Restoring Multidrug-Resistant Escherichia coli Sensitivity to Ampicillin in Combination with (-)-Epigallocatechin Gallate.

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES
Anong Kiddee, Atchariya Yosboonruang, Achiraya Siriphap, Grissana Pook-In, Chittakun Suwancharoen, Acharaporn Duangjai, Ratsada Praphasawat, Masami Suganuma, Anchalee Rawangkan
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Abstract

Multidrug-resistant (MDR) bacteria, especially Escherichia coli, are a major contributor to healthcare-associated infections globally, posing significant treatment challenges. This study explores the efficacy of (-)-epigallocatechin gallate (EGCG), a natural constituent of green tea, in combination with ampicillin (AMP) to restore the effectiveness of AMP against 40 isolated MDR E. coli strains. Antimicrobial activity assays were conducted to determine the minimum inhibitory concentrations (MIC) of EGCG using the standard microdilution technique. Checkerboard assays were employed to assess the potential synergistic effects of EGCG combined with AMP. The pharmacodynamic effects of the combination were evaluated through time-kill assays. Outer membrane disruption was analyzed by measuring DNA and protein leakage and with assessments using N-phenyl-1-naphthylamine (NPN) and rhodamine 123 (Rh123) fluorescence dyes. Biofilm eradication studies involved biofilm formation assays and preformed biofilm biomass and viability assays. Scanning electron microscopy (SEM) was used to examine changes in cellular morphology. The results indicated that EGCG demonstrated activity against all isolates, with MICs ranging from 0.5 to 2 mg/mL, while AMP exhibited MIC values between 1.25 and 50 mg/mL. Importantly, the EGCG-AMP combination showed enhanced efficacy compared to either treatment alone, as indicated by a fractional inhibitory concentration index between 0.009 and 0.018. The most pronounced synergy was observed in 13 drug-resistant strains, where the MIC for EGCG dropped to 8 µg/mL (from 1 mg/mL alone) and that for AMP to 50 µg/mL (from 50 mg/mL alone), achieving a 125-fold and 1000-fold reduction, respectively. Time-kill assays revealed that the bactericidal effect of the EGCG-AMP combination occurred within 2 h. The mechanism of EGCG action includes the disruption of membrane permeability and biofilm eradication in a dose-dependent manner. SEM confirmed that the combination treatment consistently outperformed the individual treatments. This study underscores the potential of restoring AMP efficacy in combination with EGCG as a promising strategy for treating MDR E. coli infections.

恢复多重耐药大肠杆菌对氨苄西林联合(-)-表没食子儿茶素没食子酸酯的敏感性。
耐多药(MDR)细菌,特别是大肠杆菌,是全球卫生保健相关感染的主要因素,对治疗构成重大挑战。本研究探讨了(-)-表没食子儿茶素没食子酸酯(EGCG),绿茶的一种天然成分,与氨苄西林(AMP)联合使用,恢复AMP对40株分离的耐多药大肠杆菌菌株的有效性。采用标准微量稀释法测定EGCG的最低抑菌浓度(MIC)。采用棋盘法评估EGCG与AMP联合的潜在协同效应,并通过时间杀伤法评估联合的药效学效应。采用n -苯基-1-萘胺(NPN)和罗丹明123 (Rh123)荧光染料测定DNA和蛋白质渗漏量,分析外膜破坏情况。生物膜根除研究包括生物膜形成分析和预成型生物膜生物量和活力分析。用扫描电镜(SEM)观察细胞形态的变化。结果表明,EGCG对所有菌株都有活性,MIC值在0.5 ~ 2mg /mL之间,AMP的MIC值在1.25 ~ 50mg /mL之间。重要的是,EGCG-AMP联合治疗比单独治疗更有效,分数抑制浓度指数在0.009和0.018之间。在13株耐药菌株中观察到最明显的协同作用,其中EGCG的MIC降至8µg/mL(从单独的1 mg/mL), AMP降至50µg/mL(从单独的50 mg/mL),分别实现125倍和1000倍的降低。时间杀伤实验表明,EGCG- amp联合作用在2 h内发生杀菌作用。EGCG的作用机制包括破坏膜通透性和消灭生物膜,并呈剂量依赖性。扫描电镜证实,联合治疗始终优于单独治疗。这项研究强调了恢复AMP与EGCG联合治疗耐多药大肠杆菌感染的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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