Nishikawa Y, Xuan X, Kimura M, Otsuka H
Department of Global Agricultural Sciences, Graduate School of Agricultural and Life Science, University of Tokyo, Japan.
J Vet Med Sci. 1999 Oct;61(10):1113-7. doi: 10.1292/jvms.61.1113.
A recombinant canine herpesvirus (CHV) which expressed glycoprotein B (gB) of pseudorabies virus (PrV) was constructed. The antigenicity of the PrV gB expressed by the recombinant CHV is similar to that of the native PrV. The expressed PrV gB was shown to be transported to the surface of infected cells as judged by an indirected immunofluorescence test. Antibodies raised in mice immunized with the recombinant CHV neutralized the infectivity of PrV in vitro. It is known that the authentic PrV gB exists as a glycoprotein complex, which consists of gBa, gBb and gBc. In MDCK cells, PrV gB expressed by the recombinant CHV was processed like authentic PrV gB, suggesting that the cleavage mechanism of PrV gB depends on a functional cleavage domain from PrV gB gene and protease from infected cells.
构建了一种表达伪狂犬病病毒(PrV)糖蛋白B(gB)的重组犬疱疹病毒(CHV)。重组CHV表达的PrV gB的抗原性与天然PrV相似。通过间接免疫荧光试验判断,所表达的PrV gB被转运至感染细胞表面。用重组CHV免疫的小鼠产生的抗体在体外中和了PrV的感染性。已知天然PrV gB以糖蛋白复合物的形式存在,该复合物由gBa、gBb和gBc组成。在MDCK细胞中,重组CHV表达的PrV gB的加工方式与天然PrV gB相同,这表明PrV gB的切割机制取决于PrV gB基因的功能性切割结构域和感染细胞中的蛋白酶。