Wattal C, Oberoi J K
Department of Clinical Microbiology & Immunology, Sir Ganga Ram Hospital (SGRH), Rajinder Nagar, New Delhi, 110060, India.
Eur J Clin Microbiol Infect Dis. 2016 Jan;35(1):75-82. doi: 10.1007/s10096-015-2510-y. Epub 2015 Nov 19.
The study addresses the utility of Matrix Assisted Laser Desorption/Ionisation Time-Of-Flight mass spectrometry (MALDI-TOF MS) using VITEK MS and the VITEK 2 antimicrobial susceptibility testing (AST) system for direct identification (ID) and timely AST from positive blood culture bottles using a lysis-filtration method (LFM). Between July and December 2014, a total of 140 non-duplicate mono-microbial blood cultures were processed. An aliquot of positive blood culture broth was incubated with lysis buffer before the bacteria were filtered and washed. Micro-organisms recovered from the filter were first identified using VITEK MS and its suspension was used for direct AST by VITEK 2 once the ID was known. Direct ID and AST results were compared with classical methods using solid growth. Out of the 140 bottles tested, VITEK MS resulted in 70.7 % correct identification to the genus and/ or species level. For the 103 bottles where identification was possible, there was agreement in 97 samples (94.17 %) with classical culture. Compared to the routine method, the direct AST resulted in category agreement in 860 (96.5 %) of 891 bacteria-antimicrobial agent combinations tested. The results of direct ID and AST were available 16.1 hours before those of the standard approach on average. The combined use of VITEK MS and VITEK 2 directly on samples from positive blood culture bottles using a LFM technique can result in rapid and reliable ID and AST results in blood stream infections to result in early institution of targeted treatment. The combination of LFM and AST using VITEK 2 was found to expedite AST more reliably.
本研究探讨了使用VITEK MS基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)和VITEK 2抗菌药物敏感性试验(AST)系统,通过裂解过滤法(LFM)对阳性血培养瓶进行直接鉴定(ID)和及时AST的效用。在2014年7月至12月期间,共处理了140份非重复的单微生物血培养样本。在过滤和洗涤细菌之前,将一份阳性血培养肉汤与裂解缓冲液一起孵育。从滤膜上回收的微生物首先使用VITEK MS进行鉴定,一旦获得鉴定结果,其悬浮液就用于VITEK 2直接进行AST。将直接ID和AST结果与使用固体培养的经典方法进行比较。在测试的140个培养瓶中,VITEK MS在属和/或种水平上的正确鉴定率为70.7%。对于103个可以进行鉴定的培养瓶,有97个样本(94.17%)与经典培养结果一致。与常规方法相比,直接AST在891种细菌-抗菌药物组合测试中有860种(96.5%)类别相符。直接ID和AST结果平均比标准方法提前16.1小时获得。使用LFM技术将VITEK MS和VITEK 2直接联合用于阳性血培养瓶样本,可在血流感染中快速可靠地获得ID和AST结果,从而尽早开始针对性治疗。发现LFM与使用VITEK 2的AST相结合能更可靠地加快AST检测。