Department of Microbiology and Immunology, University of Arkansas for Medical Sciencesgrid.241054.6, Little Rock, Arkansas, USA.
J Bacteriol. 2022 Aug 16;204(8):e0015222. doi: 10.1128/jb.00152-22. Epub 2022 Jul 11.
Production of capsular polysaccharides in Staphylococcus aureus is transcriptionally regulated by a control region of the operon that consists of SigA- and SigB-dependent promoters. A large number of regulators have been shown to affect gene expression. However, regulation of capsule is only partially understood. Here we found that SarZ was another regulator that activated the genes through the SigA-dependent promoter. Gel electrophoresis mobility shift experiments revealed that SarZ is bound to a broad region of the promoter including the SigA-dependent promoter but mainly the downstream region. We demonstrated that activation of expression by SarZ was independent of MgrA, which also activated capsule through the SigA-dependent promoter. Our results further showed that oxidative stress with hydrogen peroxide (HO) treatments enhanced SarZ activation of expression, indicating that SarZ is able to sense oxidative stress to regulate capsule production. Expression of virulence genes in Staphylococcus aureus is affected by environmental cues and is regulated by a surprisingly large number of regulators. Much is still unknown about how virulence factors are regulated by environment cues at the molecular level. Capsule is an antiphagocytic virulence factor that is highly regulated. In this study, we found SarZ was an activator of capsule and that the regulation of capsule by SarZ was affected by oxidative stress. These results provide an example of how a virulence factor could be regulated in response to an environmental cue. As the host oxidative defense system plays an important role against S. aureus, this study contributes to a better understanding of virulence gene regulation and staphylococcal pathogenesis.
金黄色葡萄球菌荚膜多糖的产生受 操纵子的控制区转录调控,该控制区由 SigA 和 SigB 依赖性启动子组成。大量调节剂已被证明会影响 基因表达。然而,荚膜的调控机制尚不完全清楚。在这里,我们发现 SarZ 是另一种通过 SigA 依赖性启动子激活 基因的调节剂。凝胶电泳迁移率变动实验表明,SarZ 结合于 启动子的一个广泛区域,包括 SigA 依赖性启动子,但主要是下游区域。我们证明了 SarZ 通过 SigA 依赖性启动子激活 表达是不依赖于 MgrA 的。我们的结果还表明,过氧化氢 (HO) 处理的氧化应激增强了 SarZ 对 表达的激活作用,表明 SarZ 能够感知氧化应激来调节荚膜的产生。金黄色葡萄球菌毒力基因的表达受环境线索的影响,并受大量调节剂的调控。关于环境线索如何在分子水平上调节毒力因子的信息仍然知之甚少。荚膜是一种抗吞噬的毒力因子,其调控非常复杂。在这项研究中,我们发现 SarZ 是荚膜的激活剂,并且 SarZ 对荚膜的调节受氧化应激的影响。这些结果为一种毒力因子如何响应环境线索进行调节提供了一个范例。由于宿主的氧化防御系统在抵抗金黄色葡萄球菌方面起着重要作用,因此本研究有助于更好地理解毒力基因的调控和金黄色葡萄球菌的发病机制。