• English
    • Српски
    • Српски (Serbia)
  • English 
    • English
    • Српски
    • Српски (Serbia)
  • Login
View Item 
  •   DSpace Home
  • NIV-NS
  • Zbornici
  • View Item
  •   DSpace Home
  • NIV-NS
  • Zbornici
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

TaqMan based qPCR assay for specific detection of Sheeppox virus

Thumbnail
View/Open
taqmvd19.pdf (1.223Mb)
Date
2019
Author
Vidanović, Dejan
Šekler, Milanko
Tešović, Bojana
Matović, Kazimir
Debeljak, Zoran
Vasković, Nikola
Dmitrić, Marko
Kolarević, Mišo
Petrović, Tamaš
Metadata
Show full item record
Abstract
Sheeppox virus, together with goatpox virus and Lumpy skin disease virus, is a member of the genus Capripoxvirus, family Poxviridae. SPPV strains cause sheep pox, disease primarily in sheep but can also cause disease in goats. It is characterized by fever, generalized papules or nodules, vesicles, internal lesions and death. Mortality can be up to 100%. Sheep pox are endemic in Africa north of the Equator, the Middle East and Asia, but recently there were outbreaks in European countries Bulgaria and Greece and also in other countries such as Chinese Taipei, Israel, Kazakhstan, Kyrgyzstan, Mongolia, Morocco and Russia. Because of severity of disease and great economic importance, Sheep pox is listed to OIE notifiable diseases. Rapid detection of the virus before appearance of clinical signs would be very important in managing and for surveillance of the disease. We describe development of rapid TaqMan based real-time PCR assay for specific detection of SPPV, both field and vaccine strains. The assay does not detect GTPV or LSDV strains. Specificity of the assay was tested on 20 different SPPV, GTPV and LSDV strains with no false positive or false negative results. Sensitivity of the assay was determined comparing with Capripox qPCR assay (Bowden) and it is determined that the SPPV assay is 4 times less sensitive. Despite slightly lower sensitivity this assay can provide fast and reliable detection of the virus and differentiation from GTPV and LSDV strains without need for gel electrophoresis or nucleotide sequencing.
URI
https://repo.niv.ns.ac.rs/xmlui/handle/123456789/20
Collections
  • Zbornici

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV
 

 

Browse

All of DSpaceCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

My Account

Login

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV