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Evaluation of the Andromas Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry System for Identification of Aerobically Growing Gram-Positive Bacilli

Authors :
Olivier Join-Lambert
M. Barritault
Anne Leflèche
Xavier Nassif
Carlos Vay
Emmanuelle Bergeron
S. Vimont
Jean-Luc Beretti
A.-S. Le Guern
Brunhilde Dauphin
Josette Raymond
Hélène Guet-Revillet
Emmanuelle Bille
Marc Lecuit
A. Le Monnier
Claudia Barberis
Alexandre Leclercq
E. Farfour
Veronica Rodriguez-Nava
E. Carbonnelle
Edgar Badell
Julie Meyer
Hervé Lécuyer
Nicole Guiso
Patrick Berche
J. Leto
Agnès Ferroni
Laboratoire d'Ecologie Microbienne - UMR 5557 (LEM)
Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Ecole Nationale Vétérinaire de Lyon (ENVL)
Université de Lyon-Université de Lyon-Ecole Nationale Vétérinaire de Lyon (ENVL)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)
Source :
Journal of Clinical Microbiology, Journal of Clinical Microbiology, American Society for Microbiology, 2012, 50 (8), pp.2702-2707. ⟨10.1128/JCM.00368-12⟩
Publication Year :
2012
Publisher :
American Society for Microbiology, 2012.

Abstract

Matrix-associated laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) is a rapid and simple microbial identification method. Previous reports using the Biotyper system suggested that this technique requires a preliminary extraction step to identify Gram-positive rods (GPRs), a technical issue that may limit the routine use of this technique to identify pathogenic GPRs in the clinical setting. We tested the accuracy of the MALDI-TOF MS Andromas strategy to identify a set of 659 GPR isolates representing 16 bacterial genera and 72 species by the direct colony method. This bacterial collection included 40 C. diphtheriae , 13 C. pseudotuberculosis , 19 C. ulcerans , and 270 other Corynebacterium isolates, 32 L. monocytogenes and 24 other Listeria isolates, 46 Nocardia , 75 Actinomyces , 18 Actinobaculum , 11 Propionibacterium acnes , 18 Propionibacterium avidum , 30 Lactobacillus , 21 Bacillus , 2 Rhodococcus equi , 2 Erysipelothrix rhusiopathiae , and 38 other GPR isolates, all identified by reference techniques. Totals of 98.5% and 1.2% of non- Listeria GPR isolates were identified to the species or genus level, respectively. Except for L. grayi isolates that were identified to the species level, all other Listeria isolates were identified to the genus level because of highly similar spectra. These data demonstrate that rapid identification of pathogenic GPRs can be obtained without an extraction step by MALDI-TOF mass spectrometry.

Details

ISSN :
1098660X and 00951137
Volume :
50
Database :
OpenAIRE
Journal :
Journal of Clinical Microbiology
Accession number :
edsair.doi.dedup.....2dd20b31f6c37d1fb9f9807a6e403481
Full Text :
https://doi.org/10.1128/jcm.00368-12