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Standardization of a broth microdilution susceptibility testing method to determine minimum inhibitory concentrations of aquatic bacteria

机译:肉汤微量稀释药敏试验方法的标准化,以确定水生细菌的最低抑菌浓度

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A multiple laboratory study was conducted in accordance with the standards established by the Clinical and Laboratory Standards Institute (CLSI), formerly the National Committee for Clinical Laboratory Standards (NCCLS), for the development of quality control (QC) ranges using dilution antimicrobial susceptibility testing methods for bacterial isolates from aquatic animal species. QC ranges were established for Escherichia coli ATCC 25922 and Aeromonas salmonicida subsp. salmonicida ATCC 33658 when testing at 22, 28 and 35 degrees C (E. coli only) for 10 different antimicrobial agents (ampicillin, enrofloxacin, erythromycin, florfenicol, flumequine, gentamicin, ormetoprim/sulfadimethoxine, oxolinic acid, oxytetracycline and trimethoprim/sulfamethoxazole). Minimum inhibitory concentration (MIC) QC ranges were determined using dry- and frozen-form 96-well plates and cation-adjusted Mueller-Hinton broth. These QC ranges were accepted by the CLSI/NCCLS Subcommittee on Veterinary Antimicrobial Susceptibility Testing in January 2004. This broth microdilution testing method represents the first standardized method for determining MICs of bacterial isolates whose preferred growth temperatures are below 35 degrees C. Methods and QC ranges defined in this study will enable aquatic animal disease researchers to reliably compare quantitative susceptibility testing data between laboratories, and will be used to ensure both precision and inter-laboratory harmonization.
机译:根据临床和实验室标准协会(CLSI)(以前是国家临床实验室标准委员会(NCCLS))建立的标准,进行了多个实验室研究,目的是使用稀释抗微生物药敏试验开发质量控制(QC)范围水生动物细菌分离物的方法。建立了大肠杆菌ATCC 25922和鲑鱼气单胞菌亚种的QC范围。沙门氏菌ATCC 33658,分别在22、28和35摄氏度(仅大肠杆菌)下测试10种不同的抗菌剂(氨苄西林,恩诺沙星,红霉素,氟苯尼考,氟喹明,庆大霉素,奥美普敏/磺胺二甲恶嗪,恶唑酸,氧四环素和甲氧苄氨嘧啶) 。最小抑菌浓度(MIC)QC范围使用干燥和冷冻形式的96孔板以及经阳离子调节的Mueller-Hinton肉汤确定。这些QC范围已于2004年1月被CLSI / NCCLS兽医抗药性敏感性小组委员会接受。这种肉汤微稀释测试方法代表了确定首选生长温度低于35摄氏度的细菌分离株MIC的首个标准化方法。方法和QC范围这项研究中定义的方法将使水生动物疾病研究人员能够可靠地比较实验室之间的定量药敏试验数据,并将用于确保精确度和实验室间的协调性。

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