Reactive oxygen species accelerate de novo acquisition of antibiotic resistance in E. coli

Summary

Reactive oxygen species (ROS) produced as a secondary effect of bactericidal antibiotics are hypothesized to play a role in killing bacteria. If correct, ROS may play a role in development of de novo resistance. Here we report that single-gene knockout strains with reduced ROS scavenging exhibited enhanced ROS accumulation and more rapid acquisition of resistance when exposed to sublethal levels of bactericidal antibiotics. Consistent with this observation, the ROS scavenger thiourea in the medium decelerated resistance development. Thiourea downregulated the transcriptional level of error-prone DNA polymerase and DNA glycosylase MutM, which counters the incorporation and accumulation of 8-hydroxy-2′-deoxyguanosine (8-HOdG) in the genome. The level of 8-HOdG significantly increased following incubation with bactericidal antibiotics but decreased after treatment with the ROS scavenger thiourea. These observations suggest that in E. coli sublethal levels of ROS stimulate de novo development of resistance, providing a mechanistic basis for hormetic responses induced by antibiotics.

Graphical abstract

Highlights

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  The ROS scavenger thiourea decelerates the development of antimicrobial resistance

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  E. coli mutants with reduced ROS elimination acquire resistance faster

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  Thiourea downregulates transcription of DNA repair genes and lowers the mutation rate

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  Bactericidal antibiotics increase level of 8-hydroxy-2′-deoxyguanosine; thiourea reduces it

Abstract

Biochemistry; Microbiology; Molecular microbiology