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评价 Vitek MS v3.0 基质辅助激光解吸电离飞行时间质谱系统对分枝杆菌和诺卡氏菌属种的鉴定能力。

Evaluation of the Vitek MS v3.0 Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry System for Identification of Mycobacterium and Nocardia Species.

机构信息

Department of Esoteric Microbiology, Lab. Corp. of America Holdings, Burlington, North Carolina, USA.

ARUP Laboratories, Salt Lake City, Utah, USA.

出版信息

J Clin Microbiol. 2018 May 25;56(6). doi: 10.1128/JCM.00237-18. Print 2018 Jun.

Abstract

This multicenter study was designed to assess the accuracy and reproducibility of the Vitek MS v3.0 matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry system for identification of and species compared to DNA sequencing. A total of 963 clinical isolates representing 51 taxa were evaluated. In all, 663 isolates were correctly identified to the species level (69%), with another 231 (24%) correctly identified to the complex or group level. Fifty-five isolates (6%) could not be identified despite repeat testing. All of the tuberculous mycobacteria (45/45; 100%) and most of the nontuberculous mycobacteria (569/606; 94%) were correctly identified at least to the group or complex level. However, not all species or subspecies within the , , and complexes and within the and groups could be differentiated. Among the 312 isolates tested, 236 (76%) were correctly identified to the species level, with an additional 44 (14%) correctly identified to the complex level. Species within the and complexes could not always be differentiated. Eleven percent of the isolates (103/963) underwent repeat testing in order to get a final result. Identification of a representative set of and species was highly reproducible, with 297 of 300 (99%) replicates correctly identified using multiple kit lots, instruments, analysts, and sites. These findings demonstrate that the system is robust and has utility for the routine identification of mycobacteria and in clinical practice.

摘要

这项多中心研究旨在评估 Vitek MS v3.0 基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱系统用于鉴定 和 种与 DNA 测序相比的准确性和可重复性。共评估了代表 51 个分类群的 963 株临床分离株。在所有情况下,663 株分离株被正确鉴定到种水平(69%),另有 231 株(24%)被正确鉴定到复合体或组水平。尽管进行了重复测试,但仍有 55 株(6%)无法鉴定。所有结核分枝杆菌(45/45;100%)和大多数非结核分枝杆菌(569/606;94%)至少被正确鉴定到组或复合体水平。然而,并非所有 、 、 和 复合体以及 和 组内的种或亚种都可以区分。在测试的 312 株 中,236 株(76%)被正确鉴定到种水平,另有 44 株(14%)被正确鉴定到复合体水平。 复合体中的种并不总是可以区分。为了得到最终结果,11%的分离株(103/963)进行了重复测试。一组有代表性的 和 种的鉴定具有高度可重复性,使用多个试剂盒批次、仪器、分析人员和地点,正确鉴定了 300 个中的 297 个(99%)重复。这些发现表明该系统稳健且具有在临床实践中用于常规鉴定分枝杆菌和 的用途。

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