Yan Zhang , Yihong Wang , Baohui Yao , Zhaoxian Tan , Xinyang Chen , Rong Wang , Weihong Ji , Jiapeng Qu
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引用次数: 0
Abstract
Altitude of the plateau may affect the composition and functional diversity of animal gut microbiota. However, the specific effects of altitude on the composition, community structure, and function of the host's gut microbiota, as well as how these effects, through interactions between microbial metabolic products (e.g., SCFAs) and microbial diversity, support host adaptation to high-altitude environments, remain unclear. This study investigates the variations of gut microbial community structure and function in plateau pikas (Ochotona curzoniae) along altitude on Qinghai-Tibetan Plateau. Cecum contents were analyzed using 16S rRNA sequencing and short-chain fatty acid (SCFA) content analyses to explore the structure, function and metabolic characteristics gut microbiota across different altitudes. As altitude increases, pikas' gut microbiota diversity significantly decreased, SCFA levels did not significantly change, while both diversity and complexity of the microbiota co-occurrence networks significantly decreased. The microbial community shifted toward better suited to high-altitude environments, as significantly increased in Bacteroidetes abundance but decreased in Firmicutes abundance. The microbial community assembly process became more deterministic, and KEGG analysis revealed the upregulation of metabolic, genetic information processing, and organismal system pathways. These results indicated that the gut microbiota diversity and complexity decreased in plateau pikas with increasing altitude, along with the upregulation of key metabolic pathways, as well as the stability of SCFA levels which reflecting balanced supply-demand relationships, contribute to adaptation of high-altitude environments. These findings reveal the substantial impact of altitude on the gut microbiota of a small mammal inhabiting the plateau, providing new insights into its adaptation mechanisms to high-altitude environments.
期刊介绍:
Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology.
Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.