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氟康唑和伊曲康唑在体外药物压力下连续传代增加红色毛癣菌临床分离株的耐药性。

Increase in resistance to fluconazole and itraconazole in Trichophyton rubrum clinical isolates by sequential passages in vitro under drug pressure.

机构信息

Department of Dermatology, Venereology and Allergology, Wrocław Medical University, Wrocław, Poland.

出版信息

Mycopathologia. 2013 Aug;176(1-2):49-55. doi: 10.1007/s11046-013-9655-y. Epub 2013 Apr 18.

DOI:10.1007/s11046-013-9655-y
PMID:23595653
Abstract

Trichophyton rubrum, an anthropophilic dermatophyte fungus, is the predominant causative agent of superficial skin infections in human population. There are only scanty reports on drug susceptibility profiling of T. rubrum. Neither mechanisms for drug resistance development nor correlation between in vitro drug susceptibility and in vivo response to treatment is known for that species. In this study, changes in the in vitro susceptibilities to fluconazole (FLZ) and itraconazole (ITZ) among thirty T. rubrum clinical strains subjected to sequential passages in the presence or absence of the azoles were investigated. Each strain was passaged 12 times at 4-week intervals as three parallel cultures, maintained on a drug-free medium (1), and a medium containing FLZ (2) or ITZ (3) at subinhibitory concentrations. Susceptibility to FLZ and ITZ of the original strain and its 3 subcultures was determined by microdilution method. The MIC values of the two azoles remained unaltered for all T. rubrum strains tested, after 12 passages on a drug-free medium. Among the strains grown with FLZ, an increase in the MICs of FLZ and ITZ was noted in 17 (56.7 %) and 19 (63.3 %) strains, respectively. Increased MICs of ITZ and FLZ were demonstrated for 24 (80 %) and 20 (66.7 %) strains that were propagated with ITZ. The results indicate the capacity of T. rubrum to develop resistance toward the azoles after prolonged exposure to these drugs. Resistance of T. rubrum to azoles plays an important role in therapy failures and consequently contributes to persistence and chronicity of the infections.

摘要

红色毛癣菌,一种亲人性皮肤癣菌真菌,是人类浅部皮肤感染的主要致病因子。关于红色毛癣菌的药敏谱分析仅有少量报道。对于该菌种,耐药机制以及体外药敏与体内治疗反应之间的相关性均不清楚。在本研究中,我们研究了在氟康唑(FLZ)和伊曲康唑(ITZ)存在或不存在的情况下,连续传代对 30 株红色毛癣菌临床株的体外药敏性的变化。每个菌株在无药物的培养基(1)和含有亚抑菌浓度 FLZ(2)或 ITZ(3)的培养基中,每隔 4 周传代 12 次,分为 3 个平行培养物。采用微量稀释法测定原始菌株及其 3 个亚培养物对 FLZ 和 ITZ 的药敏性。在无药物培养基上传代 12 次后,所有红色毛癣菌菌株的两种唑类药物的 MIC 值均未改变。在含 FLZ 的菌株中,17 株(56.7%)和 19 株(63.3%)菌株的 FLZ 和 ITZ 的 MIC 值分别增加。在含 ITZ 的菌株中,24 株(80%)和 20 株(66.7%)的 ITZ 和 FLZ 的 MIC 值增加。结果表明,红色毛癣菌在长时间暴露于这些药物后,能够对唑类药物产生耐药性。红色毛癣菌对唑类药物的耐药性在治疗失败中起着重要作用,从而导致感染的持续和慢性化。

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