Using whole-genome sequencing to determine appropriate streptomycin epidemiological cutoffs for Salmonella and Escherichia coli

FEMS Microbiol Lett. 2016 Feb;363(4):fnw009. doi: 10.1093/femsle/fnw009. Epub 2016 Jan 17.

Abstract

For Enterobacteriaceae such as Salmonella spp. and Escherichia coli, no unified interpretive resistance criteria exist for streptomycin, an epidemiologically important antibiotic. As part of the National Antimicrobial Resistance Monitoring System, we had previously used a minimum inhibitory concentration of ≥ 64 μg mL(-1) as an epidemiological cutoff value (ECV) to define non-wild-type isolates. To identify whether this ECV correlated with genetic determinants of resistance, we performed whole-genome sequencing of 463 Salmonella and E. coli isolates to identify streptomycin resistance genotypes. From this analysis, we found that using a streptomycin resistance breakpoint of ≥ 64 μg mL(-1) classified over 20% of strains possessing aadA or strA/strB resistance genes as wild-type. Therefore, to improve the concordance between genotypic and phenotypic data, we propose reducing the phenotypic cutoff values to ≥ 32 μg mL(-1) for both Salmonella and E. coli, to be used widely as ECVs to categorize non-wild-type isolates.

Keywords: E. coli; Salmonella; genotyping; resistance; streptomycin; whole-genome sequencing.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Drug Resistance, Multiple, Bacterial / genetics*
  • Escherichia coli / drug effects
  • Escherichia coli / genetics*
  • Escherichia coli Infections / epidemiology
  • Genome, Bacterial / genetics
  • Genotype
  • High-Throughput Nucleotide Sequencing
  • Microbial Sensitivity Tests / standards*
  • Phenotype
  • Polymerase Chain Reaction
  • Salmonella / drug effects
  • Salmonella / genetics*
  • Salmonella Infections, Animal / epidemiology
  • Streptomycin / pharmacology*

Substances

  • Anti-Bacterial Agents
  • Streptomycin