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某些健康人类和住院 COVID-19 患者的人类胃肠道微生物群落中微生物菌株失调的早期指标。

Early indicators of microbial strain dysbiosis in the human gastrointestinal microbial community of certain healthy humans and hospitalized COVID-19 patients.

机构信息

Department of Genetics, Hugh Kaul Precision Medicine Institute, University of Alabama at Birmingham, Birmingham, AL, USA.

Department of Cell, Developmental and Integrative Biology, Hugh Kaul Precision Medicine Institute, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Sci Rep. 2022 Apr 21;12(1):6562. doi: 10.1038/s41598-022-10472-w.

Abstract

Dysbiosis in the human gastrointestinal microbial community could functionally impact microbial metabolism and colonization resistance to pathogens. To further elucidate the indicators of microbial strain dysbiosis, we have developed an analytic method that detects patterns of presence/absence of selected KEGG metabolic pathways for a selected strain (PKS). Using a metagenomic data set consisting of multiple high-density fecal samples from six normal individuals, we found three had unique PKS for important gut commensal microbes, Bacteroides vulgatus and Bacteroides uniformis, at all sample times examined. Two individuals had multiple shared PKS clusters of B. vulgatus or B. uniformis over time. Analysis of a data set of high-density fecal samples from eight COVID-19 hospitalized patients taken over a short period revealed that two patients had shared PKS clusters for B. vulgatus and one shared cluster for B. uniformis. Our analysis demonstrates that while the majority of normal individuals with no B. vulgatus or B. uniformis strain change over time have unique PKS, in some healthy humans and patients hospitalized with COVID-19, we detected shared PKS clusters at the different times suggesting a slowing down of the intrinsic rates of strain variation that could eventually lead to a dysbiosis in the microbial strain community.

摘要

人类胃肠道微生物群落的失调可能会对微生物代谢和对病原体的定植抗性产生功能性影响。为了进一步阐明微生物菌株失调的指标,我们开发了一种分析方法,用于检测选定 KEGG 代谢途径的存在/不存在模式,用于选定的菌株(PKS)。使用由六个正常人的多个高密度粪便样本组成的宏基因组数据集,我们发现其中三个个体在所有检查的样本时间都有独特的 PKS,用于重要的肠道共生微生物,脆弱拟杆菌和均匀拟杆菌。两个人在一段时间内有多个脆弱拟杆菌或均匀拟杆菌的共享 PKS 簇。对八名 COVID-19 住院患者在短时间内采集的高密度粪便样本数据集的分析表明,两名患者的脆弱拟杆菌有共享的 PKS 簇,一名患者的均匀拟杆菌有共享的 PKS 簇。我们的分析表明,虽然大多数没有脆弱拟杆菌或均匀拟杆菌菌株变化的正常人随着时间的推移具有独特的 PKS,但在一些健康人和因 COVID-19 住院的患者中,我们在不同时间检测到了共享的 PKS 簇,这表明菌株变异的内在率减慢,最终可能导致微生物菌株群落失调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a14/9023558/1281c9a2f80c/41598_2022_10472_Fig1_HTML.jpg

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