Validation of a New Web Application for Identification of Fungi by Use of Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

Author:

Normand A. C.1,Becker P.2,Gabriel F.3,Cassagne C.1,Accoceberry I.3,Gari-Toussaint M.4,Hasseine L.4,De Geyter D.5,Pierard D.5,Surmont I.6,Djenad F.1,Donnadieu J. L.7,Piarroux M.8,Ranque S.1ORCID,Hendrickx M.2,Piarroux R.1

Affiliation:

1. Laboratoire de Parasitologie-Mycologie, CHU Timone, Aix-Marseille Université, Marseille, France

2. Service of Mycology and Aerobiology, BCCM/IHEM Fungal Collection, Scientific Institute of Public Health, Brussels, Belgium

3. Centre Hospitalier Universitaire de Bordeaux, Laboratoire de Parasitologie-Mycologie, Bordeaux, France

4. Laboratoire de Parasitologie-Mycologie, CHU l'Archet 2, Nice, France

5. Department Microbiology and Infection Control, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, Belgium

6. Department of Microbiology, AZ Sint Jan, Bruges-Oostende, Belgium

7. Passerelle, Montpellier, France

8. Centre d'Epidémiologie et de Santé Publique des Armées, Marseille, France

Abstract

ABSTRACT Matrix-assisted laser desorption ionization–time of flight (MALDI-TOF) mass spectrometry has emerged as a reliable technique to identify molds involved in human diseases, including dermatophytes, provided that exhaustive reference databases are available. This study assessed an online identification application based on original algorithms and an extensive in-house reference database comprising 11,851 spectra (938 fungal species and 246 fungal genera). Validation criteria were established using an initial panel of 422 molds, including dermatophytes, previously identified via DNA sequencing (126 species). The application was further assessed using a separate panel of 501 cultured clinical isolates (88 mold taxa including dermatophytes) derived from five hospital laboratories. A total of 438 (87.35%) isolates were correctly identified at the species level, while 26 (5.22%) were assigned to the correct genus but the wrong species and 37 (7.43%) were not identified, since the defined threshold of 20 was not reached. The use of the Bruker Daltonics database included in the MALDI Biotyper software resulted in a much higher rate of unidentified isolates (39.76 and 74.30% using the score thresholds 1.7 and 2.0, respectively). Moreover, the identification delay of the online application remained compatible with real-time online queries (0.15 s per spectrum), and the application was faster than identifications using the MALDI Biotyper software. This is the first study to assess an online identification system based on MALDI-TOF spectrum analysis. We have successfully applied this approach to identify molds, including dermatophytes, for which diversity is insufficiently represented in commercial databases. This free-access application is available to medical mycologists to improve fungal identification.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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