Transcription profiling-based identification of Staphylococcus aureus genes regulated by the agr and/or sarA loci

J Bacteriol. 2001 Dec;183(24):7341-53. doi: 10.1128/JB.183.24.7341-7353.2001.

Abstract

The advent of transcription profiling technologies has provided researchers with an unprecedented ability to study biological processes. Accordingly, a custom-made Affymetrix GeneChip, constituting >86% of the Staphylococcus aureus genome, was used to identify open reading frames that are regulated by agr and/or SarA, the two best-studied regulators of the organism's virulence response. RNA extracted from wild-type cells and agr, sarA, and agr sarA mutant cells in the early-, mid-, and late-log and stationary phases of growth was analyzed. Open reading frames with transcription patterns expected of genes either up- or downregulated in an agr- and/or SarA-dependent manner were identified. Oligonucleotide microarray and Northern blot analyses confirmed that the transcription of several known virulence genes, including hla (alpha-toxin) and spa (protein A), is regulated by each effector and provided insights about the regulatory cascades involved in both alpha-hemolysin and protein A expression. Several putative virulence factors were also identified as regulated by agr and/or SarA. In addition, genes that are involved in several biological processes but which are difficult to reconcile as playing a direct role in the organism's pathogenesis also appeared to be regulated by each effector, suggesting that products of both the agr and the sarA locus are more-global transcription regulators than previously realized.

MeSH terms

  • Bacterial Proteins / metabolism*
  • Bacterial Toxins / genetics
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial
  • Genes, Bacterial*
  • Hemolysin Proteins / genetics
  • Oligonucleotide Array Sequence Analysis
  • Open Reading Frames
  • Staphylococcal Protein A / genetics
  • Staphylococcus aureus / genetics*
  • Staphylococcus aureus / pathogenicity
  • Trans-Activators*
  • Transcription Factors / metabolism*
  • Up-Regulation
  • Virulence / genetics

Substances

  • Agr protein, Staphylococcus aureus
  • Bacterial Proteins
  • Bacterial Toxins
  • DNA-Binding Proteins
  • Hemolysin Proteins
  • SarA protein, bacterial
  • Staphylococcal Protein A
  • Trans-Activators
  • Transcription Factors
  • staphylococcal alpha-toxin