Xiao Q L, Zhang Z F, He J L
Key Laboratory of Silkworm Biotechnology, Ministry of Agriculture, Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Zhenjiang 212018, China.
Sheng Wu Gong Cheng Xue Bao. 2001 May;17(3):283-7.
By cloning vp1 and vp2 genes of chicken anaemia virus into transfer vector pBacPAK8, recombinant transfer plasmids pBac-vp1 and pBac-vp2 were obtained. Then BmN cells were co-transfected with linearized baculovirus Bm-BacPAK6 DNA and above two recombinant plasmids respectively, recombinant viruses Bm-vp1 and Bm-vp2 were constructed and used to co-infect silkworms to express recombinant proteins. The results indicated that recombinant VP1 and VP2 could induce the corresponding antibody in chickens using immunofluorescence assay and the expression products could protect filial generation from the attack of CAV. Recombinant BmNPV expressing VP1 and VP2 is, therefore, a great hopeful production system for a subunit vaccine against CAV infection.
通过将鸡贫血病毒的vp1和vp2基因克隆到转移载体pBacPAK8中,获得了重组转移质粒pBac-vp1和pBac-vp2。然后将线性化的杆状病毒Bm-BacPAK6 DNA分别与上述两种重组质粒共转染BmN细胞,构建重组病毒Bm-vp1和Bm-vp2,并用于共同感染家蚕以表达重组蛋白。结果表明,重组VP1和VP2可通过免疫荧光试验在鸡体内诱导产生相应抗体,且表达产物可保护子代免受CAV的攻击。因此,表达VP1和VP2的重组BmNPV是一种非常有希望的抗CAV感染亚单位疫苗生产系统。