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Multicentre study on the reproducibility of MALDI-TOF MS for nontuberculous mycobacteria identification

The ability of MALDI-TOF for the identification of nontuberculous mycobacteria (NTM) has improved recently thanks to updated databases and optimized protein extraction procedures. Few multicentre studies on the reproducibility of MALDI-TOF have been performed so far, none on mycobacteria. The aim of...

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Detalles Bibliográficos
Autores principales: Rodriguez-Temporal, David, Alcaide, Fernando, Mareković, Ivana, O’Connor, James Anthony, Gorton, Rebecca, van Ingen, Jakko, Van den Bossche, An, Héry-Arnaud, Genevieve, Beauruelle, Clémence, Orth-Höller, Dorothea, Palacios-Gutiérrez, Juan-José, Tudó, Griselda, Bou, Germán, Ceyssens, Pieter-Jan, Garrigó, Montserrat, González-Martin, Julià, Greub, Gilbert, Hrabak, Jaroslav, Ingebretsen, André, Mediavilla-Gradolph, Maria Concepción, Oviaño, Marina, Palop, Begoña, Pranada, Arthur B., Quiroga, Lidia, Ruiz-Serrano, Maria Jesús, Rodríguez-Sánchez, Belén
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786948/
https://www.ncbi.nlm.nih.gov/pubmed/35075208
http://dx.doi.org/10.1038/s41598-022-05315-7
Descripción
Sumario:The ability of MALDI-TOF for the identification of nontuberculous mycobacteria (NTM) has improved recently thanks to updated databases and optimized protein extraction procedures. Few multicentre studies on the reproducibility of MALDI-TOF have been performed so far, none on mycobacteria. The aim of this study was to evaluate the reproducibility of MALDI-TOF for the identification of NTM in 15 laboratories in 9 European countries. A total of 98 NTM clinical isolates were grown on Löwenstein-Jensen. Biomass was collected in tubes with water and ethanol, anonymized and sent out to the 15 participating laboratories. Isolates were identified using MALDI Biotyper (Bruker Daltonics). Up to 1330 MALDI-TOF identifications were collected in the study. A score ≥ 1.6 was obtained for 100% of isolates in 5 laboratories (68.2–98.6% in the other). Species-level identification provided by MALDI-TOF was 100% correct in 8 centres and 100% correct to complex-level in 12 laboratories. In most cases, the misidentifications obtained were associated with closely related species. The variability observed for a few isolates could be due to variations in the protein extraction procedure or to MALDI-TOF system status in each centre. In conclusion, MALDI-TOF showed to be a highly reproducible method and suitable for its implementation for NTM identification.