The Yersinia Type III Secretion System as a Tool for Studying Cytosolic Innate Immune Surveillance

被引:17
作者
Schubert, Katherine Andrea [1 ]
Xu, Yue [2 ]
Shao, Feng [2 ]
Auerbuch, Victoria [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Microbiol & Environm Toxicol, Santa Cruz, CA 95064 USA
[2] Natl Inst Biol Sci, Beijing 102206, Peoples R China
来源
ANNUAL REVIEW OF MICROBIOLOGY, VOL 74, 2020 | 2020年 / 74卷
基金
美国国家卫生研究院;
关键词
Yersinia; type III secretion system; T3SS; Yop; inflammasome; ALPK1; TIFA; Pyrin; pyroptosis; GSDMD; NF-KAPPA-B; GUANYLATE-BINDING-PROTEINS; TRAF-INTERACTING PROTEIN; CELL-DEATH; INFLAMMASOME ACTIVATION; NLRP3; INFLAMMASOME; TRANSLOCATORS YOPB; INDUCED APOPTOSIS; EPITHELIAL-CELLS; PLASMA-MEMBRANE;
D O I
10.1146/annurev-micro-020518-120221
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Microbial pathogens have evolved complex mechanisms to interface with host cells in order to evade host defenses and replicate. However, mammalian innate immune receptors detect the presence of molecules unique to the microbial world or sense the activity of virulence factors, activating antimicrobial and inflammatory pathways. We focus on how studies of the major virulence factor of one group of microbial pathogens, the type III secretion system (T3SS) of human pathogenic Yersinia, have shed light on these important innate immune responses. Yersinia are largely extracellular pathogens, yet they insert T3SS cargo into target host cells that modulate the activity of cytosolic innate immune receptors. This review covers both the host pathways that detect the Yersinia T3SS and the effector proteins used by Yersinia to manipulate innate immune signaling.
引用
收藏
页码:221 / 245
页数:25
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