Multicentre study on the reproducibility of MALDI-TOF MS for nontuberculous mycobacteria identification
Rodriguez-Temporal, D.; Alcaide, F.; Mareković, I.; O’Connor, J.A.; Gorton, R.; van Ingen, J.; Van den Bossche, A.; Héry-Arnaud, G.; Beauruelle, C.; Orth-Höller, D.; Palacios-Gutiérrez, J.-J.; Tudó, G.; Bou Arévalo, Germán; Ceyssens, P.-J.; Garrigó, M.; González-Martin, J.; Greub, G.; Hrabak, J.; Ingebretsen, A.; Mediavilla-Gradolph, M.C.; Oviaño García, Marina; Palop, B.; Pranada, A.B.; Quiroga, L.; Ruiz-Serrano, M.J.; Rodríguez-Sánchez, B.
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Fecha de publicación
2022Título de revista
Scientific Reports
Tipo de contenido
Journal Article
Resumen
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.
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