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用于检测皮肤癣菌对抗真菌药物敏感性的肉汤微量稀释法(改良的CLSI M38-A)的质量控制菌株的实验室间研究。

Interlaboratory study of quality control isolates for a broth microdilution method (modified CLSI M38-A) for testing susceptibilities of dermatophytes to antifungals.

作者信息

Ghannoum M A, Arthington-Skaggs B, Chaturvedi V, Espinel-Ingroff A, Pfaller M A, Rennie R, Rinaldi M G, Walsh T J

机构信息

Center for Medical Mycology, University Hospitals/Case Western Reserve University, EMBA, 11100 Euclid Avenue, Cleveland, OH 44106-5028, USA.

出版信息

J Clin Microbiol. 2006 Dec;44(12):4353-6. doi: 10.1128/JCM.00688-06. Epub 2006 Oct 18.

Abstract

The Clinical and Laboratory Standards Institute (CLSI; formerly National Committee for Clinical Laboratory Standards, or NCCLS) M38-A standard for the susceptibility testing of filamentous fungi does not specifically address the testing of dermatophytes. In 2003, a multicenter study investigated the reproducibility of the microdilution method developed at the Center for Medical Mycology, Cleveland, Ohio, for testing the susceptibility of dermatophytes. Data from that study supported the introduction of this method for testing dermatophytes in the future version of the CLSI M38-A standard. In order for the method to be accepted by CLSI, appropriate quality control isolates needed to be identified. To that end, an interlaboratory study, involving the original six laboratories plus two additional sites, was conducted to evaluate potential candidates for quality control isolates. These candidate strains included five Trichophyton rubrum strains known to have elevated MICs to terbinafine and five Trichophyton mentagrophytes strains. Antifungal agents tested included ciclopirox, fluconazole, griseofulvin, itraconazole, posaconazole, terbinafine, and voriconazole. Based on the data generated, two quality control isolates, one T. rubrum isolate and one T. mentagrophytes isolate, were identified and submitted to the American Type Culture Collection (ATCC) for inclusion as reference strains. Ranges encompassing 95.2 to 97.9% of all data points for all seven drugs were established.

摘要

临床和实验室标准协会(CLSI;前身为国家临床实验室标准委员会,即NCCLS)关于丝状真菌药敏试验的M38 - A标准并未专门涉及皮肤癣菌的检测。2003年,一项多中心研究调查了俄亥俄州克利夫兰医学真菌学中心开发的用于检测皮肤癣菌药敏性的微量稀释法的可重复性。该研究的数据支持在CLSI M38 - A标准的未来版本中引入此方法用于检测皮肤癣菌。为使该方法被CLSI接受,需要鉴定合适的质量控制菌株。为此,开展了一项实验室间研究,参与的实验室包括最初的六个实验室以及另外两个地点,以评估质量控制菌株的潜在候选菌株。这些候选菌株包括五株已知对特比萘芬MIC值升高的红色毛癣菌菌株和五株须癣毛癣菌菌株。所测试的抗真菌药物包括环吡酮、氟康唑、灰黄霉素、伊曲康唑、泊沙康唑、特比萘芬和伏立康唑。基于所产生的数据,鉴定出两株质量控制菌株,一株红色毛癣菌菌株和一株须癣毛癣菌菌株,并提交给美国典型培养物保藏中心(ATCC)作为参考菌株收录。确定了涵盖所有七种药物95.2%至97.9%数据点的范围。

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