Regulation of type III secretion system 1 gene expression in Vibrio parahaemolyticus is dependent on interactions between ExsA, ExsC and ExsD

44Citations
Citations of this article
42Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Vibrio parahaemolyticus ExsA is the transcriptional regulator for type III secretion system 1 (T3SS 1) while ExsD blocks T3SS 1 expression. Herein we show that deletion of exsC from V. parahaemolyticus blocked synthesis of T3SS 1-dependent proteins under inducing conditions (contact with HeLa cells), while in trans complementation of the ΔexsC strain with wild-type exsC restored protein synthesis. Under non-inducing conditions (Luria broth plus salt), in trans expression of exsC in a wild-type strain resulted in synthesis and secretion of T3SS 1-dependent proteins. Deletion of exsC does not affect the synthesis of ExsA while expression of T3SS 1 genes is independent of ExsC in the absence of ExsD. Co-expression of recombinant proteins with different antigenic tags demonstrated that ExsC binds ExsD and that the N-terminal amino acids of ExsC (positions 7 to 12) are required for binding. Co-expression and purification of antigentically tagged ExsA and ExsD demonstrated that ExsD directly binds ExsA and presumably prevents ExsA from binding promoter regions of T3SS 1 genes. Collectively these data demonstrate that ExsD binds ExsA to block expression of T3SS 1 genes, while ExsC binds ExsD to permit expression of T3SS 1 genes. ExsA, ExsC and ExsD from V. parahaemolyticus appear to be functional orthologues of their Pseudomonas aeruginosa counterparts. © 2010 Landes Bioscience.

Cite

CITATION STYLE

APA

Zhou, X., Konkel, M. E., & Call, D. R. (2010). Regulation of type III secretion system 1 gene expression in Vibrio parahaemolyticus is dependent on interactions between ExsA, ExsC and ExsD. Virulence, 1(4), 260–272. https://doi.org/10.4161/viru.1.4.12318

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free