生物
炎症性肠病
细菌
微生物学
免疫学
免疫球蛋白A
结肠炎
肠道菌群
致病菌
肠粘膜
抗体
微生物群
疾病
免疫球蛋白G
遗传学
医学
病理
内科学
作者
Noah W. Palm,Marcel R. de Zoete,Thomas W. Cullen,Natasha A. Barry,Jonathan Stefanowski,Liming Hao,Patrick H. Degnan,Jianzhong Hu,Inga Peter,Wei Zhang,Elizabeth Ruggiero,Judy H. Cho,Andrew L. Goodman,Richard A. Flavell
出处
期刊:Cell
[Elsevier]
日期:2014-08-01
卷期号:158 (5): 1000-1010
被引量:1007
标识
DOI:10.1016/j.cell.2014.08.006
摘要
Specific members of the intestinal microbiota dramatically affect inflammatory bowel disease (IBD) in mice. In humans, however, identifying bacteria that preferentially affect disease susceptibility and severity remains a major challenge. Here, we used flow-cytometry-based bacterial cell sorting and 16S sequencing to characterize taxa-specific coating of the intestinal microbiota with immunoglobulin A (IgA-SEQ) and show that high IgA coating uniquely identifies colitogenic intestinal bacteria in a mouse model of microbiota-driven colitis. We then used IgA-SEQ and extensive anaerobic culturing of fecal bacteria from IBD patients to create personalized disease-associated gut microbiota culture collections with predefined levels of IgA coating. Using these collections, we found that intestinal bacteria selected on the basis of high coating with IgA conferred dramatic susceptibility to colitis in germ-free mice. Thus, our studies suggest that IgA coating identifies inflammatory commensals that preferentially drive intestinal disease. Targeted elimination of such bacteria may reduce, reverse, or even prevent disease development.
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