Evaluation of ID Fungi Plates Medium for Identification of Molds by MALDI Biotyper.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
23 04 2020
Historique:
received: 21 10 2019
accepted: 06 02 2020
pubmed: 14 2 2020
medline: 24 6 2021
entrez: 14 2 2020
Statut: epublish

Résumé

MALDI-TOF mass spectrometry (MS) identification of pathogenic filamentous fungi is often impaired by difficulties in harvesting hyphae embedded in the medium and long extraction protocols. The ID Fungi Plate (IDFP) is a novel culture method developed to address such difficulties and improve the identification of filamentous fungi by MALDI-TOF MS. We cultured 64 strains and 11 clinical samples on IDFP, Sabouraud agar-chloramphenicol (SAB), and ChromID Candida agar (CAN2). We then compared the three media for growth, ease of harvest, amount of material picked, and MALDI-TOF identification scores after either rapid direct transfer (DT) or a long ethanol-acetonitrile (EA) extraction protocol. Antifungal susceptibility testing and microscopic morphology after subculture on SAB and IDFP were also compared for ten molds. Growth rates and morphological aspects were similar for the three media. With IDFP, harvesting of fungal material for the extraction procedure was rapid and easy in 92.4% of cases, whereas it was tedious on SAB or CAN2 in 65.2% and 80.3% of cases, respectively. The proportion of scores above 1.7 (defined as acceptable identification) were comparable for both extraction protocols using IDFP (

Identifiants

pubmed: 32051262
pii: JCM.01687-19
doi: 10.1128/JCM.01687-19
pmc: PMC7180245
pii:
doi:

Substances chimiques

Culture Media 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2020 American Society for Microbiology.

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Auteurs

Marie Gladys Robert (MG)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France mrobert2@chu-grenoble.fr mcornet@chu-grenoble.fr.
Team Host-Pathogen Interactions and Immunity to Infection, Institute for Advanced Biosciences, INSERM U1209, CNRS UMR5309, Université Grenoble Alpes, Grenoble, France.

Charlotte Romero (C)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France.

Céline Dard (C)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France.
Team Host-Pathogen Interactions and Immunity to Infection, Institute for Advanced Biosciences, INSERM U1209, CNRS UMR5309, Université Grenoble Alpes, Grenoble, France.

Cécile Garnaud (C)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France.
Université Grenoble Alpes, CNRS, Grenoble INP, CHU Grenoble Alpes, TIMC, Grenoble, France.

Odile Cognet (O)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France.

Thomas Girard (T)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France.

Tahinamandranto Rasamoelina (T)

Université Grenoble Alpes, CNRS, Grenoble INP, CHU Grenoble Alpes, TIMC, Grenoble, France.
Centre d'Infectiologie Charles Mérieux, Ankatso, Université d'Antananarivo, Antananarivo, Madagascar.

Muriel Cornet (M)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France mrobert2@chu-grenoble.fr mcornet@chu-grenoble.fr.
Université Grenoble Alpes, CNRS, Grenoble INP, CHU Grenoble Alpes, TIMC, Grenoble, France.

Danièle Maubon (D)

Laboratoire de Parasitologie et Mycologie, CHU Grenoble Alpes, Grenoble, France.
Université Grenoble Alpes, CNRS, Grenoble INP, CHU Grenoble Alpes, TIMC, Grenoble, France.

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Classifications MeSH