Contribution of integrons, and SmeABC and SmeDEF efflux pumps to multidrug resistance in clinical isolates of Stenotrophomonas maltophilia (vol 53, pg 518, 2004)
被引:1
作者:
Chang, LL
论文数: 0引用数: 0
h-index: 0
机构:Department of Microbiology, Kaohsiung Medical University, Kaohsiung
Chang, LL
Chen, HF
论文数: 0引用数: 0
h-index: 0
机构:Department of Microbiology, Kaohsiung Medical University, Kaohsiung
Chen, HF
Chang, CY
论文数: 0引用数: 0
h-index: 0
机构:Department of Microbiology, Kaohsiung Medical University, Kaohsiung
Chang, CY
Lee, TM
论文数: 0引用数: 0
h-index: 0
机构:Department of Microbiology, Kaohsiung Medical University, Kaohsiung
Lee, TM
Wu, WJ
论文数: 0引用数: 0
h-index: 0
机构:Department of Microbiology, Kaohsiung Medical University, Kaohsiung
Wu, WJ
机构:
[1] Department of Microbiology, Kaohsiung Medical University, Kaohsiung
[2] Department of Food Science/Technol., Tajen Institute of Technology, Pingtung
[3] Department of Urology, Kaohsiung Medical University, Kaohsiung
Objectives: The contribution of integrons and efflux pumps to multidrug resistance in Stenotrophomonas maltophilia was evaluated. Materials and methods: Ninety-three S. maltophilia clinical isolates were studied. PCR and direct sequencing were used to detect the presence of integrons. Real-time PCR was performed to assess and quantify the expression of the Sme efflux pumps of S. maltophilia. Results: Class 1 integrons were detected in 22% of clinical isolates and carried cassettes conferring resistance mainly to aminoglycosides and trimethoprim. The small multidrug resistance gene, smr, was found on class 1 integrons in six isolates. Thirty-one percent of the isolates overexpressed the smeDEF gene, as compared with a control strain, and 59% overexpressed the smeABC gene. Extrusion of ciprofloxacin and meropenem was specific to the SmeABC and SmeDEF pumps, respectively. Conclusion: SmeABC and SmeDEF efflux pumps play important roles in resistance of S. maltophilia to ciprofloxacin and meropenem.
引用
收藏
页码:553 / 553
页数:1
相关论文
共 1 条
[1]
Chang LL, 2004, J ANTIMICROB CHEMOTH, V53, P518, DOI 10.1093/jac/dkh094