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Detection of Mycobacterium ulcerans by real-time PCR with improved primers
BACKGROUND: Buruli ulcer is a severe skin disease caused by Mycobacterium ulcerans. Real-time PCR targeting the IS2404 sequence has been used as a reliable and rapid method for the diagnosis of Buruli ulcer and detection of M. ulcerans in the environment. The genome of M. ulcerans contains hundreds...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009631/ https://www.ncbi.nlm.nih.gov/pubmed/27610043 http://dx.doi.org/10.1186/s41182-016-0028-3 |
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author | Shinoda, Noriko Nakamura, Hajime Watanabe, Mineo |
author_facet | Shinoda, Noriko Nakamura, Hajime Watanabe, Mineo |
author_sort | Shinoda, Noriko |
collection | PubMed |
description | BACKGROUND: Buruli ulcer is a severe skin disease caused by Mycobacterium ulcerans. Real-time PCR targeting the IS2404 sequence has been used as a reliable and rapid method for the diagnosis of Buruli ulcer and detection of M. ulcerans in the environment. The genome of M. ulcerans contains hundreds of IS2404 copies, which have variability in certain sequences. Therefore, the design of new primers specific to conserved IS2404 regions may potentially improve the sensitivity of M. ulcerans detection and, consequently, the diagnosis of Buruli ulcer, thus ensuring timely treatment of the disease. RESULTS: In silico analysis indicates that DNA sequences of the IS2404 elements are highly variable within a single strain. As the binding sites of conventional IS2404-specific primers used for M. ulcerans detection contain polymorphic sequences, we designed new primers, which enabled the detection of M. ulcerans by real-time PCR with higher sensitivity and similar specificity with respect to that of conventional primers. However, the increase in sensitivity with the new primers depended on the M. ulcerans strain. CONCLUSIONS: The results suggest that real-time PCR based on the new primers could improve Buruli ulcer diagnosis and M. ulcerans detection in environmental samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s41182-016-0028-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5009631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50096312016-09-08 Detection of Mycobacterium ulcerans by real-time PCR with improved primers Shinoda, Noriko Nakamura, Hajime Watanabe, Mineo Trop Med Health Research BACKGROUND: Buruli ulcer is a severe skin disease caused by Mycobacterium ulcerans. Real-time PCR targeting the IS2404 sequence has been used as a reliable and rapid method for the diagnosis of Buruli ulcer and detection of M. ulcerans in the environment. The genome of M. ulcerans contains hundreds of IS2404 copies, which have variability in certain sequences. Therefore, the design of new primers specific to conserved IS2404 regions may potentially improve the sensitivity of M. ulcerans detection and, consequently, the diagnosis of Buruli ulcer, thus ensuring timely treatment of the disease. RESULTS: In silico analysis indicates that DNA sequences of the IS2404 elements are highly variable within a single strain. As the binding sites of conventional IS2404-specific primers used for M. ulcerans detection contain polymorphic sequences, we designed new primers, which enabled the detection of M. ulcerans by real-time PCR with higher sensitivity and similar specificity with respect to that of conventional primers. However, the increase in sensitivity with the new primers depended on the M. ulcerans strain. CONCLUSIONS: The results suggest that real-time PCR based on the new primers could improve Buruli ulcer diagnosis and M. ulcerans detection in environmental samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s41182-016-0028-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-19 /pmc/articles/PMC5009631/ /pubmed/27610043 http://dx.doi.org/10.1186/s41182-016-0028-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Shinoda, Noriko Nakamura, Hajime Watanabe, Mineo Detection of Mycobacterium ulcerans by real-time PCR with improved primers |
title | Detection of Mycobacterium ulcerans by real-time PCR with improved primers |
title_full | Detection of Mycobacterium ulcerans by real-time PCR with improved primers |
title_fullStr | Detection of Mycobacterium ulcerans by real-time PCR with improved primers |
title_full_unstemmed | Detection of Mycobacterium ulcerans by real-time PCR with improved primers |
title_short | Detection of Mycobacterium ulcerans by real-time PCR with improved primers |
title_sort | detection of mycobacterium ulcerans by real-time pcr with improved primers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009631/ https://www.ncbi.nlm.nih.gov/pubmed/27610043 http://dx.doi.org/10.1186/s41182-016-0028-3 |
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