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P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard
POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM: OBJECTIVE: Mycetoma is a neglected tropical skin disease, caused by 70 different causative agents. For most of the causative agents, molecular identification is the only reliable method to identify the species level. In practice, ultrasound...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515937/ http://dx.doi.org/10.1093/mmy/myac072.P445 |
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author | Siddig, Emmanuel Nyuykonge, Bertrand Mhmoud, Najwa Abdallah, Omnia Bahar, Mustafa Ahmed, Eiman Nyaoke, Borna Zijlstra, Eduard Verbon, Annelies Bakhiet, Sahar Fahal, Ahmed van de Sande, Wendy |
author_facet | Siddig, Emmanuel Nyuykonge, Bertrand Mhmoud, Najwa Abdallah, Omnia Bahar, Mustafa Ahmed, Eiman Nyaoke, Borna Zijlstra, Eduard Verbon, Annelies Bakhiet, Sahar Fahal, Ahmed van de Sande, Wendy |
author_sort | Siddig, Emmanuel |
collection | PubMed |
description | POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM: OBJECTIVE: Mycetoma is a neglected tropical skin disease, caused by 70 different causative agents. For most of the causative agents, molecular identification is the only reliable method to identify the species level. In practice, ultrasound, histopathology, culturing, and species-specific PCRs are most commonly used for species identification. However, the performance of these different tests was not validated using molecular identification by sequencing barcoding genes. METHODS: In this study, we validated the performance of the most commonly used diagnostic tools including culture, histopathology, Ultrasound and two species-specific PCR for Madurella mycetomatis on 222 patients suspected of fungal mycetoma by M. mycetomatis; the sensitivity, specificity, and accuracy of each method was calculated. RESULTS: From the 222 patients, 154 (69.3%) were correctly identified by ultrasound, histology, culture, and both species-specific PCRs. For five patients all tests were negative and for three only the ultrasound was indicative of mycetoma. For the other 60 patients, at least one of the assays was negative for M. mycetomatis. The two species-specific PCRs were the most sensitive and specific, followed by culture and histology. Ultrasound was the least specific as it only allows to differentiate between actinomycetoma and eumycetoma. However, with ultrasound, an identification could be obtained in 9.38 min. PCR took 3.76 h, histology 8.5 days, and culturing 21 days. CONCLUSION: We concluded that PCR directly on DNA isolated from grains is the most rapid and reliable diagnostic tool to identify M. mycetomatis from eumycetoma grains to use species-specific PCRs. In order to shorten the time to identification of other causative agents, the focus should be on developing more molecular assays for those species. |
format | Online Article Text |
id | pubmed-9515937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95159372022-09-28 P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard Siddig, Emmanuel Nyuykonge, Bertrand Mhmoud, Najwa Abdallah, Omnia Bahar, Mustafa Ahmed, Eiman Nyaoke, Borna Zijlstra, Eduard Verbon, Annelies Bakhiet, Sahar Fahal, Ahmed van de Sande, Wendy Med Mycol Oral Presentations POSTER SESSION 3, SEPTEMBER 23, 2022, 12:30 PM - 1:30 PM: OBJECTIVE: Mycetoma is a neglected tropical skin disease, caused by 70 different causative agents. For most of the causative agents, molecular identification is the only reliable method to identify the species level. In practice, ultrasound, histopathology, culturing, and species-specific PCRs are most commonly used for species identification. However, the performance of these different tests was not validated using molecular identification by sequencing barcoding genes. METHODS: In this study, we validated the performance of the most commonly used diagnostic tools including culture, histopathology, Ultrasound and two species-specific PCR for Madurella mycetomatis on 222 patients suspected of fungal mycetoma by M. mycetomatis; the sensitivity, specificity, and accuracy of each method was calculated. RESULTS: From the 222 patients, 154 (69.3%) were correctly identified by ultrasound, histology, culture, and both species-specific PCRs. For five patients all tests were negative and for three only the ultrasound was indicative of mycetoma. For the other 60 patients, at least one of the assays was negative for M. mycetomatis. The two species-specific PCRs were the most sensitive and specific, followed by culture and histology. Ultrasound was the least specific as it only allows to differentiate between actinomycetoma and eumycetoma. However, with ultrasound, an identification could be obtained in 9.38 min. PCR took 3.76 h, histology 8.5 days, and culturing 21 days. CONCLUSION: We concluded that PCR directly on DNA isolated from grains is the most rapid and reliable diagnostic tool to identify M. mycetomatis from eumycetoma grains to use species-specific PCRs. In order to shorten the time to identification of other causative agents, the focus should be on developing more molecular assays for those species. Oxford University Press 2022-09-20 /pmc/articles/PMC9515937/ http://dx.doi.org/10.1093/mmy/myac072.P445 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Oral Presentations Siddig, Emmanuel Nyuykonge, Bertrand Mhmoud, Najwa Abdallah, Omnia Bahar, Mustafa Ahmed, Eiman Nyaoke, Borna Zijlstra, Eduard Verbon, Annelies Bakhiet, Sahar Fahal, Ahmed van de Sande, Wendy P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
title | P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
title_full | P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
title_fullStr | P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
title_full_unstemmed | P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
title_short | P445 Clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
title_sort | p445 clinical evaluation of the performance of the most commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the golden standard |
topic | Oral Presentations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515937/ http://dx.doi.org/10.1093/mmy/myac072.P445 |
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