首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparison of two alternative microdilution procedures with the National Committee for Clinical Laboratory Standards reference macrodilution method M27-P for in vitro testing of fluconazole-resistant and -susceptible isolates of Candida albicans.
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Comparison of two alternative microdilution procedures with the National Committee for Clinical Laboratory Standards reference macrodilution method M27-P for in vitro testing of fluconazole-resistant and -susceptible isolates of Candida albicans.

机译:两种替代微量稀释程序与美国国家临床实验室标准委员会的标准宏观稀释方法M27-P的比较用于体外检测耐氟康唑和敏感的白色念珠菌分离株。

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摘要

The National Committee for Clinical Laboratory Standards has proposed a reference broth macrodilution method for in vitro antifungal susceptibility testing of yeasts (the M27-P method). This method is cumbersome and time-consuming and includes MIC endpoint determination by the visual and subjective inspection of growth inhibition after 48 h of incubation. Two alternative microdilution procedures for MIC endpoint determination, a spectrophotometric MIC endpoint test that evaluates 80% growth inhibition by the drug and a colorimetric method with an oxidation-reduction indicator (Alamar Blue), were compared with the M27-P method for fluconazole susceptibility testing of 45 susceptible and resistant isolates of Candida albicans. The spectrophotometric method was performed with RPMI 1640 medium with 2% glucose, and the other two tests were performed with plain RPMI 1640 medium. All tests were incubated at 35 degrees C. Excellent agreement was demonstrated between the M27-P method and both 24-h microdilution tests (97.7%) as well as between the two microdilution tests (95.5%). Also, there was agreement in the detection in vivo of fluconazole resistance by the three methods. These preliminary data indicate that both microdilution methods may serve as less subjective alternatives to the M27-P method for the determination of fluconazole MIC endpoints.
机译:全国临床实验室标准委员会已经提出了用于酵母体外抗真菌药敏试验的参考肉汤大量稀释方法(M27-P方法)。该方法麻烦且耗时,并且包括在孵育48小时后通过目视和主观检查生长抑制来确定MIC终点。比较了两种用于MIC终点测定的微量稀释方法,分光光度法MIC终点测试(评估该药物对80%生长的抑制作用)和带氧化还原指示剂的比色法(Alamar Blue),与M27-P方法进行氟康唑敏感性测试的比较45种敏感的白色念珠菌耐药菌株。分光光度法是使用含2%葡萄糖的RPMI 1640培养基进行的,其他两项测试是使用普通RPMI 1640培养基进行的。所有测试均在35摄氏度下孵育。在M27-P方法与两个24小时微量稀释测试(97.7%)以及两个微量稀释测试(95.5%)之间均表现出极好的一致性。另外,通过三种方法在体内检测氟康唑耐药性方面也达成了共识。这些初步数据表明,两种微量稀释方法都可以作为M27-P方法在确定氟康唑MIC终点方面的主观选择。

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