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PMID: 11985718 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

LcrQ and SycH function together at the Ysc type III secretion system in Yersinia pestis to impose a hierarchy of secretion.

Molecular microbiology ·Vol. 43 ·No. 2 ·2002-01-00 ·Pages 411-23

Wulff-Strobel CR, Williams AW, Straley SC

Abstract

LcrQ is a regulatory protein unique to Yersinia. Previous study in Yersinia pseudotuberculosis and Yersinia enterocolitica prompted the model in which LcrQ negatively regulates the expression of a set of virulence proteins called Yops, and its secretion upon activation of the Yop secretion (Ysc) type III secretion system permits full induction of Yops expression. In this study, we tested the hypothesis that LcrQ's effects on Yops expression might be indirect. Excess LcrQ was found to exert an inhibitory effect specifically at the level of Yops secretion, independent of production, and a normal inner Ysc gate protein LcrG was required for this activity. However, overexpression of LcrQ did not prevent YopH secretion, suggesting that LcrQ's effects at the Ysc discriminate among the Yops. We tested this idea by determining the effects of deletion or overexpression of LcrQ, YopH and their common chaperone SycH on early Yop secretion through the Ysc. Together, our findings indicated that LcrQ is not a negative regulator directly, but it acts in partnership with SycH at the Ysc gate to control the entry of a set of Ysc secretion substrates. A hierarchy of YopH secretion before YopE appears to be imposed by SycH in conjunction with both LcrQ and YopH. LcrQ and SycH in addition influenced the deployment of LcrV, a component of the Yops delivery mechanism. Accordingly, LcrQ appears to be a central player in determining the substrate specificity of the Ysc.

MeSH Terms
Antigens, Bacterial/metabolism Bacterial Outer Membrane Proteins/genetics,metabolism Bacterial Proteins/genetics,metabolism Gene Expression Molecular Chaperones/genetics,metabolism Mutagenesis Pore Forming Cytotoxic Proteins Protein Tyrosine Phosphatases/metabolism Yersinia pestis/genetics,metabolism
Chemicals
Antigens, Bacterial Bacterial Outer Membrane Proteins Bacterial Proteins LcrG protein, Yersinia LcrV protein, Yersinia Molecular Chaperones Pore Forming Cytotoxic Proteins SycH protein, Yersinia yopE protein, Yersinia lcrQ protein, Yersinia pseudotuberculosis Protein Tyrosine Phosphatases yopH protein, Yersinia
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wulff-Strobel Christine R
Department of Microbiology and Immunology, University of Kentucky, Lexington 40536-0298, USA.
Williams Andrew W
Straley Susan C
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2002-01-00
Pages
411-23
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIAID NIH HHS · AI21017 · United States
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