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Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus
BACKGROUND: Orf virus (ORFV) is the causative agent of Orf (also known as contagious ecthyma or contagious papular dermatitis), a severe infectious skin disease in goats, sheep and other ruminants. The rapid detection of ORFV is of great importance in disease control and highly needed. A isothermal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668657/ https://www.ncbi.nlm.nih.gov/pubmed/26631157 http://dx.doi.org/10.1186/s12985-015-0440-z |
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author | Yang, Yang Qin, Xiaodong Wang, Guangxiang Zhang, Yuen Shang, Youjun Zhang, Zhidong |
author_facet | Yang, Yang Qin, Xiaodong Wang, Guangxiang Zhang, Yuen Shang, Youjun Zhang, Zhidong |
author_sort | Yang, Yang |
collection | PubMed |
description | BACKGROUND: Orf virus (ORFV) is the causative agent of Orf (also known as contagious ecthyma or contagious papular dermatitis), a severe infectious skin disease in goats, sheep and other ruminants. The rapid detection of ORFV is of great importance in disease control and highly needed. A isothermal molecular diagnostic approach, termed recombinase polymerase amplification (RPA), is considered as an novel and rapid alternative techonology to PCR assay. RESULTS: In the present study, a novel fluorescent probe based on RPA assay (ORFV exo RPA assay) was developed. The developed ORFV exo RPA assay was capable of as low as 100 copies of ORFV DNA /reaction and was highly specific, with no cross-reaction with closely related viruses (capripox virus, foot-and-mouth disease virus or peste des petits ruminants virus). Further assessment with clinical samples showed that the developed ORFV exo RPA assay has good correlation with qPCR assays for detection of ORFV. CONCLUSIONS: These results suggest that the developed ORFV exo RPA assay is suitable for rapid detection of ORFV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-015-0440-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4668657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46686572015-12-04 Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus Yang, Yang Qin, Xiaodong Wang, Guangxiang Zhang, Yuen Shang, Youjun Zhang, Zhidong Virol J Methodology BACKGROUND: Orf virus (ORFV) is the causative agent of Orf (also known as contagious ecthyma or contagious papular dermatitis), a severe infectious skin disease in goats, sheep and other ruminants. The rapid detection of ORFV is of great importance in disease control and highly needed. A isothermal molecular diagnostic approach, termed recombinase polymerase amplification (RPA), is considered as an novel and rapid alternative techonology to PCR assay. RESULTS: In the present study, a novel fluorescent probe based on RPA assay (ORFV exo RPA assay) was developed. The developed ORFV exo RPA assay was capable of as low as 100 copies of ORFV DNA /reaction and was highly specific, with no cross-reaction with closely related viruses (capripox virus, foot-and-mouth disease virus or peste des petits ruminants virus). Further assessment with clinical samples showed that the developed ORFV exo RPA assay has good correlation with qPCR assays for detection of ORFV. CONCLUSIONS: These results suggest that the developed ORFV exo RPA assay is suitable for rapid detection of ORFV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-015-0440-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-02 /pmc/articles/PMC4668657/ /pubmed/26631157 http://dx.doi.org/10.1186/s12985-015-0440-z Text en © Yang et al. 2015 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 | Methodology Yang, Yang Qin, Xiaodong Wang, Guangxiang Zhang, Yuen Shang, Youjun Zhang, Zhidong Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus |
title | Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus |
title_full | Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus |
title_fullStr | Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus |
title_full_unstemmed | Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus |
title_short | Development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of Orf virus |
title_sort | development of a fluorescent probe-based recombinase polymerase amplification assay for rapid detection of orf virus |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668657/ https://www.ncbi.nlm.nih.gov/pubmed/26631157 http://dx.doi.org/10.1186/s12985-015-0440-z |
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