The nucleoid occlusion protein SlmA is a direct transcriptional activator of chitobiose utilization in Vibrio cholerae

PLoS Genet. 2017 Jul 6;13(7):e1006877. doi: 10.1371/journal.pgen.1006877. eCollection 2017 Jul.

Abstract

Chitin utilization by the cholera pathogen Vibrio cholerae is required for its persistence and evolution via horizontal gene transfer in the marine environment. Genes involved in the uptake and catabolism of the chitin disaccharide chitobiose are encoded by the chb operon. The orphan sensor kinase ChiS is critical for regulation of this locus, however, the mechanisms downstream of ChiS activation that result in expression of the chb operon are poorly understood. Using an unbiased transposon mutant screen, we uncover that the nucleoid occlusion protein SlmA is a regulator of the chb operon. SlmA has not previously been implicated in gene regulation. Also, SlmA is a member of the TetR family of proteins, which are generally transcriptional repressors. In vitro, we find that SlmA binds directly to the chb operon promoter, and in vivo, we show that this interaction is required for transcriptional activation of this locus and for chitobiose utilization. Using point mutations that disrupt distinct functions of SlmA, we find that DNA-binding, but not nucleoid occlusion, is critical for transcriptional activation. This study identifies a novel role for SlmA as a transcriptional regulator in V. cholerae in addition to its established role as a cell division licensing factor.

MeSH terms

  • Bacterial Proteins / genetics*
  • Binding Sites
  • Chitin / metabolism
  • Cholera / genetics*
  • Cholera / microbiology
  • DNA-Binding Proteins / genetics
  • Disaccharides / biosynthesis
  • Disaccharides / genetics*
  • Escherichia coli / genetics
  • Gene Expression Regulation, Bacterial
  • Gene Transfer, Horizontal / genetics
  • Humans
  • Operon / genetics*
  • Point Mutation
  • Promoter Regions, Genetic
  • Transcriptional Activation / genetics*
  • Vibrio cholerae / genetics*
  • Vibrio cholerae / pathogenicity

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Disaccharides
  • SlmA protein, Vibrio cholerae
  • Chitin
  • chitobiose