应对 mcr 介导的多粘菌素抗药性的辅助策略。

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RSC medicinal chemistry Pub Date : 2024-11-01 DOI:10.1039/d4md00654b
Madison R Nuske, Junlang Zhong, Renjie Huang, Vijayalekshmi Sarojini, Jack L Y Chen, Christopher J Squire, Mark A T Blaskovich, Ivanhoe K H Leung
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引用次数: 0

摘要

移动性可乐定耐药性(mcr)基因的出现是造成全球抗生素耐药性危机的一个明显威胁。mcr 编码一种磷脂酰乙醇胺(pEtN)转移酶,可催化 pEtN 分子从磷脂酰乙醇胺转移到脂质 A(脂多糖(LPS)的头部基团)。这将中和 LPS 的整体负电荷,防止多粘菌素与细菌膜结合。我们相信,多粘菌素佐剂的开发可能是延长这类重要的最后抗生素使用时间的一种有前途的方法。本综述讨论了在确定、设计和开发佐剂以恢复这些耐药细菌对多粘菌素的敏感性方面的最新进展,重点关注 MCR 抑制剂以及调节多粘菌素耐药性的替代方法。
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Adjuvant strategies to tackle mcr-mediated polymyxin resistance.

The emergence of the mobile colistin resistance (mcr) gene is a demonstrable threat contributing to the worldwide antibiotic resistance crisis. The gene is encoded on plasmids and can easily spread between different bacterial strains. mcr encodes a phosphoethanolamine (pEtN) transferase, which catalyses the transfer of the pEtN moiety from phosphatidylethanolamine to lipid A, the head group of lipopolysaccharides (LPS). This neutralises the overall negative charge of the LPS and prevents the binding of polymyxins to bacterial membranes. We believe that the development of polymyxin adjuvants could be a promising approach to prolong the use of this important class of last-resort antibiotics. This review discusses recent progress in the identification, design and development of adjuvants to restore polymyxin sensitivity in these resistant bacteria, and focuses on both MCR inhibitors as well as alternative approaches that modulate polymyxin resistance.

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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
期刊最新文献
Back cover Property-based optimisation of PROTACs. A practical guide for the assay-dependent characterisation of irreversible inhibitors. Adjuvant strategies to tackle mcr-mediated polymyxin resistance. Synthesis and antifungal evaluation of new azole derivatives containing 1,2,3-triazole.
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