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肠球菌属细胞应对细胞壁压力时的 PASTA 激酶和双组分信号传导的汇聚

Convergence of PASTA Kinase and Two-Component Signaling in Response to Cell Wall Stress in Enterococcus faecalis.

机构信息

Department of Microbiology and Immunology, Center for Infectious Disease Research, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Department of Microbiology and Immunology, Center for Infectious Disease Research, Medical College of Wisconsin, Milwaukee, Wisconsin, USA

出版信息

J Bacteriol. 2018 May 24;200(12). doi: 10.1128/JB.00086-18. Print 2018 Jun 15.

Abstract

Two common signal transduction mechanisms used by bacteria to sense and respond to changing environments are two-component systems (TCSs) and eukaryote-like Ser/Thr kinases and phosphatases (eSTK/Ps). is a Gram-positive bacterium and a serious opportunistic pathogen that relies on both a TCS and an eSTK/P pathway for intrinsic resistance to cell wall-targeting antibiotics. The TCS consists of a histidine kinase (CroS) and a response regulator (CroR) that become activated upon exposure of cells to cell wall-targeting antibiotics, leading to a modulation of gene expression. The eSTK/P pathway consists of a transmembrane kinase (IreK) and its cognate phosphatase (IreP), which act antagonistically to mediate antibiotic resistance through an unknown mechanism. Because both CroS/R and IreK/P contribute to enterococcal resistance toward cell wall-targeting antibiotics, we hypothesized that these signaling systems are intertwined. To test this hypothesis, we analyzed CroR phosphorylation and CroS/R-dependent gene expression to probe the influence of IreK and IreP on CroS/R signaling. In addition, we analyzed the phosphorylation state of CroS, which revealed the IreK-dependent phosphorylation of a Thr residue important for CroS function. Our results are consistent with a model in which IreK positively influences CroR-dependent gene expression through the phosphorylation of CroS to promote antimicrobial resistance in Two-component signaling systems (TCSs) and eukaryote-like Ser/Thr kinases (eSTKs) are used by bacteria to sense and adapt to changing environments. Understanding how these pathways are regulated to promote bacterial survival is critical for a more complete understanding of bacterial stress responses and physiology. The opportunistic pathogen relies on both a TCS (CroS/R) and an eSTK (IreK) for intrinsic resistance to cell wall-targeting antibiotics. We probed the relationship between CroS/R and IreK, revealing the convergence of IreK and the sensor kinase CroS to enhance signaling through CroS/R and increase antimicrobial resistance in This newly described example of eSTK/TCS convergence adds to our understanding of the signaling networks mediating antimicrobial resistance in .

摘要

两种常见的细菌感知和响应环境变化的信号转导机制是双组分系统(TCS)和真核样丝氨酸/苏氨酸激酶和磷酸酶(eSTK/Ps)。 是一种革兰氏阳性菌,也是一种严重的机会性病原体,它依赖于 TCS 和 eSTK/P 途径来固有地抵抗细胞壁靶向抗生素。TCS 由组氨酸激酶(CroS)和应答调节子(CroR)组成,当细胞暴露于细胞壁靶向抗生素时,它们会被激活,导致基因表达的调节。eSTK/P 途径由跨膜激酶(IreK)和其同源磷酸酶(IreP)组成,它们通过未知的机制拮抗作用来介导抗生素抗性。由于 CroS/R 和 IreK/P 都有助于肠球菌对细胞壁靶向抗生素的抗性,我们假设这些信号系统是相互交织的。为了验证这一假设,我们分析了 CroR 磷酸化和 CroS/R 依赖性基因表达,以探讨 IreK 和 IreP 对 CroS/R 信号的影响。此外,我们还分析了 CroS 的磷酸化状态,结果表明 IreK 依赖于 Thr 残基的磷酸化,该残基对 CroS 功能很重要。我们的结果与以下模型一致:IreK 通过 CroS 的磷酸化正向影响 CroR 依赖性基因表达,以促进 双组分信号系统(TCSs)和真核样丝氨酸/苏氨酸激酶(eSTKs)被细菌用来感知和适应不断变化的环境。了解这些途径如何被调节以促进细菌存活,对于更全面地理解细菌应激反应和生理学至关重要。机会性病原体 依赖于 TCS(CroS/R)和 eSTK(IreK)来固有地抵抗细胞壁靶向抗生素。我们探讨了 CroS/R 和 IreK 之间的关系,揭示了 IreK 和传感器激酶 CroS 的收敛,以增强通过 CroS/R 的信号,并增加 在这个新描述的 eSTK/TCS 收敛的例子中,增加了我们对介导 中抗菌药物抗性的信号网络的理解。

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