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

dc.contributor.author
Rodriguez Temporal, David
dc.contributor.author
Alcaide Fernández de Vega, Fernando
dc.contributor.author
Mareković, Ivana
dc.contributor.author
O’Connor, James Anthony
dc.contributor.author
Gorton, Rebecca
dc.contributor.author
Ingen, Jakko van
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Bossche, An van den
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Héry-Arnaud, Genevieve
dc.contributor.author
Beauruelle, Clémence
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Orth-Höller, Dorothea
dc.contributor.author
Palacios Gutiérrez, Juan José
dc.contributor.author
Tudó i Vilanova, Griselda
dc.contributor.author
Bou, Germán
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Ceyssens, Pieter-Jan
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Garrigó, Montserrat
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González Martín, Julián
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Greub, Gilbert
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Hrabak, Jaroslav
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Ingebretsen, André
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Mediavilla Gradolph, Maria Concepción
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Oviaño, Marina
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Palop, Begoña
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Pranada, Arthur B.
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Quiroga, Lidia
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Ruiz Serrano, Maria Jesús
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Rodríguez Sánchez, Belén
dc.date.issued
2022-02-11T16:34:35Z
dc.date.issued
2022-02-11T16:34:35Z
dc.date.issued
2022-01-24
dc.date.issued
2022-02-11T10:48:33Z
dc.identifier
2045-2322
dc.identifier
https://hdl.handle.net/2445/183115
dc.identifier
35075208
dc.description.abstract
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 Lowenstein-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.
dc.format
7 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Springer Science and Business Media LLC
dc.relation
Reproducció del document publicat a: https://doi.org/10.1038/s41598-022-05315-7
dc.relation
Scientific Reports, 2022, vol 12, num 1
dc.relation
https://doi.org/10.1038/s41598-022-05315-7
dc.rights
cc by (c) Rodriguez Temporal, David et al, 2022
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Fonaments Clínics)
dc.subject
Malalties del pulmó
dc.subject
Bacteris patògens
dc.subject
Pulmonary diseases
dc.subject
Pathogenic bacteria
dc.title
Multicentre study on the reproducibility of MALDI-TOF MS for nontuberculous mycobacteria identification
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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