Infection and Drug Resistance (Aug 2022)

The Risk of Emerging Resistance to Trimethoprim/Sulfamethoxazole in Staphylococcus aureus

  • Sato T,
  • Ito R,
  • Kawamura M,
  • Fujimura S

Journal volume & issue
Vol. Volume 15
pp. 4779 – 4784

Abstract

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Takumi Sato, Ryota Ito, Masato Kawamura, Shigeru Fujimura Division of Clinical Infectious Diseases & Chemotherapy, Tohoku Medical and Pharmaceutical University, Sendai, JapanCorrespondence: Takumi Sato, Division of Clinical Infectious Diseases & Chemotherapy, Tohoku Medical and Pharmaceutical University, 4-4-1 Komatsushima, Aoba-ku, Sendai, 981-8558, Japan, Tel/Fax +81227270176, Email [email protected]: Due to the spread of community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA), the demand for trimethoprim/sulfamethoxazole (SXT) is increasing in the world. It is not clear whether the resistant strain emerges by overuse of SXT. We investigated here the emergent risk of the SXT-resistant mutant in S. aureus by an in vitro SXT exposure experiment.Methods: A total of 40 S. aureus clinical isolates (20 MSSA and 20 MRSA isolates) were exposed to sub-MIC of SXT for consecutive days, and MIC of SXT was determined every day. In addition, the dfrB DNA sequencing was performed to detect the mutation in the SXT-resistant strain.Results: The SXT-resistant strain began to emerge on the eighth day and accounted for 45% (18/40 clinical isolates) after 14 days. Moreover, one half of these resistant strains showed F98Y mutation in DfrB to retain SXT-resistance without selective pressure.Conclusion: The emergent risk was SXT exposure of 14 days or more.Keywords: Staphylococcus aureus, antimicrobial resistance, trimethoprim/sulfamethoxazole, dfrB

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