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一种新型商业比色微量稀释法与标准方法用于念珠菌属和新型隐球菌体外药敏试验的比较。

Comparison of a new commercial colorimetric microdilution method with a standard method for in-vitro susceptibility testing of Candida spp. and Cryptococcus neoformans.

作者信息

Davey K G, Szekely A, Johnson E M, Warnock D W

机构信息

PHLS Mycology Reference Laboratory, Public Health Laboratory, Bristol, UK.

出版信息

J Antimicrob Chemother. 1998 Oct;42(4):439-44. doi: 10.1093/jac/42.4.439.

Abstract

The Sensititre Yeast One method (AccuMed International Ltd, East Grinstead, UK) is a microplate-based procedure that incorporates an oxidation-reduction indicator, Alamar Blue, for the in-vitro testing of five antifungal agents (amphotericin B, fluconazole, itraconazole, ketoconazole and flucytosine). We compared this colorimetric method with a standard broth microdilution test, performed according to US National Committee for Clinical Laboratory Standards document M27-A guidelines, for determining the in-vitro susceptibilities of 180 isolates of Candida spp. (50 Candida albicans, 50 Candida glabrata, ten Candida kefyr, 20 Candida krusei, ten Candida lusitaniae, 20 Candida parapsilosis and 20 Candida tropicalis) and 20 isolates of Cryptococcus neoformans. The overall agreement between the results of the two methods (colorimetric MICs within +/- two log2 dilutions of standard MICs) were 99% for amphotericin B, 96.5% for flucytosine, 93% for itraconazole, 91.5% for fluconazole and 85.5% for ketoconazole. The overall levels of agreement between the two methods were > or = 94% for six of the eight species tested, the exceptions being C. neoformans and C. tropicalis where the overall agreement was 89% and 80% respectively. The poorest agreement between the results for individual agents was seen with C. tropicalis and the three azole agents (60-75% of colorimetric MICs within +/- two log2 dilutions of standard MICs), and C. neoformans for ketoconazole (50%). The Yeast One method appears to be a suitable alternative procedure for routine antifungal susceptibility testing of Candida spp. and C. neoformans.

摘要

Sensititre酵母一步法(AccuMed国际有限公司,英国东格林斯特德)是一种基于微孔板的方法,该方法采用氧化还原指示剂阿拉玛蓝,用于体外检测五种抗真菌药物(两性霉素B、氟康唑、伊曲康唑、酮康唑和氟胞嘧啶)。我们将这种比色法与根据美国国家临床实验室标准委员会M27-A指南进行的标准肉汤微量稀释试验进行了比较,以确定180株念珠菌属菌株(50株白色念珠菌、50株光滑念珠菌、10株克柔念珠菌、20株克鲁斯念珠菌、10株葡萄牙念珠菌、20株近平滑念珠菌和20株热带念珠菌)和20株新型隐球菌的体外敏感性。两种方法的结果(比色法测定的最低抑菌浓度在标准最低抑菌浓度的±两个log2稀释范围内)总体一致性为:两性霉素B为99%,氟胞嘧啶为96.5%,伊曲康唑为93%,氟康唑为91.5%,酮康唑为85.5%。在所测试的八个菌种中,有六个菌种两种方法的总体一致性≥94%,例外的是新型隐球菌和热带念珠菌,其总体一致性分别为89%和80%。对于个别药物,热带念珠菌与三种唑类药物(比色法测定的最低抑菌浓度在标准最低抑菌浓度的±两个log2稀释范围内的比例为60 - 75%)以及新型隐球菌与酮康唑(50%)之间的一致性最差。酵母一步法似乎是念珠菌属和新型隐球菌常规抗真菌药敏试验的一种合适替代方法。

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