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

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作者
Tesfaye Rufael Chibssa
Tirumala Bharani K. Settypalli
Francisco J. Berguido
Reingard Grabherr
Angelika Loitsch
Eeva Tuppurainen
Nick Nwankpa
Karim Tounkara
Hafsa Madani
Amel Omani
Mariane Diop
Giovanni Cattoli
Adama Diallo
Charles Euloge Lamien
机构
[1] Joint FAO/IAEA Agricultural and Biotechnology laboratory,Animal Production and Health Laboratory
[2] Division of Nuclear Techniques in Food and Agriculture,Institute of Biotechnology
[3] Department of Nuclear Sciences and Applications,Institute for Veterinary Disease Control
[4] International Atomic Energy Agency,Institut National de la Médecine Vétérinaire
[5] University of Natural Resources and Life Sciences (BOKU),Laboratoire National d’Elevage et de Recherches Vétérinaires
[6] National Animal Health Diagnostic and Investigation Center (NAHDIC),UMR CIRAD INRA
[7] Austrian Agency for Health and Food Safety (AGES),undefined
[8] Independent veterinary consultant,undefined
[9] African Union Pan African Veterinary Vaccine Centre,undefined
[10] (AU-PANVAC),undefined
[11] Laboratoire Central Vétérinaire d’Alger,undefined
[12] Institut Sénégalais de Recherches Agricoles (ISRA),undefined
[13] BP 2057 Dakar-Hann,undefined
[14] Animal,undefined
[15] Santé,undefined
[16] Territoires,undefined
[17] Risques et Ecosystèmes (ASTRE),undefined
[18] 24 Montpellier cedex 05,undefined
来源
Scientific Reports | / 9卷
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摘要
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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