Luong Thanh T, Dunman Paul M, Murphy Ellen, Projan Steven J, Lee Chia Y
Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, 4301 W. Markham St., Slot 511, Little Rock, AR 72205, USA.
J Bacteriol. 2006 Mar;188(5):1899-910. doi: 10.1128/JB.188.5.1899-1910.2006.
MgrA has been shown to affect multiple Staphylococcus aureus genes involved in virulence and antibiotic resistance. To comprehensively identify the target genes regulated by mgrA, we employed a microarray method to analyze the transcription profiles of S. aureus Newman, its isogeneic mgrA mutant, and an MgrA-overproducing derivative. We compared genes that were differentially expressed at exponential or early stationary growth phases. Our results showed that MgrA affected an impressive number of genes, 175 of which were positively regulated and 180 of which were negatively regulated in an mgrA-specific manner. The target genes included all functional categories. The microarray results were validated by real-time reverse transcription-PCR quantitation of a set of selected genes from different functional categories. Our data also indicate that mgrA regulates virulence factors in a fashion analogous to that of the accessory gene regulatory locus (agr). Accordingly, exoproteins are upregulated and surface proteins are downregulated by the regulator, suggesting that mgrA may function in concert with agr. The fact that a large number of genes are regulated by mgrA implies that MgrA is a major global regulator in S. aureus.
MgrA已被证明会影响金黄色葡萄球菌中多个与毒力和抗生素耐药性相关的基因。为了全面鉴定受MgrA调控的靶基因,我们采用微阵列方法分析了金黄色葡萄球菌Newman菌株、其同基因mgrA突变体以及MgrA过表达衍生物的转录谱。我们比较了在指数生长期或早期稳定生长期差异表达的基因。我们的结果表明,MgrA影响了大量基因,其中175个基因以MgrA特异性方式被正向调控,180个基因被负向调控。靶基因涵盖了所有功能类别。通过对一组来自不同功能类别的选定基因进行实时逆转录PCR定量分析,验证了微阵列结果。我们的数据还表明,mgrA调控毒力因子的方式与辅助基因调控位点(agr)类似。因此,该调节因子上调胞外蛋白并下调表面蛋白,这表明mgrA可能与agr协同发挥作用。大量基因受mgrA调控这一事实意味着MgrA是金黄色葡萄球菌中的一个主要全局调节因子。