The Evolution of Heteroresistance via Small Colony Variants in Escherichia coli Following Long Term Exposure to Bacteriostatic Antibiotics.

Teresa Gil-Gil, Brandon A Berryhill, Joshua A Manuel, Andrew P Smith, Ingrid C McCall, Fernando Baquero, Bruce R Levin
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Abstract

Traditionally, bacteriostatic antibiotics are agents able to arrest bacterial growth. Despite being traditionally viewed as unable to kill bacterial cells, when they are used clinically the outcome of these drugs is frequently as effective as when a bactericidal drug is used. We explore the dynamics of Escherichia coli after exposure to two ribosome-targeting bacteriostatic antibiotics, chloramphenicol and azithromycin, for thirty days. The results of our experiments provide evidence that bacteria exposed to these drugs replicate, evolve, and generate a sub-population of small colony variants (SCVs) which are resistant to multiple drugs. These SCVs contribute to the evolution of heteroresistance and rapidly revert to a susceptible state once the antibiotic is removed. Stated another way, exposure to bacteriostatic drugs selects for the evolution of heteroresistance in populations previously lacking this trait. More generally, our results question the definition of bacteriostasis as populations exposed to bacteriostatic drugs are replicating despite the lack of net growth.

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长期暴露于抑菌抗生素后大肠杆菌小菌落变异的异源抗性进化。
传统上,抑菌抗生素是能够阻止细菌生长的药物。尽管这些药物不能杀死细菌细胞,但在临床上使用时,其效果往往与使用杀菌药物一样有效。我们研究了暴露于两种核糖体靶向抑菌抗生素(氯霉素和阿奇霉素)30天后大肠杆菌的动态。我们的实验结果提供了证据,表明暴露于这些药物的细菌复制、进化并产生对多种药物耐药的小菌落变异(scv)亚群。这些scv促进了异源耐药的进化,一旦抗生素被移除,它们就会迅速恢复到易感状态。换句话说,暴露于抑菌药物选择了在以前缺乏这种特性的人群中进化出异源耐药性。更一般地说,我们的结果质疑抑菌作用的定义,因为尽管缺乏净增长,但暴露于抑菌药物的种群正在复制。
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