Targeting virulence: can we make evolution-proof drugs?

被引:422
作者
Allen, Richard C. [1 ]
Popat, Roman [1 ]
Diggle, Stephen P. [2 ]
Brown, Sam P. [1 ]
机构
[1] Univ Edinburgh, Ctr Immun Infect & Evolut, Sch Biol Sci, Edinburgh EH9 3JY, Midlothian, Scotland
[2] Univ Nottingham, Ctr Biomol Sci, Sch Life Sci, Nottingham NG7 2RD, England
基金
英国自然环境研究理事会; 英国工程与自然科学研究理事会; 英国惠康基金;
关键词
QUORUM-SENSING INHIBITORS; PSEUDOMONAS-AERUGINOSA; ESCHERICHIA-COLI; ANTIBIOTIC-RESISTANCE; SOCIAL EVOLUTION; INFECTION; COOPERATION; BACTERIA; IDENTIFICATION; PROTEIN;
D O I
10.1038/nrmicro3232
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Antivirulence drugs are a new type of therapeutic drug that target virulence factors, potentially revitalising the drug-development pipeline with new targets. As antivirulence drugs disarm the pathogen, rather than kill or halt pathogen growth, it has been hypothesized that they will generate much weaker selection for resistance than traditional antibiotics. However, recent studies have shown that mechanisms of resistance to antivirulence drugs exist, seemingly damaging the 'evolution-proof' claim. In this Opinion article, we highlight a crucial distinction between whether resistance can emerge and whether it will spread to a high frequency under drug selection. We argue that selection for resistance can be reduced, or even reversed, using appropriate combinations of target and treatment environment, opening a path towards the development of evolutionarily robust novel therapeutics.
引用
收藏
页码:300 / 308
页数:9
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