Perturbation of the gut microbiome by Prevotella spp. enhances host susceptibility to mucosal inflammation

被引:230
|
作者
Iljazovic, Aida [1 ]
Roy, Urmi [1 ]
Galvez, Eric J. C. [1 ,2 ]
Lesker, Till R. [1 ]
Zhao, Bei [1 ]
Gronow, Achim [1 ]
Amend, Lena [1 ]
Will, Sabine E. [3 ]
Hofmann, Julia D. [4 ]
Pils, Marina C. [5 ]
Schmidt-Hohagen, Kerstin [4 ]
Neumann-Schaal, Meina [3 ]
Strowig, Till [1 ,2 ,6 ]
机构
[1] Helmholtz Ctr Infect Res, Dept Microbial Immune Regulat, Braunschweig, Germany
[2] Hannover Med Sch, Hannover, Germany
[3] Leibniz Inst DSMZ German Collect Microorganisms &, Bacterial Metabol, Braunschweig, Germany
[4] Tech Univ Carolo Wilhelmina Braunschweig, Dept Bioinformat & Biochem, BRICS, Braunschweig, Germany
[5] Helmholtz Ctr Infect Res, Mouse Pathol, Braunschweig, Germany
[6] Ctr Individualised Infect Med, Hannover, Germany
关键词
CHAIN FATTY-ACIDS; CROHNS-DISEASE; EPITHELIAL-CELLS; BARRIER FUNCTION; COLITIS; BUTYRATE; INDUCE; MICE; COLONIZATION; METABOLITES;
D O I
10.1038/s41385-020-0296-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Diverse microbial signatures within the intestinal microbiota have been associated with intestinal and systemic inflammatory diseases, but whether these candidate microbes actively modulate host phenotypes or passively expand within the altered microbial ecosystem is frequently not known. Here we demonstrate that colonization of mice with a member of the genus Prevotella, which has been previously associated to colitis in mice, exacerbates intestinal inflammation. Our analysis revealed that Prevotella intestinalis alters composition and function of the ecosystem resulting in a reduction of short-chain fatty acids, specifically acetate, and consequently a decrease in intestinal IL-18 levels during steady state. Supplementation of IL-18 to Prevotella-colonized mice was sufficient to reduce intestinal inflammation. Hence, we conclude that intestinal Prevotella colonization results in metabolic changes in the microbiota, which reduce IL-18 production and consequently exacerbate intestinal inflammation, and potential systemic autoimmunity.
引用
收藏
页码:113 / 124
页数:12
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