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Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus
BACKGROUND: Orf virus (ORFV) is the causative agent of a severe infectious skin disease (also known as contagious ecthyma) in goats, sheep and other small ruminants. Importantly, ORFV also infect humans which causes a public health concern in the context of changing environment and increase in human...
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/PMC4799565/ https://www.ncbi.nlm.nih.gov/pubmed/26993468 http://dx.doi.org/10.1186/s12985-016-0502-x |
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author | Yang, Yang Qin, Xiaodong Wang, Guangxiang Jin, Jiaxin Shang, Youjun Zhang, Zhidong |
author_facet | Yang, Yang Qin, Xiaodong Wang, Guangxiang Jin, Jiaxin Shang, Youjun Zhang, Zhidong |
author_sort | Yang, Yang |
collection | PubMed |
description | BACKGROUND: Orf virus (ORFV) is the causative agent of a severe infectious skin disease (also known as contagious ecthyma) in goats, sheep and other small ruminants. Importantly, ORFV also infect humans which causes a public health concern in the context of changing environment and increase in human populations. The rapid detection is critical in effective control of the disease and urgently needed. RESULTS: A novel “point of care” molecular amplification assay for rapid visual detection of ORFV was developed based on isothermoal recombinase polymerase amplification (RPA) technology in combination with a simpler lateral flow immunoassay strip (ORFV RPA- LFD assay). The developed ORFV RPA- LFD assay was able to detect ORFV in less than 25 min. This assay was highly sensitive, with detection limit of as low as 80 copies/reaction, and highly specific, with no cross-reactions with capripox virus, foot-and-mouth disease virus and peste des petits ruminants virus. Furthermore, the ORFV RPA- LFD assay has good correlation with qPCR assay for detection of ORFV present in clinical samples. CONCLUSIONS: The developed ORFV RPA-LFD assay was a sensitive and specific method for rapid detection of ORFV, and has great potential as an onsite molecular diagnostic tool in control of Orf. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-016-0502-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4799565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47995652016-03-20 Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus Yang, Yang Qin, Xiaodong Wang, Guangxiang Jin, Jiaxin Shang, Youjun Zhang, Zhidong Virol J Methodology BACKGROUND: Orf virus (ORFV) is the causative agent of a severe infectious skin disease (also known as contagious ecthyma) in goats, sheep and other small ruminants. Importantly, ORFV also infect humans which causes a public health concern in the context of changing environment and increase in human populations. The rapid detection is critical in effective control of the disease and urgently needed. RESULTS: A novel “point of care” molecular amplification assay for rapid visual detection of ORFV was developed based on isothermoal recombinase polymerase amplification (RPA) technology in combination with a simpler lateral flow immunoassay strip (ORFV RPA- LFD assay). The developed ORFV RPA- LFD assay was able to detect ORFV in less than 25 min. This assay was highly sensitive, with detection limit of as low as 80 copies/reaction, and highly specific, with no cross-reactions with capripox virus, foot-and-mouth disease virus and peste des petits ruminants virus. Furthermore, the ORFV RPA- LFD assay has good correlation with qPCR assay for detection of ORFV present in clinical samples. CONCLUSIONS: The developed ORFV RPA-LFD assay was a sensitive and specific method for rapid detection of ORFV, and has great potential as an onsite molecular diagnostic tool in control of Orf. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-016-0502-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-19 /pmc/articles/PMC4799565/ /pubmed/26993468 http://dx.doi.org/10.1186/s12985-016-0502-x Text en © Yang et al. 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 | Methodology Yang, Yang Qin, Xiaodong Wang, Guangxiang Jin, Jiaxin Shang, Youjun Zhang, Zhidong Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus |
title | Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus |
title_full | Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus |
title_fullStr | Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus |
title_full_unstemmed | Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus |
title_short | Development of an isothermoal amplification-based assay for rapid visual detection of an Orf virus |
title_sort | development of an isothermoal amplification-based assay for rapid visual detection of an orf virus |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799565/ https://www.ncbi.nlm.nih.gov/pubmed/26993468 http://dx.doi.org/10.1186/s12985-016-0502-x |
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