Metabolic dependent and independent pH-drop shuts down VirSR quorum sensing in Clostridium perfringens

J Biosci Bioeng. 2018 May;125(5):525-531. doi: 10.1016/j.jbiosc.2017.12.019. Epub 2018 Jan 17.

Abstract

Clostridium perfringens produces various exotoxins and enzymes that cause food poisoning and gas gangrene. The genes involved in virulence are regulated by the agr-like quorum sensing (QS) system, which consists of a QS signal synthesis system and a VirSR two-component regulatory system (VirSR TCS) which is a global regulatory system composed of signal sensor kinase (VirS) and response regulator (VirR). We found that the perfringolysin O gene (pfoA) was transiently expressed during mid-log phase of bacterial growth; its expression was rapidly shut down thereafter, suggesting the existence of a self-quorum quenching (sQQ) system. The sQQ system was induced by the addition of stationary phase culture supernatant (SPCS). Activity of the sQQ system was heat stable, and was present following filtration through the ultrafiltration membrane, suggesting that small molecules acted as sQQ agents. In addition, sQQ was also induced by pure acetic and butyric acids at concentrations equivalent to those in the stationary phase culture, suggesting that organic acids produced by C. perfringens were involved in sQQ. In pH-controlled batch culture, sQQ was greatly diminished; expression level of pfoA extended to late-log growth phase, and was eventually increased by one order of magnitude. Furthermore, hydrochloric acid induced sQQ at the same pH as was used in organic acids. SPCS also suppressed the expression of genes regulated by VirSR TCS. Overall, the expression of virulence factors of C. perfringens was downregulated by the sQQ system, which was mediated by primary acidic metabolites and acidic environments. This suggested the possibility of pH-controlled anti-virulence strategies.

Keywords: Acidic pH; Autoinducing peptide; Clostridium perfringens; Quorum quenching; Quorum sensing; VirS/VirR two-component regulatory system.

MeSH terms

  • Acids / pharmacology*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bacterial Toxins / genetics
  • Clostridium perfringens / drug effects*
  • Clostridium perfringens / genetics
  • Clostridium perfringens / metabolism*
  • Gene Expression Regulation, Bacterial / drug effects
  • Genes, Regulator / drug effects
  • Genes, Regulator / physiology
  • Hemolysin Proteins / genetics
  • Hydrogen-Ion Concentration
  • Metabolic Networks and Pathways / drug effects
  • Metabolic Networks and Pathways / genetics
  • Metabolic Networks and Pathways / physiology*
  • Phosphotransferases / genetics
  • Phosphotransferases / metabolism
  • Quorum Sensing / drug effects*
  • Quorum Sensing / genetics
  • Quorum Sensing / physiology*
  • Virulence Factors / genetics

Substances

  • Acids
  • Bacterial Proteins
  • Bacterial Toxins
  • Hemolysin Proteins
  • Virulence Factors
  • Clostridium perfringens theta-toxin
  • Phosphotransferases