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首页> 外文期刊>Journal of Clinical Microbiology >Comparison of a New Colorimetric Assay with the NCCLS Broth Microdilution Method (M-27A) for Antifungal Drug MIC Determination
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Comparison of a New Colorimetric Assay with the NCCLS Broth Microdilution Method (M-27A) for Antifungal Drug MIC Determination

机译:NCLLS肉汤微稀释法(M-27A)用于真菌药物MIC测定的新比色测定法的比较

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摘要

We evaluated a new microtiter assay for antifungal susceptibility testing based on a colorimetric reaction to monitor fungal substrate utilization. This new method (rapid susceptibility assay [RSA]) provides quantitative endpoint readings in less than 8 h compared with visual determination of MIC by the National Committee for Clinical Laboratory Standards (NCCLS) broth microdilution method, which requires a minimum of 48 h of incubation. In this study, we tested clinical isolates from each of the following species: Candida albicans (20 isolates), C. glabrata (20 isolates),C. krusei (19 isolates), C. tropicalis (19 isolates), and C. parapsilosis (28 isolates). RSA and NCCLS broth dilution methods were used to determine the MICs of amphotericin B, fluconazole, itraconazole, and 5-flucytosine for all 106 isolates. RPMI 1640 medium buffered with morpholinopropanesulfonic acid was used for both methods; however, glucose and inoculum concentrations in the RSA were modified. RSA MICs were determined as the lowest drug concentration that prevented glucose consumption by the organism after 6 h of incubation. MICs obtained from the RSA were compared with those obtained from the NCCLS M-27A method read at 24 and 48 h. MIC pairs were considered in agreement when the difference between the pairs was within 2 twofold dilutions. For the 106 isolates tested, amphotericin B and 5-flucytosine demonstrated the highest agreement in MICs between the two methods (100 and 98%, respectively), whereas fluconazole and itraconazole produced less favorable MIC agreement (63.2 and 61.3%, respectively). The azole MIC differences between the two methods were significantly reduced when lower inocula were used with a prolonged incubation time. This preliminary comparison suggests that this rapid procedure may be a reliable tool for the in vitro determination of MICs of amphotericin B and 5-flucytosine and warrants further evaluation.
机译:我们基于比色反应来监测真菌底物利用率,评估了一种新的微量滴定法用于抗真菌药敏试验。与国家临床实验室标准委员会(NCCLS)肉汤微量稀释法目测测定MIC相比,这种新方法(快速药敏试验[RSA])可在不到8小时的时间内提供定量终点读数,该方法最少需要48小时的培养时间。在这项研究中,我们测试了以下每个物种的临床分离株:白色念珠菌(20个分离株), C。 glabrata (20个分离株), C。 krusei (19个分离株), C。 Tropicalis (19个分离株)和 C。副滑落症(28株)。使用RSA和NCCLS肉汤稀释方法确定所有106个分离株的两性霉素B,氟康唑,伊曲康唑和5-氟胞嘧啶的MIC。两种方法均使用以吗啉代丙烷磺酸缓冲的RPMI 1640培养基。但是,RSA中的葡萄糖和接种物浓度被修改。将RSA MIC确定为在孵育6小时后阻止有机体消耗葡萄糖的最低药物浓度。将从RSA获得的MIC与在24和48小时读取的从NCCLS M-27A方法获得的MIC进行比较。当两对之间的差异在2倍稀释度之内时,认为MIC对是一致的。对于所测试的106株分离物,两性霉素B和5-氟胞嘧啶在两种方法中的MIC中显示出最高的一致性(分别为100%和98%),而氟康唑和伊曲康唑产生的MIC一致性较差(分别为63.2%和61.3%)。当使用较低的接种量并延长孵育时间时,两种方法之间的唑MIC差异显着降低。初步比较表明,该快速程序可能是体外测定两性霉素B和5-氟胞嘧啶MIC的可靠工具,因此有必要进行进一步评估。

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