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Madurella real-time PCR, a novel approach for eumycetoma diagnosis
The genus Madurella comprising four species, M. fahalii, M. mycetomatis, M. pseudomycetomatis, and M. tropicana, represents the prevalent cause of eumycetoma worldwide. The four species are phenotypically similar and cause an invariable clinical picture, but differ markedly in their susceptibility t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986762/ https://www.ncbi.nlm.nih.gov/pubmed/31940343 http://dx.doi.org/10.1371/journal.pntd.0007845 |
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author | Arastehfar, Amir Lim, Wilson Daneshnia, Farnaz van de Sande, Wendy W. J. Fahal, Ahmed H. Desnos-Ollivier, Marie de Hoog, Gerrit S. Boekhout, Teun Ahmed, Sarah. A. |
author_facet | Arastehfar, Amir Lim, Wilson Daneshnia, Farnaz van de Sande, Wendy W. J. Fahal, Ahmed H. Desnos-Ollivier, Marie de Hoog, Gerrit S. Boekhout, Teun Ahmed, Sarah. A. |
author_sort | Arastehfar, Amir |
collection | PubMed |
description | The genus Madurella comprising four species, M. fahalii, M. mycetomatis, M. pseudomycetomatis, and M. tropicana, represents the prevalent cause of eumycetoma worldwide. The four species are phenotypically similar and cause an invariable clinical picture, but differ markedly in their susceptibility to antifungal drugs, and epidemiological pattern. Therefore, specific identification is required for optimal management of Madurella infection and to reveal proper epidemiology of the species. In this study, a novel multiplex real-time PCR targeting the four Madurella species was developed and standardized. Evaluation of the assay using reference strains of the target and non-target species resulted in 100% specificity, high analytical reproducibility (R2 values >0.99) and a lowest detection limit of 3 pg target DNA. The accuracy of the real-time PCR was further assessed using biopsies from eumycetoma suspected patients. Unlike culture and DNA sequencing as gold standard diagnostic methods, the real-time PCR yielded accurate diagnosis with specific identification of the causative species in three hours compared to one or two weeks required for culture. The novel method reduces turnaround time as well as labor intensity and high costs associated with current reference methods. |
format | Online Article Text |
id | pubmed-6986762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69867622020-02-18 Madurella real-time PCR, a novel approach for eumycetoma diagnosis Arastehfar, Amir Lim, Wilson Daneshnia, Farnaz van de Sande, Wendy W. J. Fahal, Ahmed H. Desnos-Ollivier, Marie de Hoog, Gerrit S. Boekhout, Teun Ahmed, Sarah. A. PLoS Negl Trop Dis Research Article The genus Madurella comprising four species, M. fahalii, M. mycetomatis, M. pseudomycetomatis, and M. tropicana, represents the prevalent cause of eumycetoma worldwide. The four species are phenotypically similar and cause an invariable clinical picture, but differ markedly in their susceptibility to antifungal drugs, and epidemiological pattern. Therefore, specific identification is required for optimal management of Madurella infection and to reveal proper epidemiology of the species. In this study, a novel multiplex real-time PCR targeting the four Madurella species was developed and standardized. Evaluation of the assay using reference strains of the target and non-target species resulted in 100% specificity, high analytical reproducibility (R2 values >0.99) and a lowest detection limit of 3 pg target DNA. The accuracy of the real-time PCR was further assessed using biopsies from eumycetoma suspected patients. Unlike culture and DNA sequencing as gold standard diagnostic methods, the real-time PCR yielded accurate diagnosis with specific identification of the causative species in three hours compared to one or two weeks required for culture. The novel method reduces turnaround time as well as labor intensity and high costs associated with current reference methods. Public Library of Science 2020-01-15 /pmc/articles/PMC6986762/ /pubmed/31940343 http://dx.doi.org/10.1371/journal.pntd.0007845 Text en © 2020 Arastehfar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Arastehfar, Amir Lim, Wilson Daneshnia, Farnaz van de Sande, Wendy W. J. Fahal, Ahmed H. Desnos-Ollivier, Marie de Hoog, Gerrit S. Boekhout, Teun Ahmed, Sarah. A. Madurella real-time PCR, a novel approach for eumycetoma diagnosis |
title | Madurella real-time PCR, a novel approach for eumycetoma diagnosis |
title_full | Madurella real-time PCR, a novel approach for eumycetoma diagnosis |
title_fullStr | Madurella real-time PCR, a novel approach for eumycetoma diagnosis |
title_full_unstemmed | Madurella real-time PCR, a novel approach for eumycetoma diagnosis |
title_short | Madurella real-time PCR, a novel approach for eumycetoma diagnosis |
title_sort | madurella real-time pcr, a novel approach for eumycetoma diagnosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986762/ https://www.ncbi.nlm.nih.gov/pubmed/31940343 http://dx.doi.org/10.1371/journal.pntd.0007845 |
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