| Literature DB >> 30446925 |
Bina Mishra1, Piyali Mondal2, C L Patel3, Insha Zafir3, Rachna Gangwar3, Neha Singh2, Joyshikh Sonowal2, Deepanker Bisht2, Amit Ranjan Sahu2, Mumtaz Baig4, Basavaraj Sajjanar2, R K Singh2, Ravi Kumar Gandham2,5.
Abstract
Sheeppox disease is associated with significant losses in sheep production world over. The sheep pox virus, the goatpox virus, and the lumpy skin disease virus cannot be distinguished by conventional serological tests. Identification of these pathogens needs molecular methods. In this study, seven genes viz. EEV maturation protein-F12L, Virion protein-D3R, RNA polymerase subunit-A5R, Virion core protein-A10L, EEV glycoprotein-A33R, VARV B22R homologue, and Kelch like protein-A55R that cover the start, middle, and end of the genome were selected. These genes were amplified from Roumanian-Fanar vaccine strain and Jaipur virulent strain, cloned, and sequenced. On analysis with the available database sequences, VARV B22R homologue was identified as a marker for phylogenetic reconstruction for classifying the sheeppox viruses of the ungulates. Further, divergence time dating with VARV B22R gene accurately predicted the sheeppox disease outbreak involving Jaipur virulent strain.Entities:
Keywords: Capripoxvirus; Divergence time dating; Goatpox virus; Lumpy skin disease virus; Phylogeny; Sheeppox virus
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Year: 2018 PMID: 30446925 DOI: 10.1007/s11262-018-1613-9
Source DB: PubMed Journal: Virus Genes ISSN: 0920-8569 Impact factor: 2.198