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Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media

Nontuberculous mycobacteria (NTM) identification is essential for establishing the relevance of the isolate and for appropriate antimicrobial therapy. Traditionally, NTM identification is performed by using Line Probe Assays (LPA), a costly and time-consuming technique requiring trained personnel. M...

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Autores principales: Pastrone, Lisa, Curtoni, Antonio, Criscione, Giulia, Scaiola, Francesca, Bottino, Paolo, Guarrasi, Luisa, Iannaccone, Marco, Timke, Markus, Costa, Cristina, Cavallo, Rossana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9866535/
https://www.ncbi.nlm.nih.gov/pubmed/36677412
http://dx.doi.org/10.3390/microorganisms11010120
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author Pastrone, Lisa
Curtoni, Antonio
Criscione, Giulia
Scaiola, Francesca
Bottino, Paolo
Guarrasi, Luisa
Iannaccone, Marco
Timke, Markus
Costa, Cristina
Cavallo, Rossana
author_facet Pastrone, Lisa
Curtoni, Antonio
Criscione, Giulia
Scaiola, Francesca
Bottino, Paolo
Guarrasi, Luisa
Iannaccone, Marco
Timke, Markus
Costa, Cristina
Cavallo, Rossana
author_sort Pastrone, Lisa
collection PubMed
description Nontuberculous mycobacteria (NTM) identification is essential for establishing the relevance of the isolate and for appropriate antimicrobial therapy. Traditionally, NTM identification is performed by using Line Probe Assays (LPA), a costly and time-consuming technique requiring trained personnel. MALDI-TOF MS is a promising tool for NTM identification, and its use is rapidly growing. We evaluated the newly introduced MBT Mycobacteria kit (MBT) and the MycoEx preparation protocol (Bruker Daltonics, Germany) for NTM MALDI-TOF MS identification using LPA results as a reference. Fifty NTM grown on 7H11 agar and MGIT broth were analyzed with both protocols using the Bruker Microflex(®) LT MALDI-TOF MS (Bruker Daltonics) instrument. MBT and MycoEx provided identification results in 97.0% and 95.0% of the cases, respectively. With both protocols, 100% of the provided results agreed with LPA with no registered mismatch. MBT achieved an elevated number of highly probable identifications (88.0% vs. 83.0%) and a higher reproducibility rate of correct results (86.6% vs. 75.8%) in comparison to MycoEx. This study provides results about MBT performance for liquid and solid media, underlining the strengths and weakness under different conditions. Our results suggest that MALDI-TOF MS could provide a great advantage for timely and cost-saving NTM identification with potential implications for patient outcome.
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spelling pubmed-98665352023-01-22 Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media Pastrone, Lisa Curtoni, Antonio Criscione, Giulia Scaiola, Francesca Bottino, Paolo Guarrasi, Luisa Iannaccone, Marco Timke, Markus Costa, Cristina Cavallo, Rossana Microorganisms Article Nontuberculous mycobacteria (NTM) identification is essential for establishing the relevance of the isolate and for appropriate antimicrobial therapy. Traditionally, NTM identification is performed by using Line Probe Assays (LPA), a costly and time-consuming technique requiring trained personnel. MALDI-TOF MS is a promising tool for NTM identification, and its use is rapidly growing. We evaluated the newly introduced MBT Mycobacteria kit (MBT) and the MycoEx preparation protocol (Bruker Daltonics, Germany) for NTM MALDI-TOF MS identification using LPA results as a reference. Fifty NTM grown on 7H11 agar and MGIT broth were analyzed with both protocols using the Bruker Microflex(®) LT MALDI-TOF MS (Bruker Daltonics) instrument. MBT and MycoEx provided identification results in 97.0% and 95.0% of the cases, respectively. With both protocols, 100% of the provided results agreed with LPA with no registered mismatch. MBT achieved an elevated number of highly probable identifications (88.0% vs. 83.0%) and a higher reproducibility rate of correct results (86.6% vs. 75.8%) in comparison to MycoEx. This study provides results about MBT performance for liquid and solid media, underlining the strengths and weakness under different conditions. Our results suggest that MALDI-TOF MS could provide a great advantage for timely and cost-saving NTM identification with potential implications for patient outcome. MDPI 2023-01-03 /pmc/articles/PMC9866535/ /pubmed/36677412 http://dx.doi.org/10.3390/microorganisms11010120 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pastrone, Lisa
Curtoni, Antonio
Criscione, Giulia
Scaiola, Francesca
Bottino, Paolo
Guarrasi, Luisa
Iannaccone, Marco
Timke, Markus
Costa, Cristina
Cavallo, Rossana
Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media
title Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media
title_full Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media
title_fullStr Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media
title_full_unstemmed Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media
title_short Evaluation of Two Different Preparation Protocols for MALDI-TOF MS Nontuberculous Mycobacteria Identification from Liquid and Solid Media
title_sort evaluation of two different preparation protocols for maldi-tof ms nontuberculous mycobacteria identification from liquid and solid media
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9866535/
https://www.ncbi.nlm.nih.gov/pubmed/36677412
http://dx.doi.org/10.3390/microorganisms11010120
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