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多黏菌素与依康唑联合应用对多重耐药鲍曼不动杆菌及其持续生存菌的协同抗菌作用。

Synergistic Antimicrobial Effect of Colistin in Combination with Econazole against Multidrug-Resistant Acinetobacter baumannii and Its Persisters.

机构信息

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Konggrid.35030.35, Kowloon, Hong Kong.

State Key Lab of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

出版信息

Microbiol Spectr. 2022 Jun 29;10(3):e0093722. doi: 10.1128/spectrum.00937-22. Epub 2022 Apr 25.

Abstract

Colistin is a last-line antibiotic which acts by causing membrane permeabilization in Gram-negative bacteria. However, its clinical value has been limited by its toxicity and the emergence of resistant organisms. In this study, we showed that econazole and colistin can act synergistically to produce a strong antimicrobial effect sufficient for eradication of starvation-induced tolerant and multidrug-resistant populations of Acinetobacter baumannii, a notorious pathogen causing recalcitrant infections, both and in mouse infection models. Investigation of the underlying mechanism showed that, while colistin disrupts the membrane structure, econazole causes the dissipation of proton motive force, eliciting a vicious cycle of membrane structural damages and disruption of membrane protein functions, and eventually cell death. This drug combination therefore achieves our goal of using a much smaller dosage of colistin to produce a much stronger antimicrobial effect to tackle the problems of toxicity and resistance associated with colistin usage. Findings described in this study constitute concrete evidence that it is possible to significantly enhance the antimicrobial activity of colistin by using an antifungal drug, econazole, as a colistin adjuvant. We showed that this drug combination can kill not only multidrug-resistant A. baumannii but also the tolerant subpopulation of such strains known as persisters, which may cause chronic and recurrent infections in clinical settings. The synergistic killing effect of the econazole and colistin combination was also observable in mouse infection models at a very low concentration, suggesting that such a drug combination has high potential to be used clinically. Findings in this study therefore have important implications for enhancing its clinical application potential as well as developing new approaches to enhance treatment effectiveness and reduce suffering in patients.

摘要

黏菌素是一种最后一线抗生素,通过在革兰氏阴性菌中引起膜通透性来发挥作用。然而,其临床价值受到毒性和耐药生物体出现的限制。在这项研究中,我们表明,酮康唑和黏菌素可以协同作用,产生强大的抗菌作用,足以消除饥饿诱导的耐多药鲍曼不动杆菌的耐受和多药耐药群体,这是一种引起顽固感染的臭名昭著的病原体,无论是在 和小鼠感染模型中。对潜在机制的研究表明,虽然黏菌素破坏膜结构,但酮康唑会导致质子动力势耗散,引发膜结构损伤和膜蛋白功能破坏的恶性循环,最终导致细胞死亡。因此,这种药物组合实现了我们的目标,即用更小剂量的黏菌素产生更强的抗菌效果,以解决与黏菌素使用相关的毒性和耐药性问题。本研究中的发现提供了具体证据,表明通过使用抗真菌药物酮康唑作为黏菌素佐剂,可以显著增强黏菌素的抗菌活性。我们表明,这种药物组合不仅可以杀死多药耐药的鲍曼不动杆菌,还可以杀死这种菌株的耐受亚群,即所谓的持久性细菌,这些细菌可能在临床环境中引起慢性和复发性感染。酮康唑和黏菌素组合的协同杀菌作用在小鼠感染模型中也可以在非常低的浓度下观察到,这表明这种药物组合具有很高的临床应用潜力。因此,本研究的结果对提高其临床应用潜力以及开发新方法以提高治疗效果和减轻患者痛苦具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4348/9241926/b2bd6c93953a/spectrum.00937-22-f001.jpg

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