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

被引:504
作者
Dunman, PM
Murphy, E
Haney, S
Palacios, D
Tucker-Kellogg, G
Wu, S
Brown, EL
Zagursky, RJ
Shlaes, D
Projan, SJ
机构
[1] Wyeth Ayerst Res, Dept Infect Dis, Pearl River, NY 10965 USA
[2] Wyeth Ayerst Res, Dept Genom, Cambridge, MA 02140 USA
[3] Wyeth Ayerst Res, Monmouth Jct, NJ 08852 USA
[4] Wyeth Lederle Vaccines, W Henrietta, NY 14586 USA
关键词
D O I
10.1128/JB.183.24.7341-7353.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页码:7341 / 7353
页数:13
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