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肠道微生物定殖的保守遗传基础。

Conserved genetic basis for microbial colonization of the gut.

作者信息

Liu Menghan, Blattman Sydney B, Takahashi Mai, Mandayam Nandan, Jiang Wenyan, Oikonomou Panos, Tavazoie Sohail F, Tavazoie Saeed

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

Laboratory of Systems Cancer Biology, The Rockefeller University, New York, NY 10065, USA.

出版信息

Cell. 2025 May 1;188(9):2505-2520.e22. doi: 10.1016/j.cell.2025.03.010. Epub 2025 Apr 4.

DOI:10.1016/j.cell.2025.03.010
PMID:40187346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12048274/
Abstract

Despite the fundamental importance of gut microbes, the genetic basis of their colonization remains largely unexplored. Here, by applying cross-species genotype-habitat association at the tree-of-life scale, we identify conserved microbial gene modules associated with gut colonization. Across thousands of species, we discovered 79 taxonomically diverse putative colonization factors organized into operonic and non-operonic modules. They include previously characterized colonization pathways such as autoinducer-2 biosynthesis and novel processes including tRNA modification and translation. In vivo functional validation revealed YigZ (IMPACT family) and tRNA hydroxylation protein-P (TrhP) are required for E. coli intestinal colonization. Overexpressing YigZ alone is sufficient to enhance colonization of the poorly colonizing MG1655 E. coli by >100-fold. Moreover, natural allelic variations in YigZ impact inter-strain colonization efficiency. Our findings highlight the power of large-scale comparative genomics in revealing the genetic basis of microbial adaptations. These broadly conserved colonization factors may prove critical for understanding gastrointestinal (GI) dysbiosis and developing therapeutics.

摘要

尽管肠道微生物至关重要,但其定殖的遗传基础在很大程度上仍未得到探索。在此,通过在生命树尺度上应用跨物种基因型-栖息地关联分析,我们鉴定出了与肠道定殖相关的保守微生物基因模块。在数千个物种中,我们发现了79个分类学上不同的假定定殖因子,它们被组织成操纵子和非操纵子模块。其中包括先前已被表征的定殖途径,如自诱导物-2生物合成,以及包括tRNA修饰和翻译在内的新过程。体内功能验证表明,YigZ(IMPACT家族)和tRNA羟基化蛋白-P(TrhP)是大肠杆菌在肠道定殖所必需的。单独过表达YigZ就足以使定殖能力较差的MG1655大肠杆菌的定殖能力增强100倍以上。此外,YigZ中的天然等位基因变异会影响菌株间的定殖效率。我们的研究结果凸显了大规模比较基因组学在揭示微生物适应性遗传基础方面的强大作用。这些广泛保守的定殖因子可能对于理解胃肠道功能紊乱和开发治疗方法至关重要。