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Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice
Suckling CD1 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 d...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
1983
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087107/ https://www.ncbi.nlm.nih.gov/pubmed/6195997 http://dx.doi.org/10.1007/BF01309260 |
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author | Pearson, J. Mims, C. A. |
author_facet | Pearson, J. Mims, C. A. |
author_sort | Pearson, J. |
collection | PubMed |
description | Suckling CD1 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 bothin vivo andin 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. |
format | Online Article Text |
id | pubmed-7087107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1983 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-70871072020-03-23 Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice Pearson, J. Mims, C. A. Arch Virol Original Papers Suckling CD1 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 bothin vivo andin 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. Springer-Verlag 1983 /pmc/articles/PMC7087107/ /pubmed/6195997 http://dx.doi.org/10.1007/BF01309260 Text en © Springer-Verlag 1983 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Papers Pearson, J. Mims, C. A. Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice |
title | Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice |
title_full | Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice |
title_fullStr | Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice |
title_full_unstemmed | Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice |
title_short | Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice |
title_sort | selective vulnerability of neural cells and age-related susceptibility to oc43 virus in mice |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087107/ https://www.ncbi.nlm.nih.gov/pubmed/6195997 http://dx.doi.org/10.1007/BF01309260 |
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