Biological cost of fosfomycin resistance in Escherichia coli in a murine model of urinary tract infection

Int J Med Microbiol. 2017 Dec;307(8):452-459. doi: 10.1016/j.ijmm.2017.09.019. Epub 2017 Sep 29.

Abstract

Prevalence of fosfomycin resistance in E. coli clinical isolates from UTIs remains very low. Our hypothesis was that fosfomycin resistance may be associated with a biological cost. Three groups of strains of E. coli belonging to the B2 phylogenetic group were used: clinical wild-type (WT) isolates, clinical multidrug-resistant isolates and in vitro fosfomycin-resistant derivatives from the uropathogen clinical strain E. coli CFT073. In each group fosfomycin-susceptible and -resistant isolates were compared. In vitro, we found a significantly decreased growth rate for fosfomycin-resistant strains as compared with susceptible strains in the WT group. In a murine model of ascending UTI, there was a significant reduction in infection rates with fosfomycin-resistant isolates as compared with susceptible ones, in all 3 study groups, ranging from 28 to 39% (P<0.03). All fosfomycin-susceptible clinical strains were virulent in vivo (13/13), while fosfomycin-resistant clinical strains were either virulent (2/7) or non-virulent (5/7) (P<0.002). This difference was not explained by the number of virulence factors or pathogenicity-associated islands. In conclusion, fosfomycin resistance appears to carry some biological cost in E. coli, which may explain in part the apparent paradox of the low prevalence of fosfomycin resistance despite a high rate of spontaneous mutants.

Keywords: Antibiotic resistance; E. coli; Fitness; Fosfomycin; UTI; Virulence.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Disease Models, Animal
  • Drug Resistance, Bacterial*
  • Escherichia coli / drug effects*
  • Escherichia coli / genetics
  • Escherichia coli / growth & development
  • Escherichia coli / pathogenicity
  • Escherichia coli Infections / drug therapy
  • Escherichia coli Infections / microbiology*
  • Female
  • Fosfomycin / pharmacology*
  • Genetic Fitness*
  • Mice, Inbred CBA
  • Urinary Tract Infections / drug therapy
  • Urinary Tract Infections / microbiology*
  • Virulence

Substances

  • Anti-Bacterial Agents
  • Fosfomycin