Bile salt receptor complex activates a pathogenic type III secretion system

被引:1
作者
Li, Peng [1 ]
Rivera-Cancel, Giomar [1 ]
Kinch, Lisa N. [2 ]
Salomon, Dor [1 ]
Tomchick, Diana R. [3 ,4 ]
Grishin, Nick V. [2 ,3 ,4 ]
Orth, Kim [1 ,2 ,3 ]
机构
[1] Univ Texas Southwestern Med Ctr, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr, Howard Hughes Med Inst, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr, Dept Biochem, Dallas, TX 75390 USA
[4] Univ Texas Southwestern Med Ctr, Dept Biophys, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
LIPID-BINDING PROTEIN; VIBRIO-PARAHAEMOLYTICUS; ENVIRONMENTAL SIGNALS; VIRULENCE FACTORS; DATA REDUCTION; CHOLERAE; IDENTIFICATION; INTEGRATION; EXPRESSION; TOXR;
D O I
10.7554/elife.15718
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bile is an important component of the human gastrointestinal tract with an essential role in food absorption and antimicrobial activities. Enteric bacterial pathogens have developed strategies to sense bile as an environmental cue to regulate virulence genes during infection. We discovered that Vibrio parahaemolyticus VtrC, along with VtrA and VtrB, are required for activating the virulence type III secretion system 2 in response to bile salts. The VtrA/VtrC complex activates VtrB in the presence of bile salts. The crystal structure of the periplasmic domains of the VtrA/VtrC heterodimer reveals a beta-barrel with a hydrophobic inner chamber. A co-crystal structure of VtrA/VtrC with bile salt, along with biophysical and mutational analysis, demonstrates that the hydrophobic chamber binds bile salts and activates the virulence network. As part of a family of conserved signaling receptors, VtrA/VtrC provides structural and functional insights into the evolutionarily conserved mechanism used by bacteria to sense their environment.
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页数:26
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