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BrpA Is Involved in Regulation of Cell Envelope Stress Responses in Streptococcus mutans

机译:BrpA参与调节变形链球菌中的细胞膜应力反应。

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摘要

Previous studies have shown that BrpA plays a major role in acid and oxidative stress tolerance and biofilm formation by Streptococcus mutans. Mutant strains lacking BrpA also display increased autolysis and decreased viability, suggesting a role for BrpA in cell envelope integrity. In this study, we examined the impact of BrpA deficiency on cell envelope stresses induced by envelope-active antimicrobials. Compared to the wild-type strain UA159, the BrpA-deficient mutant (TW14D) was significantly more susceptible to antimicrobial agents, especially lipid II inhibitors. Several genes involved in peptidoglycan synthesis were identified by DNA microarray analysis as downregulated in TW14D. Luciferase reporter gene fusion assays also revealed that expression of brpA is regulated in response to environmental conditions and stresses induced by exposure to subinhibitory concentrations of cell envelope antimicrobials. In a Galleria mellonella (wax worm) model, BrpA deficiency was shown to diminish the virulence of S. mutans OMZ175, which, unlike S. mutans UA159, efficiently kills the worms. Collectively, these results suggest that BrpA plays a role in the regulation of cell envelope integrity and that deficiency of BrpA adversely affects the fitness and diminishes the virulence of OMZ175, a highly invasive strain of S. mutans.
机译:先前的研究表明,BrpA在变形链球菌对酸和氧化应激的耐受性以及生物膜形成中起主要作用。缺乏BrpA的突变株也显示出增加的自溶作用和降低的生存能力,表明BrpA在细胞包膜完整性中的作用。在这项研究中,我们检查了BrpA缺乏症对包膜活性抗微生物剂诱导的细胞包膜应力的影响。与野生型UA159菌株相比,缺乏BrpA的突变体(TW14D)对抗菌剂特别是脂质II抑制剂更敏感。通过DNA芯片分析鉴定了与肽聚糖合成有关的几个基因,这些基因在TW14D中被下调。萤光素酶报道基因融合试验还显示,响应环境条件和暴露于亚抑制浓度的细胞包膜抗微生物剂诱导的应激,对brpA的表达进行调节。在梅勒拱廊(蜡蠕虫)模型中,BrpA缺乏症可降低变形链球菌OMZ175的毒力,与变形链球菌UA159不同,OMZ175可有效杀死蠕虫。总体而言,这些结果表明,BrpA在调节细胞包膜完整性中起作用,而BrpA的缺乏会不利地影响健康并降低变形链球菌高侵害性菌株OMZ175的毒力。

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