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。

IF 12.7 1区 生物学 Q1 MICROBIOLOGY
Alexandra Brante, Paulina Bustos, Claudio Ortega-Muñoz, Eliana Paola Acuña Gómez, Vicenzo Brante, Rodolfo Farlora
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引用次数: 0

摘要

背景:环境变异性塑造了亚南极地区微生物群落的组成和功能,但其对微生物基因表达和宿主-微生物组相互作用的影响仍知之甚少。鳃是水生生物与其环境之间的主要界面,其中蕴藏着多种动态微生物群落,在宿主生理中起着重要作用。利用亚转录组学方法,本研究旨在探索巴塔哥尼亚峡湾非生物波动对南部帝王蟹(Lithodes santolla) holobiont鳃相关微生物组功能的影响。通过评估微生物组成和基因表达的变化,本研究旨在揭示与微生物代谢调节和宿主恢复力相关的功能途径。这些发现为海洋物种微生物组驱动的功能反应提供了见解,并可能为环境变化下的保护策略提供信息。结果:从balena Sound和Choiseul Bay两个环境不同的地点收集的个体的微生物基因表达谱显示微生物组成略有差异,变形菌门在两个地点都占主导地位。功能注释确定了涉及能量产生、应激反应和微生物相互作用的关键代谢途径,突出了对环境波动的独特适应机制。差异表达分析揭示了碳固定、离子运输和氧化应激反应的变化,表明这些生理反应可以通过环境条件来模拟。此外,宿主相关转录本在免疫调节和代谢稳态途径中表现出差异富集,表明微生物组对宿主生理有介导作用。结论:这些发现首次揭示了环境因素与圣多拉微生物功能之间的动态关系,突出了鳃相关微生物组可塑性在适应变化的栖息地中的重要性。这些结果提高了我们对亚南极环境中微生物驱动的功能响应的理解,为评估这些波动生态系统中全息生物的恢复力提供了有价值的视角。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
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.
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