Class 1 integrons increase trimethoprim-sulfamethoxazole MICs against epidemiologically unrelated Stenotrophomonas maltophilia isolates

Antimicrob Agents Chemother. 2004 Feb;48(2):666-9. doi: 10.1128/AAC.48.2.666-669.2004.

Abstract

Twenty-five plasmid-specified antimicrobial resistance determinants common to gram-negative bacilli from nosocomial infection were investigated from 31 Stenotrophomonas maltophilia isolates. Twenty-four clones were identified by pulsed-field gel electrophoresis, and in three clones that exhibited an increased trimethoprim-sulfamethoxazole MIC, the sul1 determinant was found. These results support not only the higher spread of class 1 integrons compared to other mechanisms but also the potential limitation of using trimethoprim-sulfamethoxazole for therapy of severe S. maltophilia infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cross Infection / microbiology
  • Genes, Bacterial / genetics
  • Genotype
  • Gram-Negative Bacterial Infections / microbiology*
  • Humans
  • Integrons / genetics*
  • Microbial Sensitivity Tests
  • Multigene Family / genetics
  • Plasmids / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stenotrophomonas maltophilia / drug effects*
  • Stenotrophomonas maltophilia / genetics*
  • Trimethoprim, Sulfamethoxazole Drug Combination / pharmacology*

Substances

  • Trimethoprim, Sulfamethoxazole Drug Combination