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使用多酚表没食子儿茶素没食子酸酯(EGCG)恢复抗生素氨曲南对多药耐药临床分离株的活性。

Restoring the activity of the antibiotic aztreonam using the polyphenol epigallocatechin gallate (EGCG) against multidrug-resistant clinical isolates of .

机构信息

Department of Pathology and Infectious Diseases, School of Veterinary Medicine, University of Surrey, Guildford, UK.

German Centre for Infection Research (DZIF), partner site Bonn-Cologne, 38124 Braunschweig, Germany.

出版信息

J Med Microbiol. 2019 Oct;68(10):1552-1559. doi: 10.1099/jmm.0.001060.

Abstract

. is an important Gram-negative pathogen that is intrinsically multidrug-resistant (MDR) and frequently associated with healthcare-associated outbreaks. With increasing resistance to antibiotics and with very few novel drugs under development, clinicians often use combinations to treat critically ill patients.. The aim of this study was to evaluate the ability of epigallocatechin (EGCG) to restore the activity of aztreonam against clinical MDR strains of .. Checkerboard and time-kill kinetic assays were performed to assess synergy and the model of infection was used to test the efficacy of the combination . Accumulation assays were performed to gain insight into the mechanism of action.. The results demonstrate that synergy between aztreonam and EGCG exists [fractional inhibitory concentration indices (FICIs) 0.02-0.5], with the combination affording significantly (=<0.05) enhanced bacterial killing, with a >3 log reduction in colony-forming units ml at 24 h. EGCG was able to restore susceptibility to aztreonam to a level equal to or below the breakpoint set by the European Committee for Antimicrobial Susceptibility Testing. In , the combination was superior to monotherapy, with increased larval survival observed (94 % vs ≤63 %). We also demonstrated the relatively low toxicity of EGCG to human keratinocytes and larvae. Accumulation assay data suggest that the mechanism of synergy may be due to EGCG increasing the uptake of aztreonam.. EGCG was able to restore the activity of aztreonam against MDR . The data presented support further evaluation of the aztreonam-EGCG combination and highlight its potential for use in clinical medicine.

摘要

. 是一种重要的革兰氏阴性病原体,具有固有耐多药(MDR)特性,并且经常与医疗机构相关的暴发有关。随着抗生素耐药性的增加,并且几乎没有新的药物在开发中,临床医生经常使用组合来治疗重症患者。. 本研究旨在评估表没食子儿茶素没食子酸酯(EGCG)恢复氨曲南对临床 MDR 株的活性的能力。 采用棋盘和时间杀伤动力学测定评估协同作用,并采用感染模型测试联合用药的疗效。 进行累积测定以深入了解作用机制。. 结果表明,氨曲南和 EGCG 之间存在协同作用 [分数抑菌浓度指数(FICI)0.02-0.5],联合用药可显著(=<0.05)增强细菌杀伤作用,在 24 小时内使菌落形成单位 ml 的减少> 3 对数。 EGCG 能够将对氨曲南的敏感性恢复到等于或低于欧洲抗菌药物敏感性测试委员会设定的折点。 在 中,联合用药优于单药治疗,观察到幼虫存活率增加(94%对≤63%)。 我们还证明了 EGCG 对人角质形成细胞和幼虫的相对低毒性。 累积测定数据表明协同作用的机制可能是由于 EGCG 增加了氨曲南的摄取。. EGCG 能够恢复氨曲南对 MDR 的活性。 所提供的数据支持进一步评估氨曲南-EGCG 联合用药,并强调其在临床医学中的应用潜力。

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