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抗生素杂合体:下一代针对革兰氏阴性病原体的药物和佐剂?

Antibiotic Hybrids: the Next Generation of Agents and Adjuvants against Gram-Negative Pathogens?

机构信息

Department of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada.

Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada

出版信息

Clin Microbiol Rev. 2018 Mar 14;31(2). doi: 10.1128/CMR.00077-17. Print 2018 Apr.

Abstract

The global incidence of drug-resistant Gram-negative bacillary infections has been increasing, and there is a dire need to develop novel strategies to overcome this problem. Intrinsic resistance in Gram-negative bacteria, such as their protective outer membrane and constitutively overexpressed efflux pumps, is a major survival weapon that renders them refractory to current antibiotics. Several potential avenues to overcome this problem have been at the heart of antibiotic drug discovery in the past few decades. We review some of these strategies, with emphasis on antibiotic hybrids either as stand-alone antibacterial agents or as adjuvants that potentiate a primary antibiotic in Gram-negative bacteria. Antibiotic hybrid is defined in this review as a synthetic construct of two or more pharmacophores belonging to an established agent known to elicit a desired antimicrobial effect. The concepts, advances, and challenges of antibiotic hybrids are elaborated in this article. Moreover, we discuss several antibiotic hybrids that were or are in clinical evaluation. Mechanistic insights into how tobramycin-based antibiotic hybrids are able to potentiate legacy antibiotics in multidrug-resistant Gram-negative bacilli are also highlighted. Antibiotic hybrids indeed have a promising future as a therapeutic strategy to overcome drug resistance in Gram-negative pathogens and/or expand the usefulness of our current antibiotic arsenal.

摘要

全球范围内耐药革兰氏阴性杆菌感染的发病率一直在上升,因此迫切需要开发新的策略来解决这一问题。革兰氏阴性菌固有的耐药性,如它们保护性的外膜和组成型过表达的外排泵,是一种主要的生存武器,使它们对目前的抗生素产生耐药性。在过去几十年的抗生素药物发现中,有几个潜在的途径被认为可以克服这一问题。我们回顾了其中的一些策略,重点介绍了抗生素杂合体,无论是作为独立的抗菌剂还是作为佐剂,都可以增强革兰氏阴性菌中主要抗生素的作用。在本综述中,抗生素杂合体被定义为两个或多个药效团的合成构建体,这些药效团属于已知具有所需抗菌作用的已建立药物。本文详细阐述了抗生素杂合体的概念、进展和挑战。此外,我们还讨论了几种正在或已经进行临床评估的抗生素杂合体。本文还强调了妥布霉素类抗生素杂合体如何能够增强多药耐药革兰氏阴性杆菌中传统抗生素的作用的机制见解。抗生素杂合体确实有一个光明的未来,作为一种治疗策略,可以克服革兰氏阴性病原体的耐药性,和/或扩大我们目前抗生素库的用途。

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