Assessment of trimethoprim-sulfamethoxazole susceptibility testing methods for fastidious Haemophilus spp

Clin Microbiol Infect. 2020 Jul;26(7):944.e1-944.e7. doi: 10.1016/j.cmi.2019.11.022. Epub 2019 Dec 4.

Abstract

Objectives: To compare the determinants of trimethoprim-sulfamethoxazole resistance with established susceptibility values for fastidious Haemophilus spp., to provide recommendations for optimal trimethoprim-sulfamethoxazole measurement.

Methods: We collected 50 strains each of Haemophilus influenzae and Haemophilus parainfluenzae at Bellvitge University Hospital. Trimethoprim-sulfamethoxazole susceptibility was tested by microdilution, E-test and disc diffusion using both Mueller-Hinton fastidious (MH-F) medium and Haemophilus test medium (HTM) following EUCAST and CLSI criteria, respectively. Mutations in folA, folP and additional determinants of resistance were identified in whole-genome-sequenced isolates.

Results: Strains presented generally higher rates of trimethoprim-sulfamethoxazole resistance when grown on HTM than on MH-F, independent of the methodology used (average MIC 2.6-fold higher in H. influenzae and 1.2-fold higher in H. parainfluenzae). The main resistance-related determinants were as follows: I95L and F154S/V in folA; 3- and 15-bp insertions and substitutions in folP; acquisition of sul genes; and FolA overproduction potentially linked to mutations in -35 and -10 promoter motifs. Of note, 2 of 19 H. influenzae strains (10.5%) and 9 of 33 H. parainfluenzae strains (27.3%) with mutations and assigned as resistant by microdilution were inaccurately considered susceptible by disc diffusion. This misinterpretation was resolved by raising the clinical resistance breakpoint of the EUCAST guidelines to ≤30 mm.

Conclusions: Given the routine use of disc diffusion, a significant number of strains could potentially be miscategorized as susceptible to trimethoprim-sulfamethoxazole despite having resistance-related mutations. A simple modification to the current clinical resistance breakpoint given by the EUCAST guideline for MH-F ensures correct interpretation and correlation with the reference standard method of microdilution.

Keywords: Antimicrobial susceptibility testing methods; EUCAST; Haemophilus influenzae; Haemophilus parainfluenzae; Resistance-related determinants; Trimethoprim-sulfamethoxazole; clinical resistance breakpoint.

Publication types

  • Comparative Study

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins / genetics*
  • Culture Media / chemistry
  • Drug Resistance, Multiple, Bacterial*
  • Haemophilus Infections / microbiology*
  • Haemophilus influenzae / drug effects
  • Haemophilus influenzae / genetics*
  • Haemophilus parainfluenzae / drug effects
  • Haemophilus parainfluenzae / genetics*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Microbial Sensitivity Tests
  • Mutation
  • Promoter Regions, Genetic
  • Trimethoprim, Sulfamethoxazole Drug Combination / pharmacology
  • Whole Genome Sequencing

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Culture Media
  • Trimethoprim, Sulfamethoxazole Drug Combination