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多粘菌素与细菌细胞膜:抗菌活性及耐药机制综述

Polymyxins and Bacterial Membranes: A Review of Antibacterial Activity and Mechanisms of Resistance.

作者信息

Ayoub Moubareck Carole

机构信息

College of Natural and Health Sciences, Zayed University, Dubai 19282, UAE.

出版信息

Membranes (Basel). 2020 Aug 8;10(8):181. doi: 10.3390/membranes10080181.

DOI:10.3390/membranes10080181
PMID:32784516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7463838/
Abstract

Following their initial discovery in the 1940s, polymyxin antibiotics fell into disfavor due to their potential clinical toxicity, especially nephrotoxicity. However, the dry antibiotic development pipeline, together with the rising global prevalence of infections caused by multidrug-resistant (MDR) Gram-negative bacteria have both rejuvenated clinical interest in these polypeptide antibiotics. Parallel to the revival of their use, investigations into the mechanisms of action and resistance to polymyxins have intensified. With an initial known effect on biological membranes, research has uncovered the detailed molecular and chemical interactions that polymyxins have with Gram-negative outer membranes and lipopolysaccharide structure. In addition, genetic and epidemiological studies have revealed the basis of resistance to these agents. Nowadays, resistance to polymyxins in MDR Gram-negative pathogens is well elucidated, with chromosomal as well as plasmid-encoded, transferrable pathways. The aims of the current review are to highlight the important chemical, microbiological, and pharmacological properties of polymyxins, to discuss their mechanistic effects on bacterial membranes, and to revise the current knowledge about Gram-negative acquired resistance to these agents. Finally, recent research, directed towards new perspectives for improving these old agents utilized in the 21st century, to combat drug-resistant pathogens, is summarized.

摘要

自20世纪40年代首次发现多粘菌素类抗生素以来,由于其潜在的临床毒性,尤其是肾毒性,这类抗生素逐渐失宠。然而,抗生素研发进展缓慢,加之全球范围内多重耐药革兰氏阴性菌引起的感染日益普遍,这两者都重新唤起了临床对这些多肽类抗生素的兴趣。随着多粘菌素类抗生素重新投入使用,对其作用机制和耐药性的研究也日益深入。最初已知多粘菌素类抗生素对生物膜有作用,如今研究已经揭示了它们与革兰氏阴性菌外膜和脂多糖结构之间详细的分子和化学相互作用。此外,遗传学和流行病学研究也揭示了对这些药物耐药的基础。如今,多重耐药革兰氏阴性病原体对多粘菌素类抗生素的耐药情况已得到充分阐明,包括染色体介导以及质粒编码的可转移耐药途径。本综述的目的是强调多粘菌素类抗生素重要的化学、微生物学和药理学特性,讨论它们对细菌膜的作用机制,并梳理目前关于革兰氏阴性菌对这些药物获得性耐药的认识。最后,总结了近期旨在为改进这些在21世纪用于对抗耐药病原体的老药提供新视角的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f216/7463838/abb82da6f3ea/membranes-10-00181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f216/7463838/2fee8703c27e/membranes-10-00181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f216/7463838/abb82da6f3ea/membranes-10-00181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f216/7463838/2fee8703c27e/membranes-10-00181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f216/7463838/abb82da6f3ea/membranes-10-00181-g002.jpg

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