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亚致死抗生素处理通过自由基诱导的突变导致多药耐药性。

Sublethal antibiotic treatment leads to multidrug resistance via radical-induced mutagenesis.

机构信息

Howard Hughes Medical Institute, Boston University, Boston, MA 02215, USA.

出版信息

Mol Cell. 2010 Feb 12;37(3):311-20. doi: 10.1016/j.molcel.2010.01.003.

Abstract

Antibiotic resistance arises through mechanisms such as selection of naturally occurring resistant mutants and horizontal gene transfer. Recently, oxidative stress has been implicated as one of the mechanisms whereby bactericidal antibiotics kill bacteria. Here, we show that sublethal levels of bactericidal antibiotics induce mutagenesis, resulting in heterogeneous increases in the minimum inhibitory concentration for a range of antibiotics, irrespective of the drug target. This increase in mutagenesis correlates with an increase in ROS and is prevented by the ROS scavenger thiourea and by anaerobic conditions, indicating that sublethal concentrations of antibiotics induce mutagenesis by stimulating the production of ROS. We demonstrate that these effects can lead to mutant strains that are sensitive to the applied antibiotic but resistant to other antibiotics. This work establishes a radical-based molecular mechanism whereby sublethal levels of antibiotics can lead to multidrug resistance, which has important implications for the widespread use and misuse of antibiotics.

摘要

抗生素耐药性的产生机制包括自然存在的耐药突变体的选择和水平基因转移。最近,氧化应激被认为是杀菌抗生素杀死细菌的机制之一。在这里,我们表明,亚致死水平的杀菌抗生素会诱导突变,导致一系列抗生素的最低抑菌浓度发生不均匀的增加,而与药物靶标无关。这种突变的增加与 ROS 的增加相关,并且可以通过 ROS 清除剂硫脲和厌氧条件来预防,表明亚致死浓度的抗生素通过刺激 ROS 的产生来诱导突变。我们证明,这些效应可能导致对应用抗生素敏感但对其他抗生素耐药的突变株。这项工作建立了一个基于自由基的分子机制,通过该机制,亚致死水平的抗生素可以导致多药耐药性,这对广泛使用和滥用抗生素具有重要意义。

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