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Abstract
A recombinant goatpox virus was constructed in which an enhanced green fluorescent protein gene was inserted under the control of the 11K late promoter, a guanine phosphoribosyltransferase gene was inserted under the control of the 7.5K early/late promoter, and exogenous genes were inserted into an intergenic region between loci gp_24 and gp_24.5 of the recombinant genome. Analysis of protein expression showed that LT cells infected with only the recombinant virus produced specific fluorescence. A comparative growth assay demonstrated the stability of the recombinant virus at the replication level. These results suggest that the intergenic region is not essential for replication of goatpox virus.
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1 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Division of Livestock Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin, People’s Republic of China (GRID:grid.38587.31); Xinjiang Academy of Animal Science, Institute of Veterinary Medicine, Ürümqi, People’s Republic of China (GRID:grid.410754.3) (ISNI:0000000417634106)
2 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Division of Livestock Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin, People’s Republic of China (GRID:grid.38587.31)
3 Xinjiang Academy of Animal Science, Institute of Veterinary Medicine, Ürümqi, People’s Republic of China (GRID:grid.410754.3) (ISNI:0000000417634106)





