, morphotype, size, spore formation, and disease-relatedness. The comparison of community traits of the Amoebozoa with sympatric but highly divergent Cercozoa (Rhizaria) revealed both convergent evolution of morphology or locomotion and distinct differences in habitat preference and feeding selectivity. Amoebozoa seem to be rather unselective in their prey choice compared to Cercozoa. Indeed, the feeding preferences of Amoebozoa appeared to be related to cell size, whereas Cercozoa selectively feed on prey. Applications to metatranscriptomic data from soil, litter, and bark surfaces revealed differences in the average community trait compositions and ecosystem functioning, such as an increased proportion of disease-related Amoebozoa in soil or different proportions of nutrition types of Amoebozoa and Cercozoa on bark. This database will facilitate ecological analyses of sequencing data and improve our understanding of the diversity of adaptations of Amoebozoa to the environment and their functional roles in ecosystems.
Additional Links: PMID-41165014
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@article {pmid41165014,
year = {2025},
author = {Freudenthal, J and Schlegel, M and Bonkowski, M and Dumack, K},
title = {A Novel Protistan Trait Database Reveals Functional Redundancy and Complementarity in Terrestrial Protists (Amoebozoa and Rhizaria).},
journal = {Molecular ecology resources},
volume = {},
number = {},
pages = {e70064},
doi = {10.1111/1755-0998.70064},
pmid = {41165014},
issn = {1755-0998},
support = {221301018//Deutsche Forschungsgemeinschaft/ ; 447013012//Deutsche Forschungsgemeinschaft/ ; SPP 1991//Deutsche Forschungsgemeinschaft/ ; },
abstract = {The inclusion of functional traits of protists in environmental sequencing surveys, in addition to the traditional taxonomic framework, is essential for a better understanding of their roles and impacts on ecosystem processes. We provide a database of functional traits for a widespread and important clade of protists-the Amoebozoa-based on extensive literature research in eight trait categories: Habitat, locomotion, nutrition, morphology, morphotype, size, spore formation, and disease-relatedness. The comparison of community traits of the Amoebozoa with sympatric but highly divergent Cercozoa (Rhizaria) revealed both convergent evolution of morphology or locomotion and distinct differences in habitat preference and feeding selectivity. Amoebozoa seem to be rather unselective in their prey choice compared to Cercozoa. Indeed, the feeding preferences of Amoebozoa appeared to be related to cell size, whereas Cercozoa selectively feed on prey. Applications to metatranscriptomic data from soil, litter, and bark surfaces revealed differences in the average community trait compositions and ecosystem functioning, such as an increased proportion of disease-related Amoebozoa in soil or different proportions of nutrition types of Amoebozoa and Cercozoa on bark. This database will facilitate ecological analyses of sequencing data and improve our understanding of the diversity of adaptations of Amoebozoa to the environment and their functional roles in ecosystems.},
}
RevDate: 2025-10-30
CmpDate: 2025-10-30
Assembly and co-occurrence networks of nitrogen-fixing bacteria associated with epiphyllous liverworts in fragmented tropical forests.
ISME communications, 5(1):ycaf173.
Understanding the spatial dynamics of plant-associated microbial communities is increasingly urgent in the context of habitat loss and the biodiversity crisis. However, the influence of reduced habitat size and connectivity on the assembly mechanisms underlying microbial associations is fundamental to advancing microbial ecology and conservation. In the Brazilian Amazon, we investigated nitrogen-fixing (diazotrophic) bacterial communities associated with two epiphyllous liverworts, Cololejeunea surinamensis and Radula flaccida, across 11 forest sites within the Biological Dynamics of Forest Fragments Project landscape. Using amplicon sequencing targeting the nitrogenase gene (nifH), we characterized diazotroph community diversity, inferred assembly mechanisms through null models, and analyzed co-occurrence network structure. Host-specific associations were evident: C. surinamensis predominantly hosted Hassallia, while R. flaccida was primarily associated with Fischerella. Despite habitat fragmentation, diazotrophic richness and composition remained similar across habitats of different sizes, consistent with strong homogenizing dispersal. Network analyses revealed that smaller fragments harbored more modular communities with fewer module hubs, pronounced shifts in key species relative abundance, and reduced network robustness. Our findings underscore the influence of habitat size on the stability of liverwort-associated diazotrophs, with smaller fragments exhibiting lower key species specificity and disruption of microbe-microbe interactions. Our results emphasize the importance of conserving large, connected forest habitats to maintain the functional integrity of phyllosphere N-fixing microbiota.
Additional Links: PMID-41164406
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@article {pmid41164406,
year = {2025},
author = {Sierra, AM and Escolástico-Ortiz, DA and Zartman, CE and Derome, N and Lovejoy, C and Villarreal A, JC},
title = {Assembly and co-occurrence networks of nitrogen-fixing bacteria associated with epiphyllous liverworts in fragmented tropical forests.},
journal = {ISME communications},
volume = {5},
number = {1},
pages = {ycaf173},
pmid = {41164406},
issn = {2730-6151},
abstract = {Understanding the spatial dynamics of plant-associated microbial communities is increasingly urgent in the context of habitat loss and the biodiversity crisis. However, the influence of reduced habitat size and connectivity on the assembly mechanisms underlying microbial associations is fundamental to advancing microbial ecology and conservation. In the Brazilian Amazon, we investigated nitrogen-fixing (diazotrophic) bacterial communities associated with two epiphyllous liverworts, Cololejeunea surinamensis and Radula flaccida, across 11 forest sites within the Biological Dynamics of Forest Fragments Project landscape. Using amplicon sequencing targeting the nitrogenase gene (nifH), we characterized diazotroph community diversity, inferred assembly mechanisms through null models, and analyzed co-occurrence network structure. Host-specific associations were evident: C. surinamensis predominantly hosted Hassallia, while R. flaccida was primarily associated with Fischerella. Despite habitat fragmentation, diazotrophic richness and composition remained similar across habitats of different sizes, consistent with strong homogenizing dispersal. Network analyses revealed that smaller fragments harbored more modular communities with fewer module hubs, pronounced shifts in key species relative abundance, and reduced network robustness. Our findings underscore the influence of habitat size on the stability of liverwort-associated diazotrophs, with smaller fragments exhibiting lower key species specificity and disruption of microbe-microbe interactions. Our results emphasize the importance of conserving large, connected forest habitats to maintain the functional integrity of phyllosphere N-fixing microbiota.},
}
RevDate: 2025-10-30
CmpDate: 2025-10-30
Correction: Phase angle associates with severity and mortality in acute-on-chronic liver failure.
Frontiers in medicine, 12:1695643.
[This corrects the article DOI: 10.3389/fmed.2025.1541795.].
Additional Links: PMID-41164176
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@article {pmid41164176,
year = {2025},
author = {Cai, S and Lin, L and Cai, Y and Wang, C and Lin, Y and Zhou, J and Zhou, F and Chen, M},
title = {Correction: Phase angle associates with severity and mortality in acute-on-chronic liver failure.},
journal = {Frontiers in medicine},
volume = {12},
number = {},
pages = {1695643},
doi = {10.3389/fmed.2025.1695643},
pmid = {41164176},
issn = {2296-858X},
abstract = {[This corrects the article DOI: 10.3389/fmed.2025.1541795.].},
}
RevDate: 2025-10-30
CmpDate: 2025-10-30
Thermomonospora spp. are implicated in the biodegradation of long-chain aliphatic polyester bioplastics during thermophilic composting.
Frontiers in microbiology, 16:1671731.
Biodegradable plastics are an important component for achieving a circular polymer economy. To be considered biodegradable at the regulatory level, plastics must pass standardized tests, for example under industrial composting conditions at 58 °C (ISO 14855-1). Although such tests are frequently applied, little is known about the microorganisms catalyzing these degradation processes. Recently, bioplastics with properties similar to polyethylene, Long-Chain Aliphatic Polyesters (LCAP), for example polyester 1,18-octadecanediol-alt-1,18-octadecanedioic acid (abbreviated PE-18,18), were shown to biodegrade under industrial composting conditions. In this work, we analyzed the microbial communities that had developed in the compost treatments at the end of the biodegradation test for three different LCAPs (PE-18,18, PE-12,12 and PE-2,18) relative to the untreated controls, via amplicon-sequencing of bacterial 16S and fungal ITS2 rDNA. This revealed significant treatment-induced shifts in the bacterial communities (p < 0.05), with Pseudonocardia and Thermomonospora ASVs enriched in all LCAP-treated samples compared to the controls (p ≤ 0.0001), while no pronounced shifts were observed for the fungal community. Thermomonospora sequences showed high similarity to T. curvata DSM43183, which encodes the known polyester hydrolase Tcur1278, and the presence of gene tcur1278 was confirmed in LCAP-treated samples via PCR. Enzyme assays with heterologously expressed and partially purified Tcur1278 demonstrated its activity on PE-2,18 LCAP, releasing up to 230 μmol of soluble monomers over 48 h at 50 °C. Hence, our study implicated Thermomonospora species in LCAP degradation during thermophilic composting, based on taxonomic enrichment, and provided evidence linking the detected phylotypes to Tcur1278, the first bacterial enzyme demonstrated to depolymerize LCAP. It thereby is the first evidence for an ecological relevance of Tcur1278-encoding Thermomonospora phylotypes for bioplastic degradation in situ.
Additional Links: PMID-41164007
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@article {pmid41164007,
year = {2025},
author = {Lerner, H and Eck, M and Link, C and Witt, T and Battagliarin, G and Mecking, S and Schleheck, D},
title = {Thermomonospora spp. are implicated in the biodegradation of long-chain aliphatic polyester bioplastics during thermophilic composting.},
journal = {Frontiers in microbiology},
volume = {16},
number = {},
pages = {1671731},
pmid = {41164007},
issn = {1664-302X},
abstract = {Biodegradable plastics are an important component for achieving a circular polymer economy. To be considered biodegradable at the regulatory level, plastics must pass standardized tests, for example under industrial composting conditions at 58 °C (ISO 14855-1). Although such tests are frequently applied, little is known about the microorganisms catalyzing these degradation processes. Recently, bioplastics with properties similar to polyethylene, Long-Chain Aliphatic Polyesters (LCAP), for example polyester 1,18-octadecanediol-alt-1,18-octadecanedioic acid (abbreviated PE-18,18), were shown to biodegrade under industrial composting conditions. In this work, we analyzed the microbial communities that had developed in the compost treatments at the end of the biodegradation test for three different LCAPs (PE-18,18, PE-12,12 and PE-2,18) relative to the untreated controls, via amplicon-sequencing of bacterial 16S and fungal ITS2 rDNA. This revealed significant treatment-induced shifts in the bacterial communities (p < 0.05), with Pseudonocardia and Thermomonospora ASVs enriched in all LCAP-treated samples compared to the controls (p ≤ 0.0001), while no pronounced shifts were observed for the fungal community. Thermomonospora sequences showed high similarity to T. curvata DSM43183, which encodes the known polyester hydrolase Tcur1278, and the presence of gene tcur1278 was confirmed in LCAP-treated samples via PCR. Enzyme assays with heterologously expressed and partially purified Tcur1278 demonstrated its activity on PE-2,18 LCAP, releasing up to 230 μmol of soluble monomers over 48 h at 50 °C. Hence, our study implicated Thermomonospora species in LCAP degradation during thermophilic composting, based on taxonomic enrichment, and provided evidence linking the detected phylotypes to Tcur1278, the first bacterial enzyme demonstrated to depolymerize LCAP. It thereby is the first evidence for an ecological relevance of Tcur1278-encoding Thermomonospora phylotypes for bioplastic degradation in situ.},
}
RevDate: 2025-10-29
The contribution of the Midichloria mitochondrii endosymbiont to Borrelia infection dynamics.
Trends in parasitology pii:S1471-4922(25)00293-4 [Epub ahead of print].
Recent studies have revealed a positive correlation between the presence of the Midichloria mitochondrii endosymbiont and Borrelia species in the tick vector, suggesting potential interactions that may influence pathogen infection and the transmission dynamics of Lyme borreliosis. This article discusses the possible mechanistic pathways underlying these interactions.
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@article {pmid41162221,
year = {2025},
author = {Hodžić, A},
title = {The contribution of the Midichloria mitochondrii endosymbiont to Borrelia infection dynamics.},
journal = {Trends in parasitology},
volume = {},
number = {},
pages = {},
doi = {10.1016/j.pt.2025.10.003},
pmid = {41162221},
issn = {1471-5007},
abstract = {Recent studies have revealed a positive correlation between the presence of the Midichloria mitochondrii endosymbiont and Borrelia species in the tick vector, suggesting potential interactions that may influence pathogen infection and the transmission dynamics of Lyme borreliosis. This article discusses the possible mechanistic pathways underlying these interactions.},
}
RevDate: 2025-10-29
CmpDate: 2025-10-29
The domestic cat microbiome: mapping knowledge gaps through scientometric analysis in feline microbial research.
Veterinary research communications, 50(1):6.
In this study, we present the first comprehensive scientometric analysis of research on the domestic cat microbiome, providing a transparent and data-driven overview of the field. We examined 282 publications on the microbiome of domestic cats (Felis catus) to uncover dominant research themes, methodological patterns, microbial niches, and knowledge gaps. Our results reveal a sharp rise in publications since 2012, with a peak in 2024, where most work is concentrated in high-income countries and driven by a small number of academic institutions. Current efforts are heavily focused on the bacterial gut microbiome, typically using genomic tools for taxonomic profiling in comparative designs. In contrast, research on other microbial communities (e.g., oral or skin), non-bacterial taxa, functional analyses, and behavioural outcomes remains scarce, with behavioural studies virtually absent. Although some studies report health-related effects, mainly positive or neutral, the functional roles of the microbiota and their possible influence on feline behaviour remain largely unexplored. By mapping these trends and gaps, our study provides a strategic framework for advancing microbiome research in domestic cats. These findings highlight priority areas and methodological opportunities that can guide future investigations, foster interdisciplinary collaboration, and ultimately deepen our understanding of the intricate links between microbial ecology, feline health, and behaviour. Studies connecting the microbiome with feline diseases, behaviour, and diet are strongly encouraged, given their high applicability to everyday animal care and management. Such research has the potential to improve both feline health and welfare, while also strengthening the human-cat bond.
Additional Links: PMID-41160321
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@article {pmid41160321,
year = {2025},
author = {de Azevedo, CS and Schork, IG and Passos, LF and Goodhead, I and Young, RJ},
title = {The domestic cat microbiome: mapping knowledge gaps through scientometric analysis in feline microbial research.},
journal = {Veterinary research communications},
volume = {50},
number = {1},
pages = {6},
pmid = {41160321},
issn = {1573-7446},
mesh = {Animals ; Cats/microbiology ; *Microbiota ; *Gastrointestinal Microbiome ; },
abstract = {In this study, we present the first comprehensive scientometric analysis of research on the domestic cat microbiome, providing a transparent and data-driven overview of the field. We examined 282 publications on the microbiome of domestic cats (Felis catus) to uncover dominant research themes, methodological patterns, microbial niches, and knowledge gaps. Our results reveal a sharp rise in publications since 2012, with a peak in 2024, where most work is concentrated in high-income countries and driven by a small number of academic institutions. Current efforts are heavily focused on the bacterial gut microbiome, typically using genomic tools for taxonomic profiling in comparative designs. In contrast, research on other microbial communities (e.g., oral or skin), non-bacterial taxa, functional analyses, and behavioural outcomes remains scarce, with behavioural studies virtually absent. Although some studies report health-related effects, mainly positive or neutral, the functional roles of the microbiota and their possible influence on feline behaviour remain largely unexplored. By mapping these trends and gaps, our study provides a strategic framework for advancing microbiome research in domestic cats. These findings highlight priority areas and methodological opportunities that can guide future investigations, foster interdisciplinary collaboration, and ultimately deepen our understanding of the intricate links between microbial ecology, feline health, and behaviour. Studies connecting the microbiome with feline diseases, behaviour, and diet are strongly encouraged, given their high applicability to everyday animal care and management. Such research has the potential to improve both feline health and welfare, while also strengthening the human-cat bond.},
}
MeSH Terms:
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Animals
Cats/microbiology
*Microbiota
*Gastrointestinal Microbiome
RevDate: 2025-10-29
Selective Decontamination of the Digestive Tract during Ventilation in the ICU.
The New England journal of medicine [Epub ahead of print].
BACKGROUND: Whether selective decontamination of the digestive tract (SDD) reduces mortality among patients undergoing mechanical ventilation and whether it adversely affects microbial ecology in the intensive care unit (ICU) remain unclear. In an earlier analysis of data from Australia, SDD did not result in a lower incidence of in-hospital death than standard care, but data from the full international trial are needed.
METHODS: We randomly assigned ICUs in Australia and Canada to use SDD or to continue standard care for two 12-month periods in patients undergoing mechanical ventilation. Patients in the SDD group received specific oral and gastric antimicrobial interventions for the duration of ventilation and an intravenous antibiotic agent for the first 4 days after enrollment. All other patients in the ICU were included in an observational ecologic assessment. Previously reported data from Australia are now combined with data from Canada. The primary outcome was in-hospital death from any cause at 90 days. The secondary clinical outcomes, assessed at 90 days, were death in the ICU and the number of days alive and free of mechanical ventilation, ICU admission, and hospitalization. Microbiologic secondary outcomes included new positive cultures for bloodstream infections and antibiotic-resistant organisms. For the ecologic assessment, the microbiologic outcomes were tested for noninferiority (noninferiority margin, 2 percentage points).
RESULTS: In this trial involving 20,000 patients in 26 ICUs, 9289 patients were enrolled in the randomized trial and 10,711 were included in the ecologic assessment. At 90 days, 1175 of 4215 patients (27.9%) in the SDD group and 1494 of 5065 (29.5%) in the standard-care group had died before hospital discharge (odds ratio, 0.93; 95% confidence interval [CI], 0.84 to 1.05; P = 0.27). New bloodstream infections occurred in 4.9% of the patients in the SDD group and in 6.8% of those in the standard-care group (adjusted mean difference, -1.30 percentage points; 95% CI, -2.55 to -0.05); antibiotic-resistant organisms were cultured in 16.8% and 26.8%, respectively (adjusted mean difference, -9.60 percentage points; 95% CI, -12.40 to -6.80). In the ecologic assessment, noninferiority of SDD was not confirmed for the development of new antibiotic-resistant organisms. Adverse events considered to be related to SDD or standard care were reported in 12 patients (0.3%) in the SDD group and in no patients in the standard-care group. Serious adverse events occurred in 47 patients (1.1%) and 59 patients (1.2%), respectively.
CONCLUSIONS: Among critically ill patients undergoing mechanical ventilation, SDD did not result in a lower incidence of in-hospital death than standard care. (Funded by the National Health and Medical Research Council of Australia and the Canadian Institutes of Health Research; ClinicalTrials.gov number, NCT02389036.).
Additional Links: PMID-41159880
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@article {pmid41159880,
year = {2025},
author = {, and Cuthbertson, BH and Billot, L and Campbell, MK and Daneman, N and Davis, JS and Delaney, A and Devaux, A and Ferguson, ND and Finfer, SR and Fowler, R and Gordon, AC and Hammond, NE and Klein, G and Li, Q and Marshall, J and Micallef, S and Murthy, S and Mysore, J and Naik, C and Patel, C and Pinto, R and Rose, L and Seppelt, IM and Venkatesh, B and Young, PJ and Myburgh, JA},
title = {Selective Decontamination of the Digestive Tract during Ventilation in the ICU.},
journal = {The New England journal of medicine},
volume = {},
number = {},
pages = {},
doi = {10.1056/NEJMoa2506398},
pmid = {41159880},
issn = {1533-4406},
support = {1084244//National Health and Medical Research Council/ ; MYG-151210/CAPMC/CIHR/Canada ; PJT-153367/CAPMC/CIHR/Canada ; },
abstract = {BACKGROUND: Whether selective decontamination of the digestive tract (SDD) reduces mortality among patients undergoing mechanical ventilation and whether it adversely affects microbial ecology in the intensive care unit (ICU) remain unclear. In an earlier analysis of data from Australia, SDD did not result in a lower incidence of in-hospital death than standard care, but data from the full international trial are needed.
METHODS: We randomly assigned ICUs in Australia and Canada to use SDD or to continue standard care for two 12-month periods in patients undergoing mechanical ventilation. Patients in the SDD group received specific oral and gastric antimicrobial interventions for the duration of ventilation and an intravenous antibiotic agent for the first 4 days after enrollment. All other patients in the ICU were included in an observational ecologic assessment. Previously reported data from Australia are now combined with data from Canada. The primary outcome was in-hospital death from any cause at 90 days. The secondary clinical outcomes, assessed at 90 days, were death in the ICU and the number of days alive and free of mechanical ventilation, ICU admission, and hospitalization. Microbiologic secondary outcomes included new positive cultures for bloodstream infections and antibiotic-resistant organisms. For the ecologic assessment, the microbiologic outcomes were tested for noninferiority (noninferiority margin, 2 percentage points).
RESULTS: In this trial involving 20,000 patients in 26 ICUs, 9289 patients were enrolled in the randomized trial and 10,711 were included in the ecologic assessment. At 90 days, 1175 of 4215 patients (27.9%) in the SDD group and 1494 of 5065 (29.5%) in the standard-care group had died before hospital discharge (odds ratio, 0.93; 95% confidence interval [CI], 0.84 to 1.05; P = 0.27). New bloodstream infections occurred in 4.9% of the patients in the SDD group and in 6.8% of those in the standard-care group (adjusted mean difference, -1.30 percentage points; 95% CI, -2.55 to -0.05); antibiotic-resistant organisms were cultured in 16.8% and 26.8%, respectively (adjusted mean difference, -9.60 percentage points; 95% CI, -12.40 to -6.80). In the ecologic assessment, noninferiority of SDD was not confirmed for the development of new antibiotic-resistant organisms. Adverse events considered to be related to SDD or standard care were reported in 12 patients (0.3%) in the SDD group and in no patients in the standard-care group. Serious adverse events occurred in 47 patients (1.1%) and 59 patients (1.2%), respectively.
CONCLUSIONS: Among critically ill patients undergoing mechanical ventilation, SDD did not result in a lower incidence of in-hospital death than standard care. (Funded by the National Health and Medical Research Council of Australia and the Canadian Institutes of Health Research; ClinicalTrials.gov number, NCT02389036.).},
}
RevDate: 2025-10-29
Development of a CRISPR/Cas9-induced gene editing system for Pseudoalteromonas fuliginea and its applications in functional genomics.
Applied and environmental microbiology [Epub ahead of print].
Pseudoalteromonas has been used as a model system to study cold adaptation and is of widespread interest in biotechnology and ecology. To explore its physiological responses to extreme cold, uncover functional genes, and clarify their ecological roles, efficient genetic tools are essential. However, existing genetic manipulation methods in Pseudoalteromonas rely on traditional homology-based recombination, which is laborious and time-consuming in this bacterial system. Consequently, improving editing efficiency is crucial for advancing both basic research and applied potential. Here, we established a CRISPR/Cas9 system in Pseudoalteromonas and carried out an extensive investigation of the Type II CRISPR/Cas9 platform for gene editing in Pseudoalteromonas fuliginea, a representative species thriving in the frigid polar oceans. To validate the feasibility of the CRISPR/Cas system in P. fuliginea, multiple genes were selected as targets, and the gene editing effects were confirmed through phenotypic changes or gene expression. We have successfully achieved both gene knockouts and insertions in P. fuliginea, encompassing the deletion of genes such as fliJ, indA, and genes encoding Pf sRNAs, as well as the in vivo insertion of 3×FLAG and the gfp gene. The average CRISPR/Cas9 gene editing efficiency in P. fuliginea exceeded 70%. In summary, we developed an efficient CRISPR/Cas9-based editing system in P. fuliginea, which can be utilized to accelerate the development of Pseudoalteromonas as a model system for addressing fundamental questions related to extreme environmental adaptation and to fulfill its potential biotechnological applications.IMPORTANCEPseudoalteromonas fuliginea is a marine bacterium with great potential for ecological and biotechnological research, yet its genetic manipulation has long been a technical challenge. In this study, we developed a gene editing system based on CRISPR technology that enables efficient and precise genome modification in this organism. Using this system, we successfully deleted, inserted, and tagged multiple genes, including regulatory and non-coding elements, with high success rates. Notably, several of these genes are linked to key traits such as motility and stress response, which contribute to microbial adaptation in polar environments. This tool allows researchers to directly test gene function and study microbial adaptation in cold marine environments. The ability to perform reliable genetic edits in P. fuliginea opens new possibilities for its use as a model organism and will support future advances in microbial ecology, environmental microbiology, and marine biotechnology.
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@article {pmid41159723,
year = {2025},
author = {Duan, Z and Yang, R and Lai, T and Jiang, W and Zhang, J and Chen, B and Liao, L},
title = {Development of a CRISPR/Cas9-induced gene editing system for Pseudoalteromonas fuliginea and its applications in functional genomics.},
journal = {Applied and environmental microbiology},
volume = {},
number = {},
pages = {e0177125},
doi = {10.1128/aem.01771-25},
pmid = {41159723},
issn = {1098-5336},
abstract = {Pseudoalteromonas has been used as a model system to study cold adaptation and is of widespread interest in biotechnology and ecology. To explore its physiological responses to extreme cold, uncover functional genes, and clarify their ecological roles, efficient genetic tools are essential. However, existing genetic manipulation methods in Pseudoalteromonas rely on traditional homology-based recombination, which is laborious and time-consuming in this bacterial system. Consequently, improving editing efficiency is crucial for advancing both basic research and applied potential. Here, we established a CRISPR/Cas9 system in Pseudoalteromonas and carried out an extensive investigation of the Type II CRISPR/Cas9 platform for gene editing in Pseudoalteromonas fuliginea, a representative species thriving in the frigid polar oceans. To validate the feasibility of the CRISPR/Cas system in P. fuliginea, multiple genes were selected as targets, and the gene editing effects were confirmed through phenotypic changes or gene expression. We have successfully achieved both gene knockouts and insertions in P. fuliginea, encompassing the deletion of genes such as fliJ, indA, and genes encoding Pf sRNAs, as well as the in vivo insertion of 3×FLAG and the gfp gene. The average CRISPR/Cas9 gene editing efficiency in P. fuliginea exceeded 70%. In summary, we developed an efficient CRISPR/Cas9-based editing system in P. fuliginea, which can be utilized to accelerate the development of Pseudoalteromonas as a model system for addressing fundamental questions related to extreme environmental adaptation and to fulfill its potential biotechnological applications.IMPORTANCEPseudoalteromonas fuliginea is a marine bacterium with great potential for ecological and biotechnological research, yet its genetic manipulation has long been a technical challenge. In this study, we developed a gene editing system based on CRISPR technology that enables efficient and precise genome modification in this organism. Using this system, we successfully deleted, inserted, and tagged multiple genes, including regulatory and non-coding elements, with high success rates. Notably, several of these genes are linked to key traits such as motility and stress response, which contribute to microbial adaptation in polar environments. This tool allows researchers to directly test gene function and study microbial adaptation in cold marine environments. The ability to perform reliable genetic edits in P. fuliginea opens new possibilities for its use as a model organism and will support future advances in microbial ecology, environmental microbiology, and marine biotechnology.},
}
RevDate: 2025-10-29
Honey as a Functional Food: Evaluating Its Antimicrobial Properties and Bacterial Safety Concerns.
Foodborne pathogens and disease [Epub ahead of print].
Honey is increasingly recognized as a functional food with intrinsic antimicrobial properties. Its complex chemical makeup, high sugar content, low water activity, acidic pH, hydrogen peroxide generation, and a spectrum of bioactive phytochemicals create a multifaceted defense against microbial growth, yet honey also harbors diverse microorganisms, including potential pathogens, underscoring the need for robust quality control and safety considerations across production, processing, and storage. This study synthesizes current evidence on the antimicrobial mechanisms of honey and evaluates bacterial safety concerns, with emphasis on probiotic potential and risks associated with pathogens such as Clostridium botulinum, to inform safe use and innovative functional food applications. A comprehensive review of existing literature and honey-specific data was conducted to collate chemical, microbiological, and safety-related parameters. Key antimicrobial mechanisms (osmotic pressure, acidic environment, hydrogen peroxide production, and bioactive compounds such as methylglyoxal in certain varieties) were mapped to their effects on diverse microbes. Safety considerations, contamination pathways, and regulatory frameworks were qualitatively assessed to identify critical control points. Honey's antimicrobial activity arises from synergistic interactions among sugars, pH, hydrogen peroxide, enzymes, and phytochemicals, yielding broad-spectrum inhibition. Beneficial lactic acid bacteria from honey and bees contribute probiotic potential, while the risk of contamination by pathogens necessitates stringent hygiene, processing controls, and adherence to quality standards. Processors can leverage nonthermal and thermal reduction methods to balance safety with the preservation of bioactive components. Honey remains a robust functional food with antimicrobial advantages and probiotic opportunities, provided that meticulous quality control and regulatory compliance are maintained to mitigate safety risks for vulnerable populations. Future work should optimize honey-based probiotic formulations and establish standardized safety protocols across the supply chain.
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@article {pmid41159286,
year = {2025},
author = {Shirani, K and Mottaghi, A and Shabani, M},
title = {Honey as a Functional Food: Evaluating Its Antimicrobial Properties and Bacterial Safety Concerns.},
journal = {Foodborne pathogens and disease},
volume = {},
number = {},
pages = {},
doi = {10.1177/15353141251392181},
pmid = {41159286},
issn = {1556-7125},
abstract = {Honey is increasingly recognized as a functional food with intrinsic antimicrobial properties. Its complex chemical makeup, high sugar content, low water activity, acidic pH, hydrogen peroxide generation, and a spectrum of bioactive phytochemicals create a multifaceted defense against microbial growth, yet honey also harbors diverse microorganisms, including potential pathogens, underscoring the need for robust quality control and safety considerations across production, processing, and storage. This study synthesizes current evidence on the antimicrobial mechanisms of honey and evaluates bacterial safety concerns, with emphasis on probiotic potential and risks associated with pathogens such as Clostridium botulinum, to inform safe use and innovative functional food applications. A comprehensive review of existing literature and honey-specific data was conducted to collate chemical, microbiological, and safety-related parameters. Key antimicrobial mechanisms (osmotic pressure, acidic environment, hydrogen peroxide production, and bioactive compounds such as methylglyoxal in certain varieties) were mapped to their effects on diverse microbes. Safety considerations, contamination pathways, and regulatory frameworks were qualitatively assessed to identify critical control points. Honey's antimicrobial activity arises from synergistic interactions among sugars, pH, hydrogen peroxide, enzymes, and phytochemicals, yielding broad-spectrum inhibition. Beneficial lactic acid bacteria from honey and bees contribute probiotic potential, while the risk of contamination by pathogens necessitates stringent hygiene, processing controls, and adherence to quality standards. Processors can leverage nonthermal and thermal reduction methods to balance safety with the preservation of bioactive components. Honey remains a robust functional food with antimicrobial advantages and probiotic opportunities, provided that meticulous quality control and regulatory compliance are maintained to mitigate safety risks for vulnerable populations. Future work should optimize honey-based probiotic formulations and establish standardized safety protocols across the supply chain.},
}
RevDate: 2025-10-29
CmpDate: 2025-10-29
Linking microbial ecology to the cycling of neutral and acidic polysaccharides in pustular mats from Shark Bay, Western Australia.
Frontiers in microbiology, 16:1684648.
Cyanobacteria and other microbes in peritidal microbial mats have produced extracellular polymeric substances (EPS) for more than two billion years. The production and degradation of EPS contributes to the biogeochemical cycling of carbon and carbonate precipitation within modern microbial mats, but key microbes involved in the cycling of EPS remain unidentified. Here, we investigate the cycling of EPS in the peritidal pustular mats of Shark Bay, Western Australia. We characterize the chemical composition of EPS produced by cyanobacterial enrichment cultures under natural and UV-stress conditions and link these findings to the metabolic potential for EPS production and degradation encoded in 84 metagenome-assembled genomes (MAGs) from the mat community. We further identify the key microbial degraders of specific acidic and neutral polysaccharides in this community by cultivating enrichment cultures on seven commercially available polysaccharides representative of those present in the mats and assessing the dominant taxa. All sequenced Cyanobacteria MAGs have the potential to synthesize mannose, fucose, glucose, arabinose, rhamnose, galactose, xylose, N-acetylglucosamine, galacturonic acid and glucuronic acid. Biochemical analyses confirm the presence of nearly all these monosaccharides in the hydrolysates of EPS extracted from UV- and non-UV exposed cyanobacterial enrichments. Ultraviolet radiation influences the structure and composition of EPS by reducing the hydration, potentially due to cross-linking among polymers in EPS and increasing the relative abundances of uronic acids and xylose in polysaccharides. Analyses of carbohydrate-active enzymes (CAZymes) in the MAGs and of 16S rRNA sequences from experimental polysaccharide enrichments point to major roles for Bacteroidetes, Planctomycetes, and Verrucomicrobia in the cycling of acidic EPS. These experiments reveal a complex interplay among microbial community composition, CAZyme diversity, environmental stressors, and EPS cycling, which together shape carbon flow and biomineralization in pustular mats in Shark Bay.
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@article {pmid41158777,
year = {2025},
author = {Skoog, EJ and Cutts, E and Bosak, T},
title = {Linking microbial ecology to the cycling of neutral and acidic polysaccharides in pustular mats from Shark Bay, Western Australia.},
journal = {Frontiers in microbiology},
volume = {16},
number = {},
pages = {1684648},
pmid = {41158777},
issn = {1664-302X},
abstract = {Cyanobacteria and other microbes in peritidal microbial mats have produced extracellular polymeric substances (EPS) for more than two billion years. The production and degradation of EPS contributes to the biogeochemical cycling of carbon and carbonate precipitation within modern microbial mats, but key microbes involved in the cycling of EPS remain unidentified. Here, we investigate the cycling of EPS in the peritidal pustular mats of Shark Bay, Western Australia. We characterize the chemical composition of EPS produced by cyanobacterial enrichment cultures under natural and UV-stress conditions and link these findings to the metabolic potential for EPS production and degradation encoded in 84 metagenome-assembled genomes (MAGs) from the mat community. We further identify the key microbial degraders of specific acidic and neutral polysaccharides in this community by cultivating enrichment cultures on seven commercially available polysaccharides representative of those present in the mats and assessing the dominant taxa. All sequenced Cyanobacteria MAGs have the potential to synthesize mannose, fucose, glucose, arabinose, rhamnose, galactose, xylose, N-acetylglucosamine, galacturonic acid and glucuronic acid. Biochemical analyses confirm the presence of nearly all these monosaccharides in the hydrolysates of EPS extracted from UV- and non-UV exposed cyanobacterial enrichments. Ultraviolet radiation influences the structure and composition of EPS by reducing the hydration, potentially due to cross-linking among polymers in EPS and increasing the relative abundances of uronic acids and xylose in polysaccharides. Analyses of carbohydrate-active enzymes (CAZymes) in the MAGs and of 16S rRNA sequences from experimental polysaccharide enrichments point to major roles for Bacteroidetes, Planctomycetes, and Verrucomicrobia in the cycling of acidic EPS. These experiments reveal a complex interplay among microbial community composition, CAZyme diversity, environmental stressors, and EPS cycling, which together shape carbon flow and biomineralization in pustular mats in Shark Bay.},
}
RevDate: 2025-10-29
CmpDate: 2025-10-29
Distinct Gut and Skin Microbiomes of a Carnivorous Caecilian Larva (Ichthyophis bannanicus) Show Ecological and Phylogenetic Divergence from Anuran Tadpoles.
Microorganisms, 13(10): pii:microorganisms13102405.
The amphibian microbiome plays a vital role in host health, yet the bacterial communities of caecilians (Order: Gymnophiona) remain largely uncharacterised. We investigated this by providing the first characterisation of the gut and skin microbiome of larval Ichthyophis bannanicus, a carnivorous caecilian, using 16S rRNA gene metabarcoding. Our analyses show distinct communities between the faecal samples and skin, with significant enrichment of Laribacter in faeces and Flavobacterium on skin. Despite significant variation in their community structures, the core genera Escherichia-Shigella were shared between both regions, suggesting similar microbial exchange in the aquatic environments. Skin bacterial diversity exhibited relatively higher richness, but lower evenness than that of faeces. Further, the skin bacterial community exhibited more complex interactions, suggesting stronger resilience to changes. The relationships and interactions of skin and faecal bacterial communities suggest their interactive effects on the host's overall health. Compared with anuran tadpoles, the I. bannanicus larval microbiome showed taxonomic overlap, but possessed certain unique core bacteria. This work on an understudied amphibian lineage is foundational, highlighting how diet, phylogeny, and aquatic environment shape microbial communities and informing future research into amphibian health and disease.
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@article {pmid41156863,
year = {2025},
author = {Rajput, AP and Sun, D and Zhou, S and Meegaskumbura, M},
title = {Distinct Gut and Skin Microbiomes of a Carnivorous Caecilian Larva (Ichthyophis bannanicus) Show Ecological and Phylogenetic Divergence from Anuran Tadpoles.},
journal = {Microorganisms},
volume = {13},
number = {10},
pages = {},
doi = {10.3390/microorganisms13102405},
pmid = {41156863},
issn = {2076-2607},
support = {Guangxi University's startup-funding to Madhava Meegaskumbura;Postdoctoral Project funding to Amrapali Prithvisingh Rajput//Guangxi University/ ; },
abstract = {The amphibian microbiome plays a vital role in host health, yet the bacterial communities of caecilians (Order: Gymnophiona) remain largely uncharacterised. We investigated this by providing the first characterisation of the gut and skin microbiome of larval Ichthyophis bannanicus, a carnivorous caecilian, using 16S rRNA gene metabarcoding. Our analyses show distinct communities between the faecal samples and skin, with significant enrichment of Laribacter in faeces and Flavobacterium on skin. Despite significant variation in their community structures, the core genera Escherichia-Shigella were shared between both regions, suggesting similar microbial exchange in the aquatic environments. Skin bacterial diversity exhibited relatively higher richness, but lower evenness than that of faeces. Further, the skin bacterial community exhibited more complex interactions, suggesting stronger resilience to changes. The relationships and interactions of skin and faecal bacterial communities suggest their interactive effects on the host's overall health. Compared with anuran tadpoles, the I. bannanicus larval microbiome showed taxonomic overlap, but possessed certain unique core bacteria. This work on an understudied amphibian lineage is foundational, highlighting how diet, phylogeny, and aquatic environment shape microbial communities and informing future research into amphibian health and disease.},
}
RevDate: 2025-10-29
CmpDate: 2025-10-29
Pediococcus pentosaceus OL77 Enhances Oat (Avena sativa) Silage Fermentation Under Cold Conditions.
Microorganisms, 13(10): pii:microorganisms13102248.
Ensiling forage under low-temperature conditions often leads to poor fermentation and nutrient losses. This study evaluated the effects of a cold-tolerant Pediococcus pentosaceus OL77 strain on oat silage. Silages were prepared with or without Pediococcus pentosaceus inoculation (1 × 10[5] cfu/g FM). After 90 days, OL77-treated silage showed markedly higher lactic acid (45.83 vs. 30.51 g/kg DM), lower pH (3.88 vs. 4.443), and better preservation of WSC (64.68 vs. 47.60 g/kg DM) and crude protein (89.26 vs. 65.52 g/kg DM) than the control. Microbial analysis revealed accelerated colonization by Pediococcus, reduced bacterial diversity, and faster stabilization of the fermentation process. Functional predictions indicated enhanced carbohydrate and energy metabolism. These findings demonstrate that OL77 can effectively improve fermentation quality and nutrient preservation of oat silage under low-temperature conditions, offering a practical inoculant option for cold regions.
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@article {pmid41156709,
year = {2025},
author = {Liu, X and Zhao, G and Bai, J and Qu, X and Chai, J and Lin, D},
title = {Pediococcus pentosaceus OL77 Enhances Oat (Avena sativa) Silage Fermentation Under Cold Conditions.},
journal = {Microorganisms},
volume = {13},
number = {10},
pages = {},
doi = {10.3390/microorganisms13102248},
pmid = {41156709},
issn = {2076-2607},
support = {32160810//National Natural Science Foundation of China/ ; },
abstract = {Ensiling forage under low-temperature conditions often leads to poor fermentation and nutrient losses. This study evaluated the effects of a cold-tolerant Pediococcus pentosaceus OL77 strain on oat silage. Silages were prepared with or without Pediococcus pentosaceus inoculation (1 × 10[5] cfu/g FM). After 90 days, OL77-treated silage showed markedly higher lactic acid (45.83 vs. 30.51 g/kg DM), lower pH (3.88 vs. 4.443), and better preservation of WSC (64.68 vs. 47.60 g/kg DM) and crude protein (89.26 vs. 65.52 g/kg DM) than the control. Microbial analysis revealed accelerated colonization by Pediococcus, reduced bacterial diversity, and faster stabilization of the fermentation process. Functional predictions indicated enhanced carbohydrate and energy metabolism. These findings demonstrate that OL77 can effectively improve fermentation quality and nutrient preservation of oat silage under low-temperature conditions, offering a practical inoculant option for cold regions.},
}
RevDate: 2025-10-28
Propane-driven efficient BPA degradation in groundwater: Transformation pathways, microbial ecology and enzymatic mechanisms in a membrane biofilm reactor.
Journal of hazardous materials, 499:140214 pii:S0304-3894(25)03133-4 [Epub ahead of print].
The widespread occurrence of bisphenol A (BPA) in groundwater has raised growing concern due to its endocrine-disrupting effects. This study demonstrates for the first time that a propane-fed membrane biofilm reactor (C3H8-MBfR) achieved efficient BPA degradation, with rates up to 1157.8 ± 42.7 μg·L[-1]·d[-1]. In-situ withdrawal experiments confirmed that propane is essential for maintaining degradation performance. Transformation products (TPs) analysis revealed hydroxylation, oxidative skeletal rearrangement, ipso substitution, and ring-cleavage steps consistent with stepwise detoxification. ECOSAR-based toxicity predictions indicated that BPA degradation potentially leads to a reduced overall ecological risk, although minor toxic TPs might still pose residual risks. Multi-omic profiling identified a metabolically diverse microbial consortium dominated by J033 sp., Methyloversatilis discipulorum (M. discipulorum), Macondimonas, and Gemmobacter sp., which expressed key oxidative enzymes including cytochrome P450 (CYP450), particulate methane monooxygenase (pMMO), and propane monooxygenase (PrMO). Enzymatic inhibition assays supported their crucial roles in BPA transformation. The generated intermediates were subsequently transformed by these upstream oxidizers together with downstream degraders, such as M. discipulorum. These findings reveal a previously unrecognized, enzyme-driven network for BPA degradation in the C3H8-fed biofilm, offering a sustainable strategy for mitigating endocrine disrupting compounds from groundwater.
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@article {pmid41151518,
year = {2025},
author = {Ouyang, S and Zhao, HP and Lai, CY},
title = {Propane-driven efficient BPA degradation in groundwater: Transformation pathways, microbial ecology and enzymatic mechanisms in a membrane biofilm reactor.},
journal = {Journal of hazardous materials},
volume = {499},
number = {},
pages = {140214},
doi = {10.1016/j.jhazmat.2025.140214},
pmid = {41151518},
issn = {1873-3336},
abstract = {The widespread occurrence of bisphenol A (BPA) in groundwater has raised growing concern due to its endocrine-disrupting effects. This study demonstrates for the first time that a propane-fed membrane biofilm reactor (C3H8-MBfR) achieved efficient BPA degradation, with rates up to 1157.8 ± 42.7 μg·L[-1]·d[-1]. In-situ withdrawal experiments confirmed that propane is essential for maintaining degradation performance. Transformation products (TPs) analysis revealed hydroxylation, oxidative skeletal rearrangement, ipso substitution, and ring-cleavage steps consistent with stepwise detoxification. ECOSAR-based toxicity predictions indicated that BPA degradation potentially leads to a reduced overall ecological risk, although minor toxic TPs might still pose residual risks. Multi-omic profiling identified a metabolically diverse microbial consortium dominated by J033 sp., Methyloversatilis discipulorum (M. discipulorum), Macondimonas, and Gemmobacter sp., which expressed key oxidative enzymes including cytochrome P450 (CYP450), particulate methane monooxygenase (pMMO), and propane monooxygenase (PrMO). Enzymatic inhibition assays supported their crucial roles in BPA transformation. The generated intermediates were subsequently transformed by these upstream oxidizers together with downstream degraders, such as M. discipulorum. These findings reveal a previously unrecognized, enzyme-driven network for BPA degradation in the C3H8-fed biofilm, offering a sustainable strategy for mitigating endocrine disrupting compounds from groundwater.},
}
RevDate: 2025-10-28
Mediated electron transfer in five prevalent human oral microbial species.
Bioelectrochemistry (Amsterdam, Netherlands), 168:109149 pii:S1567-5394(25)00252-X [Epub ahead of print].
An increasing number of microbial species within the human body, many of which are pathogenic, are being reported as "electroactive". However, the mechanisms and kinetics of extracellular electron transfer (EET) and its putative ecological relevance remain understudied. We utilized rotating disk electrodes (RDEs) to assess mediated electron transfer (MET) in five oral species via their ability to reduce riboflavin and ferricyanide. The use of both mediators was confirmed in Streptococcus mutans, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis, while A. viscosus only reduced riboflavin. Kinetics of EET (turnover rate per cell) were slow with riboflavin (kcat, RF< 10[4] s[-1]) in all species but F. nucleatum, whereas ferricyanide resulted in fast kinetics (kcat, Ferri(app)> 10[4] s[-1]) in all but S. mutans. Due to its central role in oral biofilms and association to systemic diseases, MET was further characterized in F. nucleatum. Apparent Michaelis-Menten kinetics showed Km values of (0.57 ± 0.16 and 10.43 ± 0.91) μM for ferricyanide and riboflavin. The presence of mediators enhanced acetate production compared to mediator-free controls; when ferricyanide was used, butyrate and formate production was triggered only after its depletion. Finally, the putative molecular mechanisms enabling MET in F. nucleatum are discussed.
Additional Links: PMID-41151427
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@article {pmid41151427,
year = {2025},
author = {Hernández-Villamor, D and Jeaidi, A and Boydens, R and Rabaey, K and Van de Wiele, T and Prévoteau, A},
title = {Mediated electron transfer in five prevalent human oral microbial species.},
journal = {Bioelectrochemistry (Amsterdam, Netherlands)},
volume = {168},
number = {},
pages = {109149},
doi = {10.1016/j.bioelechem.2025.109149},
pmid = {41151427},
issn = {1878-562X},
abstract = {An increasing number of microbial species within the human body, many of which are pathogenic, are being reported as "electroactive". However, the mechanisms and kinetics of extracellular electron transfer (EET) and its putative ecological relevance remain understudied. We utilized rotating disk electrodes (RDEs) to assess mediated electron transfer (MET) in five oral species via their ability to reduce riboflavin and ferricyanide. The use of both mediators was confirmed in Streptococcus mutans, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis, while A. viscosus only reduced riboflavin. Kinetics of EET (turnover rate per cell) were slow with riboflavin (kcat, RF< 10[4] s[-1]) in all species but F. nucleatum, whereas ferricyanide resulted in fast kinetics (kcat, Ferri(app)> 10[4] s[-1]) in all but S. mutans. Due to its central role in oral biofilms and association to systemic diseases, MET was further characterized in F. nucleatum. Apparent Michaelis-Menten kinetics showed Km values of (0.57 ± 0.16 and 10.43 ± 0.91) μM for ferricyanide and riboflavin. The presence of mediators enhanced acetate production compared to mediator-free controls; when ferricyanide was used, butyrate and formate production was triggered only after its depletion. Finally, the putative molecular mechanisms enabling MET in F. nucleatum are discussed.},
}
RevDate: 2025-10-28
CmpDate: 2025-10-28
Signatures and likely sources of the male pregnancy microbiome in wild bay pipefish (Syngnathus leptorhynchus).
Animal microbiome, 7(1):112.
BACKGROUND: Understanding the origin and structure of microbiomes and their associations with ecologically significant host traits is essential for understanding the evolution of host-microbe interactions. These interactions support a wide range of physiological processes important for development, survival, and reproduction. Syngnathid fishes (seahorses, pipefish, and seadragons) represent a compelling system for investigating host-microbiome interactions due to their unique evolution of male pregnancy. Males harbor a fitness-critical brood pouch that provides embryos with protection, osmoregulation, and nutrient exchange through a placenta-like structure, all while requiring the male to modulate his immune system to accommodate developing offspring. These features create a tightly regulated internal environment where microbial interactions could be especially influential to supporting a successful pregnancy. While we have some understanding of the physiological and genetic factors underlying brood pouch development and maintenance, the role of the microbiome and host-microbe interactions in male pregnancy has remained underexplored across the broader diversity of Syngnathidae species and geographic regions. To investigate this relationship further, and for the first time sampling microbiota from a wild syngnathid population, we characterized microbiomes of the bay pipefish (Syngnathus leptorhynchus) using high-throughput 16S rRNA gene sequencing. We quantified microbial community diversity and composition across the brood pouch, embryos, ovaries, gills, intestines, and outer skin body tissues, focusing on sex-specific (brood pouch, embryo, ovary) and sex-shared (gill, intestine, skin) tissues, and variation in pregnancy stage (non-pregnant, early, mid, and late pregnancy).
RESULTS: We found that the male brood pouch microbiome was distinct from all other body sites (ovaries, embryos, gills, intestines, and outer skin) in community composition, and in that it exhibited the highest richness and phylogenetic diversity of microbes of any site on average, possibly supporting a specialized environment for embryonic development. Moreover, we found that microbial diversity was lower in non-pregnant brood pouches compared to each pregnancy stage (non-pregnant, early, mid, and late pregnancy) but found no significant differences among the pregnancy stages. Female ovaries had the lowest microbial richness and phylogenetic diversity compared to nonpregnant brood pouches, pregnant brood pouches, and embryos. Source tracking analysis using fast expectation-maximization for microbial source tracking (FEAST) indicated that the male outer skin serves as a significant microbial source for both the pregnant brood pouch and developing embryos, establishing a strong paternal influence on the offsprings’ microbial communities. Overall, we identified Proteobacteria, Bacteroidota, Cyanobacteria, Planctomycetota, and Actinobacteriota as the dominant phyla spanning all surveyed bay pipefish tissue sites, consistent with previous teleost fish microbiome studies. Analysis of core microbiome and indicator species further revealed that sequences classified as Methylotenera_A_557637 (two species), GCA-2862085 sp., Yoonia_491068 sp., Pla163 sp007750655, and Roseibacillus_B sp. show relatively high abundance and specificity with respect to the male brood pouch, suggesting that these taxa may have functional connections to the biology of male pregnancy.
CONCLUSIONS: These findings reveal insights into the microbial ecology of a unique reproductive system in its natural environment, highlighting the paternal microbiome’s potential functional role in shaping the developing offspring. Our results also indicate a likely influence of both environmental and host-specific factors in shaping the bay pipefish microbiome, but there is need for future research on the functional implications of these microbial communities, especially in the brood pouch during pregnancy, and with respect to offspring viability and fitness.
SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-025-00476-y.
Additional Links: PMID-41146339
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@article {pmid41146339,
year = {2025},
author = {Barker, EM and Small, CM and Bassham, S and Beck, EA and Currey, MC and Healey, HM and Johnson, BD and Cresko, WA and Jones, AG},
title = {Signatures and likely sources of the male pregnancy microbiome in wild bay pipefish (Syngnathus leptorhynchus).},
journal = {Animal microbiome},
volume = {7},
number = {1},
pages = {112},
pmid = {41146339},
issn = {2524-4671},
abstract = {BACKGROUND: Understanding the origin and structure of microbiomes and their associations with ecologically significant host traits is essential for understanding the evolution of host-microbe interactions. These interactions support a wide range of physiological processes important for development, survival, and reproduction. Syngnathid fishes (seahorses, pipefish, and seadragons) represent a compelling system for investigating host-microbiome interactions due to their unique evolution of male pregnancy. Males harbor a fitness-critical brood pouch that provides embryos with protection, osmoregulation, and nutrient exchange through a placenta-like structure, all while requiring the male to modulate his immune system to accommodate developing offspring. These features create a tightly regulated internal environment where microbial interactions could be especially influential to supporting a successful pregnancy. While we have some understanding of the physiological and genetic factors underlying brood pouch development and maintenance, the role of the microbiome and host-microbe interactions in male pregnancy has remained underexplored across the broader diversity of Syngnathidae species and geographic regions. To investigate this relationship further, and for the first time sampling microbiota from a wild syngnathid population, we characterized microbiomes of the bay pipefish (Syngnathus leptorhynchus) using high-throughput 16S rRNA gene sequencing. We quantified microbial community diversity and composition across the brood pouch, embryos, ovaries, gills, intestines, and outer skin body tissues, focusing on sex-specific (brood pouch, embryo, ovary) and sex-shared (gill, intestine, skin) tissues, and variation in pregnancy stage (non-pregnant, early, mid, and late pregnancy).
RESULTS: We found that the male brood pouch microbiome was distinct from all other body sites (ovaries, embryos, gills, intestines, and outer skin) in community composition, and in that it exhibited the highest richness and phylogenetic diversity of microbes of any site on average, possibly supporting a specialized environment for embryonic development. Moreover, we found that microbial diversity was lower in non-pregnant brood pouches compared to each pregnancy stage (non-pregnant, early, mid, and late pregnancy) but found no significant differences among the pregnancy stages. Female ovaries had the lowest microbial richness and phylogenetic diversity compared to nonpregnant brood pouches, pregnant brood pouches, and embryos. Source tracking analysis using fast expectation-maximization for microbial source tracking (FEAST) indicated that the male outer skin serves as a significant microbial source for both the pregnant brood pouch and developing embryos, establishing a strong paternal influence on the offsprings’ microbial communities. Overall, we identified Proteobacteria, Bacteroidota, Cyanobacteria, Planctomycetota, and Actinobacteriota as the dominant phyla spanning all surveyed bay pipefish tissue sites, consistent with previous teleost fish microbiome studies. Analysis of core microbiome and indicator species further revealed that sequences classified as Methylotenera_A_557637 (two species), GCA-2862085 sp., Yoonia_491068 sp., Pla163 sp007750655, and Roseibacillus_B sp. show relatively high abundance and specificity with respect to the male brood pouch, suggesting that these taxa may have functional connections to the biology of male pregnancy.
CONCLUSIONS: These findings reveal insights into the microbial ecology of a unique reproductive system in its natural environment, highlighting the paternal microbiome’s potential functional role in shaping the developing offspring. Our results also indicate a likely influence of both environmental and host-specific factors in shaping the bay pipefish microbiome, but there is need for future research on the functional implications of these microbial communities, especially in the brood pouch during pregnancy, and with respect to offspring viability and fitness.
SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-025-00476-y.},
}
RevDate: 2025-10-28
CmpDate: 2025-10-28
Evaluation of Wood Decay and Identification of Fungi Found in the USS Cairo, a Historic American Civil War Ironclad Gunboat.
Journal of fungi (Basel, Switzerland), 11(10): pii:jof11100732.
Studies of microbial degradation of historic woods are essential to help protect and preserve these important cultural properties. The USS Cairo is a historic Civil War gunboat and one of the first steam-powered and ironclad ships used in the American Civil War. Built in 1861, the ship sank in the Yazoo River of Mississippi in 1862 after a mine detonated and tore a hole in the port bow. The ship remained on the river bottom and was gradually buried with sediments for over 98 years. After recovery of the ship, it remained exposed to the environment before the first roofed structure was completed in 1980, and it has been displayed under a tensile fabric canopy with open sides at the Vicksburg National Military Park in Vicksburg, Mississippi. Concerns over the long-term preservation of the ship initiated this investigation to document the current condition of the wooden timbers, identify the fungi that may be present, and determine the elemental composition resulting from past wood-preservative treatments. Micromorphological characteristics observed using scanning electron microscopy showed that many of the timbers were in advanced stages of degradation. Eroded secondary cell walls leaving a weak framework of middle lamella were commonly observed. Soft rot attack was prevalent, and evidence of white and brown rot degradation was found in some wood. DNA extraction and sequencing of the ITS region led to the identification of a large group of diverse fungi that were isolated from ship timbers. Soft rot fungi, including Alternaria, Chaetomium, Cladosporium, Curvularia, Xylaria and others, and white rot fungi, including Bjerkandera, Odontoefibula, Phanerodontia, Phlebiopsis, Trametes and others, were found. No brown rot fungi were isolated. Elemental analyses using induced coupled plasma spectroscopy revealed elevated levels of all elements as compared to sound modern types of wood. High concentrations of boron, copper, iron, lead, zinc and other elements were found, and viable fungi were isolated from this wood. Biodegradation issues are discussed to help long-term conservation efforts to preserve the historic ship for future generations.
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@article {pmid41149922,
year = {2025},
author = {Blanchette, RA and Held, BW and Chemello, C and Mardikian, P},
title = {Evaluation of Wood Decay and Identification of Fungi Found in the USS Cairo, a Historic American Civil War Ironclad Gunboat.},
journal = {Journal of fungi (Basel, Switzerland)},
volume = {11},
number = {10},
pages = {},
doi = {10.3390/jof11100732},
pmid = {41149922},
issn = {2309-608X},
support = {no number//US National Park Service/ ; Hatch project MIN22-089//USDA/ ; },
abstract = {Studies of microbial degradation of historic woods are essential to help protect and preserve these important cultural properties. The USS Cairo is a historic Civil War gunboat and one of the first steam-powered and ironclad ships used in the American Civil War. Built in 1861, the ship sank in the Yazoo River of Mississippi in 1862 after a mine detonated and tore a hole in the port bow. The ship remained on the river bottom and was gradually buried with sediments for over 98 years. After recovery of the ship, it remained exposed to the environment before the first roofed structure was completed in 1980, and it has been displayed under a tensile fabric canopy with open sides at the Vicksburg National Military Park in Vicksburg, Mississippi. Concerns over the long-term preservation of the ship initiated this investigation to document the current condition of the wooden timbers, identify the fungi that may be present, and determine the elemental composition resulting from past wood-preservative treatments. Micromorphological characteristics observed using scanning electron microscopy showed that many of the timbers were in advanced stages of degradation. Eroded secondary cell walls leaving a weak framework of middle lamella were commonly observed. Soft rot attack was prevalent, and evidence of white and brown rot degradation was found in some wood. DNA extraction and sequencing of the ITS region led to the identification of a large group of diverse fungi that were isolated from ship timbers. Soft rot fungi, including Alternaria, Chaetomium, Cladosporium, Curvularia, Xylaria and others, and white rot fungi, including Bjerkandera, Odontoefibula, Phanerodontia, Phlebiopsis, Trametes and others, were found. No brown rot fungi were isolated. Elemental analyses using induced coupled plasma spectroscopy revealed elevated levels of all elements as compared to sound modern types of wood. High concentrations of boron, copper, iron, lead, zinc and other elements were found, and viable fungi were isolated from this wood. Biodegradation issues are discussed to help long-term conservation efforts to preserve the historic ship for future generations.},
}
RevDate: 2025-10-28
CmpDate: 2025-10-28
Temporal Dynamics of Bacterial Communities in Ectropis grisescens Following Cryogenic Mortality.
Insects, 16(10): pii:insects16101040.
Ectropis grisescens (Lepidoptera: Geometridae) is a destructive pest in tea plantations, leading to significant economic losses through defoliation. Existing control strategies, including chemical insecticides and biological agents, are often limited by environmental concerns, resistance, and variable efficacy. Recent evidence suggests that bacteria influence insect physiology and could be leveraged for pest management, but the postmortem microbial ecology of E. grisescens remains uncharacterized. In this study, we employed 16S rRNA sequencing to investigate temporal changes in the bacterial communities of E. grisescens cadavers at 0, 7, and 21 days following cryogenic mortality. Our results indicate a time-dependent decline in microbial diversity, while species richness initially increased before subsequent reduction. The dominant endosymbiont Wolbachia gradually diminished after host death, whereas Enterobacter remained abundant. Notably, non-dominant genera including Lysinibacillus and Sporosarcina exhibited a transient increase in abundance at day 7 before reverting to control levels by day 21. This study presents the first comprehensive analysis of postmortem microbial succession in a lepidopteran system, highlighting dynamic shifts in bacterial composition and offering potential avenues for microbiome-based pest management strategies.
Additional Links: PMID-41148908
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PubMed:
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@article {pmid41148908,
year = {2025},
author = {Zhang, X and Wang, Z and Feng, G and Xiao, Q and Tang, M},
title = {Temporal Dynamics of Bacterial Communities in Ectropis grisescens Following Cryogenic Mortality.},
journal = {Insects},
volume = {16},
number = {10},
pages = {},
doi = {10.3390/insects16101040},
pmid = {41148908},
issn = {2075-4450},
support = {31700613 and CAAS-ASTIP-TRICAAS//the National Natural Science Foundation of China and the Innovative Program of the Chinese Academy of Agricultural Sciences/ ; },
abstract = {Ectropis grisescens (Lepidoptera: Geometridae) is a destructive pest in tea plantations, leading to significant economic losses through defoliation. Existing control strategies, including chemical insecticides and biological agents, are often limited by environmental concerns, resistance, and variable efficacy. Recent evidence suggests that bacteria influence insect physiology and could be leveraged for pest management, but the postmortem microbial ecology of E. grisescens remains uncharacterized. In this study, we employed 16S rRNA sequencing to investigate temporal changes in the bacterial communities of E. grisescens cadavers at 0, 7, and 21 days following cryogenic mortality. Our results indicate a time-dependent decline in microbial diversity, while species richness initially increased before subsequent reduction. The dominant endosymbiont Wolbachia gradually diminished after host death, whereas Enterobacter remained abundant. Notably, non-dominant genera including Lysinibacillus and Sporosarcina exhibited a transient increase in abundance at day 7 before reverting to control levels by day 21. This study presents the first comprehensive analysis of postmortem microbial succession in a lepidopteran system, highlighting dynamic shifts in bacterial composition and offering potential avenues for microbiome-based pest management strategies.},
}
RevDate: 2025-10-28
Linking nutrient availability and community size to stochasticity in microbial community assembly.
FEMS microbiology ecology pii:8305078 [Epub ahead of print].
Both deterministic (e.g. species-environment interactions) and stochastic processes (e.g. random birth and death events) shape communities, but it remains poorly understood which environmental conditions promote stochasticity. Here we investigated interactive effects of nutrient availability and community size on stochasticity in order to predict how eutrophication and biomass loss shift the balance between predictable and random community dynamics. For this, we used freshwater bacterial communities in a microcosm experiment where communities were diluted to varying sizes and exposed to low, intermediate and high nutrient concentrations. Stochasticity was estimated with null modelling and as beta-diversity among replicate communities. At low nutrient concentrations, deterministic processes dominated, especially in smaller communities, which had the lowest diversity and abundance. In contrast, higher nutrient concentrations increased stochasticity. In contrast to theoretical predictions, this was particularly the case in larger communities with the highest diversity and abundance, likely due to stochastic initial growth. The findings underline how nutrient availability and community size jointly influence stochastic assembly processes, with important consequences for bacterial diversity and ecosystem functioning under environmental change.
Additional Links: PMID-41147699
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@article {pmid41147699,
year = {2025},
author = {Bick, B and Lumpi, T and Lindström, ES and Langenheder, S},
title = {Linking nutrient availability and community size to stochasticity in microbial community assembly.},
journal = {FEMS microbiology ecology},
volume = {},
number = {},
pages = {},
doi = {10.1093/femsec/fiaf110},
pmid = {41147699},
issn = {1574-6941},
abstract = {Both deterministic (e.g. species-environment interactions) and stochastic processes (e.g. random birth and death events) shape communities, but it remains poorly understood which environmental conditions promote stochasticity. Here we investigated interactive effects of nutrient availability and community size on stochasticity in order to predict how eutrophication and biomass loss shift the balance between predictable and random community dynamics. For this, we used freshwater bacterial communities in a microcosm experiment where communities were diluted to varying sizes and exposed to low, intermediate and high nutrient concentrations. Stochasticity was estimated with null modelling and as beta-diversity among replicate communities. At low nutrient concentrations, deterministic processes dominated, especially in smaller communities, which had the lowest diversity and abundance. In contrast, higher nutrient concentrations increased stochasticity. In contrast to theoretical predictions, this was particularly the case in larger communities with the highest diversity and abundance, likely due to stochastic initial growth. The findings underline how nutrient availability and community size jointly influence stochastic assembly processes, with important consequences for bacterial diversity and ecosystem functioning under environmental change.},
}
RevDate: 2025-10-27
CmpDate: 2025-10-27
Flagellar location determines the stability of bacterial surface entrapment.
Proceedings of the National Academy of Sciences of the United States of America, 122(44):e2506380122.
Surface interactions play a crucial role in shaping the motility patterns and ecological adaptations of swimming bacteria. Previous studies have primarily focused on peritrichous bacteria like Escherichia coli, whose multiple flagella form a bundle during swimming, allowing them to remain trapped at surfaces for extended periods. However, this surface entrapment phenomenon varies significantly among different bacterial species, despite all fitting into the simplified theoretical models of pusher-type bacteria, suggesting that key factors remain unidentified. Here, we demonstrate that flagellar location is a critical determinant of surface entrapment stability in pusher-type bacteria. Using fluorescently labeled Pseudomonas aeruginosa, we show that cells with a single lateral flagellum exhibit substantially longer surface residence times compared to those with a single polar flagellum, despite similar cell morphology and swimming speeds. Through direct visualization of bacterial orientation angles relative to surfaces, we reveal that this difference results from the distinct bending directions of the flagellar hook-the flexible joint connecting the rigid filament to the cell body. The hook-generated torque resists reorientation differently depending on flagellar location, facilitating surface escape for polar-flagellated bacteria while enhancing entrapment for lateral-flagellated bacteria. Our findings highlight the previously overlooked importance of flagellar placement in bacterial surface interactions, providing insights for understanding microbial ecology and designing biomimetic microswimmers.
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@article {pmid41144669,
year = {2025},
author = {Tao, A and Fu, S and Zhang, R and Yuan, J},
title = {Flagellar location determines the stability of bacterial surface entrapment.},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
volume = {122},
number = {44},
pages = {e2506380122},
doi = {10.1073/pnas.2506380122},
pmid = {41144669},
issn = {1091-6490},
support = {12090053//MOST | National Natural Science Foundation of China (NSFC)/ ; },
mesh = {*Flagella/physiology ; *Pseudomonas aeruginosa/physiology ; Escherichia coli/physiology ; },
abstract = {Surface interactions play a crucial role in shaping the motility patterns and ecological adaptations of swimming bacteria. Previous studies have primarily focused on peritrichous bacteria like Escherichia coli, whose multiple flagella form a bundle during swimming, allowing them to remain trapped at surfaces for extended periods. However, this surface entrapment phenomenon varies significantly among different bacterial species, despite all fitting into the simplified theoretical models of pusher-type bacteria, suggesting that key factors remain unidentified. Here, we demonstrate that flagellar location is a critical determinant of surface entrapment stability in pusher-type bacteria. Using fluorescently labeled Pseudomonas aeruginosa, we show that cells with a single lateral flagellum exhibit substantially longer surface residence times compared to those with a single polar flagellum, despite similar cell morphology and swimming speeds. Through direct visualization of bacterial orientation angles relative to surfaces, we reveal that this difference results from the distinct bending directions of the flagellar hook-the flexible joint connecting the rigid filament to the cell body. The hook-generated torque resists reorientation differently depending on flagellar location, facilitating surface escape for polar-flagellated bacteria while enhancing entrapment for lateral-flagellated bacteria. Our findings highlight the previously overlooked importance of flagellar placement in bacterial surface interactions, providing insights for understanding microbial ecology and designing biomimetic microswimmers.},
}
MeSH Terms:
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*Flagella/physiology
*Pseudomonas aeruginosa/physiology
Escherichia coli/physiology
RevDate: 2025-10-27
Comparative analysis of dietary fiber impact on bile acid metabolism and gut microbiota composition in mice.
Npj gut and liver, 2(1):26.
Dietary fiber is essential for health but remains under-consumed in Western diets. Fiber types differ in their physicochemical properties, which influence gastrointestinal function, bile acid (BA) metabolism, and gut microbiota composition. C57Bl/6 mice were fed control or 10% (w/w) fiber diets containing cellulose, chitin, resistant starch, pectin, inulin, β-glucan, psyllium, dextrin, or raffinose. All fibers reduced bacterial diversity, while most increased Akkermansia muciniphila abundance. Cellulose/chitin and inulin/β-glucan/raffinose formed distinct microbiome clusters. Rikenellaceae correlated positively with taurine-conjugated BAs levels. BA concentrations were reduced across tissues. Taurine conjugates showed inverse liver-intestine distribution. Inulin and β-glucan resulted in the highest taurine conjugate levels and reduced intestinal taurine-conjugated BAs concentrations, suggesting enhanced bile salt hydrolase (BSH) activity. Resistant starch had a minimal effect. Psyllium most strongly impacted BA- and taurine-related gene expression, cecum size and weight loss. Dietary fibers distinctly modulate BA metabolism and gut microbiota, with implications for metabolic health and targeted therapies.
Additional Links: PMID-41140797
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Citation:
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@article {pmid41140797,
year = {2025},
author = {Zöchling, A and Séneca, J and Pjevac, P and Auñon-Lopez, A and Zebeli, Q and Pignitter, M and Duszka, K},
title = {Comparative analysis of dietary fiber impact on bile acid metabolism and gut microbiota composition in mice.},
journal = {Npj gut and liver},
volume = {2},
number = {1},
pages = {26},
pmid = {41140797},
issn = {3004-9806},
abstract = {Dietary fiber is essential for health but remains under-consumed in Western diets. Fiber types differ in their physicochemical properties, which influence gastrointestinal function, bile acid (BA) metabolism, and gut microbiota composition. C57Bl/6 mice were fed control or 10% (w/w) fiber diets containing cellulose, chitin, resistant starch, pectin, inulin, β-glucan, psyllium, dextrin, or raffinose. All fibers reduced bacterial diversity, while most increased Akkermansia muciniphila abundance. Cellulose/chitin and inulin/β-glucan/raffinose formed distinct microbiome clusters. Rikenellaceae correlated positively with taurine-conjugated BAs levels. BA concentrations were reduced across tissues. Taurine conjugates showed inverse liver-intestine distribution. Inulin and β-glucan resulted in the highest taurine conjugate levels and reduced intestinal taurine-conjugated BAs concentrations, suggesting enhanced bile salt hydrolase (BSH) activity. Resistant starch had a minimal effect. Psyllium most strongly impacted BA- and taurine-related gene expression, cecum size and weight loss. Dietary fibers distinctly modulate BA metabolism and gut microbiota, with implications for metabolic health and targeted therapies.},
}
RevDate: 2025-10-27
CmpDate: 2025-10-27
StrataSeq: A Workflow for Rapid Development of Molecular Databases for Hard-To-Identify Species.
Ecology and evolution, 15(10):e72375.
Biodiversity loss necessitates improved monitoring of small, species-rich taxa, such as protists, phyto- and zooplankton and terrestrial invertebrates. Traditional biomonitoring is often infeasible for these taxa due to complex morphology and few taxonomists. DNA-based approaches offer promising solutions by enabling rapid species identification. However, the effectiveness of these methods depends on the completeness of molecular reference databases, which remain incomplete, particularly for remote and biodiverse regions. To address this, we propose the StrataSeq workflow, a systematic approach to optimise the generation of DNA reference databases for hard-to-identify taxa. Reference sequences allow us to connect molecular operational taxonomic units to a wealth of information available for many described taxa. StrataSeq consists of four key steps: (1) Habitat-stratified sample subsetting selects a minimal but ecologically representative sample set by stratifying along key environmental gradients. (2) Prioritising morphospecies involves sorting specimens into morphospecies and ranking them based on their occurrence across samples, prioritising common taxa for detailed identification. (3) Detailed morphological identification focuses on common morphospecies to maximise taxonomic coverage while minimising effort. (4) Reference DNA sequence generation targets taxa lacking molecular references, with sequenced specimens deposited as museum vouchers. We benchmarked the StrataSeq workflow using two datasets of Collembola from grassland soils in Germany. In comparison with a species list generated by a more labour-intensive traditional approach (identification of randomly selected individuals from all samples), the StrataSeq workflow captured 69% of species but required only 22% of the effort. StrataSeq is adaptable to various organism groups and environmental settings, including both spatial and temporal gradients. The workflow enhances the cost-effectiveness of generating reference DNA databases, supporting improved biodiversity monitoring and ecological research. StrataSeq offers a scalable solution to accelerate the completion of molecular databases, thereby improving biomonitoring and ecosystem assessments under global change pressures.
Additional Links: PMID-41140306
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Citation:
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@article {pmid41140306,
year = {2025},
author = {Merges, AK and Manning, P and Baulechner, D and John, K and Zaitsev, A and Wolters, V and Baranski, D and Grossart, HP and Woodhouse, J and Schneider, C and Bálint, M},
title = {StrataSeq: A Workflow for Rapid Development of Molecular Databases for Hard-To-Identify Species.},
journal = {Ecology and evolution},
volume = {15},
number = {10},
pages = {e72375},
pmid = {41140306},
issn = {2045-7758},
abstract = {Biodiversity loss necessitates improved monitoring of small, species-rich taxa, such as protists, phyto- and zooplankton and terrestrial invertebrates. Traditional biomonitoring is often infeasible for these taxa due to complex morphology and few taxonomists. DNA-based approaches offer promising solutions by enabling rapid species identification. However, the effectiveness of these methods depends on the completeness of molecular reference databases, which remain incomplete, particularly for remote and biodiverse regions. To address this, we propose the StrataSeq workflow, a systematic approach to optimise the generation of DNA reference databases for hard-to-identify taxa. Reference sequences allow us to connect molecular operational taxonomic units to a wealth of information available for many described taxa. StrataSeq consists of four key steps: (1) Habitat-stratified sample subsetting selects a minimal but ecologically representative sample set by stratifying along key environmental gradients. (2) Prioritising morphospecies involves sorting specimens into morphospecies and ranking them based on their occurrence across samples, prioritising common taxa for detailed identification. (3) Detailed morphological identification focuses on common morphospecies to maximise taxonomic coverage while minimising effort. (4) Reference DNA sequence generation targets taxa lacking molecular references, with sequenced specimens deposited as museum vouchers. We benchmarked the StrataSeq workflow using two datasets of Collembola from grassland soils in Germany. In comparison with a species list generated by a more labour-intensive traditional approach (identification of randomly selected individuals from all samples), the StrataSeq workflow captured 69% of species but required only 22% of the effort. StrataSeq is adaptable to various organism groups and environmental settings, including both spatial and temporal gradients. The workflow enhances the cost-effectiveness of generating reference DNA databases, supporting improved biodiversity monitoring and ecological research. StrataSeq offers a scalable solution to accelerate the completion of molecular databases, thereby improving biomonitoring and ecosystem assessments under global change pressures.},
}
RevDate: 2025-10-26
CmpDate: 2025-10-26
Optimization of Doses of Antibiotics and Cuminaldehyde to Combat Methicillin-Resistant Staphylococcus aureus (MRSA): A Study With Machine Learning.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 133(10):e70076.
Methicillin-resistant Staphylococcus aureus (MRSA), a drug-resistant organism, can cause a spectrum of infections in the human host involving biofilm. Therefore, novel therapeutic approaches need to be explored to mitigate this persistent infection. This study investigated a combinatorial approach that incorporates cuminaldehyde (a phytochemical) alongside aminoglycoside antibiotics (gentamicin and tobramycin) to improve antibiofilm efficacy by addressing multiple targets. In this regard, to achieve precise dosing of the chosen compounds for effective biofilm management, different machine learning models, namely multiple linear regression (MLR), polynomial regression (PR), artificial neural network regression (ANNR), and support vector regression (SVR), were employed. The results suggested that ANNR exhibited a strong association between the predicted and experimental observations (R[2] = 98.07). Furthermore, the ANNR model, followed by genetic algorithm (GA), recommended that the combinatorial doses of the selected compounds [cuminaldehyde (40 μg/mL); gentamicin (0.5 μg/mL); and tobramycin (0.035 μg/mL)] could show the highest antibiofilm activity against MRSA. Additionally, this study revealed that the combination of the mentioned compounds at their recommended doses not only accumulated intracellular reactive oxygen species (ROS) but also increased the cell membrane permeability of MRSA. Thus, this study provides a promising foundation for developing novel therapeutic strategies against MRSA biofilm through an AI-driven approach.
Additional Links: PMID-41139509
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PubMed:
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@article {pmid41139509,
year = {2025},
author = {Roy, R and Gogoi, UR and Das, M and Paul, P and Chakraborty, P and Das, S and Sarkar, S and Gupta, AD and Malik, M and Sarker, RK and Tribedi, P},
title = {Optimization of Doses of Antibiotics and Cuminaldehyde to Combat Methicillin-Resistant Staphylococcus aureus (MRSA): A Study With Machine Learning.},
journal = {APMIS : acta pathologica, microbiologica, et immunologica Scandinavica},
volume = {133},
number = {10},
pages = {e70076},
doi = {10.1111/apm.70076},
pmid = {41139509},
issn = {1600-0463},
support = {TNU/R&D/M P/2021/008//The Neotia University/ ; TNU/R&D/M/12//The Neotia University/ ; },
mesh = {*Methicillin-Resistant Staphylococcus aureus/drug effects/physiology ; *Anti-Bacterial Agents/pharmacology/administration & dosage ; Biofilms/drug effects ; *Machine Learning ; Tobramycin/pharmacology/administration & dosage ; Humans ; Microbial Sensitivity Tests ; Gentamicins/pharmacology/administration & dosage ; Staphylococcal Infections/drug therapy/microbiology ; *Benzaldehydes/pharmacology/administration & dosage ; },
abstract = {Methicillin-resistant Staphylococcus aureus (MRSA), a drug-resistant organism, can cause a spectrum of infections in the human host involving biofilm. Therefore, novel therapeutic approaches need to be explored to mitigate this persistent infection. This study investigated a combinatorial approach that incorporates cuminaldehyde (a phytochemical) alongside aminoglycoside antibiotics (gentamicin and tobramycin) to improve antibiofilm efficacy by addressing multiple targets. In this regard, to achieve precise dosing of the chosen compounds for effective biofilm management, different machine learning models, namely multiple linear regression (MLR), polynomial regression (PR), artificial neural network regression (ANNR), and support vector regression (SVR), were employed. The results suggested that ANNR exhibited a strong association between the predicted and experimental observations (R[2] = 98.07). Furthermore, the ANNR model, followed by genetic algorithm (GA), recommended that the combinatorial doses of the selected compounds [cuminaldehyde (40 μg/mL); gentamicin (0.5 μg/mL); and tobramycin (0.035 μg/mL)] could show the highest antibiofilm activity against MRSA. Additionally, this study revealed that the combination of the mentioned compounds at their recommended doses not only accumulated intracellular reactive oxygen species (ROS) but also increased the cell membrane permeability of MRSA. Thus, this study provides a promising foundation for developing novel therapeutic strategies against MRSA biofilm through an AI-driven approach.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Methicillin-Resistant Staphylococcus aureus/drug effects/physiology
*Anti-Bacterial Agents/pharmacology/administration & dosage
Biofilms/drug effects
*Machine Learning
Tobramycin/pharmacology/administration & dosage
Humans
Microbial Sensitivity Tests
Gentamicins/pharmacology/administration & dosage
Staphylococcal Infections/drug therapy/microbiology
*Benzaldehydes/pharmacology/administration & dosage
RevDate: 2025-10-24
Accelerated adaptive laboratory evolution: A tool for evolutionary biotechnology.
Biotechnology advances pii:S0734-9750(25)00227-7 [Epub ahead of print].
Adaptive laboratory evolution (ALE) is a powerful strategy for enhancing microbial traits by harnessing the principles of natural selection in controlled environments. It has enabled significant advances in microbial growth, stress tolerance, and product yield across a variety of organisms, while also providing insight into evolutionary mechanisms. However, the traditional ALE workflow is time- and resource-intensive, relying on prolonged cultivation to allow beneficial mutations to emerge and be maintained in the population. To improve this, a range of evolutionary engineering tools have been developed to accelerate ALE by increasing mutation rates and genetic diversity in evolving strains. In this review, we explore the core parameters that shape ALE, such as selection pressure, transfer method, and passage size, and provide a comprehensive overview of both established and emerging acceleration methods. These techniques are categorized based on portability (applicability across different microorganisms), genomic targetability (specificity of mutagenesis), and reliability (minimal off-target mutations and mutational reproducibility), with the resulting framework for selecting the most suitable approach summarized in Table 3 at the end of the review. We highlight the growing potential of accelerated ALE and outline future directions, including the integration of genome-wide and targeted mutagenesis, computational modeling, laboratory automation, and broader application beyond model organisms. This review aims to streamline the use of accelerated ALE, unlocking its true potential for advancing microbial strain engineering.
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@article {pmid41135758,
year = {2025},
author = {Declerck, L and Bouchon, F and Demeester, W and Guidi, C and De Mey, M},
title = {Accelerated adaptive laboratory evolution: A tool for evolutionary biotechnology.},
journal = {Biotechnology advances},
volume = {},
number = {},
pages = {108741},
doi = {10.1016/j.biotechadv.2025.108741},
pmid = {41135758},
issn = {1873-1899},
abstract = {Adaptive laboratory evolution (ALE) is a powerful strategy for enhancing microbial traits by harnessing the principles of natural selection in controlled environments. It has enabled significant advances in microbial growth, stress tolerance, and product yield across a variety of organisms, while also providing insight into evolutionary mechanisms. However, the traditional ALE workflow is time- and resource-intensive, relying on prolonged cultivation to allow beneficial mutations to emerge and be maintained in the population. To improve this, a range of evolutionary engineering tools have been developed to accelerate ALE by increasing mutation rates and genetic diversity in evolving strains. In this review, we explore the core parameters that shape ALE, such as selection pressure, transfer method, and passage size, and provide a comprehensive overview of both established and emerging acceleration methods. These techniques are categorized based on portability (applicability across different microorganisms), genomic targetability (specificity of mutagenesis), and reliability (minimal off-target mutations and mutational reproducibility), with the resulting framework for selecting the most suitable approach summarized in Table 3 at the end of the review. We highlight the growing potential of accelerated ALE and outline future directions, including the integration of genome-wide and targeted mutagenesis, computational modeling, laboratory automation, and broader application beyond model organisms. This review aims to streamline the use of accelerated ALE, unlocking its true potential for advancing microbial strain engineering.},
}
RevDate: 2025-10-24
Could extracts from spent mushroom materials transform reclaimed water quality? - A pilot study on pathogen suppression, antimicrobial chemical removal, and plant growth enhancement.
Journal of environmental management, 395:127688 pii:S0301-4797(25)03664-3 [Epub ahead of print].
Additional Links: PMID-41135394
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PubMed:
Citation:
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@article {pmid41135394,
year = {2025},
author = {Khalil, S and Ugolini, V and Forsbacka, J and Karlsson, M and Vetukuri, RR and Lai, FY},
title = {Could extracts from spent mushroom materials transform reclaimed water quality? - A pilot study on pathogen suppression, antimicrobial chemical removal, and plant growth enhancement.},
journal = {Journal of environmental management},
volume = {395},
number = {},
pages = {127688},
doi = {10.1016/j.jenvman.2025.127688},
pmid = {41135394},
issn = {1095-8630},
}
RevDate: 2025-10-24
CmpDate: 2025-10-24
Exclusive Effects of Moxibustion on Gut Microbiota: Protocol for a Focused Systematic Review and Meta-Analysis.
JMIR research protocols, 14:e73317 pii:v14i1e73317.
BACKGROUND: The gut microbiota (GM) plays a critical role in systemic health, influencing immune, metabolic, and neurological functions. There is emerging evidence suggesting that moxibustion, a traditional thermal therapy, may modulate the GM to restore microbial homeostasis, yet its exclusive effects remain undifferentiated from those of combined therapies such as acupuncture. Previous meta-analyses lack mechanistic specificity, necessitating a focused evaluation of moxibustion's impact on microbial ecology.
OBJECTIVE: This systematic review and meta-analysis aims to quantify moxibustion-induced changes in GM diversity, taxonomic composition, and functional metabolites (eg, short-chain fatty acids).
METHODS: We will systematically search the PubMed, Web of Science, Cochrane Library, China National Knowledge Infrastructure, Wanfang, and VIP databases from inception to December 31, 2024, using keywords such as "moxibustion," "gut microbiota," and "intestinal flora." Eligible preclinical (animal) and clinical (human) studies evaluating stand-alone moxibustion interventions on the GM will be included. Primary outcomes include microbial α diversity indexes (Shannon and Simpson) and relative abundance of key taxa (eg, Firmicutes and Bacteroidetes). Risk of bias will be assessed using the Systematic Review Center for Laboratory Animal Experimentation risk-of-bias tool for animal studies and the modified Collaborative Approach to Meta-Analysis and Review of Animal Data from Experimental Studies criteria for human trials. Pooled effect estimates for continuous outcomes (eg, diversity indexes and taxa ratios) will be calculated using the ratio of means with 95% CIs. Statistical analyses will be conducted in RevMan (version 5.4) and R (metafor package), with data archived on Figshare for reproducibility.
RESULTS: As of March 2025, the literature search and screening have been completed, and 31 studies meeting the inclusion criteria have been identified. The comprehensive analysis is scheduled to be completed by October 2025, with results anticipated to be published in late 2025. On the basis of previous work, an anticipated result is that moxibustion may reduce pathogenic genera such as Ruminococcus while enhancing beneficial genera, effects that are expected to be associated with improved intestinal barrier integrity and anti-inflammatory responses.
CONCLUSIONS: This protocol provides a rigorous framework to evaluate moxibustion's unique role in GM modulation, bridging traditional medicine with microbiome science. The results will inform optimized, nonpharmacological strategies for managing microbiome-associated chronic diseases and guide future research priorities.
Additional Links: PMID-41135049
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PubMed:
Citation:
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@article {pmid41135049,
year = {2025},
author = {Zhang, X and Guo, Y and Shi, J and Zang, Q and Li, Y},
title = {Exclusive Effects of Moxibustion on Gut Microbiota: Protocol for a Focused Systematic Review and Meta-Analysis.},
journal = {JMIR research protocols},
volume = {14},
number = {},
pages = {e73317},
doi = {10.2196/73317},
pmid = {41135049},
issn = {1929-0748},
mesh = {*Moxibustion/methods ; *Gastrointestinal Microbiome/physiology ; Humans ; Meta-Analysis as Topic ; Systematic Reviews as Topic ; Animals ; Research Design ; },
abstract = {BACKGROUND: The gut microbiota (GM) plays a critical role in systemic health, influencing immune, metabolic, and neurological functions. There is emerging evidence suggesting that moxibustion, a traditional thermal therapy, may modulate the GM to restore microbial homeostasis, yet its exclusive effects remain undifferentiated from those of combined therapies such as acupuncture. Previous meta-analyses lack mechanistic specificity, necessitating a focused evaluation of moxibustion's impact on microbial ecology.
OBJECTIVE: This systematic review and meta-analysis aims to quantify moxibustion-induced changes in GM diversity, taxonomic composition, and functional metabolites (eg, short-chain fatty acids).
METHODS: We will systematically search the PubMed, Web of Science, Cochrane Library, China National Knowledge Infrastructure, Wanfang, and VIP databases from inception to December 31, 2024, using keywords such as "moxibustion," "gut microbiota," and "intestinal flora." Eligible preclinical (animal) and clinical (human) studies evaluating stand-alone moxibustion interventions on the GM will be included. Primary outcomes include microbial α diversity indexes (Shannon and Simpson) and relative abundance of key taxa (eg, Firmicutes and Bacteroidetes). Risk of bias will be assessed using the Systematic Review Center for Laboratory Animal Experimentation risk-of-bias tool for animal studies and the modified Collaborative Approach to Meta-Analysis and Review of Animal Data from Experimental Studies criteria for human trials. Pooled effect estimates for continuous outcomes (eg, diversity indexes and taxa ratios) will be calculated using the ratio of means with 95% CIs. Statistical analyses will be conducted in RevMan (version 5.4) and R (metafor package), with data archived on Figshare for reproducibility.
RESULTS: As of March 2025, the literature search and screening have been completed, and 31 studies meeting the inclusion criteria have been identified. The comprehensive analysis is scheduled to be completed by October 2025, with results anticipated to be published in late 2025. On the basis of previous work, an anticipated result is that moxibustion may reduce pathogenic genera such as Ruminococcus while enhancing beneficial genera, effects that are expected to be associated with improved intestinal barrier integrity and anti-inflammatory responses.
CONCLUSIONS: This protocol provides a rigorous framework to evaluate moxibustion's unique role in GM modulation, bridging traditional medicine with microbiome science. The results will inform optimized, nonpharmacological strategies for managing microbiome-associated chronic diseases and guide future research priorities.},
}
MeSH Terms:
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*Moxibustion/methods
*Gastrointestinal Microbiome/physiology
Humans
Meta-Analysis as Topic
Systematic Reviews as Topic
Animals
Research Design
RevDate: 2025-10-23
CARD14 signaling in intestinal epithelial cells induces intestinal inflammation and intestinal transit delay.
EMBO molecular medicine [Epub ahead of print].
CARD14 is an intracellular NF-κB signaling mediator in the skin, and rare CARD14 variants have been associated with psoriasis and atopic dermatitis. CARD14 is also expressed in intestinal epithelial cells (IEC). However, its function in the intestine remains unknown. We demonstrate here that transgenic mice expressing the psoriasis-associated gain-of-function human CARD14(E138A) mutant specifically in IEC show mild intestinal inflammation, without epithelial damage. Moreover, CARD14(E138A)[IEC] mice show a drastic reduction in intestinal motility, often associated with rectal prolapse. Enteric neuronal survival and functionality are unaffected in CARD14(E138A)[IEC] mice. Transcriptome analysis of IEC from CARD14(E138A)[IEC] mice reveals decreased expression of antimicrobial peptides by Paneth cells, accompanied by microbial dysbiosis and increased susceptibility to enteric bacterial infection. Our findings suggest that gain-of-function CARD14 mutations may not only predispose patients to psoriasis but also mild intestinal inflammation, reduced intestinal motility, and increased sensitivity to intestinal infection. CARD14(E138A)[IEC] mice are also a valuable tool for further investigation of IEC-intrinsic molecular processes involved in intestinal inflammation and motility disorders.
Additional Links: PMID-41131424
PubMed:
Citation:
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@article {pmid41131424,
year = {2025},
author = {Aidarova, A and Carels, M and Haegman, M and Driege, Y and Timmermans, S and Van Damme, E and Aguilera-Lizarraga, J and Viola, MF and de Cássia Collaço, R and Manils, J and Ley, SC and Bosmans, F and Van de Wiele, T and Boeckxstaens, G and Libert, C and Beyaert, R and Afonina, IS},
title = {CARD14 signaling in intestinal epithelial cells induces intestinal inflammation and intestinal transit delay.},
journal = {EMBO molecular medicine},
volume = {},
number = {},
pages = {},
pmid = {41131424},
issn = {1757-4684},
support = {G035517N//Fonds Wetenschappelijk Onderzoek (FWO)/ ; 3G0I1422//Fonds Wetenschappelijk Onderzoek (FWO)/ ; G000220N//Fonds Wetenschappelijk Onderzoek (FWO)/ ; 12Z3922N//Fonds Wetenschappelijk Onderzoek (FWO)/ ; G0A7T24N//Fonds Wetenschappelijk Onderzoek (FWO)/ ; 3G086521//Fonds Wetenschappelijk Onderzoek (FWO)/ ; 3S003122//Strategic Basic Research grants from FWO/ ; 3179K5620//Strategic Basic Research grants from FWO/ ; 01G00419//Ghent University grant GOA/ ; 01M00121//Methusalem/ ; 2024/01/511//Universiteit Gent (UGent)/ ; 365C06721//Stichting Tegen Kanker (Fondation Contre le Cancer)/ ; 222487/Z/21/Z//Wellcome Trust Investigator/ ; },
abstract = {CARD14 is an intracellular NF-κB signaling mediator in the skin, and rare CARD14 variants have been associated with psoriasis and atopic dermatitis. CARD14 is also expressed in intestinal epithelial cells (IEC). However, its function in the intestine remains unknown. We demonstrate here that transgenic mice expressing the psoriasis-associated gain-of-function human CARD14(E138A) mutant specifically in IEC show mild intestinal inflammation, without epithelial damage. Moreover, CARD14(E138A)[IEC] mice show a drastic reduction in intestinal motility, often associated with rectal prolapse. Enteric neuronal survival and functionality are unaffected in CARD14(E138A)[IEC] mice. Transcriptome analysis of IEC from CARD14(E138A)[IEC] mice reveals decreased expression of antimicrobial peptides by Paneth cells, accompanied by microbial dysbiosis and increased susceptibility to enteric bacterial infection. Our findings suggest that gain-of-function CARD14 mutations may not only predispose patients to psoriasis but also mild intestinal inflammation, reduced intestinal motility, and increased sensitivity to intestinal infection. CARD14(E138A)[IEC] mice are also a valuable tool for further investigation of IEC-intrinsic molecular processes involved in intestinal inflammation and motility disorders.},
}
RevDate: 2025-10-23
Microbial network assembly in bat flies with differing host specificity from North Africa.
International microbiology : the official journal of the Spanish Society for Microbiology [Epub ahead of print].
The study investigates the microbial composition of bat flies (Diptera: Nycteribiidae) collected from Myotis punicus in Algeria, focusing on the diversity and dynamics of their microbiota through network analysis. The analysis targets two genera, Nycteribia and Penicillidia, comparing oioxenous and stenoxenous species to understand host specificity's influence on microbial communities. Utilizing 16S rRNA sequencing, alpha and beta diversity metrics, and co-occurrence networks, the study assesses microbial diversity, community composition, and the impact of specific bacteria (endosymbionts, commensals, and pathogens) on network stability. Results reveal significant microbial community variations between genera and species, with N. latreillii exhibiting the most complex network. We showed that host specificity and feeding strategies significantly influence microbial diversity and interactions within bat flies. Robustness analysis through node removal simulations identifies the roles of key bacteria, such as Wolbachia, Arsenophonus, and Bartonella, in maintaining network stability. Findings highlight the complex interplay between these microorganisms and their hosts, offering insights into microbial ecology and vector-pathogen dynamics. The research underscores the importance of bat flies in shaping pathogen transmission networks, contributing valuable knowledge to wildlife ecology, disease control, and conservation strategies.
Additional Links: PMID-41131131
PubMed:
Citation:
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@article {pmid41131131,
year = {2025},
author = {Corduneanu, A and Bendjeddou, ML and Sándor, AD and Mihalca, AD and Hornok, S and Péter, Á and Khelfaoui, F and Aželytè, J and Obregon, D and Mateos-Hernández, L and Maitre, A and Abuin-Denis, L and Wu-Chuang, A and Kratou, M and Ben Said, M and Cabezas-Cruz, A},
title = {Microbial network assembly in bat flies with differing host specificity from North Africa.},
journal = {International microbiology : the official journal of the Spanish Society for Microbiology},
volume = {},
number = {},
pages = {},
pmid = {41131131},
issn = {1618-1905},
support = {14/2022-2024//Ministerul Cercetării şi Inovării/ ; 1500107//Hungarian Research Network/ ; NTP-NFTÖ-20-B-0094//Hungarian Ministry of Human Resources, Hungary/ ; SGCE - RAPPORT No 0300//Collectivité de Corse/ ; ANR-10-LABX-62-IBEID//Agence Nationale de la Recherche/ ; },
abstract = {The study investigates the microbial composition of bat flies (Diptera: Nycteribiidae) collected from Myotis punicus in Algeria, focusing on the diversity and dynamics of their microbiota through network analysis. The analysis targets two genera, Nycteribia and Penicillidia, comparing oioxenous and stenoxenous species to understand host specificity's influence on microbial communities. Utilizing 16S rRNA sequencing, alpha and beta diversity metrics, and co-occurrence networks, the study assesses microbial diversity, community composition, and the impact of specific bacteria (endosymbionts, commensals, and pathogens) on network stability. Results reveal significant microbial community variations between genera and species, with N. latreillii exhibiting the most complex network. We showed that host specificity and feeding strategies significantly influence microbial diversity and interactions within bat flies. Robustness analysis through node removal simulations identifies the roles of key bacteria, such as Wolbachia, Arsenophonus, and Bartonella, in maintaining network stability. Findings highlight the complex interplay between these microorganisms and their hosts, offering insights into microbial ecology and vector-pathogen dynamics. The research underscores the importance of bat flies in shaping pathogen transmission networks, contributing valuable knowledge to wildlife ecology, disease control, and conservation strategies.},
}
RevDate: 2025-10-23
Anaerobic fungi - effective warriors in lignocellulosic biomass degradation and fermentation.
FEMS microbiology ecology pii:8300365 [Epub ahead of print].
The significant advancements in understanding the roles of anaerobic fungi within microbial ecology have opened numerous avenues for biotechnological exploitation, particularly in enhancing the productivity of livestock. The efficient, unique, and complex enzyme systems of anaerobic fungi play a determining role in the metabolic conversion of lignocellulosic plant matter into animal products such as milk and meat by mammalian herbivores. Mitigation of methane emissions through microbial or dietary strategies in ruminants is a major environmental climate change issue. In turn, controlled management of the inter-kingdom syntrophic interactions among the eukaryotic anaerobic fungi, prokaryotic bacteria and archaea can lead to the production of valuable biofuels, (biomethane, biohydrogen, bioethanol), and organic acids. These products can also serve as building blocks in numerous processes to generate high value chemicals in circular bioeconomy.
Additional Links: PMID-41129402
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PubMed:
Citation:
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@article {pmid41129402,
year = {2025},
author = {Kovács, E and Szűcs, C and Juhász-Erdélyi, A and Bagi, Z and Kovács, KL},
title = {Anaerobic fungi - effective warriors in lignocellulosic biomass degradation and fermentation.},
journal = {FEMS microbiology ecology},
volume = {},
number = {},
pages = {},
doi = {10.1093/femsec/fiaf108},
pmid = {41129402},
issn = {1574-6941},
abstract = {The significant advancements in understanding the roles of anaerobic fungi within microbial ecology have opened numerous avenues for biotechnological exploitation, particularly in enhancing the productivity of livestock. The efficient, unique, and complex enzyme systems of anaerobic fungi play a determining role in the metabolic conversion of lignocellulosic plant matter into animal products such as milk and meat by mammalian herbivores. Mitigation of methane emissions through microbial or dietary strategies in ruminants is a major environmental climate change issue. In turn, controlled management of the inter-kingdom syntrophic interactions among the eukaryotic anaerobic fungi, prokaryotic bacteria and archaea can lead to the production of valuable biofuels, (biomethane, biohydrogen, bioethanol), and organic acids. These products can also serve as building blocks in numerous processes to generate high value chemicals in circular bioeconomy.},
}
RevDate: 2025-10-23
CmpDate: 2025-10-23
Effects of Facility Cultivation Shaping Soil Microbial Community Structure in Jujube Orchard.
Microbial ecology, 88(1):112.
Facility cultivation systems provide protection for jujube (Ziziphus jujuba) against rain-induced fruit cracking during the maturation and regulate the fruit ripening process. Prolonged cultivation within these controlled environments may alter the soil microbial community structure, potentially detrimentally affecting plant growth and fruit quality. There is a lack of information regarding the arbuscular mycorrhizal fungi (AMF) and bacterial communities in orchards under facility conditions. This study compared the soil bacterial and AMF communities in jujube orchards under greenhouse and rain shelter conditions. Greenhouse cultivation significantly increased soil organic carbon (SOC), total nitrogen (TN), and electrical conductivity, while it decreased soil pH compared to rain shelters. These changes were associated with reduced α-diversity indices in both bacterial and AMF communities. Non-metric multidimensional scaling analysis demonstrated distinct differences between bacteria and AMF communities under the two cultivation types. The phyla Actinobacteria, Gemmatimonadetes, and Rokubacteria were identified as key contributors to the observed alterations in the bacterial community, while variations in the genus Glomus and Paraglomus were responsible for changes in the AMF communities between the two cultivation types. Redundancy analysis revealed that pH was the primary factor shaping microbial community structure across the two cultivation types. Using a Zi-Pi plot, we identified several keystone ASVs, which showed a positive correlation with pH, SOC, and TN. The findings highlight the significant impact of cultivation type on soil microbial community structure and function, which has important implications for optimizing cultivation practices and ensuring sustainable jujube production.
Additional Links: PMID-41128906
PubMed:
Citation:
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@article {pmid41128906,
year = {2025},
author = {Ma, Z and Wang, J and Huang, C and Cao, Y and Sun, Y and Hu, Y and Basit, MF and Huang, J},
title = {Effects of Facility Cultivation Shaping Soil Microbial Community Structure in Jujube Orchard.},
journal = {Microbial ecology},
volume = {88},
number = {1},
pages = {112},
pmid = {41128906},
issn = {1432-184X},
support = {2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 2019YFD1001605//National Key Research and Development Program of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; 31870584//National Natural Science Foundation of China/ ; XJCYTX-01//Xinjiang Jujube Industrial Technology System/ ; XJCYTX-01//Xinjiang Jujube Industrial Technology System/ ; XJCYTX-01//Xinjiang Jujube Industrial Technology System/ ; XJCYTX-01//Xinjiang Jujube Industrial Technology System/ ; XJCYTX-01//Xinjiang Jujube Industrial Technology System/ ; },
mesh = {*Soil Microbiology ; *Ziziphus/microbiology/growth & development ; *Bacteria/classification/genetics/isolation & purification ; Soil/chemistry ; *Mycorrhizae/classification/genetics/isolation & purification ; *Microbiota ; Nitrogen/analysis ; *Agriculture/methods ; Carbon/analysis ; Hydrogen-Ion Concentration ; Biodiversity ; },
abstract = {Facility cultivation systems provide protection for jujube (Ziziphus jujuba) against rain-induced fruit cracking during the maturation and regulate the fruit ripening process. Prolonged cultivation within these controlled environments may alter the soil microbial community structure, potentially detrimentally affecting plant growth and fruit quality. There is a lack of information regarding the arbuscular mycorrhizal fungi (AMF) and bacterial communities in orchards under facility conditions. This study compared the soil bacterial and AMF communities in jujube orchards under greenhouse and rain shelter conditions. Greenhouse cultivation significantly increased soil organic carbon (SOC), total nitrogen (TN), and electrical conductivity, while it decreased soil pH compared to rain shelters. These changes were associated with reduced α-diversity indices in both bacterial and AMF communities. Non-metric multidimensional scaling analysis demonstrated distinct differences between bacteria and AMF communities under the two cultivation types. The phyla Actinobacteria, Gemmatimonadetes, and Rokubacteria were identified as key contributors to the observed alterations in the bacterial community, while variations in the genus Glomus and Paraglomus were responsible for changes in the AMF communities between the two cultivation types. Redundancy analysis revealed that pH was the primary factor shaping microbial community structure across the two cultivation types. Using a Zi-Pi plot, we identified several keystone ASVs, which showed a positive correlation with pH, SOC, and TN. The findings highlight the significant impact of cultivation type on soil microbial community structure and function, which has important implications for optimizing cultivation practices and ensuring sustainable jujube production.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Soil Microbiology
*Ziziphus/microbiology/growth & development
*Bacteria/classification/genetics/isolation & purification
Soil/chemistry
*Mycorrhizae/classification/genetics/isolation & purification
*Microbiota
Nitrogen/analysis
*Agriculture/methods
Carbon/analysis
Hydrogen-Ion Concentration
Biodiversity
RevDate: 2025-10-23
Nitrogen fixation under declining Arctic sea ice.
Communications earth & environment, 6(1):811.
With climate change-induced sea ice decline in the Arctic Ocean, nitrogen is expected to become an increasingly important determinant of primary productivity. Nitrogen fixation is the conversion of molecular nitrogen to bioavailable ammonium by microorganisms called diazotrophs. Here, we report nitrogen fixation rates, diazotroph composition, and expression under different stages of declining sea ice in the Central Arctic Ocean (multiyear ice, five stations) and the Eurasian Arctic (marginal ice zone, seven stations). Nitrogen fixation in the Central Arctic Ocean was positively correlated with primary production, ranging from 0.4 ± 0.1 to 2.5 ± 0.87 nmol N L[-1] d[-1]. Along two transects across the marginal ice zone, nitrogen fixation varied between days and ice regime from below detection up to 5.3 ± 3.65 nmol N L[-1] d[-1] associated with an ice-edge phytoplankton bloom. We show nitrogen fixation in sea ice-covered waters of the Arctic Ocean and provide insight into present and active non-cyanobacterial diazotrophs in the region.
Additional Links: PMID-41127647
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Citation:
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@article {pmid41127647,
year = {2025},
author = {von Friesen, LW and Farnelid, H and von Appen, WJ and Benavides, M and Grosso, O and Laber, CP and Schüttler, J and Sundbom, M and Torres-Valdés, S and Bertilsson, S and Peeken, I and Snoeijs-Leijonmalm, P and Riemann, L},
title = {Nitrogen fixation under declining Arctic sea ice.},
journal = {Communications earth & environment},
volume = {6},
number = {1},
pages = {811},
pmid = {41127647},
issn = {2662-4435},
abstract = {With climate change-induced sea ice decline in the Arctic Ocean, nitrogen is expected to become an increasingly important determinant of primary productivity. Nitrogen fixation is the conversion of molecular nitrogen to bioavailable ammonium by microorganisms called diazotrophs. Here, we report nitrogen fixation rates, diazotroph composition, and expression under different stages of declining sea ice in the Central Arctic Ocean (multiyear ice, five stations) and the Eurasian Arctic (marginal ice zone, seven stations). Nitrogen fixation in the Central Arctic Ocean was positively correlated with primary production, ranging from 0.4 ± 0.1 to 2.5 ± 0.87 nmol N L[-1] d[-1]. Along two transects across the marginal ice zone, nitrogen fixation varied between days and ice regime from below detection up to 5.3 ± 3.65 nmol N L[-1] d[-1] associated with an ice-edge phytoplankton bloom. We show nitrogen fixation in sea ice-covered waters of the Arctic Ocean and provide insight into present and active non-cyanobacterial diazotrophs in the region.},
}
RevDate: 2025-10-23
CmpDate: 2025-10-23
Developing and validating a nomogram for predicting endoscopic hemostasis failure in cirrhotic patients with esophageal variceal bleeding.
Frontiers in medicine, 12:1670759.
BACKGROUND AND AIMS: This study aimed to create and validate a model to predict the failure of endoscopic hemostasis in Chinese cirrhosis patients with acute esophagogastric variceal bleeding (EGVB), enabling early identification of high-risk individuals.
METHODS: A retrospective study analyzed 296 cirrhotic patients with EGVB who received emergency endoscopic therapy from January 2020 to February 2025. Patients were divided into success (n = 273) and failure (n = 23, defined as bleeding recurrence within 5 days) groups. LASSO regression optimized variable selection, and multivariate logistic regression identified independent predictors to create a nomogram. Internal validation used Bootstrap resampling (500 iterations). Model performance was assessed using ROC curves, calibration plots, and decision curve analysis (DCA), and compared with CTP (Child-Turcotte-Pugh), MELD (Model for End-Stage Liver Disease), and Rockall scores.
RESULTS: The cumulative incidence of endoscopic failure was observed to be 7.8%. Independent predictors identified included a shock index (SI) > 1.2 (OR = 5.447), the presence of a red color (RC) sign (OR = 10.005), active bleeding observed during endoscopy (OR = 5.962), and the CTP (OR = 1.584). The nomogram exhibited superior discriminatory power with an AUC of 0.890 (95% CI: 0.820-0.960), outperforming the CTP (AUC = 0.771, 95% CI: 0.656-0.886; P < 0.001), MELD (AUC = 0.733, 95% CI: 0.616-0.849; P < 0.001), and Rockall (AUC = 0.656, 95% CI: 0.545-0.768; P < 0.001). Calibration was satisfactory as indicated by the Hosmer-Lemeshow test (χ[2] = 10.021, P = 0.263). DCA demonstrated a clinical net benefit across a broad range of thresholds.
CONCLUSION: A validated nomogram that integrates the SI, RC sign, active bleeding, and CTP provides an effective prediction of the risk of endoscopic hemostasis failure in patients with cirrhotic EGVB, thereby facilitating timely intervention.
Additional Links: PMID-41127399
PubMed:
Citation:
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@article {pmid41127399,
year = {2025},
author = {Guo, Y and Ouyang, H and Su, J and Zhong, M and Huang, W and Huang, M and Xie, C},
title = {Developing and validating a nomogram for predicting endoscopic hemostasis failure in cirrhotic patients with esophageal variceal bleeding.},
journal = {Frontiers in medicine},
volume = {12},
number = {},
pages = {1670759},
pmid = {41127399},
issn = {2296-858X},
abstract = {BACKGROUND AND AIMS: This study aimed to create and validate a model to predict the failure of endoscopic hemostasis in Chinese cirrhosis patients with acute esophagogastric variceal bleeding (EGVB), enabling early identification of high-risk individuals.
METHODS: A retrospective study analyzed 296 cirrhotic patients with EGVB who received emergency endoscopic therapy from January 2020 to February 2025. Patients were divided into success (n = 273) and failure (n = 23, defined as bleeding recurrence within 5 days) groups. LASSO regression optimized variable selection, and multivariate logistic regression identified independent predictors to create a nomogram. Internal validation used Bootstrap resampling (500 iterations). Model performance was assessed using ROC curves, calibration plots, and decision curve analysis (DCA), and compared with CTP (Child-Turcotte-Pugh), MELD (Model for End-Stage Liver Disease), and Rockall scores.
RESULTS: The cumulative incidence of endoscopic failure was observed to be 7.8%. Independent predictors identified included a shock index (SI) > 1.2 (OR = 5.447), the presence of a red color (RC) sign (OR = 10.005), active bleeding observed during endoscopy (OR = 5.962), and the CTP (OR = 1.584). The nomogram exhibited superior discriminatory power with an AUC of 0.890 (95% CI: 0.820-0.960), outperforming the CTP (AUC = 0.771, 95% CI: 0.656-0.886; P < 0.001), MELD (AUC = 0.733, 95% CI: 0.616-0.849; P < 0.001), and Rockall (AUC = 0.656, 95% CI: 0.545-0.768; P < 0.001). Calibration was satisfactory as indicated by the Hosmer-Lemeshow test (χ[2] = 10.021, P = 0.263). DCA demonstrated a clinical net benefit across a broad range of thresholds.
CONCLUSION: A validated nomogram that integrates the SI, RC sign, active bleeding, and CTP provides an effective prediction of the risk of endoscopic hemostasis failure in patients with cirrhotic EGVB, thereby facilitating timely intervention.},
}
RevDate: 2025-10-22
CmpDate: 2025-10-23
A reference metagenome sequence of the lichen Cladonia rangiformis.
BMC biology, 23(1):319.
BACKGROUND: Lichens are an ancient symbiosis comprising the thalli of lichen-forming fungi, their photoautotrophic partners, and their microbiome. So far, they were poorly studied at the genome sequence level. Here, we present a reference metagenome for the holobiont of Cladonia rangiformis, aiming to illuminate the genomic complexity and evolutionary interactions within lichen symbioses.
RESULTS: Using long-read sequences from an entire symbiotic complex, plus short-read libraries from 28 additional diverse European lichen samples, we were able to separate genome sequences of 20 individual species. We constructed chromosome-scale assemblies of the C. rangiformis fungus and its trebouxioid green algal photobiont Asterochloris mediterranea. The genome of the fungus comprises ~ 22% transposable elements and is highly compartmentalized into genic regions and large TE-derived segments which show extensive signatures of repeat-induced point mutations (RIP). We found that A. mediterranea centromeres are predominantly derived from two interacting retrotransposon families. We also identified strong candidates for genes that were horizontally transferred from bacteria to both alga and fungus. Furthermore, we isolated 18 near-complete bacterial genomes, of which 13 are enriched in the lichen compared to surrounding soil. Analysis of gene content in fungus, algae, and bacteria identified 22 distinct biosynthetic gene cluster categories for known secondary metabolites.
CONCLUSIONS: Our findings revealed that the thalli of C. rangiformis have a highly complex microbiome, comprising a mix of species that may include opportunists, ecologically obligate symbionts and possibly even lichen-beneficial bacteria. This study provides the first chromosome-scale genomic framework for a lichen holobiont, offering a foundational resource for future research into metagenomics, symbiosis, and microbial ecology in lichens.
Additional Links: PMID-41126179
PubMed:
Citation:
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@article {pmid41126179,
year = {2025},
author = {Heuberger, M and Wehrkamp, CM and Pfammatter, A and Poretti, M and Graf, JP and Herger, A and Isaksson, J and Schlagenhauf, E and Honegger, R and Wicker, T and Sotiropoulos, AG},
title = {A reference metagenome sequence of the lichen Cladonia rangiformis.},
journal = {BMC biology},
volume = {23},
number = {1},
pages = {319},
pmid = {41126179},
issn = {1741-7007},
support = {310030_212428//Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung/ ; },
mesh = {*Lichens/genetics/microbiology ; *Metagenome ; Symbiosis/genetics ; *Genome, Fungal ; *Ascomycota/genetics ; Chlorophyta/genetics ; },
abstract = {BACKGROUND: Lichens are an ancient symbiosis comprising the thalli of lichen-forming fungi, their photoautotrophic partners, and their microbiome. So far, they were poorly studied at the genome sequence level. Here, we present a reference metagenome for the holobiont of Cladonia rangiformis, aiming to illuminate the genomic complexity and evolutionary interactions within lichen symbioses.
RESULTS: Using long-read sequences from an entire symbiotic complex, plus short-read libraries from 28 additional diverse European lichen samples, we were able to separate genome sequences of 20 individual species. We constructed chromosome-scale assemblies of the C. rangiformis fungus and its trebouxioid green algal photobiont Asterochloris mediterranea. The genome of the fungus comprises ~ 22% transposable elements and is highly compartmentalized into genic regions and large TE-derived segments which show extensive signatures of repeat-induced point mutations (RIP). We found that A. mediterranea centromeres are predominantly derived from two interacting retrotransposon families. We also identified strong candidates for genes that were horizontally transferred from bacteria to both alga and fungus. Furthermore, we isolated 18 near-complete bacterial genomes, of which 13 are enriched in the lichen compared to surrounding soil. Analysis of gene content in fungus, algae, and bacteria identified 22 distinct biosynthetic gene cluster categories for known secondary metabolites.
CONCLUSIONS: Our findings revealed that the thalli of C. rangiformis have a highly complex microbiome, comprising a mix of species that may include opportunists, ecologically obligate symbionts and possibly even lichen-beneficial bacteria. This study provides the first chromosome-scale genomic framework for a lichen holobiont, offering a foundational resource for future research into metagenomics, symbiosis, and microbial ecology in lichens.},
}
MeSH Terms:
show MeSH Terms
hide MeSH Terms
*Lichens/genetics/microbiology
*Metagenome
Symbiosis/genetics
*Genome, Fungal
*Ascomycota/genetics
Chlorophyta/genetics
RevDate: 2025-10-22
Higher variability of bacterial communities across space than over time in Antarctic lakes, and contrasting assembly processes.
Applied and environmental microbiology [Epub ahead of print].
As sentinels of environmental changes, Antarctic lakes are ideal systems for studying the temporal and spatial dynamics of microbial communities. However, the relative magnitude and underlying mechanisms driving these variations remain poorly understood. Studying the spatiotemporal variation of microbial communities is crucial to provide a robust baseline for predicting ecosystem responses to global changes. Here, we investigated the spatial and inter-annual variation of bacterial community structure and their underlying assembly processes across sediment and water habitats in 11 lakes on the Fildes Peninsula, Maritime Antarctica, sampled during austral summers from 2017 to 2023, using 16S rRNA gene sequencing. The communities primarily clustered by habitat, with higher diversity in sediment (characterized by Rhodoferax, Intraporangiaceae, and Vicinamibacterales) compared to water (characterized by Polaromonas, Flavovacterium, and Sporichthyaceae). Spatial turnover of communities dominated over inter-annual variation in both habitats. Accordingly, the temporal core microbiome showed greater stability than the spatial core. The conserved bacterial communities (core communities) over time and across space exhibited a strikingly similar taxonomic composition. Community assembly processes differed between habitats, with a stronger contribution of dispersal limitation in sediment, versus ecological drift in water, as expected from the differences in connectivity within each habitat. Spatial and temporal variations in sediment were driven by globally similar assembly processes. In contrast, in water communities, different assembly processes explained the spatial and temporal variation. These insights emphasize the need to consider both spatial and temporal scales and various habitat types when predicting future bacterial dynamics in Antarctic lakes in a changing environment.IMPORTANCEUnderstanding the inherent baseline microbial dynamics in Antarctic lakes is crucial for predicting their responses to environmental changes. Our findings underscore the predominance of spatial (rather than inter-annual) factors in shaping bacterial communities and highlight the slightly higher contribution of stochastic processes in sediment compared to water habitats. The stochastic processes differed considerably among habitats. The greater stability of the temporal core microbiome suggests a certain degree of resilience toward possible seasonal fluctuations between the inter-annual sampling dates. In water, dispersal limitation and homogeneous selection played a greater role in the spatial than in the temporal turnover of communities, whereas environmental filtering exerted a stronger influence over time. Future studies should integrate both spatial and temporal dimensions in evaluating microbial community variability to improve forecasting of ecosystem shifts in response to global change and thus provide a better baseline for Antarctic biodiversity conservation and management.
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@article {pmid41124090,
year = {2025},
author = {Ahumada, D and Schwob, G and Osorio, M and Astorga, MS and Lavergne, C and Olgun, N and Thalasso, F and Poulin, E and Orlando, J and Cabrol, L},
title = {Higher variability of bacterial communities across space than over time in Antarctic lakes, and contrasting assembly processes.},
journal = {Applied and environmental microbiology},
volume = {},
number = {},
pages = {e0107925},
doi = {10.1128/aem.01079-25},
pmid = {41124090},
issn = {1098-5336},
abstract = {As sentinels of environmental changes, Antarctic lakes are ideal systems for studying the temporal and spatial dynamics of microbial communities. However, the relative magnitude and underlying mechanisms driving these variations remain poorly understood. Studying the spatiotemporal variation of microbial communities is crucial to provide a robust baseline for predicting ecosystem responses to global changes. Here, we investigated the spatial and inter-annual variation of bacterial community structure and their underlying assembly processes across sediment and water habitats in 11 lakes on the Fildes Peninsula, Maritime Antarctica, sampled during austral summers from 2017 to 2023, using 16S rRNA gene sequencing. The communities primarily clustered by habitat, with higher diversity in sediment (characterized by Rhodoferax, Intraporangiaceae, and Vicinamibacterales) compared to water (characterized by Polaromonas, Flavovacterium, and Sporichthyaceae). Spatial turnover of communities dominated over inter-annual variation in both habitats. Accordingly, the temporal core microbiome showed greater stability than the spatial core. The conserved bacterial communities (core communities) over time and across space exhibited a strikingly similar taxonomic composition. Community assembly processes differed between habitats, with a stronger contribution of dispersal limitation in sediment, versus ecological drift in water, as expected from the differences in connectivity within each habitat. Spatial and temporal variations in sediment were driven by globally similar assembly processes. In contrast, in water communities, different assembly processes explained the spatial and temporal variation. These insights emphasize the need to consider both spatial and temporal scales and various habitat types when predicting future bacterial dynamics in Antarctic lakes in a changing environment.IMPORTANCEUnderstanding the inherent baseline microbial dynamics in Antarctic lakes is crucial for predicting their responses to environmental changes. Our findings underscore the predominance of spatial (rather than inter-annual) factors in shaping bacterial communities and highlight the slightly higher contribution of stochastic processes in sediment compared to water habitats. The stochastic processes differed considerably among habitats. The greater stability of the temporal core microbiome suggests a certain degree of resilience toward possible seasonal fluctuations between the inter-annual sampling dates. In water, dispersal limitation and homogeneous selection played a greater role in the spatial than in the temporal turnover of communities, whereas environmental filtering exerted a stronger influence over time. Future studies should integrate both spatial and temporal dimensions in evaluating microbial community variability to improve forecasting of ecosystem shifts in response to global change and thus provide a better baseline for Antarctic biodiversity conservation and management.},
}
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