Skip to main content
Springer Nature - PMC COVID-19 Collection logoLink to Springer Nature - PMC COVID-19 Collection
. 1983;78(1):81–88. doi: 10.1007/BF01310860

Antigenic relationships of murine coronaviruses

J C Childs 1, S A Stohlman 3, L Kingsford 1, R Russell 1
PMCID: PMC7086718  PMID: 6316876

Summary

Two serological tests were used to examine the antigenic relationships between murine hepatitis viruses that cause different diseases in mice. Antisera prepared by immunization of mice with the individual viruses were tested for their ability to neutralize both the homologous immunogen and the other viruses. By a plaque reduction neutralization test, each antiserum was found to be specific for the immunizing virus; however, there was substantial cross-reactivity, indicating the viruses were closely related. By kinetic neutralization, two of the viruses tested, MHV-JHM and MHV-2, were found to be antigenically distinct. MHV-3 and MHV-A59 were found to be antigenically very similar but distinct. These data show that kinetic neutralization is a more precise method for determining the antigenic relationships between murine coronaviruses.

Keywords: Hepatitis, Infectious Disease, Hepatitis Virus, Serological Test, Neutralization Test

Footnotes

With 1 Figure

References

  • 1.Collins A. R., Knobler R. L., Powell H. R., Buchmeier M. J. Monoclonal antibodies to murine hepatitis virus-4 (Strain JHM) define the viral glycoprotein responsible for attachment and cell-cell fusion. Virology. 1982;119:358–371. doi: 10.1016/0042-6822(82)90095-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Gledhill A. W., Niven J. S. F. Latent virus as exemplified by mouse hepatitis virus (MHV) Vet. Rev. Annot. 1955;1:82–90. [Google Scholar]
  • 3.Hierholzer J. C., Broderson J. R., Murphy F. New strain of mouse hepatitis virus as the cause of lethal enteritis in infant mice. Infect. Immun. 1979;24:508–522. doi: 10.1128/iai.24.2.508-522.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Hirano N., Fujiwara K., Hino S., Matumoto M. Replication and plaque formation of mouse hepatitis virus (MHV-2) in mouse cell line DBT culture. Arch. Virol. 1974;44:298–302. doi: 10.1007/BF01240618. [DOI] [PubMed] [Google Scholar]
  • 5.Karjalainen K., Makela O. A Mendelian idiotype is demonstrable in the heteroclitic anti-NP antibodies of the mouse. Eur. J. Immunol. 1978;8:105–112. doi: 10.1002/eji.1830080207. [DOI] [PubMed] [Google Scholar]
  • 6.Lai M. M. C., Stohlman S. A. The RNA of mouse hepatitis virus. J. Virol. 1978;26:236–242. doi: 10.1128/jvi.26.2.236-242.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Lai M. M. C., Stohlman S. A. Comparative analysis of RNA genomes of mouse hepatitis viruses. J. Virol. 1981;38:661–670. doi: 10.1128/jvi.38.2.661-670.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Lai M. M. C., Brayton P. R., Armen R. C., Patton C., Pugh C., Stohlman S. A. Mouse hepatitis virus A59: mRNA structure and genetic localization of the sequence divergence from hepatotropic strain MHV-3. J. Virol. 1981;39:823–834. doi: 10.1128/jvi.39.3.823-834.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Robb J., Bond C. W. Pathogenic murine coronaviruses. I. Characterization of biological behaviorin vitro and virus-specific intracellular RNA of strongly neurotropic JHM and weakly neurotropic A59 viruses. Virology. 1979;94:352–370. doi: 10.1016/0042-6822(79)90467-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Siddell S., Wege H., ter Meulen V. The structure and replication of coronaviruses. Curr. Topics Microbiol. Immunol. 1982;99:131–163. doi: 10.1007/978-3-642-68528-6_4. [DOI] [PubMed] [Google Scholar]
  • 11.Stohlman S. A., Eylar O. R., Wisseman C. L. Dengue viral antigens in host cell membranes. Acta Virol. 1978;22:31–36. [PubMed] [Google Scholar]
  • 12.Stohlman S. A., Frelinger J. A., Weiner L. P. Resistance to fatal central nervous system disease by mouse hepatitis virus, strain JHM. II. Adherent cell mediated protection. J. Immunol. 1980;124:1733–1739. [PubMed] [Google Scholar]
  • 13.Stohlman S. A., Weiner L. P. Chronic central nervous system demyelination in mice after JHM virus infection. Neurol. 1981;31:38–44. doi: 10.1212/wnl.31.1.38. [DOI] [PubMed] [Google Scholar]
  • 14.Taguchi F., Makino S., Fujiwara K. Antigenic differentiation of mouse hepatitis virus by neutralization test. Microbiol. Immunol. 1982;26:741–745. doi: 10.1111/j.1348-0421.1982.tb00218.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Wege H., Stephanson R., Koga M., Wege H., ter Meulen V. Genetic variation of neutropic and non-neurotropic murine coronaviruses. J. gen. Virol. 1981;54:67–74. doi: 10.1099/0022-1317-54-1-67. [DOI] [PubMed] [Google Scholar]
  • 16.Wege H., Siddell S., ter Meulen V. The biology and pathogenesis of coronaviruses. Curr. Topics Microbiol. Immunol. 1982;99:165–200. doi: 10.1007/978-3-642-68528-6_5. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Virology are provided here courtesy of Nature Publishing Group

RESOURCES