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人类肠道微生物组的泛基因组揭示了遗传多样性与应激反应之间的联系。

Pangenomes of human gut microbiota uncover links between genetic diversity and stress response.

机构信息

Department of Computer Science and Applied Mathematics, The Weizmann Institute of Science, Rehovot, Israel; Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot, Israel.

Department of Computer Science and Applied Mathematics, The Weizmann Institute of Science, Rehovot, Israel; Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot, Israel; Lis Maternity and Women's Hospital, Sourasky Medical Center, Tel Aviv, Israel.

出版信息

Cell Host Microbe. 2024 Oct 9;32(10):1744-1757.e2. doi: 10.1016/j.chom.2024.08.017. Epub 2024 Sep 30.

Abstract

The genetic diversity of the gut microbiota has a central role in host health. Here, we created pangenomes for 728 human gut prokaryotic species, quadrupling the genes of strain-specific genomes. Each of these species has a core set of a thousand genes, differing even between closely related species, and an accessory set of genes unique to the different strains. Functional analysis shows high strain variability associates with sporulation, whereas low variability is linked with antibiotic resistance. We further map the antibiotic resistome across the human gut population and find 237 cases of extreme resistance even to last-resort antibiotics, with a predominance among Enterobacteriaceae. Lastly, the presence of specific genes in the microbiota relates to host age and sex. Our study underscores the genetic complexity of the human gut microbiota, emphasizing its significant implications for host health. The pangenomes and antibiotic resistance map constitute a valuable resource for further research.

摘要

肠道微生物群的遗传多样性在宿主健康中起着核心作用。在这里,我们为 728 种人类肠道原核生物创建了泛基因组,将菌株特异性基因组的基因数量增加了四倍。这些物种中的每一个都有一组千个核心基因,即使是在密切相关的物种之间也存在差异,还有一组特定于不同菌株的附加基因。功能分析表明,高菌株变异性与孢子形成有关,而低变异性与抗生素耐药性有关。我们进一步在人类肠道群体中绘制抗生素抗性组图谱,发现即使是对最后手段的抗生素也存在 237 种极端耐药情况,其中肠杆菌科占主导地位。最后,微生物群中特定基因的存在与宿主年龄和性别有关。我们的研究强调了人类肠道微生物群的遗传复杂性,强调了其对宿主健康的重要意义。泛基因组和抗生素耐药性图谱构成了进一步研究的宝贵资源。

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