Sublethal Antibiotic Treatment Leads to Multidrug Resistance via Radical-Induced Mutagenesis

被引:746
作者
Kohanski, Michael A. [1 ,2 ,3 ,4 ,5 ]
DePristo, Mark A. [2 ,3 ,4 ,6 ]
Collins, James J. [1 ,2 ,3 ,4 ,5 ,7 ]
机构
[1] Boston Univ, Howard Hughes Med Inst, Boston, MA 02215 USA
[2] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[3] Boston Univ, Ctr BioDynam, Boston, MA 02215 USA
[4] Boston Univ, Ctr Adv Biotechnol, Boston, MA 02215 USA
[5] Boston Univ, Sch Med, Boston, MA 02118 USA
[6] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
[7] Harvard Univ, Wyss Inst Biologically Inspired Engn, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI; HYDROGEN-PEROXIDE; OXIDATIVE DAMAGE; STAPHYLOCOCCUS-AUREUS; SUPEROXIDE-DISMUTASE; MUTATION-RATES; DNA; BACTERIA; CIPROFLOXACIN; EVOLUTION;
D O I
10.1016/j.molcel.2010.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:311 / 320
页数:10
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