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首页> 外文期刊>Journal of bacteriology >An Extracytoplasmic Function Sigma/Anti-Sigma Factor System Regulates Hypochlorous Acid Resistance and Impacts Expression of the Type IV Secretion System in Brucella melitensis
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An Extracytoplasmic Function Sigma/Anti-Sigma Factor System Regulates Hypochlorous Acid Resistance and Impacts Expression of the Type IV Secretion System in Brucella melitensis

机译:外晶功能Sigma /抗Σ系数系统调节次氯酸耐酸性,并影响IV型分泌系统在Brucella melitensis的影响

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The intracellular bacterial pathogen Brucella causes persistent infections in various mammalian species. To survive and replicate within macrophages, these bacteria must be able to withstand oxidative stresses and express the type IV secretion system (T4SS) to evade host immune responses. The extracytoplasmic function (ECF) sigma factor system is a major signal transduction mechanism in bacteria that senses environmental cues and responds by regulating gene expression. In this study, we defined an ECF σ bcrS and its cognate anti-σ factor abcS in Brucella melitensis M28 by conserved domain analysis and a protein interaction assay. BcrS directly activates an adjacent operon, bcrXQP , that encodes a methionine-rich peptide and a putative methionine sulfoxide reductase system, whereas AbcS is a negative regulator of bcrS and bcrXQP . The bcrS - abcS and bcrXQP operons can be induced by hypochlorous acid and contribute to hypochlorous acid resistance in vitro . Next, RNA sequencing analysis and genome-wide recognition sequence search identified the regulons of BcrS and AbcS. Interestingly, we found that BcrS positively influences T4SS expression in an AbcS-dependent manner and that AbcS also affects T4SS expression independently of BcrS. Last, we demonstrate that abcS is required for the maintenance of persistent infection, while bcrS is dispensable in a mouse infection model. Collectively, we conclude that BcrS and AbcS influence expression of multiple genes responsible for Brucella virulence traits. IMPORTANCE Brucella is a notorious intracellular pathogen that induces chronic infections in animals and humans. To survive and replicate within macrophages, these bacteria require a capacity to withstand oxidative stresses and to express the type IV secretion system (T4SS) to combat host immune responses. In this study, we characterized an extracytoplasmic function sigma/anti-sigma factor system that regulates resistance to reactive chlorine species and T4SS expression, thereby establishing a potential link between two crucial virulence traits of Brucella . Furthermore, the anti-sigma factor AbcS contributes to Brucella persistent infection of mice. Thus, this work provides novel insights into Brucella virulence regulation as well as a potential drug target for fighting Brucella infections.
机译:细胞内细菌病原体Brucella会导致各种哺乳动物物种中的持续感染。为了在巨噬细胞内生存并复制,这些细菌必须能够承受氧化应激并表达IV型分泌系统(T4S)以逃避宿主免疫应答。外晶功能(ECF)Sigma系数系统是细菌的主要信号转导机制,可通过调节基因表达来感测环境提示和响应。在该研究中,通过保守的结构域分析和蛋白质相互作用测定,我们在Brucella melitensis M28中定义了ECFσBCR及其同源抗Σ因子ABC和蛋白质相互作用测定。 BCRS直接激活相邻的操作股,BCRXQP,它们编码富含甲硫氨酸的肽和推定的甲硫氨酸亚砜还原酶系统,而ABC是BCRS和BCRXQP的负调节剂。 BCRS - ABCs和BCRXQP操纵子可以通过次氯酸诱导,并有助于体外次氯酸耐性。接下来,RNA测序分析和基因组识别序列搜索确定了BCR和ABC的调节件。有趣的是,我们发现BCRS以ABCS依赖的方式积极地影响T4SS表达,并且ABC也影响T4SS表达式独立于BCRS。最后,我们证明了维持持续感染所需的ABC,而BCR在小鼠感染模型中可以分配。共同,我们得出结论,BCR和ABCS影响负责Brucella毒力特征的多种基因的表达。重要的布鲁氏菌是一种臭名昭着的细胞内病原体,可诱导动物和人类的慢性感染。为了在巨噬细胞内生存并复制,这些细菌需要承受氧化应激的能力,并表达IV型分泌系统(T4S)以对抗宿主免疫应答。在本研究中,我们表征了一种细胞膜功能Sigma /抗Σ系数系统,其调节对反应性氯物种和T4SS表达的抗性,从而建立了Brucella的两个至关重要的毒力特征之间的潜在联系。此外,抗Σ因子ABC有助于对小鼠的Brucella持续的感染。因此,这项工作为Brucella毒力调节提供了新颖的洞察力以及用于抗Brucella感染的潜在药物靶标。

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