@article{mbs:/content/journal/jgv/10.1099/0022-1317-73-5-1065, author = "Taguchi, Fumihiro and Ikeda, Toshio and Shida, Hisatoshi", title = "Molecular cloning and expression of a spike protein of neurovirulent murine coronavirus JHMV variant c1-2", journal= "Journal of General Virology", year = "1992", volume = "73", number = "5", pages = "1065-1072", doi = "https://doi.org/10.1099/0022-1317-73-5-1065", url = "https://www.microbiologyresearch.org/content/journal/jgv/10.1099/0022-1317-73-5-1065", publisher = "Microbiology Society", issn = "1465-2099", type = "Journal Article", abstract = "A cDNA encoding the spike (S) protein of the neurovirulent murine coronavirus JHMV variant c1-2 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 c1-2 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 c1-2 virus infection, but also in rabbit RK13 cells, which are not susceptible to c1-2 virus infection. This result suggests the possibility that RK13 cells have binding sites for the c1-2 virus S protein.", }