Homeostasis between gut-associated microorganisms and the immune system in Drosophila

被引:35
|
作者
You, Hyejin [1 ,2 ]
Lee, Won Jun [3 ]
Lee, Won-Jae [1 ]
机构
[1] Seoul Natl Univ, Natl Creat Res Initiat, Ctr Symbiosyst, Sch Biol Sci, Seoul 151742, South Korea
[2] Ewha Womans Univ, Dept Life Sci, Seoul 120750, South Korea
[3] Ewha Womans Univ, Coll Hlth Sci, Seoul 120750, South Korea
基金
新加坡国家研究基金会;
关键词
PEPTIDOGLYCAN RECOGNITION; ESCHERICHIA-COLI; HOST-DEFENSE; DUAL OXIDASE; PGRP-LE; MICROBIOTA; BACTERIA; INFECTION; COMMENSAL; MELANOGASTER;
D O I
10.1016/j.coi.2014.06.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The metabolic activities of a given gut bacterium or gut commensal community fluctuate in a manner largely depending on the physicochemical parameters within the gut niche. Recognition of the bacterial metabolic status in situ, by a sensing of the gut metabolites as a signature of a specific bacterial metabolic activity, has been suggested to be a highly beneficial means for the host to maintain gut-microbe homeostasis. Recently, analysis of Drosophila gut immunity revealed that bacterial-derived uracil and uracil-modulated intestinal reactive oxygen species (ROS) generation play a pivotal role in diverse aspects of host microbe interactions, such as pathogen clearance, commensal protection, intestinal cell regeneration, colitogenesis, and possibly also interorgan immunological communication. A deeper understanding of the role of uracil in Drosophila immunity will provide additional insight into the molecular mechanisms underlying host microbe symbiosis and dysbiosis.
引用
收藏
页码:48 / 53
页数:6
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