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A novel anti-virulence gene revealed by proteomic analysis in Shigella flexneri 2a

机译:通过弗氏志贺氏菌2a蛋白质组学分析揭示了一种新的抗毒力基因

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Background Shigella flexneri is a gram-negative, facultative pathogen that causes the majority of communicable bacterial dysenteries in developing countries. The virulence factors of S. flexneri have been shown to be produced at 37 degrees C but not at 30 degrees C. To discover potential, novel virulence-related proteins of S. flexneri, we performed differential in-gel electrophoresis (DIGE) analysis to measure changes in the expression profile that are induced by a temperature increase. Results The ArgT protein was dramatically down-regulated at 37 degrees C. In contrast, the ArgT from the non-pathogenic E. coli did not show this differential expression as in S. flexneri, which suggested that argT might be a potential anti-virulence gene. Competitive invasion assays in HeLa cells and in BALB/c mice with argT mutants were performed, and the results indicated that the over-expression of ArgTY225D would attenuate the virulence of S. flexneri. A comparative proteomic analysis was subsequently performed to investigate the effects of ArgT in S. flexneri at the molecular level. We show that HtrA is differentially expressed among different derivative strains. Conclusion Gene argT is a novel anti-virulence gene that may interfere with the virulence of S. flexneri via the transport of specific amino acids or by affecting the expression of the virulence factor, HtrA.
机译:背景弗氏志贺氏菌是革兰氏阴性,兼性病原体,可导致发展中国家的大多数传染性细菌性痢疾。已显示弗氏链球菌的毒力因子是在37摄氏度而不是30摄氏度下产生的。为了发现弗氏链球菌的新型毒力相关蛋白,我们进行了差异凝胶电泳(DIGE)分析测量由温度升高引起的表达谱变化。结果ArgT蛋白在37摄氏度时显着下调。相反,来自非病原性大肠杆菌的ArgT并未像弗氏链球菌那样显示出这种差异表达,这表明argT可能是潜在的抗毒力基因。在HeLa细胞和带有argT突变体的BALB / c小鼠中进行了竞争性侵袭试验,结果表明ArgTY225D的过表达会减弱弗氏链球菌的毒力。随后进行了比较蛋白质组学分析,以在分子水平上研究ArgT在弗氏链球菌中的作用。我们表明,HtrA在不同的衍生菌株之间差异表达。结论argT基因是一种新型的抗毒力基因,可能通过转运特定氨基酸或影响毒力因子HtrA的表达而干扰弗氏链球菌的毒力。

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