Shah Mayank D, Kharkar Prashant S, Sahu Niteshkumar U, Peerzada Zoya, Desai Krutika B
Sunandan Divatia School of Science, SVKM's NMIMS (Deemed to be University) Mumbai 400056 India.
Institute of Chemical Technology, Category I Deemed to be University (MHRD/UGC) Mumbai-400019 India.
RSC Adv. 2019 Dec 4;9(69):40228-40239. doi: 10.1039/c9ra06612h. eCollection 2019 Dec 3.
The emergence of multidrug-resistant (MDR) bacterial strains in the last decade is astonishingly alarming. Many of the widely used antibiotics have failed to exhibit clinical efficacy against such strains. Eventually we will exhaust all the resources in our antibiotic armamentarium. As a need of the hour, novel strategies are desperately required not only to curb, but also to reverse, the development of resistance in these pathogens, thereby maintaining their sensitivity towards current antibiotics. Intervention of bacterial virulence, rather than killing them, by inhibiting specific pathways/targets has emerged as a novel approach to tackle the drug resistance problem. The bacterial virulence is regulated quorum-sensing, a cell-cell communication process precisely controlled by autoinducer molecules such as acyl homoserine lactone (AHL). The present study aimed at identifying promising quorum-sensing inhibitors in , an opportunistic human pathogen especially associated with nosocomial infections, yielding four potential hits. Out of these, potassium 2-methoxy-4-vinylphenolate was the most potent quorum-sensing inhibitor targeting LasIR/RhlIR circuitry. It also inhibited biofilm formation, various virulence factors like LasA protease, LasB elastase and pyocyanin, and motility of bacteria like swarming and twitching.
在过去十年中,多重耐药(MDR)细菌菌株的出现令人震惊地敲响了警钟。许多广泛使用的抗生素已无法对这类菌株展现出临床疗效。最终,我们将耗尽抗生素库中的所有资源。作为当务之急,迫切需要新的策略,不仅要遏制,而且要扭转这些病原体耐药性的发展,从而维持它们对现有抗生素的敏感性。通过抑制特定途径/靶点来干预细菌毒力而非杀死它们,已成为解决耐药性问题的一种新方法。细菌毒力受群体感应调节,群体感应是一种由酰基高丝氨酸内酯(AHL)等自诱导分子精确控制的细胞间通讯过程。本研究旨在鉴定在一种尤其与医院感染相关的机会性人类病原体中具有前景的群体感应抑制剂,得到了四个潜在的有效化合物。其中,2-甲氧基-4-乙烯基苯酚钾是针对LasIR/RhlIR信号传导通路最有效的群体感应抑制剂。它还抑制生物膜形成、多种毒力因子如LasA蛋白酶、LasB弹性蛋白酶和绿脓菌素,以及细菌的运动性如群集运动和震颤运动。