首页> 外文期刊>Journal of Clinical Microbiology >Influence of Different Media, Incubation Times, and Temperatures for Determining the MICs of Seven Antifungal Agents against Paracoccidioides brasiliensis by Microdilution
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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,孵育时间和温度测定7次抗真菌剂的MIC通过微量缺失测定尿嘧啶酰脱乙酰吡啶胺

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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:用巴西副,paracoccidioidomycosis的病原体,MIC测定法已用可变协议进行的,同时采用大量稀释和微量稀释试验和包括接种物制备温度的差异,使用的媒体,孵育期,和。第二十一条副球的临床和环境分离用两性霉素B,伊曲康唑,酮康唑,氟康唑,复方磺胺甲恶唑,磺胺甲恶唑,甲氧苄啶,特比萘芬和测试,根据国家委员会临床实验室标准(全国委员会临床实验室标准化,文档M27- A2,2002年),以修饰如3个培养基配方(RPMI 1640培养基,麦克维和莫顿[MVM]介质,和改性的Mueller-Hinton [MMH]介质),两个保温温度(室温[25至28℃]和37℃),和三个潜伏期(7,10,和15天)。抗真菌活性也被列为杀菌或抑制真菌。最佳结果是在保温后,将其选作标准的温育时间为15天获得。对于大多数个体分离物在相同的温度随所使用的不同的媒体改变生长的时间长度相同的MIC( P <0.05)。的菌株,81%显示出从酵母到在RPMI 1640培养基中的菌丝体的形式在37℃下,独立抗真菌药的存在的过渡。 MMH介质似乎是与P.巴西的抗真菌药物药敏试验,除了磺胺甲恶唑和合适的介质磺胺甲恶唑 - 甲氧苄啶的组合,为此,MVM介质得到更好的结果。温育温度的影响的MIC,用,在一般情况下,较高的MIC比在37 25℃(菌丝体形式)℃( P <0.05)。根据我们的结果,我们初步提出的抗真菌药物对副球药敏试验微量稀释试验协议。

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