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The Effect of the Potential PhoQ Histidine Kinase Inhibitors on Shigella flexneri Virulence

机译:潜在的PhoQ组氨酸激酶抑制剂对弗氏志贺氏菌毒力的影响

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摘要

PhoQ/PhoP is an important two-component system that regulates Shigella virulence. We explored whether the PhoQ/PhoP system is a promising target for new antibiotics against S. flexneri infection. By using a high-throughput screen and enzymatic activity coupled assay, four compounds were found as potential PhoQ inhibitors. These compounds not only inhibited the activity of SF-PhoQc autophosphorylation but also displayed high binding affinities to the SF-PhoQc protein in the Surface Plasmon Resonance response. A S. flexneri cell invasion assay showed that three of these potential PhoQ inhibitors inhibit the invasion of HeLa cells by S. flexneri 9380. In a Mouse Sereny test, mice inoculated with S. flexneri 9380 pre-treated with the potential PhoQ inhibitors 1, 2, 3 or 4 displayed no inflammation, whereas mice inoculated with S. flexneri 9380 alone displayed severe keratoconjunctival inflammation. All four potential PhoQ inhibitors showed no significant cytotoxicity or hemolytic activity. These data suggest that the four potential PhoQ inhibitors inhibited the virulence of S. flexneri and that PhoQ/PhoP is a promising target for the development of drugs against S. flexneri infection.
机译:PhoQ / PhoP是调节志贺氏菌毒力的重要两组分系统。我们探讨了PhoQ / PhoP系统是否是针对弗氏链球菌感染的新型抗生素的有希望的靶标。通过高通量筛选和酶活性偶联测定,发现了四种化合物作为潜在的PhoQ抑制剂。这些化合物不仅抑制了SF-PhoQc自磷酸化的活性,而且在表面等离振子共振反应中显示出对SF-PhoQc蛋白的高结合亲和力。弗氏链球菌的细胞入侵试验表明,这些潜在的PhoQ抑制剂中的三种抑制弗氏链球菌9380侵袭HeLa细胞。在Mouse Sereny测试中,接种弗氏链球菌9380的小鼠用潜在的PhoQ抑制剂预处理1, 2、3、4没有显示出炎症,而单独接种弗氏链球菌9380的小鼠显示出严重的角膜结膜炎症。所有四种潜在的PhoQ抑制剂均未显示明显的细胞毒性或溶血活性。这些数据表明四种潜在的PhoQ抑制剂抑制了弗氏链球菌的毒性,并且PhoQ / PhoP是开发抗弗氏链球菌感染的药物的有希望的目标。

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