Surti Malvi, Patel Mitesh, Binsuwaidan Reem, Adnan Mohd, Alshammari Nawaf, Fatima Syeda Bushra, Reddy Mandadi Narsimha
Research and Development Cell (RDC), Parul University, Waghodia, Vadodara, Gujarat, 391760, India.
Department of Biotechnology, Parul Institute of Applied Sciences, Parul University, Waghodia, Vadodara, Gujarat, 391760, India.
Int Microbiol. 2025 Jul 2. doi: 10.1007/s10123-025-00689-w.
This study evaluates the antibacterial, antibiofilm, and anti-quorum-sensing (QS) properties of ilimaquinone (IQ) against Gram-positive and Gram-negative pathogens. The agar cup diffusion method revealed significant bacterial inhibition, with minimum inhibitory (MIC) and bactericidal (MBC) concentrations ranging from 6.25 to 25 μM and 12.5 to 50 μM, respectively. IQ exhibited dose-dependent biofilm inhibition, demonstrating its potential as an anti-biofilm agent. QS inhibition was assessed by pigment suppression in Chromobacterium violaceum (violacein), Serratia marcescens (prodigiosin), and Pseudomonas aeruginosa (pyocyanin, pyoverdine), reducing their production by 73.33%, 53.68%, 57.13%, and 62.42%, respectively, at sub-MIC concentrations. IQ also inhibited QS-regulated virulence factors in P. aeruginosa, including LasA protease, elastase, rhamnolipid, and extracellular polymeric substance (EPS) production, disrupting biofilm formation. Molecular docking and dynamics analysis confirmed strong binding affinities of IQ to key QS and biofilm-associated proteins (EsaI, PilY1, LasA, PilT, LasR, RhlR, LasI, PqsR, CviR, and CviR'), highlighting its mechanistic role in QS inhibition. These findings suggest that IQ is a promising antibacterial and anti-QS compound with potential therapeutic applications for managing bacterial infections and biofilm-related complications.
本研究评估了异香豆素(IQ)对革兰氏阳性和革兰氏阴性病原体的抗菌、抗生物膜和抗群体感应(QS)特性。琼脂杯扩散法显示出显著的细菌抑制作用,最低抑菌浓度(MIC)和杀菌浓度(MBC)分别为6.25至25μM和12.5至50μM。IQ表现出剂量依赖性的生物膜抑制作用,证明了其作为抗生物膜剂的潜力。通过抑制紫色杆菌(紫菌素)、粘质沙雷氏菌(灵菌红素)和铜绿假单胞菌(绿脓菌素、绿脓杆菌素)中的色素来评估QS抑制作用,在亚MIC浓度下,它们的产量分别降低了73.33%、53.68%、57.13%和62.42%。IQ还抑制了铜绿假单胞菌中QS调节的毒力因子,包括LasA蛋白酶、弹性蛋白酶、鼠李糖脂和细胞外聚合物(EPS)的产生,破坏了生物膜的形成。分子对接和动力学分析证实了IQ与关键的QS和生物膜相关蛋白(EsaI、PilY1、LasA、PilT、LasR、RhlR、LasI、PqsR、CviR和CviR')具有很强的结合亲和力,突出了其在QS抑制中的作用机制。这些发现表明,IQ是一种有前景的抗菌和抗QS化合物,在治疗细菌感染和生物膜相关并发症方面具有潜在的治疗应用价值。