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首页> 外文期刊>Molecular & cellular proteomics: MCP >Differential Secretomics of Streptococcus pyogenes Reveals a Novel Peroxide Regulator (PerR)-regulated Extracellular Virulence Factor Mitogen Factor3 (MF3)
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Differential Secretomics of Streptococcus pyogenes Reveals a Novel Peroxide Regulator (PerR)-regulated Extracellular Virulence Factor Mitogen Factor3 (MF3)

机译:化脓性链球菌的不同分泌组学揭示了一种新型的过氧化物调节剂(PerR)调节的细胞外致病因子丝裂原因子3(MF3)。

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Streptococcus pyogenes is a human pathogen that causes various diseases. Numerous virulence factors secreted by S. pyogenes are involved in pathogenesis. The peroxide regulator (PerR) is associated with the peroxide resistance response and pathogenesis, but little is known about the regulation of the secretome involved in virulence. To investigate how PerR regulates the expression of the S. pyogenes secretome involved in virulence, a perR deficient mutant was used for comparative secretomic analysis with a wild-type strain. The conditioned medium containing secreted proteins of a wild-type strain and a perR deficient mutant at the stationary phase were collected for two-dimensional gel electrophoresis analysis, where protease inhibitors were applied to avoid the degradation of extracellular proteins. Differentially expressed protein spots were identified by liquid chromatography electrospray ionization tandem MS. More than 330 protein spots were detected on each gel. We identified 25 unique up-regulated proteins and 13 unique down-regulated proteins that were directly or indirectly controlled by the PerR regulator. Among these identified proteins, mitogen factor 3 (MF3), was selected to verify virulence and the expression of gene products. The data showed that MF3 protein levels in conditioned medium, as measured by immunoblot analysis, correlated well with protein levels determined by two-dimensional gel electrophoresis analysis. We also demonstrated that PerR bound to the promoter region of the mf3 gene. The result of an infection model showed that virulence was attenuated in the mf3 deficient mutant. Additional growth data of the wild-type strain and the mf3 deficient mutant suggested that MF3 played a role in digestion of exogenous DNA for promoting growth. To summarize, we conclude that PerR can positively regulate the expression of the secreted protein MF3 that contributes to the virulence in S. pyogenes. The analysis of the PerR-regulated secretome provided key information for the elucidation of the host-pathogen interactions and might assist in the development of potential chemotherapeutic strategies to prevent or treat streptococcal diseases.
机译:化脓性链球菌是引起多种疾病的人类病原体。化脓性链球菌分泌的许多毒力因子参与发病机理。过氧化物调节剂(PerR)与过氧化物抗性反应和发病机理有关,但对与毒力有关的分泌组的调节知之甚少。为了研究PerR如何调节参与毒力的化脓性链球菌分泌基因组的表达,将perR缺陷型突变体用于与野生型菌株的比较分泌组学分析。收集含有野生型菌株的分泌蛋白和固定相上的perR缺陷突变体的条件培养基,以进行二维凝胶电泳分析,在其中应用蛋白酶抑制剂以避免细胞外蛋白的降解。通过液相色谱电喷雾串联MS鉴定差异表达的蛋白斑点。在每种凝胶上检测到330多个蛋白质斑点。我们确定了25种独特的上调蛋白和13种独特的下调蛋白,这些蛋白直接或间接地受PerR调节剂控制。在这些鉴定出的蛋白质中,选择了有丝分裂原因子3(MF3)来验证毒力和基因产物的表达。数据显示,通过免疫印迹分析测得的条件培养基中的MF3蛋白水平与通过二维凝胶电泳分析确定的蛋白水平具有很好的相关性。我们还证明PerR绑定到mf3基因的启动子区域。感染模型的结果表明,mf3缺陷型突变体的毒力减弱。野生型菌株和mf3缺陷型突变体的其他生长数据表明,MF3在消化外源DNA中起到促进生长的作用。总而言之,我们得出的结论是,PerR可以正向调节分泌化脓性链球菌中毒力的分泌蛋白MF3的表达。 PerR调节的分泌物组的分析为阐明宿主与病原体的相互作用提供了关键信息,并且可能有助于开发预防或治疗链球菌疾病的潜在化学治疗策略。

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