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Title: Bile salt receptor complex activates a pathogenic type III secretion system

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.
Authors:
 [1] ;  [1] ;  [2] ;  [1] ; ORCiD logo [3] ;  [4] ; ORCiD logo [5]
  1. Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, United States
  2. Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, United States
  3. Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, United States, Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, United States
  4. Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, United States, Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, United States, Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, United States
  5. Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, United States, Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, United States, Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, United States
Publication Date:
Grant/Contract Number:
AC02-06CH11357
Type:
Published Article
Journal Name:
eLife
Additional Journal Information:
Journal Volume: 5; Related Information: CHORUS Timestamp: 2017-10-18 20:28:29; Journal ID: ISSN 2050-084X
Publisher:
eLife Sciences Publications, Ltd.
Sponsoring Org:
USDOE
Country of Publication:
United States
Language:
English
OSTI Identifier:
1260282
Alternate Identifier(s):
OSTI ID: 1260283