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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the Bruker Biotyper and Vitek MS Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry Systems for Identification of Nonfermenting Gram-Negative Bacilli Isolated from Cultures from Cystic Fibrosis Patients
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Evaluation of the Bruker Biotyper and Vitek MS Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry Systems for Identification of Nonfermenting Gram-Negative Bacilli Isolated from Cultures from Cystic Fibrosis Patients

机译:布鲁克生物鉴定仪和Vitek MS基质辅助激光解吸电离的飞行时间质谱系统的鉴定,用于鉴定从囊性纤维化患者培养物中分离出来的非发酵革兰氏阴性杆菌

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The Bruker Biotyper and Vitek MS matrix-assisted laser desorption ionization–time of flight (MALDI-TOF) mass spectrometry (MS) instruments were evaluated for the identification of nonfermenting Gram-negative bacilli (NFGNB) by a blinded comparison to conventional biochemical or molecular methods. Two hundred NFGNB that were recovered from cultures from cystic fibrosis patients in the University of Iowa Health Care (UIHC) Microbiology Laboratory between 1 January 2006 and 31 October 2010 were sent to Mayo Clinic for analysis with the Bruker Biotyper (software version 3.0) and to bioMérieux for testing with Vitek MS (SARAMIS database version 3.62). If two attempts at direct colony testing failed to provide an acceptable MALDI-TOF identification, an extraction procedure was performed. The MS identifications from both of these systems were provided to UIHC for comparison to the biochemical or molecular identification that had been reported in the patient record. Isolates with discordant results were analyzed by 16S rRNA gene sequencing at UIHC. After discrepancy testing, the Bruker Biotyper result agreed with the biochemical or molecular method, with 72.5% of isolates to the species level, 5.5% to the complex level, and 19% to the genus level (3% not identified). The level of agreement for Vitek MS was 80% species, 3.5% complex, 6% genus, and 3.5% family (7% not identified). Both MS systems provided rapid (≤3 min per isolate) and reliable identifications. The agreement of combined species/complex/genus-level identification with the reference method was higher for the Bruker Biotyper (97% versus 89.5%, P = 0.004) but required an extraction step more often. Species-level agreement with the reference method was similar for both MS systems (72.5% and 80%, P = 0.099).
机译:通过与常规生化或分子生物学方法进行盲目比较,评估了布鲁克生物识别仪和Vitek MS基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱(MS)仪器,以鉴定非发酵性革兰氏阴性杆菌(NFGNB)。方法。 2006年1月1日至2010年10月31日之间,在爱荷华大学医疗保健(UIHC)微生物学实验室从囊性纤维化患者的培养物中回收的200 NFGNB被送至Mayo Clinic进行分析,使用Bruker Biotyper(软件版本3.0)和bioMérieux用于使用Vitek MS(SARAMIS数据库版本3.62)进行测试。如果两次直接菌落测试的尝试未能提供可接受的MALDI-TOF鉴定,则执行提取程序。来自这两个系统的MS鉴定均提供给UIHC,用于与患者记录中报告的生化或分子鉴定进行比较。通过UIHC的16S rRNA基因测序分析了结果不一致的分离株。经过差异测试后,Bruker Biotyper的结果与生化或分子方法相符,其中72.5%的分离物达到物种水平,5.5%的复杂水平,19%的属水平(3%未鉴定)。 Vitek MS的协议水平为80%物种,3.5%复合物,6%属和3.5%家族(未确定7%)。两种质谱系统都能提供快速(每个分离株≤3分钟)和可靠的鉴定结果。对于Bruker Biotyper,与参考方法相结合的物种/复合物/属水平鉴定的一致性更高(97%比89.5%, P = 0.004),但需要更频繁的提取步骤。在两种MS系统中,参考方法的物种水平一致性都相似(72.5%和80%, P = 0.099)。

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