An HRM Assay to Differentiate Sheeppox Virus Vaccine Strains from Sheeppox Virus Field Isolates and other Capripoxvirus Species

Tesfaye Rufael(International Atomic Energy Agency), Tirumala Bharani K. Settypalli(International Atomic Energy Agency), Francisco J. Berguido(International Atomic Energy Agency), Reingard Grabherr(BOKU University), Angelika Loitsch(Austrian Agency for Health and Food Safety), Eeva Tuppurainen, Nick Nwankpa(African Union), Karim Tounkara(African Union), Hafsa Madani(Higher National Veterinary School), Amel Omani(Higher National Veterinary School), Mariane Diop(Institut Sénégalais de Recherches Agricoles), Giovanni Cattoli(International Atomic Energy Agency), Adama Diallo(Centre de Coopération Internationale en Recherche Agronomique pour le Développement), Charles Euloge Lamien(International Atomic Energy Agency)
Scientific Reports
April 30, 2019
Cited by 29Open Access
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Abstract

Sheep poxvirus (SPPV), goat poxvirus (GTPV) and lumpy skin disease virus (LSDV) affect small ruminants and cattle causing sheeppox (SPP), goatpox (GTP) and lumpy skin disease (LSD) respectively. In endemic areas, vaccination with live attenuated vaccines derived from SPPV, GTPV or LSDV provides protection from SPP and GTP. As live poxviruses may cause adverse reactions in vaccinated animals, it is imperative to develop new diagnostic tools for the differentiation of SPPV field strains from attenuated vaccine strains. Within the capripoxvirus (CaPV) homolog of the variola virus B22R gene, we identified a unique region in SPPV vaccines with two deletions of 21 and 27 nucleotides and developed a High-Resolution Melting (HRM)-based assay. The HRM assay produces four distinct melting peaks, enabling the differentiation between SPPV vaccines, SPPV field isolates, GTPV and LSDV. This HRM assay is sensitive, specific, and provides a cost-effective means for the detection and classification of CaPVs and the differentiation of SPPV vaccines from SPPV field isolates.


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