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取代吲哚衍生物与临床使用抗生素对耐药菌的协同作用。

Synergistic action of substituted indole derivatives and clinically used antibiotics against drug-resistant bacteria.

机构信息

Departments of Chemistry and Biology, New Mexico Tech, 801 Leroy Place, Socorro, NM 87801, USA.

Department of Chemistry and Biochemistry, Texas State University, San Marcos, TX 78666, USA.

出版信息

Future Microbiol. 2020 May;15(8):579-590. doi: 10.2217/fmb-2019-0094. Epub 2020 Jun 2.

Abstract

The current report describes the discovery of indole derivatives that synergize with standard antibiotics. The antibacterial activities were determined using an optimized time-kill method, while viability of mammalian cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The synergy is observed with methicillin- and vancomycin-resistant bacterial strains, against which the standard antibiotics show no activities of their own. Our indole derivatives in combination with antibiotics lack toxicity toward mammalian cells, do not promote the evolution of resistance of in comparison to clinically established antibiotics, and likely work by permeabilizing bacterial cell membranes. The above-mentioned findings demonstrate the potential clinical applications of our indole derivatives.

摘要

本报告描述了吲哚衍生物与标准抗生素协同作用的发现。采用优化的时间杀伤法测定抗菌活性,同时采用(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐测定法评估哺乳动物细胞的活力。协同作用观察到对耐甲氧西林和万古霉素的细菌菌株,标准抗生素对这些菌株本身没有活性。我们的吲哚衍生物与抗生素联合使用对哺乳动物细胞没有毒性,与临床已建立的抗生素相比,不会促进耐药性的进化,并且可能通过破坏细菌细胞膜起作用。上述发现表明我们的吲哚衍生物具有潜在的临床应用。

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Understanding the mechanisms and drivers of antimicrobial resistance.理解抗菌药物耐药性的机制和驱动因素。
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