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首页> 外文期刊>International Journal of Medicine and Medical Sciences >Commercial tests for in vitro antifungal susceptibility testing of Candida species compared to standard (NCCLS) broth microdilution
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Commercial tests for in vitro antifungal susceptibility testing of Candida species compared to standard (NCCLS) broth microdilution

机译:与标准(NCCLS)肉汤微稀释液相比,念珠菌种体外抗真菌药敏试验的商业测试

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  It is of value to evaluate the commercial susceptibility methods as possible alternatives to standard one for routine fungal susceptibility testing. So we aimed to compare the NCCLS microdilution method with each of commercial Etest and candifast kit. A total of 30 Candida isolates were included and species identification was confirmed by morphological appearance on Sabouraud's dextrose agar (SDA), Gram stain, and candifast kit. The in vitro antifungal susceptibility testing of amphotericin B (AMB) and fluconazole (FCZ) were performed by 3 methods (standard broth microdilution, Etest and candifast) on the tested Candida species. The overall percentage of agreement of Etest with standard method was 90% for each of AMB and FCZ. For AMB the agreement of Etest with standard broth method was 100% in tested species exceptCandida glabrata (85.7%) and Candida parapsilosis (66.6%), while the percentage of agreement of candifast was100% in all species except C. glabrata (85.7%).  For fluconazole the percentage of agreement of Etest, with the standard method, was 100% for each of C. glabrata and Candida tropicalis and was 92.8, 66.6% for Candida albicansand Candida parapsilosis respectively. The percentage of agreement of candifast method was 100% in all species except C. albicans, C. glabrata which was 92.8 and 85.7% respectively. Etest method is an alternative but cannot be considered as a substitute for the NCCLS reference method. The antifungal susceptibility method not greatly influenced by the type of tested antifungal agent.  
机译:评估商业敏感性方法作为常规真菌敏感性测试的标准方法的一种可能替代方法是很有价值的。因此,我们旨在比较NCCLS微稀释方法与每种商业Etest和candifast试剂盒。总共包括30种念珠菌分离株,通过Sabouraud的葡萄糖琼脂(SDA),革兰氏染色和candifast试剂盒的形态外观确认了物种鉴定。两性霉素B(AMB)和氟康唑(FCZ)的体外抗真菌药敏试验是通过3种方法(标准肉汤微量稀释法,Etest和Candifast)对被测大麻科物种进行的。对于AMB和FCZ,Etest与标准方法达成的协议的总百分比为90%。对于AMB,除光滑念珠菌(85.7%)和近实念珠菌(66.6%)外,被测物种的Etest与标准肉汤法的一致性为100%,而除了光滑念珠菌(85.7%)以外,所有物种中念珠菌的一致性百分比为100%。 。对于氟康唑,按照标准方法,Etest的一致性百分比分别为光滑小。和热带念珠菌的100%,分别为白色念珠菌和副寄生念珠菌的92.8、66.6%。除白色念珠菌,光滑念珠菌分别为92.8和85.7%外,candifast方法的一致性百分比在所有物种中均为100%。 Etest方法是一种替代方法,但不能视为NCCLS参考方法的替代方法。抗真菌药敏方法不受所测试抗真菌剂类型的很大影响。

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