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本文引用的文献

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Nuclease expression by Staphylococcus aureus facilitates escape from neutrophil extracellular traps.金黄色葡萄球菌的核酸酶表达促进了从中性粒细胞细胞外陷阱的逃逸。
J Innate Immun. 2010;2(6):576-86. doi: 10.1159/000319909. Epub 2010 Sep 10.
2
Pseudomonas aeruginosa produces an extracellular deoxyribonuclease that is required for utilization of DNA as a nutrient source.铜绿假单胞菌产生一种细胞外脱氧核糖核酸酶,该酶对于利用 DNA 作为营养源是必需的。
Environ Microbiol. 2010 Jun;12(6):1621-9. doi: 10.1111/j.1462-2920.2010.02208.x. Epub 2010 Mar 29.
3
A proteomic view of an important human pathogen--towards the quantification of the entire Staphylococcus aureus proteome.一种重要人类病原体的蛋白质组学观点——迈向金黄色葡萄球菌蛋白质组全定量分析。
PLoS One. 2009 Dec 4;4(12):e8176. doi: 10.1371/journal.pone.0008176.
4
Identification of immunogenic proteins from Burkholderia cepacia secretome using proteomic analysis.利用蛋白质组学分析鉴定洋葱伯克霍尔德氏菌 secretome 中的免疫原性蛋白。
Vaccine. 2010 Feb 3;28(5):1318-24. doi: 10.1016/j.vaccine.2009.11.027. Epub 2009 Nov 26.
5
Oxidative stress and metal ions regulate a ferritin-like gene, dpr, in Streptococcus pyogenes.氧化应激和金属离子调节酿脓链球菌中的一种铁蛋白样基因 dpr。
Int J Med Microbiol. 2010 Apr;300(4):259-64. doi: 10.1016/j.ijmm.2009.09.002. Epub 2009 Oct 29.
6
Molecular pathogenesis of necrotizing fasciitis.坏死性筋膜炎的分子发病机制。
Annu Rev Pathol. 2010;5:1-31. doi: 10.1146/annurev-pathol-121808-102135.
7
Clinical and microbiologic characteristics of group A streptococcal necrotizing fasciitis in children.儿童A组链球菌坏死性筋膜炎的临床和微生物学特征
Pediatr Infect Dis J. 2009 Jun;28(6):541-3. doi: 10.1097/inf.0b013e318195bb10.
8
PerR confers phagocytic killing resistance and allows pharyngeal colonization by group A Streptococcus.PerR赋予A组链球菌抗吞噬杀伤能力,并使其能够在咽部定植。
PLoS Pathog. 2008 Sep 5;4(9):e1000145. doi: 10.1371/journal.ppat.1000145.
9
Molecular and clinical characteristics of invasive group A streptococcal infection in Sweden.瑞典侵袭性A组链球菌感染的分子与临床特征
Clin Infect Dis. 2007 Aug 15;45(4):450-8. doi: 10.1086/519936. Epub 2007 Jul 10.
10
DNase Sda1 provides selection pressure for a switch to invasive group A streptococcal infection.脱氧核糖核酸酶Sda1为向侵袭性A组链球菌感染转变提供选择压力。
Nat Med. 2007 Aug;13(8):981-5. doi: 10.1038/nm1612. Epub 2007 Jul 15.

化脓链球菌差异分泌组学研究揭示了一种新型过氧化物调节因子(PerR)调控的细胞外毒力因子有丝分裂原因子 3(MF3)。

Differential secretomics of Streptococcus pyogenes reveals a novel peroxide regulator (PerR)-regulated extracellular virulence factor mitogen factor 3 (MF3).

机构信息

Department of Environmental and Occupational Health, College of Medicine, Tainan, Taiwan.

出版信息

Mol Cell Proteomics. 2011 Sep;10(9):M110.007013. doi: 10.1074/mcp.M110.007013. Epub 2011 Jun 2.

DOI:10.1074/mcp.M110.007013
PMID:21636680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3186197/
Abstract

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.

摘要

化脓链球菌是一种人类病原体,可引起多种疾病。化脓链球菌分泌的许多毒力因子参与发病机制。过氧化物调节剂(PerR)与过氧化物抗性反应和发病机制有关,但对涉及毒力的分泌组的调节知之甚少。为了研究 PerR 如何调节与毒力相关的化脓链球菌分泌组的表达,使用 perR 缺陷突变体与野生型菌株进行比较分泌组学分析。收集处于静止期的野生型菌株和 perR 缺陷突变体的条件培养基用于二维凝胶电泳分析,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质谱鉴定差异表达的蛋白斑点。每张凝胶上检测到 330 多个蛋白斑点。我们鉴定了 25 个独特的上调蛋白和 13 个独特的下调蛋白,这些蛋白直接或间接地受到 PerR 调节剂的控制。在鉴定的这些蛋白中,选择有丝分裂原因子 3(MF3)来验证毒力和基因产物的表达。数据表明,通过免疫印迹分析测量的条件培养基中 MF3 蛋白水平与二维凝胶电泳分析确定的蛋白水平很好地相关。我们还证明 PerR 与 mf3 基因的启动子区域结合。感染模型的结果表明,mf3 缺陷突变体的毒力减弱。野生型菌株和 mf3 缺陷突变体的额外生长数据表明,MF3 在促进生长的外源 DNA 消化中起作用。总之,我们得出结论,PerR 可以正向调节分泌蛋白 MF3 的表达,MF3 有助于化脓链球菌的毒力。PerR 调节的分泌组分析为阐明宿主-病原体相互作用提供了关键信息,并可能有助于开发潜在的化学治疗策略来预防或治疗链球菌病。