論文ID: 11-0428
Avian leukosis virus subgroup J poses great threat in poultry industry in China. To reduce the economic losses, a quick method for detection of ALV-J antigen is required for the diagnosis and identification of the congenitally transmitting hens. In this study, we report the production and evaluation of one monoclonal antibody (MAb) suitable for achieving these goals. The gp85 gene of avian leukosis virus subgroup J CAUHM01 China isolates was sub-cloned into the expression vectors pGEX-6p-1 and pET28a and successfully expressed in E. coli. After immunizing BALB/c mice with recombinant His-Jgp85 protein, splenic cells from immunized mice were fused with SP2/0 myeloma cells to produce hybridomas. We isolated and characterized one ALV-J gp85 specific MAb by determining its titer, affinity, and IgG subclass. In addition, we performed epitope mapping and determined the epitope for the MAb 1E3 as 81-92 aa of ALV-J gp85 protein (LPWDPQELDILG). Bioinformatics analysis and IFA studies revealed that this epitope is conserved among all ALV-J isolates and this antibody could serve as a useful reagent for ALV-J detection and diagnosis.