Abstract

The Type VI secretion system (T6SS) is a macromolecular complex widespread in Gram-negative bacteria. Although several T6SS are required for virulence towards host models, most are necessary to eliminate competitor bacteria. Other functions, such as resistance to amoeba predation, biofilm formation or adaptation to environmental conditions have also been reported. This multitude of functions is reflected by the large repertoire of regulatory mechanisms shown to control T6SS expression, production or activation. Here, we demonstrate that one T6SS gene cluster encoded within the Yersinia pseudotuberculosis genome, T6SS-4, is regulated by OmpR, the response regulator of the two-component system EnvZ-OmpR. We first identified OmpR in a transposon mutagenesis screen. OmpR does not control the expression of the four other Y. pseudotuberculosis T6SS gene clusters and of an isolated vgrG gene, and responds to osmotic stresses to bind to and activate the T6SS-4 promoter. Finally, we show that T6SS-4 promotes Y. pseudotuberculosis survival in high osmolarity conditions and resistance to deoxycholate.

Highlights

  • The Type VI secretion system (T6SS) is a macromolecular machine dedicated to the secretion of toxin proteins, widespread in Gram-negative Proteobacteria [1,2,3,4,5]

  • As previously reported in both Y. pestis and Y. pseudotuberculosis, b-galactosidase activities and GFP fluorescence confirmed that the expression of the T6SS-4 locus is activated at 28uC compared to 37uC

  • We report data regarding the control of T6SS-4 gene cluster expression

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Summary

Introduction

The Type VI secretion system (T6SS) is a macromolecular machine dedicated to the secretion of toxin proteins, widespread in Gram-negative Proteobacteria [1,2,3,4,5]. This system is highly versatile as it can target eukaryotic or prokaryotic cells [6]. Several other T6SS, including those of Pseudomonas aeruginosa, Burkholderia thailendensis, Serratia marcescens V. cholerae, Citrobacter rodentium and enteroaggregative Escherichia coli, are required to eliminate competing bacteria in mixed environments [12,13,14,15,16,17]. Additional T6SS functions have been reported such as role in stress sensing, biofilm formation or adaptation to environmental conditions, the mechanistic bases for these functions have not been clearly defined [21,22,23,24]

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