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采用Sensititre YeastOne® 稀释法与临床实验室标准协会(CLSI)M27-A3微量肉汤稀释参考方法,对102株酵母菌株测定8种抗真菌药物的最低抑菌浓度(MIC)的比较。

Comparison of the Sensititre YeastOne® dilution method with the Clinical Laboratory Standards Institute (CLSI) M27-A3 microbroth dilution reference method for determining MIC of eight antifungal agents on 102 yeast strains.

作者信息

Bertout S, Dunyach C, Drakulovski P, Reynes J, Mallié M

机构信息

UMR 145 (IRD/UM1), UFR sciences pharmaceutiques et biologiques, 15, avenue Charles-Flahault, BP 14491, 34093 Montpellier cedex 5, France.

出版信息

Pathol Biol (Paris). 2011 Feb;59(1):48-51. doi: 10.1016/j.patbio.2010.07.020. Epub 2010 Sep 16.

Abstract

The Clinical Laboratory Standards Institute ([CLSI] formerly NCCLS) reference broth microdilution testing method (protocol M27-A3) was compared with a commercially available methods (Sensititre YeastOne(®)) by testing two quality control strains and 102 isolates of Candida sp. and Cryptococcus sp. against fluconazole, itraconazole, ketoconazole, posaconazole, voriconazole, flucytosin, amphotericin B and caspofungin. Minimal inhibitory concentrations (MIC) endpoints were determined after 24h of incubation for Sensititre YeastOne(®) and after 24 and 48 h for CLSI microdilution method. Essential agreements between methods vary from 70.6 to 92.2%. Categorical agreements vary from 94.1% for 5FC to 72.6% for AMB. Sensititre YeastOne(®) reading appears to be useful for avoiding very major errors and this confirms the interest of this method for evaluating new antifungals activity in vitro.

摘要

通过对两种质控菌株以及102株念珠菌属和隐球菌属菌株进行氟康唑、伊曲康唑、酮康唑、泊沙康唑、伏立康唑、氟胞嘧啶、两性霉素B和卡泊芬净的测试,将临床实验室标准协会([CLSI],前身为NCCLS)的参考肉汤微量稀释测试方法(方案M27 - A3)与一种市售方法(Sensititre YeastOne®)进行比较。对于Sensititre YeastOne®,孵育24小时后确定最低抑菌浓度(MIC)终点;对于CLSI微量稀释法,则在孵育24小时和48小时后确定终点。两种方法之间的基本一致性在70.6%至92.2%之间。分类一致性从5FC的94.1%到AMB的72.6%不等。Sensititre YeastOne®读数似乎有助于避免非常严重的误差,这证实了该方法在体外评估新型抗真菌活性方面的价值。

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