Regulation of acetyl-CoA synthetase transcription by the CrbS/R two-component system is conserved in genetically diverse environmental pathogens

PLoS One. 2017 May 18;12(5):e0177825. doi: 10.1371/journal.pone.0177825. eCollection 2017.

Abstract

The CrbS/R two-component signal transduction system is a conserved regulatory mechanism through which specific Gram-negative bacteria control acetate flux into primary metabolic pathways. CrbS/R governs expression of acetyl-CoA synthase (acsA), an enzyme that converts acetate to acetyl-CoA, a metabolite at the nexus of the cell's most important energy-harvesting and biosynthetic reactions. During infection, bacteria can utilize this system to hijack host acetate metabolism and alter the course of colonization and pathogenesis. In toxigenic strains of Vibrio cholerae, CrbS/R-dependent expression of acsA is required for virulence in an arthropod model. Here, we investigate the function of the CrbS/R system in Pseudomonas aeruginosa, Pseudomonas entomophila, and non-toxigenic V. cholerae strains. We demonstrate that its role in acetate metabolism is conserved; this system regulates expression of the acsA gene and is required for growth on acetate as a sole carbon source. As a first step towards describing the mechanism of signaling through this pathway, we identify residues and domains that may be critical for phosphotransfer. We further demonstrate that although CrbS, the putative hybrid sensor kinase, carries both a histidine kinase domain and a receiver domain, the latter is not required for acsA transcription. In order to determine whether our findings are relevant to pathogenesis, we tested our strains in a Drosophila model of oral infection previously employed for the study of acetate-dependent virulence by V. cholerae. We show that non-toxigenic V. cholerae strains lacking CrbS or CrbR are significantly less virulent than are wild-type strains, while P. aeruginosa and P. entomophila lacking CrbS or CrbR are fully pathogenic. Together, the data suggest that the CrbS/R system plays a central role in acetate metabolism in V. cholerae, P. aeruginosa, and P. entomophila. However, each microbe's unique environmental adaptations and pathogenesis strategies may dictate conditions under which CrbS/R-mediated acs expression is most critical.

MeSH terms

  • Acetate-CoA Ligase / genetics*
  • Acetates / metabolism
  • Animals
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Conserved Sequence
  • Environment*
  • Gene Expression Regulation, Bacterial
  • Genetic Variation*
  • Hemolysin Proteins / metabolism
  • Protein Domains
  • Pseudomonas aeruginosa / cytology
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / metabolism
  • Pseudomonas aeruginosa / pathogenicity
  • Sequence Deletion
  • Sequence Homology, Nucleic Acid
  • Signal Transduction
  • Transcription, Genetic*
  • Vibrio cholerae / cytology
  • Vibrio cholerae / genetics
  • Vibrio cholerae / metabolism
  • Vibrio cholerae / pathogenicity
  • Virulence

Substances

  • Acetates
  • Bacterial Proteins
  • Hemolysin Proteins
  • Acetate-CoA Ligase

Grants and funding

The authors received funding from start up funds from Amherst College and Northern Michigan University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.