FASTinov, S.A., Matosinhos, Portugal.
Division of Microbiology, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal.
Eur J Clin Microbiol Infect Dis. 2020 Oct;39(10):1907-1914. doi: 10.1007/s10096-020-03926-4. Epub 2020 Jun 2.
The urgent need for rapid antimicrobial susceptibility is broadly apparent from government reports to the lay press. Accordingly, we developed a flow-cytometry assay (FCM) for evaluating ceftolozane-tazobactam (C/T) susceptibility directly on blood cultures (BC) requiring < 2 h from flag positivity to report. The protocol was optimized with C/T-susceptible and C/T-resistant gram-negative bacilli inoculated in BC aerobic bottles (Becton-Dickinson, USA), and afterward optimized for different C/T concentrations (1/4, 2/4, 4/4, and 8/4 mg/L) for 1 h incubation (37 °C), followed by FCM and software analysis. Fluorescent membrane permeability and membrane potential dyes were comparatively used to detect early cell lesions using the CytoFLEX cytometer (Beckman-Coulter, USA). Repeatability, reproducibility, and stability of the assay up to 48 h after BC positivity were determined. Internal validation was performed in spiked BC bottles with 130 Enterobacterales and 32 Pseudomonas aeruginosa isolates from Porto University (Portugal), including 13 ATCC isolates. Additionally, 64 gram-negative bacilli recovered from positive BC at Ramon y Cajal Hospital (Madrid, Spain) were tested. Categorical agreement (CA) and analytical errors were calculated comparing FCM with broth microdilution results. Only the membrane potential dyes clearly distinguished CT-susceptible and CT-resistant isolates. Excellent repeatability, reproducibility, and inter-method concordance was observed. Overall, CA was 99.1% using EUCAST criteria with 2 major errors and 98.7% with CLSI criteria with 2 major and 1 minor errors. A new, accurate, and ultra-rapid FCM (< 2 h) for testing C/T susceptibility gave accurate results and would expand current FCM antimicrobial susceptibility assay.
从政府向大众媒体发布的报告中广泛可见,迅速进行药敏试验的需求非常迫切。因此,我们开发了一种流式细胞术检测方法(FCM),可直接在血培养物(BC)上评估头孢他啶-他唑巴坦(C/T)的药敏性,从阳性报警到报告结果耗时不到 2 小时。该方案使用 C/T 敏感和 C/T 耐药的革兰氏阴性杆菌在 BC 需氧瓶(美国 Becton-Dickinson)中进行了优化,然后针对不同的 C/T 浓度(1/4、2/4、4/4 和 8/4mg/L)进行了 1 小时孵育(37°C)的优化,随后进行 FCM 和软件分析。使用 CytoFLEX 细胞仪(美国贝克曼库尔特)比较使用荧光膜通透性和膜电位染料检测早期细胞损伤。确定了 BC 阳性后 48 小时内该检测方法的重复性、重现性和稳定性。在波尔图大学(葡萄牙)的 130 株肠杆菌科和 32 株铜绿假单胞菌的 BC 加标瓶中进行了内部验证,包括 13 株 ATCC 分离株。此外,还对马德里 Ramon y Cajal 医院(西班牙)从阳性 BC 中分离的 64 株革兰氏阴性杆菌进行了检测。通过比较 FCM 与肉汤微量稀释结果,计算了分类一致性(CA)和分析误差。只有膜电位染料才能清楚地区分 CT 敏感和 CT 耐药的分离株。观察到极好的重复性、重现性和方法间一致性。总体而言,使用 EUCAST 标准的 CA 为 99.1%,有 2 个主要错误,使用 CLSI 标准的 CA 为 98.7%,有 2 个主要错误和 1 个次要错误。一种新的、准确的、超快速(<2 小时)的 FCM 检测 C/T 药敏性的方法提供了准确的结果,并将扩大当前的 FCM 抗菌药物敏感性检测方法。