Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Yang, Qin, Xiaodong, Wang, Guangxiang, Jin, Jiaxin, Shang, Youjun, Zhang, Zhidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
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
_version_ 1782422372948639744
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
work_keys_str_mv AT yangyang developmentofanisothermoalamplificationbasedassayforrapidvisualdetectionofanorfvirus
AT qinxiaodong developmentofanisothermoalamplificationbasedassayforrapidvisualdetectionofanorfvirus
AT wangguangxiang developmentofanisothermoalamplificationbasedassayforrapidvisualdetectionofanorfvirus
AT jinjiaxin developmentofanisothermoalamplificationbasedassayforrapidvisualdetectionofanorfvirus
AT shangyoujun developmentofanisothermoalamplificationbasedassayforrapidvisualdetectionofanorfvirus
AT zhangzhidong developmentofanisothermoalamplificationbasedassayforrapidvisualdetectionofanorfvirus