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

Author:

Body Barbara A.1,Beard Melodie A.1,Slechta E. Susan2,Hanson Kimberly E.23,Barker Adam P.23,Babady N. Esther4ORCID,McMillen Tracy4,Tang Yi-Wei45ORCID,Brown-Elliott Barbara A.6,Iakhiaeva Elena6,Vasireddy Ravikiran6,Vasireddy Sruthi6,Smith Terry6,Wallace Richard J.6,Turner S.7,Curtis L.7,Butler-Wu Susan7,Rychert Jenna2

Affiliation:

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

2. ARUP Laboratories, Salt Lake City, Utah, USA

3. University of Utah, Salt Lake City, Utah, USA

4. Memorial Sloan Kettering Cancer Center, New York, New York, USA

5. Weill Medical College of Cornell University, New York, New York, USA

6. University of Texas Health Science Center, Tyler, Texas, USA

7. University of Washington Medical Center, Seattle, Washington, USA

Abstract

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 Mycobacterium and Nocardia 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 M. tuberculosis , M. abscessus , and M. avium complexes and within the M. fortuitum and M. mucogenicum groups could be differentiated. Among the 312 Nocardia 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 N. nova and N. transvalensis 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 Mycobacterium and Nocardia 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 Nocardia in clinical practice.

Funder

BioMerieux

HHS | NIH | National Cancer Institute

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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