{"title":"环境可变性驱动的功能可塑性在鳃相关微生物组的山顶石:一个元转录组学的观点。","authors":"Alexandra Brante, Paulina Bustos, Claudio Ortega-Muñoz, Eliana Paola Acuña Gómez, Vicenzo Brante, Rodolfo Farlora","doi":"10.1186/s40168-025-02215-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Environmental variability shapes microbial community composition and function, yet its influence on microbial gene expression and host-microbiome interactions in sub-Antarctic regions remains poorly understood. Gills serve as the primary interface between aquatic organisms and their environment, harboring diverse and dynamic microbial communities that play a fundamental role in host physiology. Using a metatranscriptomic approach, this research aims to explore the influence of abiotic fluctuations in Patagonian fjords on the functional profile of the gill-associated microbiome in the southern king crab (Lithodes santolla) holobiont. By assessing shifts in microbial composition and gene expression, this research aims to uncover functional pathways linked to microbial metabolic adjustments and the host's resilience. The findings provide insights into microbiome-driven functional responses in marine species and may inform conservation strategies under environmental change.</p><p><strong>Results: </strong>Microbial gene expression profiles from individuals collected at two environmentally distinct locations, Ballena Sound and Choiseul Bay, revealed slight differences in microbial composition, with Proteobacteria dominating at both sites. Functional annotation identified key metabolic pathways involved in energy production, stress response, and microbial interactions, highlighting distinct adaptive mechanisms to environmental fluctuations. Differential expression analysis revealed shifts in carbon fixation, ion transport, and oxidative stress responses, suggesting that these physiological responses could be modeled by environmental conditions. Additionally, host-associated transcripts showed differential enrichment in immune regulation and metabolic homeostasis pathways, suggesting microbiome-mediated effects on host physiology.</p><p><strong>Conclusions: </strong>These findings offer first insights into the dynamic relationship between environmental factors and microbial functionality in L. santolla, highlighting the significance of gill-associated microbiome plasticity in adapting to changing habitats. These results improve our understanding of microbiome-driven functional responses to sub-Antarctic environments, offering valuable perspectives for assessing holobiont resilience in these fluctuating ecosystems. Video Abstract.</p>","PeriodicalId":18447,"journal":{"name":"Microbiome","volume":"13 1","pages":"197"},"PeriodicalIF":12.7000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12487024/pdf/","citationCount":"0","resultStr":"{\"title\":\"Environmental variability drives functional plasticity in the gill-associated microbiome of Lithodes santolla: a meta-transcriptomic perspective.\",\"authors\":\"Alexandra Brante, Paulina Bustos, Claudio Ortega-Muñoz, Eliana Paola Acuña Gómez, Vicenzo Brante, Rodolfo Farlora\",\"doi\":\"10.1186/s40168-025-02215-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Environmental variability shapes microbial community composition and function, yet its influence on microbial gene expression and host-microbiome interactions in sub-Antarctic regions remains poorly understood. Gills serve as the primary interface between aquatic organisms and their environment, harboring diverse and dynamic microbial communities that play a fundamental role in host physiology. Using a metatranscriptomic approach, this research aims to explore the influence of abiotic fluctuations in Patagonian fjords on the functional profile of the gill-associated microbiome in the southern king crab (Lithodes santolla) holobiont. By assessing shifts in microbial composition and gene expression, this research aims to uncover functional pathways linked to microbial metabolic adjustments and the host's resilience. The findings provide insights into microbiome-driven functional responses in marine species and may inform conservation strategies under environmental change.</p><p><strong>Results: </strong>Microbial gene expression profiles from individuals collected at two environmentally distinct locations, Ballena Sound and Choiseul Bay, revealed slight differences in microbial composition, with Proteobacteria dominating at both sites. Functional annotation identified key metabolic pathways involved in energy production, stress response, and microbial interactions, highlighting distinct adaptive mechanisms to environmental fluctuations. Differential expression analysis revealed shifts in carbon fixation, ion transport, and oxidative stress responses, suggesting that these physiological responses could be modeled by environmental conditions. Additionally, host-associated transcripts showed differential enrichment in immune regulation and metabolic homeostasis pathways, suggesting microbiome-mediated effects on host physiology.</p><p><strong>Conclusions: </strong>These findings offer first insights into the dynamic relationship between environmental factors and microbial functionality in L. santolla, highlighting the significance of gill-associated microbiome plasticity in adapting to changing habitats. These results improve our understanding of microbiome-driven functional responses to sub-Antarctic environments, offering valuable perspectives for assessing holobiont resilience in these fluctuating ecosystems. Video Abstract.</p>\",\"PeriodicalId\":18447,\"journal\":{\"name\":\"Microbiome\",\"volume\":\"13 1\",\"pages\":\"197\"},\"PeriodicalIF\":12.7000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12487024/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbiome\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s40168-025-02215-6\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiome","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s40168-025-02215-6","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Environmental variability drives functional plasticity in the gill-associated microbiome of Lithodes santolla: a meta-transcriptomic perspective.
Background: Environmental variability shapes microbial community composition and function, yet its influence on microbial gene expression and host-microbiome interactions in sub-Antarctic regions remains poorly understood. Gills serve as the primary interface between aquatic organisms and their environment, harboring diverse and dynamic microbial communities that play a fundamental role in host physiology. Using a metatranscriptomic approach, this research aims to explore the influence of abiotic fluctuations in Patagonian fjords on the functional profile of the gill-associated microbiome in the southern king crab (Lithodes santolla) holobiont. By assessing shifts in microbial composition and gene expression, this research aims to uncover functional pathways linked to microbial metabolic adjustments and the host's resilience. The findings provide insights into microbiome-driven functional responses in marine species and may inform conservation strategies under environmental change.
Results: Microbial gene expression profiles from individuals collected at two environmentally distinct locations, Ballena Sound and Choiseul Bay, revealed slight differences in microbial composition, with Proteobacteria dominating at both sites. Functional annotation identified key metabolic pathways involved in energy production, stress response, and microbial interactions, highlighting distinct adaptive mechanisms to environmental fluctuations. Differential expression analysis revealed shifts in carbon fixation, ion transport, and oxidative stress responses, suggesting that these physiological responses could be modeled by environmental conditions. Additionally, host-associated transcripts showed differential enrichment in immune regulation and metabolic homeostasis pathways, suggesting microbiome-mediated effects on host physiology.
Conclusions: These findings offer first insights into the dynamic relationship between environmental factors and microbial functionality in L. santolla, highlighting the significance of gill-associated microbiome plasticity in adapting to changing habitats. These results improve our understanding of microbiome-driven functional responses to sub-Antarctic environments, offering valuable perspectives for assessing holobiont resilience in these fluctuating ecosystems. Video Abstract.
期刊介绍:
Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.