Microbial genes and pathways in inflammatory bowel disease

被引:665
作者
Schirmer, Melanie [1 ]
Garner, Ashley [1 ]
Vlamakis, Hera [1 ,2 ]
Xavier, Ramnik J. [1 ,2 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] MIT, Ctr Microbiome Informat & Therapeut, 77 Massachusetts Ave, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
ARYL-HYDROCARBON RECEPTOR; HUMAN GUT MICROBIOME; REGULATORY T-CELLS; CROHNS-DISEASE; FECAL MICROBIOTA; HYGIENE HYPOTHESIS; ESCHERICHIA-COLI; BARRIER FUNCTION; MUCOSAL FLORA; EARLY-LIFE;
D O I
10.1038/s41579-019-0213-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Perturbations in the intestinal microbiome are implicated in inflammatory bowel disease (IBD). Studies of treatment-naive patients have identified microbial taxa associated with disease course and treatment efficacy. To gain a mechanistic understanding of how the microbiome affects gastrointestinal health, we need to move from census to function. Bacteria, including those that adhere to epithelial cells as well as several Clostridium species, can alter differentiation of T helper 17 cells and regulatory T cells. Similarly, microbial products such as short-chain fatty acids and sphingolipids also influence immune responses. Metagenomics and culturomics have identified strains of Ruminococcus gnavus and adherent invasive Escherichia coli that are linked to IBD and gut inflammation. Integrated analysis of multiomics data, including metagenomics, metatranscriptomics and metabolomics, with measurements of host response and culturomics, have great potential in understanding the role of the microbiome in IBD. In this Review, we highlight current knowledge of gut microbial factors linked to IBD pathogenesis and discuss how multiomics data from large-scale population studies in health and disease have been used to identify specific microbial strains, transcriptional changes and metabolic alterations associated with IBD.
引用
收藏
页码:497 / 511
页数:15
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