Qiao Jun, Xia Xian-Zhu, Yang Song-Tao, Hu Gui-Xue, Xie Zhi-Jing
Institute of Military Veterinary, Academy of Military Medical Sciences of PLA, Changchun 130062, China.
Wei Sheng Wu Xue Bao. 2005 Aug;45(4):588-92.
In order to construct a recombinant Canine adenovirus type 2 (CAV-2) expressing the spike glycoprotein of Canine coronavirus (CCV), the S1 gene fragment of CCV strain DXMV, encoding major antigenic region A, B, C and D of S protein, was amplified by RT-PCR and cloned into pVAX1 vector. The complete S1 expression cassette was subcloned into the shuttle vector pVAXE3, then further cloned into the backbone vector pPoly2-CAV2 containing complete genome of CAV-2. To gain the recombinant Canine adenovirus, the recombinant plasmid pCAV-2-CCV-S1 was linearized by Cla I/Asc I to release recombinant genome, and then transfected into MDCK cell. The recombinant virus CAV-2-S1 was gained through 4 passages in MDCK, which showed classical CPE of CAV-2. The expressed S1 protein of CCV, which was identified by RT-PCR and Western blot, can be specifically recognized by polyclonal antibody against CCV. The immunization in dogs indicated that the recombinant CAV-2 could effectively induce the specific antibodies against CCV and CAV.
为构建表达犬冠状病毒(CCV)刺突糖蛋白的重组犬2型腺病毒(CAV-2),通过RT-PCR扩增编码CCV DXMV株S蛋白主要抗原区域A、B、C和D的S1基因片段,并将其克隆到pVAX1载体中。将完整的S1表达盒亚克隆到穿梭载体pVAXE3中,然后进一步克隆到含有CAV-2完整基因组的骨架载体pPoly2-CAV2中。为获得重组犬腺病毒,用Cla I/Asc I将重组质粒pCAV-2-CCV-S1线性化以释放重组基因组,然后转染到MDCK细胞中。通过在MDCK中传代4次获得重组病毒CAV-2-S1,其表现出CAV-2的典型细胞病变效应。经RT-PCR和Western blot鉴定,所表达的CCV S1蛋白可被抗CCV多克隆抗体特异性识别。犬免疫实验表明,重组CAV-2可有效诱导针对CCV和CAV的特异性抗体。