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MALDI Biotyper 分枝杆菌库对非结核分枝杆菌鉴定的评估。

Evaluation of MALDI Biotyper Mycobacteria Library for Identification of Nontuberculous Mycobacteria.

机构信息

Division of Healthcare Quality Promotion, Centers for Disease Control and Preventiongrid.416738.f, Atlanta, Georgia, USA.

Division of Tuberculosis Elimination, Centers for Disease Control and Preventiongrid.416738.f, Atlanta, Georgia, USA.

出版信息

J Clin Microbiol. 2022 Sep 21;60(9):e0021722. doi: 10.1128/jcm.00217-22. Epub 2022 Aug 15.

DOI:10.1128/jcm.00217-22
PMID:35969171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9491183/
Abstract

The Bruker Biotyper matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) platform was assessed on its ability to accurately identify 314 nontuberculous mycobacteria (NTM) representing 73 species. All NTM isolates, representing 183 rapidly growing and 131 slowly growing organisms, were previously identified by Sanger DNA sequencing of the full-length 16S rRNA gene, and region V of the gene. An optimized version of the Bruker bead-beating procedure for protein extraction of NTM isolates was used to ensure high quality spectra for all NTM isolates, including less frequently encountered species. NTM spectra were analyzed using Bruker's research use only, Mycobacteria Library v6.0, supplemented by the MicrobeNet database. Identification of NTM by MALDI-TOF had an accuracy of 94% (296/314). The identification accuracy for rapidly growing mycobacteria was higher at 99% (182/183) than it was for slowly growing mycobacteria at 87% (114/131). While MALDI-TOF performed well against Sanger sequencing of the 16S rRNA gene alone, there were 11 species that required additional sequencing of . Most discrepancies between MALDI-TOF and sequencing results are likely due to underrepresentation of some species in the libraries used. Overall, the results of this study support Bruker's MALDI-TOF platform as an accurate and reliable method for the identification of NTM.

摘要

布鲁克 Biotyper 基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)平台的评估,旨在准确识别 314 株非结核分枝杆菌(NTM),代表 73 个种。所有 NTM 分离株,代表 183 株快速生长和 131 株缓慢生长的生物体,先前通过 Sanger DNA 测序全长 16S rRNA 基因和 基因区域 V 进行鉴定。采用布鲁克优化的珠磨法提取 NTM 分离株的蛋白质,以确保所有 NTM 分离株,包括较少见的物种,都能获得高质量的光谱。使用 Bruker 的研究专用版,Mycobacteria Library v6.0,辅以 MicrobeNet 数据库,对 NTM 光谱进行分析。MALDI-TOF 对 NTM 的鉴定准确率为 94%(296/314)。快速生长分枝杆菌的鉴定准确率为 99%(182/183),高于缓慢生长分枝杆菌的 87%(114/131)。虽然 MALDI-TOF 对 16S rRNA 基因的 Sanger 测序单独使用效果很好,但有 11 个种需要额外测序 基因。MALDI-TOF 与测序结果之间的大多数差异可能是由于所用文库中某些物种的代表性不足所致。总的来说,这项研究的结果支持布鲁克的 MALDI-TOF 平台作为一种准确可靠的非结核分枝杆菌鉴定方法。