Coordinate control of virulence gene expression in Francisella tularensis involves direct interaction between key regulators

J Bacteriol. 2014 Oct;196(19):3516-26. doi: 10.1128/JB.01700-14. Epub 2014 Jul 28.

Abstract

In Francisella tularensis, the putative DNA-binding protein PigR works in concert with the SspA protein family members MglA and SspA to control the expression of genes that are essential for the intramacrophage growth and survival of the organism. MglA and SspA form a complex that interacts with RNA polymerase (RNAP), and this interaction between the MglA-SspA complex and RNAP is thought to be critical to its regulatory function. How PigR works in concert with the MglA-SspA complex is not known; previously published findings differ over whether PigR interacts with the MglA-SspA complex, leading to disparate models for how PigR and the MglA-SspA complex exert their regulatory effects. Here, using a combination of genetic assays, we identify mutants of MglA and SspA that are specifically defective for interaction with PigR. Analysis of the MglA and SspA mutants in F. tularensis reveals that interaction between PigR and the MglA-SspA complex is essential in order for PigR to work coordinately with MglA and SspA to positively regulate the expression of virulence genes. Our findings uncover a surface of the MglA-SspA complex that is important for interaction with PigR and support the idea that PigR exerts its regulatory effects through an interaction with the RNAP-associated MglA-SspA complex.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adhesins, Bacterial / genetics
  • Adhesins, Bacterial / metabolism*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Francisella tularensis / genetics
  • Francisella tularensis / metabolism*
  • Francisella tularensis / pathogenicity
  • Gene Expression Regulation, Bacterial*
  • Protein Binding
  • Virulence Factors / genetics
  • Virulence Factors / metabolism*

Substances

  • Adhesins, Bacterial
  • Bacterial Proteins
  • SspA protein, bacteria
  • Virulence Factors