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将塞克硝唑重新定位为铜绿假单胞菌新型毒力因子衰减剂。

Repositioning secnidazole as a novel virulence factors attenuating agent in Pseudomonas aeruginosa.

机构信息

Department of Microbiology and Immunology, Faculty of Pharmacy, Port Said University, Egypt.

Department of Microbiology and Immunology, Faculty of Pharmacy, Zagazig University, Egypt.

出版信息

Microb Pathog. 2019 Feb;127:31-38. doi: 10.1016/j.micpath.2018.11.042. Epub 2018 Nov 27.

Abstract

Long-term treatment with antibiotics gives rise to the evolution of multi-drug resistant bacteria which are hard to be treated. Virulence factors inhibitors depend on disarming of microbial pathogens through reducing expression of virulence factors, abolishing the pathogen capability to harm the host. In the present study, the influence of secnidazole on Pseudomonas aeruginosa virulence factors expression was characterized. Production of Pseudomonas aeruginosa virulence factors such as pyocyanin, pyoverdin, elastase, rhamnolipids, proteases and hemolysins was examined following treatment of bacteria with sub-inhibitory concentration of secnidazole. Interestingly, secnidazole showed a powerful inhibitory effect on Pseudomonas aeruginosa virulence factors. Our results were further confirmed using qRT-PCR showing that there was a significant decrease in the expression of quorum sensing genes; lasI, lasR, rhlI, rhlR, pqsA and pqsR that regulate expression of virulence factors in Pseudomonas aeruginosa. Moreover, in vivo experiment using mice as infection model showed that secnidazole-treated bacteria were less capable to kill mice as compared to untreated bacteria. Importantly, there was a significant reduction in mortality in mice injected with secnidazole-treated bacteria relative to mice inoculated with untreated bacteria. In summary, our data showed that secnidazole could play a role in attenuating Pseudomonas aeruginosa through reducing virulence factors production. Moreover, our data clearly suggest that secnidazole could be involved in the treatment of Pseudomonas aeruginosa infections in order to control infection and lower the development of bacterial resistance to antibiotics.

摘要

长期使用抗生素会导致多药耐药菌的进化,这些细菌很难治疗。毒力因子抑制剂通过降低毒力因子的表达,使微生物病原体失去危害宿主的能力,从而发挥作用。在本研究中,我们研究了硝唑尼特对铜绿假单胞菌毒力因子表达的影响。用亚抑菌浓度的硝唑尼特处理细菌后,检测铜绿假单胞菌毒力因子(如绿脓菌素、吡咯烷酮、弹性蛋白酶、鼠李糖脂、蛋白酶和溶血素)的产生。有趣的是,硝唑尼特对铜绿假单胞菌毒力因子有很强的抑制作用。我们的结果进一步通过 qRT-PCR 得到证实,结果显示与铜绿假单胞菌毒力因子表达相关的群体感应基因 lasI、lasR、rhlI、rhlR、pqsA 和 pqsR 的表达显著下降。此外,我们还利用小鼠感染模型进行了体内实验,结果显示与未经处理的细菌相比,硝唑尼特处理的细菌杀死小鼠的能力较弱。重要的是,与未用硝唑尼特处理的细菌相比,用硝唑尼特处理的细菌感染的小鼠死亡率显著降低。综上所述,我们的数据表明,硝唑尼特可以通过降低毒力因子的产生来发挥减弱铜绿假单胞菌的作用。此外,我们的数据清楚地表明,硝唑尼特可以参与铜绿假单胞菌感染的治疗,以控制感染并降低细菌对抗生素耐药性的发展。

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