Species-specific recruitment of transcription factors dictates toxin expression

Nucleic Acids Res. 2020 Mar 18;48(5):2388-2400. doi: 10.1093/nar/gkz1232.

Abstract

Tight and coordinate regulation of virulence determinants is essential for bacterial biology and involves dynamic shaping of transcriptional regulatory networks during evolution. The horizontally transferred two-partner secretion system ExlB-ExlA is instrumental in the virulence of different Pseudomonas species, ranging from soil- and plant-dwelling biocontrol agents to the major human pathogen Pseudomonas aeruginosa. Here, we identify a Cro/CI-like repressor, named ErfA, which together with Vfr, a CRP-like activator, controls exlBA expression in P. aeruginosa. The characterization of ErfA regulon across P. aeruginosa subfamilies revealed a second conserved target, the ergAB operon, with functions unrelated to virulence. To gain insights into this functional dichotomy, we defined the pan-regulon of ErfA in several Pseudomonas species and found ergAB as the sole conserved target of ErfA. The analysis of 446 exlBA promoter sequences from all exlBA+ genomes revealed a wide variety of regulatory sequences, as ErfA- and Vfr-binding sites were found to have evolved specifically in P. aeruginosa and nearly each species carries different regulatory sequences for this operon. We propose that the emergence of different regulatory cis-elements in the promoters of horizontally transferred genes is an example of plasticity of regulatory networks evolving to provide an adapted response in each individual niche.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Bacterial Proteins / metabolism
  • Bacterial Toxins / metabolism*
  • Base Sequence
  • Gene Expression Regulation, Bacterial
  • Humans
  • Operon / genetics
  • Promoter Regions, Genetic
  • Protein Binding
  • Pseudomonas / genetics
  • Pseudomonas / pathogenicity
  • Repressor Proteins / metabolism
  • Species Specificity
  • Transcription Factors / metabolism*
  • Virulence

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • Repressor Proteins
  • Transcription Factors