MgrA Activates Staphylococcal Capsule via SigA-Dependent Promoter

J Bacteriol. 2020 Dec 18;203(2):e00495-20. doi: 10.1128/JB.00495-20. Print 2020 Dec 18.

Abstract

Staphylococcus aureus capsule polysaccharide is an important antiphagocytic virulence factor. The cap genes are regulated at the promoter element (Pcap) upstream of the cap operon. Pcap, which consists of a dominant SigB-dependent promoter and a weaker upstream SigA-dependent promoter, is activated by global regulator MgrA. How MgrA activates capsule is unclear. Here, we showed that MgrA directly bound to the Pcap region and affected the SigA-dependent promoter. Interestingly, an electrophoretic mobility shift assay showed that MgrA bound to a large region of Pcap, mainly downstream of the SigA-dependent promoter. We further showed that the ArlRS two-component system and the Agr quorum sensing system activated capsule primarily through MgrA in the early growth phases.IMPORTANCE The virulence of Staphylococcus aureus depends on the expression of various virulence factors, which is governed by a complex regulatory network. We have been using capsule as a model virulence factor to study virulence gene regulation in S. aureus MgrA is one of the regulators of capsule and has a major effect on capsule production. However, how MgrA regulates capsule genes is not understood. In this study, we were able to define the mechanism involving MgrA regulation of capsule. In addition, we also delineated the role of MgrA in capsule regulatory pathways involving the key virulence regulators Agr and Arl. This study further advances our understanding of virulence gene regulation in S. aureus, an important human pathogen.

Keywords: MgrA; Staphylococcus aureus; capsule; gene regulation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Bacterial Capsules / chemistry*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / physiology
  • Electrophoretic Mobility Shift Assay
  • Immunoblotting
  • Immunoglobulin A, Secretory / genetics
  • Immunoglobulin A, Secretory / physiology*
  • Mutation
  • Polysaccharides, Bacterial / genetics
  • Polysaccharides, Bacterial / physiology*
  • Promoter Regions, Genetic / physiology*
  • RNA, Bacterial / isolation & purification
  • RNA, Bacterial / physiology
  • Real-Time Polymerase Chain Reaction
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Reverse Transcription
  • Staphylococcus aureus / genetics
  • Staphylococcus aureus / pathogenicity
  • Staphylococcus aureus / physiology*
  • Virulence / genetics
  • Virulence Factors / genetics
  • Virulence Factors / physiology*

Substances

  • ArlR protein, Staphylococcus aureus
  • Bacterial Proteins
  • Immunoglobulin A, Secretory
  • Polysaccharides, Bacterial
  • RNA, Bacterial
  • RNAIII, Staphylococcus aureus
  • Recombinant Proteins
  • Virulence Factors