Peptidoglycan Sensing by the Receptor PGRP-LE in the Drosophila Gut Induces Immune Responses to Infectious Bacteria and Tolerance to Microbiota

被引:179
作者
Bosco-Drayon, Virginie [1 ]
Poidevin, Mickael [2 ]
Boneca, Ivo Gomperts [3 ,4 ]
Narbonne-Reveau, Karine [1 ]
Royet, Julien [1 ]
Charroux, Bernard [1 ]
机构
[1] Aix Marseille Univ, Inst Biol Dev Marseille Luminy, CNRS, UMR 7288, F-13288 Marseille, France
[2] Emory Univ, Dept Human Genet, Sch Med, Atlanta, GA 30322 USA
[3] Inst Pasteur, Grp Biol & Genet Bacterial Cell Wall, F-75724 Paris 15, France
[4] INSERM, Grp AVENIR, F-757015 Paris, France
关键词
DUAL OXIDASE; RECOGNITION; LC; IMD; HOMEOSTASIS; COMMENSAL; PATHWAY; REGULATOR; MAMMALS;
D O I
10.1016/j.chom.2012.06.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Gut epithelial cells contact both commensal and pathogenic bacteria, and proper responses to these bacteria require a balance of positive and negative regulatory signals. In the Drosophila intestine, peptidoglycan-recognition proteins (PGRPs), including PGRP-LE, play central roles in bacterial recognition and activation of immune responses, including induction of the IMD-NF-kappa B pathway. We show that bacteria recognition is regionalized in the Drosophila gut with various functional regions requiring different PGRPs. Specifically, peptidoglycan recognition by PGRP-LE in the gut induces NF-kappa B-dependent responses to infectious bacteria but also immune tolerance to microbiota through upregulation of pirk and PGRP-LB, which negatively regulate IMD pathway activation. Loss of PGRP-LE-mediated detection of bacteria in the gut results in systemic immune activation, which can be rescued by overexpressing PGRP-LB in the gut. Together these data indicate that PGRP-LE functions as a master gut bacterial sensor that induces balanced responses to infectious bacteria and tolerance to microbiota.
引用
收藏
页码:153 / 165
页数:13
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