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基于微阵列的金黄色葡萄球菌σB调控子分析。

Microarray-based analysis of the Staphylococcus aureus sigmaB regulon.

作者信息

Bischoff Markus, Dunman Paul, Kormanec Jan, Macapagal Daphne, Murphy Ellen, Mounts William, Berger-Bächi Brigitte, Projan Steven

机构信息

Department of Medical Microbiology, University of Zurich, CH-8028 Zurich, Switzerland.

出版信息

J Bacteriol. 2004 Jul;186(13):4085-99. doi: 10.1128/JB.186.13.4085-4099.2004.

Abstract

Microarray-based analysis of the transcriptional profiles of the genetically distinct Staphylococcus aureus strains COL, GP268, and Newman indicate that a total of 251 open reading frames (ORFs) are influenced by sigmaB activity. While sigmaB was found to positively control 198 genes by a factor of > or =2 in at least two of the three genetic lineages analyzed, 53 ORFs were repressed in the presence of sigmaB. Gene products that were found to be influenced by sigmaB are putatively involved in all manner of cellular processes, including cell envelope biosynthesis and turnover, intermediary metabolism, and signaling pathways. Most of the genes and/or operons identified as upregulated by sigmaB were preceded by a nucleotide sequence that resembled the sigmaB consensus promoter sequence of Bacillus subtilis. A conspicuous number of virulence-associated genes were identified as regulated by sigmaB activity, with many adhesins upregulated and prominently represented in this group, while transcription of various exoproteins and toxins were repressed. The data presented here suggest that the sigmaB of S. aureus controls a large regulon and is an important modulator of virulence gene expression that is likely to act conversely to RNAIII, the effector molecule of the agr locus. We propose that this alternative transcription factor may be of importance for the invading pathogen to fine-tune its virulence factor production in response to changing host environments.

摘要

基于微阵列的对基因不同的金黄色葡萄球菌菌株COL、GP268和Newman转录谱的分析表明,共有251个开放阅读框(ORF)受σB活性影响。在分析的三个遗传谱系中的至少两个谱系中,发现σB以大于或等于2的倍数正向调控198个基因,而53个ORF在有σB存在时受到抑制。被发现受σB影响的基因产物可能参与各种细胞过程,包括细胞壁生物合成和周转、中间代谢以及信号通路。大多数被鉴定为由σB上调的基因和/或操纵子之前都有一段核苷酸序列,该序列类似于枯草芽孢杆菌的σB共有启动子序列。大量与毒力相关的基因被鉴定为受σB活性调控,许多黏附素上调并在该组中占显著比例,而各种外毒素和毒素的转录则受到抑制。此处呈现的数据表明,金黄色葡萄球菌的σB控制着一个大的调控子,是毒力基因表达的重要调节因子,其作用可能与agr位点的效应分子RNAIII相反。我们提出,这种替代转录因子可能对入侵病原体在应对不断变化的宿主环境时微调其毒力因子产生具有重要意义。

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