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治疗耐药菌的下一代策略:抗生素杂合体。

Next-generation strategy for treating drug resistant bacteria: Antibiotic hybrids.

机构信息

Department of Microbiology, Government Medical College Hospital, Chandigarh, India.

出版信息

Indian J Med Res. 2019 Feb;149(2):97-106. doi: 10.4103/ijmr.IJMR_755_18.

Abstract

Resistance against nearly all antibiotics used clinically have been documented in bacteria. There is an ever-increasing danger caused by multidrug-resistant Gram-negative bacteria in both hospital and community settings. In Gram-negative bacteria, intrinsic resistance to currently available antibiotics is mainly due to overexpressed efflux pumps which are constitutively present and also presence of protective outer membrane. Combination therapy, i.e., use of two or more antibiotics, was thought to be an effective strategy because it took advantage of the additive effects of multiple antimicrobial mechanisms, lower risk of resistance development and lower mortality and improved clinical outcome. However, none of the benefits were seen in in vivo studies. Antibiotic hybrids are being used to challenge the growing drug resistance threat and increase the usefulness of current antibiotic arsenal. Antibiotic hybrids are synthetic constructs of two molecules which are covalently linked. These could be two antibiotics or antibiotic with an adjuvant (efflux pump inhibitor, siderophore, etc.) which increases the access of the antibiotics to the target. The concepts, developments and challenges in the future use of antibiotic hybrids are discussed here. Majority of the studies have been conducted on fluoroquinolones and aminoglycosides molecules. The antibiotic tobramycin has the property to enhance the action of antimicrobial agents against which the multidrug-resistant Gram-negative bacteria were earlier resistant, and thus potentiating the action of legacy antibiotics. Antibiotic hybrids may have a role as the silver bullet in Gram-negative bacteria to overcome drug resistance as well as extend the spectrum of existing antibiotics.

摘要

临床上几乎所有抗生素的耐药性都已在细菌中得到证实。在医院和社区环境中,多药耐药革兰氏阴性菌引起的危险日益增加。在革兰氏阴性菌中,对现有抗生素的固有耐药性主要是由于过度表达的外排泵,这些外排泵持续存在,并且存在保护性外膜。联合治疗,即使用两种或更多种抗生素,被认为是一种有效的策略,因为它利用了多种抗菌机制的相加作用,降低了耐药性发展的风险,降低了死亡率,并改善了临床结果。然而,在体内研究中并没有看到这些益处。抗生素杂合体被用来应对日益严重的药物耐药威胁,并提高现有抗生素武器库的实用性。抗生素杂合体是两种分子的共价连接的合成构建体。这些可以是两种抗生素,也可以是抗生素与佐剂(外排泵抑制剂、铁载体等)的组合,这可以增加抗生素到达靶标的机会。本文讨论了抗生素杂合体在未来使用中的概念、发展和挑战。大多数研究都集中在氟喹诺酮类和氨基糖苷类分子上。抗生素妥布霉素具有增强抗菌剂对先前耐药的多药耐药革兰氏阴性菌的作用的特性,从而增强了传统抗生素的作用。抗生素杂合体可能在革兰氏阴性菌中作为银弹,克服耐药性,并扩大现有抗生素的光谱。

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