Taguchi F, Ikeda T, Shida H
National Institute of Neuroscience, Tokyo, Japan.
J Gen Virol. 1992 May;73 ( Pt 5):1065-72. doi: 10.1099/0022-1317-73-5-1065.
A cDNA encoding the spike (S) protein of the neurovirulent murine coronavirus JHMV variant cl-2 was isolated and sequenced. Analysis of the cDNA revealed that the S protein consists of 1376 amino acids, as does the S protein of mouse hepatitis virus 4. We inserted the cDNA into the genome of vaccinia virus to obtain a recombinant vaccinia virus (rVV). The S protein expressed in RK13 cells infected by the rVV was shown to be electrophoretically and immunologically indistinguishable from the S protein produced in DBT cells infected with cl-2 virus. RVV infection of rats and mice induced S protein-specific antibody production detectable by immunofluorescence and neutralization. Moreover, the S protein expressed by the rVV induced syncytium formation not only in mouse DBT and L cells, which are susceptible to cl-2 virus infection, but also in rabbit RK13 cells, which are not susceptible to cl-2 virus infection. This result suggests the possibility that RK13 cells have binding sites for the cl-2 virus S protein.
分离并测序了编码神经毒力小鼠冠状病毒JHMV变异株cl-2刺突(S)蛋白的cDNA。对该cDNA的分析表明,S蛋白由1376个氨基酸组成,与小鼠肝炎病毒4的S蛋白相同。我们将该cDNA插入痘苗病毒基因组中,以获得重组痘苗病毒(rVV)。结果显示,被rVV感染的RK13细胞中表达的S蛋白在电泳和免疫方面与被cl-2病毒感染的DBT细胞中产生的S蛋白无法区分。用rVV感染大鼠和小鼠可诱导产生可通过免疫荧光和中和试验检测到的S蛋白特异性抗体。此外,rVV表达的S蛋白不仅能在易受cl-2病毒感染的小鼠DBT和L细胞中诱导合胞体形成,还能在不易受cl-2病毒感染的兔RK13细胞中诱导合胞体形成。这一结果提示RK13细胞可能具有cl-2病毒S蛋白的结合位点。