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用流式细胞术测定新型隐球菌和格特隐球菌对氟康唑的最小抑菌浓度。

Determination of the minimum inhibitory concentration of Cryptococcus neoformans and Cryptococcus gattii against fluconazole by flow cytometry.

机构信息

Evandro Chagas Clinical Research Institute (IPEC), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro.

出版信息

Med Mycol. 2014 Jan;52(1):90-8. doi: 10.3109/13693786.2013.806827.

DOI:10.3109/13693786.2013.806827
PMID:23808405
Abstract

Recent studies have used flow cytometry (FCM) as an important alternative method to determine the antifungal susceptibility of yeasts compared to the broth microdilution Clinical and Laboratory Standards Institute (CLSI) reference procedure. We present a comparative study of the broth microdilution method and flow cytometry to assess the in vitro antifungal susceptibility of Cryptococcus neoformans (n = 16) and C. gattii (n = 24) to fluconazole. The minimum inhibitory concentration (MIC) assays by flow cytometry were defined as the lowest drug concentration that showed ∼50% of the count of acridine orange negative cells compared to that of the growth control. Categorical classification showed all C. neoformans isolates were susceptible to fluconazole. Three isolates of C. gattii were susceptible dose-dependent and the remaining 21 isolates were classified as susceptible. MICs comparison of both methodologies demonstrated 100% categorical agreement of the results obtained for C. neoformans and C. gattii. The MICs obtained with the CLSI-approved method and flow cytometry were compared by the Spearman correlation test and a significant Pv = 0.001. The flow cytometric method has the advantage of analyzing a large and constant number of cells in less time, i.e., 9 h incubation for fluconazole using acridine orange versus 72 h for broth microdilution method. In conclusion, the two methods were comparable and flow cytometry method can expedite and improve the results of in vitro susceptibility tests of C. neoformans and C. gattii against fluconazole and also allows comparative studies in vitro/in vivo more rapidly, which along with clinical data, could assist in selecting the most appropriate treatment choice.

摘要

最近的研究使用流式细胞术(FCM)作为一种重要的替代方法,与肉汤微量稀释临床和实验室标准研究所(CLSI)参考程序相比,来确定酵母菌的抗真菌药敏性。我们对肉汤微量稀释法和流式细胞术进行了比较研究,以评估隐球菌(n = 16)和新型隐球菌(n = 24)对氟康唑的体外抗真菌药敏性。通过流式细胞术定义最低抑菌浓度(MIC)检测为与生长对照相比,显示吖啶橙阴性细胞计数减少约 50%的最低药物浓度。分类分类显示所有新型隐球菌分离株均对氟康唑敏感。3 株新型隐球菌为剂量依赖性敏感,其余 21 株分离株被归类为敏感。两种方法的 MIC 比较显示,新型隐球菌和新型隐球菌的结果具有 100%的分类一致性。CLSI 批准的方法和流式细胞术获得的 MIC 用 Spearman 相关检验进行比较,结果具有显著的 Pv = 0.001。流式细胞术方法的优势在于在更短的时间内分析大量且恒定数量的细胞,即吖啶橙孵育 9 小时用于氟康唑,而肉汤微量稀释法为 72 小时。总之,两种方法是可比的,流式细胞术方法可以加快和改善新型隐球菌和新型隐球菌对氟康唑的体外药敏试验结果,并且还可以更快地进行体外/体内比较研究,结合临床数据,可以帮助选择最合适的治疗选择。

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