Washington University in St. Louis School of Medicinegrid.471404.2, St. Louis, Missouri, USA.
J Clin Microbiol. 2022 May 18;60(5):e0300720. doi: 10.1128/JCM.03007-20. Epub 2022 Feb 2.
Disk diffusion is a slow but reliable standard method for measuring the antimicrobial susceptibility of microorganisms. Our objective was to improve the turnaround time for this method by reducing the time that cultures are incubated before setting up disk diffusion testing. For initial method development, clinical isolates ( = 13) and quality control strains ( = 8) of bacteria were inoculated on blood agar and were incubated at 35°C for either 6, 10, or 24 h before performing disk diffusion testing, in triplicate, using a panel of clinically appropriate antimicrobial agents. Disk diffusion zone sizes were interpreted using Clinical and Laboratory Standards Institute (CLSI) guidelines. Compared to standard 24 h of incubation, early 6-h growth had 1.3% major errors (MEs) and 1.9% very major errors (VMEs), whereas 10-h growth yielded 0.7% MEs and no VMEs. Categorical agreement with standard incubation was similar for both 6 h (96.7%) and 10 h (96.7%) growth. Inhibitory zone size from 6 h ( = 0.98) and 10 h ( = 0.99) growth correlated well with results from standard conditions. Based on these results, we performed disk diffusion under optimized conditions (6 h growth), using 100 additional clinical isolates, demonstrating a high level of categorical agreement (917 of 950 measurements [96.5%]; 95% confidence interval [CI], 95.2 to 97.5%), as well as no VMEs or MEs. Using early growth for disk diffusion testing is a simple and accurate method for susceptibility testing that can reduce time to results by as much as 18 h, compared to standard incubation, with no additional supply costs or equipment/instrumentation.
纸片扩散法是一种缓慢但可靠的标准方法,用于测量微生物的抗菌药敏性。我们的目标是通过减少培养物孵育时间来提高该方法的周转时间,从而减少设置纸片扩散试验之前的时间。在初始方法开发过程中,将临床分离株( = 13)和细菌质量控制菌株( = 8)接种在血琼脂上,并在 35°C 下孵育 6、10 或 24 小时,然后使用一组临床相关的抗菌药物进行三次重复的纸片扩散试验。使用临床和实验室标准协会 (CLSI) 指南解释纸片扩散区大小。与标准的 24 小时孵育相比,早期的 6 小时生长有 1.3%的主要错误(ME)和 1.9%的非常大错误(VME),而 10 小时生长则有 0.7%的 ME 和没有 VME。两种生长方式(6 小时和 10 小时)与标准孵育的分类一致性相似。6 小时( = 0.98)和 10 小时( = 0.99)生长的抑菌圈大小与标准条件的结果相关性良好。基于这些结果,我们使用 100 个额外的临床分离株在优化条件(6 小时生长)下进行纸片扩散,结果显示高度的分类一致性(950 次测量中有 917 次[96.5%];95%置信区间[CI],95.2 至 97.5%),没有 VME 或 ME。使用早期生长进行纸片扩散试验是一种简单而准确的药敏试验方法,与标准孵育相比,可将结果时间缩短多达 18 小时,而且没有额外的供应成本或设备/仪器。