首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the Etest and Disk Diffusion Methods for Determining Susceptibilities of 235 Bloodstream Isolates of Candida glabrata to Fluconazole and Voriconazole
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Evaluation of the Etest and Disk Diffusion Methods for Determining Susceptibilities of 235 Bloodstream Isolates of Candida glabrata to Fluconazole and Voriconazole

机译:检验和纸片扩散方法测定235种光滑念珠菌血流分离株对氟康唑和伏立康唑的敏感性的评价

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The performances of the Etest and the disk diffusion methods for testing of the susceptibilities of 235 Candida glabrata isolates to fluconazole and voriconazole were compared with that of the National Committee for Clinical Laboratory Standards (NCCLS) approved standard broth microdilution (BMD) method. The NCCLS method used RPMI 1640 broth medium, and MICs were read after incubation for 48 h at 35°C. Etest MICs were determined with RPMI 1640 agar containing 2% glucose (RPG agar) and with Mueller-Hinton agar containing 2% glucose and 0.5 μg of methylene blue per ml (MBE agar) and were read after incubation for 48 h at 35°C. Disk diffusion testing was performed with MBE agar, 25-μg fluconazole disks, and 1-μg voriconazole disks and by incubation at 35°C for 24 h. Overall agreements between the Etest and the BMD MICs obtained with RPG and MBE agars were 91 and 96%, respectively, for fluconazole and 93 and 95%, respectively, for voriconazole. Categorical agreements between the agar-based methods and BMD were 52.3 to 64.7% with fluconazole and 94.8 to 97.4% with voriconazole. The vast majority of the discrepancies by the disk diffusion and Etest methods with fluconazole were minor errors. The agar-based methods performed well in identifying isolates with resistance to fluconazole and decreased susceptibility to voriconazole.
机译:比较了Etest和圆盘扩散法测试235种光滑念珠菌分离株对氟康唑和伏立康唑的敏感性与美国国家临床实验室标准委员会(NCCLS)批准的标准肉汤微量稀释法的比较。 (BMD)方法。 NCCLS方法使用RPMI 1640肉汤培养基,在35°C孵育48小时后读取MIC。 Etest MICs用含2%葡萄糖的RPMI 1640琼脂(RPG琼脂)和含2%葡萄糖和0.5μg每毫升亚甲基蓝的Mueller-Hinton琼脂(MBE琼脂)测定,并在35°C孵育48小时后读取。使用MBE琼脂,25μg氟康唑圆盘和1μg伏立康唑圆盘并在35°C下孵育24 h进行圆盘扩散测试。使用RPG和MBE琼脂获得的Etest和BMD MIC的总体一致性,氟康唑分别为91%和96%,伏立康唑分别为93%和95%。琼脂基方法与BMD之间的分类一致性为:氟康唑为52.3%至64.7%,伏立康唑为94.8%至97.4%。磁盘扩散和Etest方法与氟康唑的绝大多数差异均为小错误。基于琼脂的方法在鉴定对氟康唑有抗性且对伏立康唑敏感性降低的分离株中表现良好。

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