Kumar Lokender, Chhibber Sanjay, Kumar Rajnish, Kumar Manoj, Harjai Kusum
Department of Microbiology, Panjab University, Chandigarh 160014, India.
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India.
Fitoterapia. 2015 Apr;102:84-95. doi: 10.1016/j.fitote.2015.02.002. Epub 2015 Feb 20.
Quorum sensing in Pseudomonas aeruginosa plays an imperative role in virulence factor, biofilm formation and antimicrobial resistance. Blocking quorum sensing pathways are viewed as viable anti-virulent therapy in association with traditional antimicrobial therapy. Anti-quorum sensing dietary phytochemicals with may prove to be a safe and viable choice as anti-virulent drug candidates. Previously, our lab proved zingerone as potent anti-biofilm agent hence; further its anti-virulent and anti-quorum activities were evaluated. Zingerone, besides decreasing swimming, swarming and twitching phenotypes of P. aeruginosa PAO1, reduced biofilm forming capacity and production of virulence factors including rhamnolipid, elastase, protease, pyocyanin, cell free and cell bound hemolysin (p<0.001) indicating anti-virulent property attributing towards attenuation of virulence of P. aeruginosa. Further zingerone not only had marked effect on the production of quorum sensing signal molecules by clinical isolates of P. aeruginosa but also showed significant interference with the activation of QS reporter strains. To study the mechanism of blocking quorum sensing cascade, in silico analysis was carried out. Anti-QS activity was attributed to interference with the ligand receptor interaction of zingerone with QS receptors (TraR, LasR, RhlR and PqsR). Zingerone showed a good comparative docking score to respective autoinducer molecules which was even higher than that of vanillin, a proven anti-quorum sensing phytochemical. The results of the present study revealed the anti-quorum sensing activity of zingerone targeting ligand-receptor interaction, hence proposing zingerone as a suitable anti-virulent drug candidate against P. aeruginosa infections.
铜绿假单胞菌中的群体感应在毒力因子、生物膜形成和抗菌耐药性方面起着至关重要的作用。与传统抗菌疗法联合使用时,阻断群体感应途径被视为一种可行的抗毒力疗法。具有抗群体感应活性的膳食植物化学物质可能被证明是作为抗毒力药物候选物的安全且可行的选择。此前,我们实验室证明姜辣素是一种有效的抗生物膜剂,因此,进一步评估了其抗毒力和抗群体感应活性。姜辣素除了降低铜绿假单胞菌PAO1的游动、群集和颤动表型外,还降低了生物膜形成能力以及包括鼠李糖脂、弹性蛋白酶、蛋白酶、绿脓菌素、游离细胞和细胞结合溶血素在内的毒力因子的产生(p<0.001),表明其具有抗毒力特性,可归因于铜绿假单胞菌毒力的减弱。此外,姜辣素不仅对铜绿假单胞菌临床分离株产生群体感应信号分子有显著影响,而且对群体感应报告菌株的激活也表现出明显干扰。为了研究阻断群体感应级联反应的机制,进行了计算机模拟分析。抗群体感应活性归因于姜辣素与群体感应受体(TraR、LasR、RhlR和PqsR)的配体 - 受体相互作用受到干扰。姜辣素与各自的自诱导分子相比显示出良好的对接分数,甚至高于香草醛(一种已证实的抗群体感应植物化学物质)。本研究结果揭示了姜辣素靶向配体 - 受体相互作用的抗群体感应活性,并因此提出姜辣素是一种针对铜绿假单胞菌感染的合适抗毒力药物候选物。