Development of a reverse genetics system for epizootic hemorrhagic disease virus and evaluation of novel strains containing duplicative gene rearrangements

• Published in: Journal of general virology 2015-09, Vol.96 (9), p.2714-2720
• Main Authors: Yang, Tao, Zhang, Jikai, Xu, Qingyuan, Sun, Encheng, Li, Junping, Lv, Shuang, Feng, Yufei, Zhang, Qin, Wang, Haixiu, Wang, Hua, Wu, Donglai
• Format: Article
• Language: English
• Subjects: Animals; Cattle; Cattle Diseases - virology; Gene Duplication; Gene Rearrangement; Hemorrhagic Disease Virus, Epizootic - genetics; Hemorrhagic Disease Virus, Epizootic - isolation & purification; Hemorrhagic Disease Virus, Epizootic - physiology; Phylogeny; Reoviridae Infections - veterinary; Reoviridae Infections - virology; Reverse Genetics - methods; Virus Replication
• ISSN: 0022-1317; 1465-2099
• DOI: 10.1099/vir.0.000192

Epizootic haemorrhagic disease is a non-contagious infectious viral disease of wild and domestic ruminants caused by epizootic hemorrhagic disease virus (EHDV). EHDV belongs to the genus Orbivirus within the family Reoviridae and is transmitted by insects of the genus Culicoides. The impact of epizootic haemorrhagic disease is underscored by its designation as a notifiable disease by the Office International des Epizooties. The EHDV genome consists of 10 linear dsRNA segments (Seg1-Seg10). Until now, no reverse genetics system (RGS) has been developed to generate replication-competent EHDV entirely from cloned cDNA, hampering detailed functional analyses of EHDV biology. Here, we report the generation of viable EHDV entirely from cloned cDNAs. A replication-competent EHDV-2 (Ibaraki BK13 strain) virus incorporating a marker mutation was rescued by transfection of BHK-21 cells with expression plasmids and in vitro synthesized RNA transcripts. Using this RGS, two additional modified EHDV-2 viruses were also generated: one that contained a duplex concatemeric Seg9 gene and another that contained a duplex concatemeric Seg10 gene. The modified EHDV-2 with a duplex Seg9 gene was genetically stable during serial passage in BHK-21 cells. In contrast, the modified EHDV-2 with a duplex Seg10 gene was unstable during serial passage, but displayed enhanced replication kinetics in vitro when compared with the WT virus. This RGS provides a new platform for the investigation of EHDV replication, pathogenesis and novel EHDV vaccines.