Predominance of dfrG as determinant of trimethoprim resistance in imported Staphylococcus aureus

D Nurjadi1, J Schäfer2, B Friedrich-Jänicke3

  • 1Department of Infectious Diseases, Medical Microbiology and Hygiene, Heidelberg University Hospital, Heidelberg, Germany.

Insights

Trimethoprim resistance in Staphylococcus aureus is often caused by the dfrG gene. Travel to South Asia increases the risk of acquiring trimethoprim-sulfamethoxazole-resistant S. aureus infections globally.

Area of Science:

  • Microbiology
  • Genetics
  • Epidemiology

Background:

  • Antimicrobial resistance is a growing global health concern.
  • Trimethoprim-sulfamethoxazole is a commonly prescribed antibiotic combination.
  • Understanding resistance mechanisms and prevalence is crucial for effective treatment.

Purpose of the Study:

  • To determine the global prevalence of trimethoprim-sulfamethoxazole resistance in Staphylococcus aureus.
  • To identify the genetic mechanisms responsible for trimethoprim resistance.
  • To assess the impact of travel on the acquisition of resistant strains.

Main Methods:

  • Analysis of Staphylococcus aureus isolates from travel-associated skin and soft-tissue infections across 13 European travel clinics.
  • Phenotypic antimicrobial susceptibility testing.
  • Genetic analysis to identify resistance determinants, focusing on dfr genes.

Main Results:

  • 38% of S. aureus isolates were resistant to trimethoprim, and 21% were resistant to trimethoprim-sulfamethoxazole.
  • The dfrG gene was identified as the primary cause of trimethoprim resistance, explaining 92% of cases.
  • Travel to South Asia was significantly associated with an increased risk of carrying trimethoprim-sulfamethoxazole-resistant S. aureus.

Conclusions:

  • The dfrG gene is the predominant genetic determinant of trimethoprim resistance in human S. aureus infections worldwide.
  • Travel plays a significant role in the global dissemination of antibiotic-resistant S. aureus.
  • Public health strategies should consider travel history in managing S. aureus infections.

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