scholarly journals Bile salt receptor complex activates a pathogenic type III secretion system

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Peng Li ◽  
Giomar Rivera-Cancel ◽  
Lisa N Kinch ◽  
Dor Salomon ◽  
Diana R Tomchick ◽  
...  

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 β-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.

2014 ◽  
Vol 464 (1) ◽  
pp. 135-144 ◽  
Author(s):  
Samira Zouhir ◽  
Joaquín Bernal-Bayard ◽  
Mar Cordero-Alba ◽  
Elena Cardenal-Muñoz ◽  
Beatriz Guimaraes ◽  
...  

We report the crystal structure of the Salmonella effector SlrP in complex with its human protein target thioredoxin Trx1. SlrP is a E3 ubiquitin ligase from the NEL family and we present evidence for the site of ubiquitination on Trx1.


2015 ◽  
Vol 71 (10) ◽  
pp. 1300-1308 ◽  
Author(s):  
Brianne J. Burkinshaw ◽  
Sergio A. Souza ◽  
Natalie C. J. Strynadka

During infection, enteropathogenicEscherichia coliassembles a complex multi-protein type III secretion system that traverses the bacterial membranes and targets the host cell membrane to directly deliver virulence or effector proteins to the host cytoplasm. As this secretion system is composed of more than 20 proteins, many of which form oligomeric associations, its assembly must be tightly regulated. A protein called the gatekeeper, or SepL, ensures that the secretion of the translocon component, which inserts into the host membrane, occurs before the secretion of effectors. The crystal structure of the gatekeeper SepL was determined and compared with the structures of SepL homologues from other bacterial pathogens in order to identify SepL residues that may be critical for its role in type III secretion-system assembly.


2016 ◽  
Author(s):  
Peng Li ◽  
Giomar Rivera-Cancel ◽  
Lisa N Kinch ◽  
Dor Salomon ◽  
Diana R Tomchick ◽  
...  

PLoS ONE ◽  
2011 ◽  
Vol 6 (4) ◽  
pp. e19208 ◽  
Author(s):  
Chiradip Chatterjee ◽  
Sundramurthy Kumar ◽  
Smarajit Chakraborty ◽  
Yih Wan Tan ◽  
Ka Yin Leung ◽  
...  

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