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Influence of Different Media Incubation Times and Temperatures for Determining the MICs of Seven Antifungal Agents against Paracoccidioides brasiliensis by Microdilution

机译:不同介质孵育时间和温度对微量稀释法测定七种抗巴西副球菌抗真菌剂MIC的影响

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摘要

MIC assays with Paracoccidioides brasiliensis, the etiological agent of paracoccidioidomycosis, had been conducted with variable protocols, employing both macrodilution and microdilution tests and including differences in inoculum preparation, media used, incubation periods, and temperatures. Twenty-one clinical and environmental isolates of Paracoccidioides were tested using amphotericin B, itraconazole, ketoconazole, fluconazole, sulfamethoxazole, sulfamethoxazole-trimethoprim, and terbinafine, according to the National Committee for Clinical Laboratory Standards (National Committee for Clinical Laboratory Standards, document M27-A2, 2002), with modifications such as three medium formulations (RPMI 1640 medium, McVeigh and Morton [MVM] medium, and modified Mueller-Hinton [MMH] medium), two incubation temperatures (room temperature [25 to 28°C] and 37°C), and three incubation periods (7, 10, and 15 days). The antifungal activities were also classified as fungicidal or fungistatic. The best results were obtained after 15 days of incubation, which was chosen as the standard incubation time. The MICs for most individual isolates grown for the same length of time at the same temperature varied with the different media used (P < 0.05). Of the isolates, 81% showed transition from the yeast to the mycelial form in RPMI 1640 medium at 37°C, independent of the presence of antifungals. MMH medium appears to be a suitable medium for susceptibility testing of antifungal drugs with P. brasiliensis, except for sulfamethoxazole and the combination of sulfamethoxazole-trimethoprim, for which the MVM medium yielded better results. The incubation temperature influenced the MICs, with, in general, higher MICs at 25°C (mycelial form) than at 37°C (P < 0.05). Based on our results, we tentatively propose a microdilution assay protocol for susceptibility testing of antifungal drugs against Paracoccidioides.
机译:使用可变稀释方案对巴西副球菌病的病原体巴西副球菌进行了MIC测定,采用了宏观稀释和微量稀释测试,包括接种物制备,使用的培养基,孵育时间和温度方面的差异。根据国家临床实验室标准委员会(国家临床实验室标准委员会,文件M27- A2,2002),并进行了修改,例如三种培养基配方(RPMI 1640培养基,McVeigh和Morton [MVM]培养基以及改良的Mueller-Hinton [MMH]培养基),两个孵育温度(室温[25至28°C]和37°C)和三个潜伏期(7、10和15天)。抗真菌活性也被分类为杀真菌的或抑真菌的。孵育15天后获得最佳结果,将其作为标准孵育时间。对于大多数分离株,在相同温度下生长相同时间长度的MIC随所用培养基的不同而不同(P <0.05)。在分离物中,有81%在37°C的RPMI 1640培养基中显示出从酵母到菌丝体的转变,与抗真菌剂的存在无关。除了磺胺甲恶唑和磺胺甲恶唑-甲氧苄氨嘧啶的组合外,MMH培养基似乎是一种适用于巴西假单胞菌抗真菌药药敏试验的培养基,MVM培养基产生了更好的结果。孵育温度影响MIC,通常在25°C(菌丝状)时的MIC高于在37°C时的MIC(P <0.05)。根据我们的结果,我们暂定提出一种微稀释测定规程,用于抗真菌药对副球菌的敏感性测试。

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