Characterization of two signal transduction systems involved in intracellular macrophage survival and environmental stress response in Enterococcus faecalis

J Mol Microbiol Biotechnol. 2008;14(1-3):59-66. doi: 10.1159/000106083.

Abstract

The intracellular survival in mouse peritoneal macrophages of 8 Enterococcus faecalis response regulator mutants was tested to assess if the corresponding 2-component signal transduction systems (TCS) are involved in the ability of E. faecalis to survive in macrophages. Three mutants (err04, err05 and err06) are more susceptible than the wild-type JH2-2 strain and 1 is more resistant (err10). Then, characterization of the TCS Err04-Ehk04 and Err06-Ehk06 reveals that the first (homolog of PhoP-PhoR of Bacillus subtilis) is induced in phosphate deprivation conditions, regulates its own expression and plays a role in the expression of pstF encoding a phosphate-binding protein. The Err06-Ehk06 is involved in oxidative stress response. A mutation in the err06 gene increases sensitivity of the bacterium to H(2)O(2). The err06-ehk06 operon is induced by H(2)O(2) stress and controlled by 2 transcriptional start sites, of which 1 is specifically active in oxidative stress conditions. We also demonstrated that the expression of the catalase gene (kat) is partly dependant of the Err06-Ehk06 TCS.

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Catalase / genetics
  • Catalase / metabolism
  • Colony Count, Microbial
  • Enterococcus faecalis / genetics
  • Enterococcus faecalis / growth & development*
  • Enterococcus faecalis / metabolism
  • Enterococcus faecalis / physiology*
  • Gene Expression Regulation, Bacterial
  • Heat-Shock Response*
  • Macrophages, Peritoneal / microbiology*
  • Mice
  • Mutation
  • Oxidative Stress
  • Phosphate-Binding Proteins / genetics
  • Phosphate-Binding Proteins / metabolism
  • Phosphates / metabolism
  • Signal Transduction*

Substances

  • Bacterial Proteins
  • Phosphate-Binding Proteins
  • Phosphates
  • Catalase