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Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis
We present an in vitro susceptibility assay for Madurella mycetomatis hyphae using resazurin for endpoint reading. Using this assay, reproducible MICs were obtained for amphotericin B, itraconazole, voriconazole, posaconazole, terbinafine, and micafungin. Results were comparable with those of a 2,3-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092548/ https://www.ncbi.nlm.nih.gov/pubmed/33318015 http://dx.doi.org/10.1128/AAC.01338-20 |
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author | Abd Algaffar, S. O. Verbon, A. van de Sande, W. W. J. Khalid, S. A. |
author_facet | Abd Algaffar, S. O. Verbon, A. van de Sande, W. W. J. Khalid, S. A. |
author_sort | Abd Algaffar, S. O. |
collection | PubMed |
description | We present an in vitro susceptibility assay for Madurella mycetomatis hyphae using resazurin for endpoint reading. Using this assay, reproducible MICs were obtained for amphotericin B, itraconazole, voriconazole, posaconazole, terbinafine, and micafungin. Results were comparable with those of a 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide salt (XTT)-based susceptibility assay. The lowest MICs were obtained for itraconazole and posaconazole (MIC(50), 0.016 µg/ml) followed by voriconazole (MIC(50), 0.063 µg/ml). Amphotericin B, micafungin, and terbinafine appeared much less effective. |
format | Online Article Text |
id | pubmed-8092548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80925482021-05-05 Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis Abd Algaffar, S. O. Verbon, A. van de Sande, W. W. J. Khalid, S. A. Antimicrob Agents Chemother Susceptibility We present an in vitro susceptibility assay for Madurella mycetomatis hyphae using resazurin for endpoint reading. Using this assay, reproducible MICs were obtained for amphotericin B, itraconazole, voriconazole, posaconazole, terbinafine, and micafungin. Results were comparable with those of a 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide salt (XTT)-based susceptibility assay. The lowest MICs were obtained for itraconazole and posaconazole (MIC(50), 0.016 µg/ml) followed by voriconazole (MIC(50), 0.063 µg/ml). Amphotericin B, micafungin, and terbinafine appeared much less effective. American Society for Microbiology 2021-02-17 /pmc/articles/PMC8092548/ /pubmed/33318015 http://dx.doi.org/10.1128/AAC.01338-20 Text en Copyright © 2021 Abd Algaffar et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Susceptibility Abd Algaffar, S. O. Verbon, A. van de Sande, W. W. J. Khalid, S. A. Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis |
title | Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis |
title_full | Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis |
title_fullStr | Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis |
title_full_unstemmed | Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis |
title_short | Development and Validation of an In Vitro Resazurin-Based Susceptibility Assay against Madurella mycetomatis |
title_sort | development and validation of an in vitro resazurin-based susceptibility assay against madurella mycetomatis |
topic | Susceptibility |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092548/ https://www.ncbi.nlm.nih.gov/pubmed/33318015 http://dx.doi.org/10.1128/AAC.01338-20 |
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