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

Author:

Farfour E.12,Leto J.3,Barritault M.12,Barberis C.4,Meyer J.1,Dauphin B.3,Le Guern A.-S.5,Leflèche A.6,Badell E.7,Guiso N.7,Leclercq A.8,Le Monnier A.8,Lecuit M.18,Rodriguez-Nava V.9,Bergeron E.9,Raymond J.110,Vimont S.11,Bille E.12,Carbonnelle E.112,Guet-Revillet H.12,Lécuyer H.12,Beretti J.-L.12,Vay C.4,Berche P.12,Ferroni A.12,Nassif X.12,Join-Lambert O.12

Affiliation:

1. Université Paris Descartes, Paris, France

2. Laboratoire de Microbiologie, Hôpital Necker-Enfants Malades, Hôpital Cochin, Hôpital Tenon, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France

3. Andromas SAS, Pépinière Paris Santé Cochin, Paris, France

4. Laboratorio de Bacteriologia, Hospital de Clínicas, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina

5. Laboratoire du Centre Médical de l'Institut Pasteur, National Centre of Reference of Corynebacteria of the Diphtheriae Complex, Institut Pasteur, Paris, France

6. Cellule d'Intervention Biologique d'Urgence, National Centre of Reference of Corynebacteria of the Diphtheriae Complex, Institut Pasteur, Paris, France

7. Molecular Prevention and Therapy of Human Diseases, National Centre of Reference of Corynebacteria of the Diphtheriae Complex, Institut Pasteur, Paris, France

8. Centre National de Référence des Listeria, Institut Pasteur, Paris, France

9. Research Group on Bacterial Opportunistic Pathogens and Environment, UMR5557-Observatoire Français des Nocardioses, Université Claude Bernard Lyon 1, Lyon, France

10. Laboratoire de Bactériologie, Hôpital Cochin, Hôpital Tenon, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France

11. Laboratoire de Bactériologie, Hôpital Tenon, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France

12. Laboratoire de Microbiologie, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France

Abstract

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.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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