普氏粪杆菌
生物
微生物群
丁酸盐
失调
肠道菌群
代谢组
慢性疲劳综合征
真细菌
队列
疾病
基因组
免疫学
生物信息学
代谢组学
医学
内科学
遗传学
细菌
基因
发酵
食品科学
作者
Cheng Guo,Xiaoyu Che,Thomas Briese,Amit Ranjan,Orchid M. Allicock,Rachel A. Yates,Aaron M. Cheng,Dana March,Mady Hornig,Anthony L. Komaroff,Susan Levine,Lucinda Bateman,Suzanne D. Vernon,Nancy G. Klimas,José G. Montoya,Daniel L. Peterson,W. Ian Lipkin,Brent L. Williams
标识
DOI:10.1016/j.chom.2023.01.004
摘要
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is characterized by unexplained debilitating fatigue, cognitive dysfunction, gastrointestinal disturbances, and orthostatic intolerance. Here, we report a multi-omic analysis of a geographically diverse cohort of 106 cases and 91 healthy controls that revealed differences in gut microbiome diversity, abundances, functional pathways, and interactions. Faecalibacterium prausnitzii and Eubacterium rectale, which are both recognized as abundant, health-promoting butyrate producers in the human gut, were reduced in ME/CFS. Functional metagenomics, qPCR, and metabolomics of fecal short-chain fatty acids confirmed a deficient microbial capacity for butyrate synthesis. Microbiome-based machine learning classifier models were robust to geographic variation and generalizable in a validation cohort. The abundance of Faecalibacterium prausnitzii was inversely associated with fatigue severity. These findings demonstrate the functional nature of gut dysbiosis and the underlying microbial network disturbance in ME/CFS, providing possible targets for disease classification and therapeutic trials.
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