Abstract

Fluoroquinolones (FQ) are the recommended antimicrobial treatment for typhoid, a severe systemic infection caused by the bacterium Salmonella enterica serovar Typhi. FQ-resistance mutations in S. Typhi have become common, hindering treatment and control efforts. Using in vitro competition experiments, we assayed the fitness of eleven isogenic S. Typhi strains with resistance mutations in the FQ target genes, gyrA and parC. In the absence of antimicrobial pressure, 6 out of 11 mutants carried a selective advantage over the antimicrobial-sensitive parent strain, indicating that FQ resistance in S. Typhi is not typically associated with fitness costs. Double-mutants exhibited higher than expected fitness as a result of synergistic epistasis, signifying that epistasis may be a critical factor in the evolution and molecular epidemiology of S. Typhi. Our findings have important implications for the management of drug-resistant S. Typhi, suggesting that FQ-resistant strains would be naturally maintained even if fluoroquinolone use were reduced. DOI: http://dx.doi.org/10.7554/eLife.01229.001.

Highlights

  • The evolution of antimicrobial resistance in bacteria is driven by the pressure of sustained exposure to antimicrobials

  • The development of specific antimicrobial resistance patterns within sentinel organisms has spawned the popular term ‘super-bug’ (Foster, 2004; Anzaldi and Skaar, 2011). This term is misleading in the sense that resistance to a specific antimicrobial typically confers a reduction in Darwinian fitness in the absence of the pressure induced by that antimicrobial (Andersson and Levin, 1999; Andersson, 2003)

  • Understanding the fitness effects of antimicrobial resistance evolution is crucial for controlling the spread of resistance, as the fitness cost induced by antimicrobial resistance is one of the few biological features of resistant organisms that can be leveraged against them

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Summary

Introduction

The evolution of antimicrobial resistance in bacteria is driven by the pressure of sustained exposure to antimicrobials. The development of specific antimicrobial resistance patterns within sentinel organisms has spawned the popular term ‘super-bug’ (Foster, 2004; Anzaldi and Skaar, 2011). This term is misleading in the sense that resistance to a specific antimicrobial typically confers a reduction in Darwinian fitness (a fitness cost) in the absence of the pressure induced by that antimicrobial (Andersson and Levin, 1999; Andersson, 2003). Understanding the fitness effects of antimicrobial resistance evolution is crucial for controlling the spread of resistance, as the fitness cost induced by antimicrobial resistance is one of the few biological features of resistant organisms that can be leveraged against them

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