Multicenter Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry Study for Identification of Clinically Relevant Nocardia spp
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Published:2016-05
Issue:5
Volume:54
Page:1251-1258
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ISSN:0095-1137
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Container-title:Journal of Clinical Microbiology
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language:en
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Short-container-title:J Clin Microbiol
Author:
Blosser Sara J.1, Drake Steven K.2, Andrasko Jennifer L.3, Henderson Christina M.1, Kamboj Kamal4, Antonara Stella1, Mijares Lilia1, Conville Patricia1, Frank Karen M.1, Harrington Susan M.3, Balada-Llasat Joan-Miquel4, Zelazny Adrian M.1
Affiliation:
1. National Institutes of Health, Department of Laboratory Medicine, Microbiology Service, Bethesda, Maryland, USA 2. National Institutes of Health, Critical Care Medicine Department, Bethesda, Maryland, USA 3. Cleveland Clinic, Pathology and Laboratory Medicine Institute, Cleveland, Ohio, USA 4. The Ohio State University Wexner Medical Center, Department of Pathology, Columbus, Ohio, USA
Abstract
ABSTRACT
This multicenter study analyzed
Nocardia
spp., including extraction, spectral acquisition, Bruker matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) identification, and score interpretation, using three
Nocardia
libraries, the Bruker, National Institutes of Health (NIH), and The Ohio State University (OSU) libraries, and compared the results obtained by each center. A standardized study protocol, 150
Nocardia
isolates, and NIH and OSU
Nocardia
MALDI-TOF MS libraries were distributed to three centers. Following standardized culture, extraction, and MALDI-TOF MS analysis, isolates were identified using score cutoffs of ≥2.0 for species/species complex-level identification and ≥1.8 for genus-level identification. Isolates yielding a score of <2.0 underwent a single repeat extraction and analysis. The overall score range for all centers was 1.3 to 2.7 (average, 2.2 ± 0.3), with common species generally producing higher average scores than less common ones. Score categorization and isolate identification demonstrated 86% agreement between centers; 118 of 150 isolates were correctly identified to the species/species complex level by all centers. Nine strains (6.0%) were not identified by any center, and six (4.0%) of these were uncommon species with limited library representation. A categorical score discrepancy among centers occurred for 21 isolates (14.0%). There was an overall benefit of 21.2% from repeat extraction of low-scoring isolates and a center-dependent benefit for duplicate spotting (range, 2 to 8.7%). Finally, supplementation of the Bruker
Nocardia
MALDI-TOF MS library with both the OSU and NIH libraries increased the genus-level and species-level identification by 18.2% and 36.9%, respectively. Overall, this study demonstrates the ability of diverse clinical microbiology laboratories to utilize MALDI-TOF MS for the rapid identification of clinically relevant
Nocardia
spp. and to implement MALDI-TOF MS libraries developed by single laboratories across institutions.
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Reference18 articles.
1. Clinical and Laboratory Features of the
Nocardia
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secA1
Gene Sequences for Identification of
Nocardia
Species 3. Conville PS, Witebsky FB. 2007. Nocardia, Rhodococcus, Gordonia, Actinomadura, Streptomyces, and other aerobic actinomycetes, p 515–542. In Murray PR, Baron EJ, Jorgensen JH, Landry ML, Pfaller MA (ed), Manual of clinical microbiology, 9th ed, vol 1. ASM Press, Washington, DC. 4. Antimicrobial susceptibility patterns of Nocardia asteroides 5. Susceptibility Profiles of Nocardia Isolates Based on Current Taxonomy
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