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In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses
Following inoculation of continuous cell lines of neural and other derivations, persistent infections are established with facility by mouse hepatitis and measles viruses. This occurs equally with the prototype MHV(3) and its neurotropic variant JHM as well as with the Edmonston vaccine and SSPE Hal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
1978
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130880/ https://www.ncbi.nlm.nih.gov/pubmed/211715 http://dx.doi.org/10.1016/0042-6822(78)90289-1 |
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author | Lucas, Alexandra Coulter, Marion Anderson, Robert Dales, Samuel Flintoff, Wayne |
author_facet | Lucas, Alexandra Coulter, Marion Anderson, Robert Dales, Samuel Flintoff, Wayne |
author_sort | Lucas, Alexandra |
collection | PubMed |
description | Following inoculation of continuous cell lines of neural and other derivations, persistent infections are established with facility by mouse hepatitis and measles viruses. This occurs equally with the prototype MHV(3) and its neurotropic variant JHM as well as with the Edmonston vaccine and SSPE Hallé measles variants. In almost every instance that the infection becomes persistent at 32.5°, virus replication is found to be thermosensitive at 39.5°; however, progeny virus derived from such infections at 32.5° is itself thermostable when replicating in the indicator, fully permissive cell lines. The new data, therefore, reveal the existence of a host-conferred interrelationship between persistence and virus restriction at elevated temperature. They indicate that the two agents with neurotropic potential, when they become established as pathogens in the nervous system, could be under close host cell regulation involving as yet unknown mechanisms. |
format | Online Article Text |
id | pubmed-7130880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1978 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71308802020-04-08 In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses Lucas, Alexandra Coulter, Marion Anderson, Robert Dales, Samuel Flintoff, Wayne Virology Article Following inoculation of continuous cell lines of neural and other derivations, persistent infections are established with facility by mouse hepatitis and measles viruses. This occurs equally with the prototype MHV(3) and its neurotropic variant JHM as well as with the Edmonston vaccine and SSPE Hallé measles variants. In almost every instance that the infection becomes persistent at 32.5°, virus replication is found to be thermosensitive at 39.5°; however, progeny virus derived from such infections at 32.5° is itself thermostable when replicating in the indicator, fully permissive cell lines. The new data, therefore, reveal the existence of a host-conferred interrelationship between persistence and virus restriction at elevated temperature. They indicate that the two agents with neurotropic potential, when they become established as pathogens in the nervous system, could be under close host cell regulation involving as yet unknown mechanisms. Published by Elsevier Inc. 1978-07-15 2004-02-23 /pmc/articles/PMC7130880/ /pubmed/211715 http://dx.doi.org/10.1016/0042-6822(78)90289-1 Text en Copyright © 1978 Published by Elsevier Inc. 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 Lucas, Alexandra Coulter, Marion Anderson, Robert Dales, Samuel Flintoff, Wayne In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
title | In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
title_full | In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
title_fullStr | In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
title_full_unstemmed | In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
title_short | In vivo and in vitro models of demyelinating diseases II. Persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
title_sort | in vivo and in vitro models of demyelinating diseases ii. persistence and host-regulated thermosensitivity in cells of neural derivation infected with mouse hepatitis and measles viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130880/ https://www.ncbi.nlm.nih.gov/pubmed/211715 http://dx.doi.org/10.1016/0042-6822(78)90289-1 |
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