Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1983;77(2-4):109-18.
doi: 10.1007/BF01309260.

Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice

Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice

J Pearson et al. Arch Virol. 1983.

Abstract

Suckling CD 1 mice infected intracerebrally or extraneurally with OC43 virus developed a lethal neurotropic infection with high titres of virus in the brain. Examination of infected brain by routine H & E staining revealed no necrosis even in extensively infected tissue. Resistance to infection developed with increasing age, and by 20 days of age mice were completely insusceptible to i.c. inoculation. Virus replication was also demonstrable by FA staining, in spinal cord, dorsal root ganglia and retina. All other tissues were insusceptible and in particular, macrophages from both susceptible and resistant mice were found to be resistant to infection both in vivo and in vitro. Immunosuppression rendered 15 day old mice more susceptible to infection but adult mice remained insusceptible. The transfer of immune or non immune spleen cells from resistant mice did not confer resistance to newborn mice. Treatment of resistant mice with anti interferon globulin (AIG) did not render them more susceptible. These results indicate that the immune response is partially responsible for the development of resistance to OC43 infection but that it is only partially protective and other factors must also be required. The basis for the unique susceptibility of neural tissues in suckling mice is being investigated.

PubMed Disclaimer

References

    1. Burks J. S., de Vald B. L., Jankovsky L. D., Gerdes J. C. Two coronaviruses isolated from central nervous system tissue of two multiple sclerosis patients. Science. 1980;209:933–934. - PubMed
    1. Cairns J. The initiation of vaccinia virus infection. Virology. 1960;11:603–623. - PubMed
    1. Gailly R., Warwick A., Bang F. B. Ontogeny of macrophage resistance to mouse hepatitisin vivo andin vitro. J. Exp. Med. 1976;125:537–547. - PMC - PubMed
    1. Levy Leblond E., Dupuy J. M. Neonatal susceptibility to MHV3 infection in mice. I. Transfer of resistance. J. Immunol. 1977;118:1219–1222. - PubMed
    1. Pickel K., Müller M. A., ter Meulen V. Analysis of age-dependent resistance to murine coronavirus JHM infection in mice. Infect. Immun. 1981;34:648–654. - PMC - PubMed

Publication types

LinkOut - more resources