Hypobaric hypoxia affects gut microbiota of rats through affected community assembly, reduced network resilience, and metabolic reprogramming.

IF 3.2 3区 生物学 Q2 MICROBIOLOGY
Xinyang Chen, Yihong Wang, Jianzhuo Feng, Huiqing Chen, Baohui Yao, Fuxin Li, Quanyu Yang, Jiapeng Qu
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Abstract

In host-microbe interactions, host diet and environmental stress are key driving factors shaping the gut microbiota. Although previous studies have shown that hypoxia affects the structure and function of the gut microbiota in rodents, most have relied on 16S rRNA gene sequencing and lacked analysis of community assembly mechanisms, co-occurrence networks, and functional pathways. Here, we used metagenomic next-generation sequencing (mNGS) to examine the gut microbiota of rats exposed to hypobaric hypoxia (WH, simulated 6000 m altitude) compared to WL group (2100 m altitude). Hypoxia significantly altered β-diversity of gut microbiota, but did not affect its α-diversity. Community assembly was primarily governed by stochastic processes, with hypoxia stress reducing their impact. Microbial co-occurrence networks were dominated by positive correlations, although network resilience and stability declined under hypoxia. Helicobacter and Eubacterium were identified as high-abundance differentiating genera, and Akkermansia muciniphila was significantly enriched in WH group. Functional analysis revealed alterations in pathways related to protein synthesis and carbohydrate metabolism, suggesting that hypoxia may affect nutrient utilization by the host. Overall, these findings provide a comprehensive view of how hypoxic stress reshapes the gut microbiota of rats, offering new insights into microbial dynamics under environmental stress.

低气压缺氧通过影响群落聚集、降低网络弹性和代谢重编程影响大鼠肠道微生物群。
在宿主-微生物相互作用中,宿主饮食和环境应激是塑造肠道微生物群的关键驱动因素。虽然已有研究表明缺氧会影响啮齿动物肠道微生物群的结构和功能,但大多数研究都依赖于16S rRNA基因测序,缺乏对群落组装机制、共现网络和功能途径的分析。在这里,我们使用宏基因组下一代测序(mNGS)来检测暴露于低气压缺氧(WH,模拟海拔6000米)的大鼠与WL组(海拔2100米)的肠道微生物群。缺氧显著改变了肠道菌群β-多样性,但不影响α-多样性。群落聚集主要受随机过程控制,低氧胁迫降低了其影响。微生物共生网络以正相关为主,但网络弹性和稳定性在缺氧条件下有所下降。Helicobacter和Eubacterium是高丰度的分化属,而Akkermansia muciniphila在WH组中显著富集。功能分析显示,与蛋白质合成和碳水化合物代谢相关的途径发生了变化,表明缺氧可能影响宿主对营养物质的利用。总的来说,这些发现提供了一个关于缺氧应激如何重塑大鼠肠道微生物群的全面观点,为环境应激下的微生物动力学提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
FEMS microbiology ecology
FEMS microbiology ecology 生物-微生物学
CiteScore
7.50
自引率
2.40%
发文量
132
审稿时长
3 months
期刊介绍: FEMS Microbiology Ecology aims to ensure efficient publication of high-quality papers that are original and provide a significant contribution to the understanding of microbial ecology. The journal contains Research Articles and MiniReviews on fundamental aspects of the ecology of microorganisms in natural soil, aquatic and atmospheric habitats, including extreme environments, and in artificial or managed environments. Research papers on pure cultures and in the areas of plant pathology and medical, food or veterinary microbiology will be published where they provide valuable generic information on microbial ecology. Papers can deal with culturable and non-culturable forms of any type of microorganism: bacteria, archaea, filamentous fungi, yeasts, protozoa, cyanobacteria, algae or viruses. In addition, the journal will publish Perspectives, Current Opinion and Controversy Articles, Commentaries and Letters to the Editor on topical issues in microbial ecology. - Application of ecological theory to microbial ecology - Interactions and signalling between microorganisms and with plants and animals - Interactions between microorganisms and their physicochemical enviornment - Microbial aspects of biogeochemical cycles and processes - Microbial community ecology - Phylogenetic and functional diversity of microbial communities - Evolutionary biology of microorganisms
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