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Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes

Three-day-old suckling mice inoculated intracerebrally (i.c.) with the 67N strain of haemagglutinating encephalomyelitis virus (HEV) showed nervous signs and died. The virus was passaged 10 times in suckling mice and was designated the MB-67N strain. The pathogenesis of MB-67N was studied with vario...

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Autores principales: Yagami, K., Hirai, K., Hirano, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 1986
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130377/
https://www.ncbi.nlm.nih.gov/pubmed/3546411
http://dx.doi.org/10.1016/0021-9975(86)90061-7
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author Yagami, K.
Hirai, K.
Hirano, N.
author_facet Yagami, K.
Hirai, K.
Hirano, N.
author_sort Yagami, K.
collection PubMed
description Three-day-old suckling mice inoculated intracerebrally (i.c.) with the 67N strain of haemagglutinating encephalomyelitis virus (HEV) showed nervous signs and died. The virus was passaged 10 times in suckling mice and was designated the MB-67N strain. The pathogenesis of MB-67N was studied with various ages of mice and inoculation routes. All mice inoculated i.c. with a large dose of virus died regardless of age, although a smaller dose caused fatal infection only in suckling mice. By intranasal, intraperitoneal and subcutaneous inoculation, the virus also killed suckling mice under 16 days old, but not older mice, even with a large dose. The susceptibility of mice for the MB-67N strain was influenced by age and inoculation routes. High titres of virus were re-isolated from the brain of diseased mice after inoculation by any route, but not from other organs. Histologically, numerous areas of severe tocal necrosis were produced in the cerebral cortex. Specific immuno-fluorescence and numerous viral particles were found in the cytoplasm of nerve cells by immuno-fluorescence staining and electron microscopy. These findings indicate that the MB-67N propagates mainly in the central nervous system and nerve cells serve as a main target of virus replication.
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spelling pubmed-71303772020-04-08 Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes Yagami, K. Hirai, K. Hirano, N. J Comp Pathol Article Three-day-old suckling mice inoculated intracerebrally (i.c.) with the 67N strain of haemagglutinating encephalomyelitis virus (HEV) showed nervous signs and died. The virus was passaged 10 times in suckling mice and was designated the MB-67N strain. The pathogenesis of MB-67N was studied with various ages of mice and inoculation routes. All mice inoculated i.c. with a large dose of virus died regardless of age, although a smaller dose caused fatal infection only in suckling mice. By intranasal, intraperitoneal and subcutaneous inoculation, the virus also killed suckling mice under 16 days old, but not older mice, even with a large dose. The susceptibility of mice for the MB-67N strain was influenced by age and inoculation routes. High titres of virus were re-isolated from the brain of diseased mice after inoculation by any route, but not from other organs. Histologically, numerous areas of severe tocal necrosis were produced in the cerebral cortex. Specific immuno-fluorescence and numerous viral particles were found in the cytoplasm of nerve cells by immuno-fluorescence staining and electron microscopy. These findings indicate that the MB-67N propagates mainly in the central nervous system and nerve cells serve as a main target of virus replication. Published by Elsevier Ltd. 1986-11 2004-09-23 /pmc/articles/PMC7130377/ /pubmed/3546411 http://dx.doi.org/10.1016/0021-9975(86)90061-7 Text en Copyright © 1986 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Yagami, K.
Hirai, K.
Hirano, N.
Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes
title Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes
title_full Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes
title_fullStr Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes
title_full_unstemmed Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes
title_short Pathogenesis of haemagglutinating encephalomyelitis virus (HEV) in mice experimentally infected by different routes
title_sort pathogenesis of haemagglutinating encephalomyelitis virus (hev) in mice experimentally infected by different routes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130377/
https://www.ncbi.nlm.nih.gov/pubmed/3546411
http://dx.doi.org/10.1016/0021-9975(86)90061-7
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