CidR and CcpA synergistically regulate staphylococcus aureus cidABC expression

Marat R. Sadykov, Ian H. Windham, Todd J. Widhelm, Vijaya Kumar Yajjala, Sean M. Watson, Jennifer L. Endres, Arissa I. Bavari, Vinai C. Thomas, Jeffrey L. Bose, Kenneth W. Bayles

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


The death and lysis of a subpopulation of Staphylococcus aureus cells during biofilm development benefit the whole bacterial population through the release of an important component of the biofilm matrix, extracellular DNA. Previously, we have demonstrated that these processes are affected by the gene products of the cidABC operon, the expression of which is controlled by the LysR-type transcriptional regulator, CidR. In this study, we characterized cis- and trans-acting elements essential for the induction of the cidABC operon. In addition to a CidR-binding site located within the cidABC promoter region, sequence analysis revealed the presence of a putative catabolite responsive element (cre box), suggestive of the involvement of the catabolite control protein A (CcpA) in the regulation of cidABC expression. This was confirmed using electrophoretic mobility shift assays and real-time reverse transcriptase PCR analysis demonstrating the direct positive control of cidABC transcription by the master regulator of carbon metabolism. Furthermore, the importance of CcpA and the identified cre site for the induction of the cidABC operon was demonstrated by examining the expression of PcidABC-lacZ reporter fusions in various mutant strains in which the genes involved in carbon metabolism and carbon catabolite repression were disrupted. Together the results of this study demonstrate the necessity of both transcriptional regulators, CidR and CcpA, for the induction of the cidABC operon and reveal the complexity of molecular interactions controlling its expression.

Original languageEnglish (US)
Article numbere00371-19
JournalJournal of bacteriology
Issue number23
StatePublished - Dec 1 2019


  • Carbon catabolite repression
  • Glycolysis
  • Regulation of gene expression
  • Staphylococcus aureus

ASJC Scopus subject areas

  • Microbiology
  • Molecular Biology


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