Transcription of exsD is repressed directly by H-NS in Vibrio parahaemolyticus

Microb Pathog. 2016 Aug:97:221-5. doi: 10.1016/j.micpath.2016.06.003. Epub 2016 Jun 8.

Abstract

Vibrio parahaemolyticus is a leading cause of seafood-associated diarrhea and gastroenteritis. This bacteria expresses a major virulence determinant called T3SS1. Expression of T3SS1 is tightly regulated by the ExsA-ExsC-ExsD regulatory system. The transcription of exsA and probably exsC is repressed directly by the H-NS protein. In this study, the regulation of exsD by H-NS was investigated using quantitative RT-PCR, primer extension, LacZ fusion, electrophoretic mobility shift, and DNase I footprinting assays. The results showed that His-H-NS protected a single region from 61 bp to 174 bp upstream of exsD against DNase I digestion, and a transcription start site located at 105 bp upstream of exsD was detected and its activity was repressed by H-NS. Therefore, a single H-NS-dependent promoter was transcribed for exsD in V. parahaemolyticus. Thus, all three genes in the ExsA-ExsC-ExsD regulatory system of T3SS1 are directly repressed by H-NS in V. parahaemolyticus.

Keywords: H-NS; T3SS1; Vibrio parahaemolyticus; exsD.

MeSH terms

  • Artificial Gene Fusion
  • Bacterial Proteins / metabolism*
  • DNA Footprinting
  • DNA-Binding Proteins / metabolism*
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial*
  • Genes, Bacterial
  • Genes, Regulator*
  • Membrane Proteins / biosynthesis*
  • Membrane Proteins / genetics
  • Real-Time Polymerase Chain Reaction
  • Transcription Initiation Site
  • Transcription, Genetic*
  • Vibrio parahaemolyticus / genetics*
  • Vibrio parahaemolyticus / metabolism*
  • beta-Galactosidase / analysis
  • beta-Galactosidase / genetics

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • H-NS protein, bacteria
  • Membrane Proteins
  • beta-Galactosidase