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MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B

Disseminated fusariosis is treated with amphotericin B and voriconazole. To determine adequate therapy, the minimal inhibitory concentration (MIC) is used. However, MIC analysis is based on visual observation and requires a long period of fungal incubation. The measure of the minimal profile change...

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Autores principales: Grizante Barião, Patrícia Helena, Cayún, Yasna, Sepúlveda, Marcela, Tonani, Ludmilla, Gonçalves de Almeida, Otavio Guilherme, Cornejo, Pablo, Dias, Nathalia, Santos, Cledir, von Zeska Kress, Marcia Regina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10383446/
https://www.ncbi.nlm.nih.gov/pubmed/37513006
http://dx.doi.org/10.3390/microorganisms11071834
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author Grizante Barião, Patrícia Helena
Cayún, Yasna
Sepúlveda, Marcela
Tonani, Ludmilla
Gonçalves de Almeida, Otavio Guilherme
Cornejo, Pablo
Dias, Nathalia
Santos, Cledir
von Zeska Kress, Marcia Regina
author_facet Grizante Barião, Patrícia Helena
Cayún, Yasna
Sepúlveda, Marcela
Tonani, Ludmilla
Gonçalves de Almeida, Otavio Guilherme
Cornejo, Pablo
Dias, Nathalia
Santos, Cledir
von Zeska Kress, Marcia Regina
author_sort Grizante Barião, Patrícia Helena
collection PubMed
description Disseminated fusariosis is treated with amphotericin B and voriconazole. To determine adequate therapy, the minimal inhibitory concentration (MIC) is used. However, MIC analysis is based on visual observation and requires a long period of fungal incubation. The measure of the minimal profile change concentration (MPCC) using MALDI-TOF MS is a quick spectral method that has presented good results in determining the antimicrobial resistance of yeasts. However, there is a lack of information on filamentous fungi. In the present work, 13 Fusarium spp. clinical isolates and two reference strains were used. MIC was obtained according to the M38-A2 protocol of the Clinical Laboratory Standards Institute, while MPPC was obtained following the initial steps of the M38-A2 protocol. Both Biotyper and the Rstudio environment were used to analyze mass spectra. For some fungal strains, the data obtained from the software MALDI Biotyper Compass 4.1 led to fuzzy heatmaps resulting in difficult interpretation, while heatmaps obtained using Rstudio tools generated better MPCC resolutions. Herein, 86.6% of the AMB MPCC values were highly correlated with the gold-standard AMB MIC. MALDI-TOF MS is a prominent tool used to determine MPCCs quicker, cost-effectively, and more accurately for Fusarium spp. strains. However, better statistical analyses could help measure the technique’s limit detection.
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spelling pubmed-103834462023-07-30 MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B Grizante Barião, Patrícia Helena Cayún, Yasna Sepúlveda, Marcela Tonani, Ludmilla Gonçalves de Almeida, Otavio Guilherme Cornejo, Pablo Dias, Nathalia Santos, Cledir von Zeska Kress, Marcia Regina Microorganisms Article Disseminated fusariosis is treated with amphotericin B and voriconazole. To determine adequate therapy, the minimal inhibitory concentration (MIC) is used. However, MIC analysis is based on visual observation and requires a long period of fungal incubation. The measure of the minimal profile change concentration (MPCC) using MALDI-TOF MS is a quick spectral method that has presented good results in determining the antimicrobial resistance of yeasts. However, there is a lack of information on filamentous fungi. In the present work, 13 Fusarium spp. clinical isolates and two reference strains were used. MIC was obtained according to the M38-A2 protocol of the Clinical Laboratory Standards Institute, while MPPC was obtained following the initial steps of the M38-A2 protocol. Both Biotyper and the Rstudio environment were used to analyze mass spectra. For some fungal strains, the data obtained from the software MALDI Biotyper Compass 4.1 led to fuzzy heatmaps resulting in difficult interpretation, while heatmaps obtained using Rstudio tools generated better MPCC resolutions. Herein, 86.6% of the AMB MPCC values were highly correlated with the gold-standard AMB MIC. MALDI-TOF MS is a prominent tool used to determine MPCCs quicker, cost-effectively, and more accurately for Fusarium spp. strains. However, better statistical analyses could help measure the technique’s limit detection. MDPI 2023-07-18 /pmc/articles/PMC10383446/ /pubmed/37513006 http://dx.doi.org/10.3390/microorganisms11071834 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
Grizante Barião, Patrícia Helena
Cayún, Yasna
Sepúlveda, Marcela
Tonani, Ludmilla
Gonçalves de Almeida, Otavio Guilherme
Cornejo, Pablo
Dias, Nathalia
Santos, Cledir
von Zeska Kress, Marcia Regina
MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B
title MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B
title_full MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B
title_fullStr MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B
title_full_unstemmed MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B
title_short MALDI-TOF MS: A Quick Method to Detect the Susceptibility of Fusarium spp. Clinical Isolates to Amphotericin B
title_sort maldi-tof ms: a quick method to detect the susceptibility of fusarium spp. clinical isolates to amphotericin b
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10383446/
https://www.ncbi.nlm.nih.gov/pubmed/37513006
http://dx.doi.org/10.3390/microorganisms11071834
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