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Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line
Subacute sclerosing panencephalitis (SSPE) is a slowly progressing fatal human disease of the central nervous system (CNS) that is associated with measles virus persistence. Virus nucleocapsids are present in the brain(1,2) and the patient is in a state of hyperimmunization towards this agent. Howev...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
1983
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094927/ https://www.ncbi.nlm.nih.gov/pubmed/6888557 http://dx.doi.org/10.1038/305153a0 |
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author | Carter, Michael J. Willcocks, Margaret M. ter Meulen, Volker |
author_facet | Carter, Michael J. Willcocks, Margaret M. ter Meulen, Volker |
author_sort | Carter, Michael J. |
collection | PubMed |
description | Subacute sclerosing panencephalitis (SSPE) is a slowly progressing fatal human disease of the central nervous system (CNS) that is associated with measles virus persistence. Virus nucleocapsids are present in the brain(1,2) and the patient is in a state of hyperimmunization towards this agent. However, although all other structural polypeptides are recognized by the immune system, there is a markedly decreased antibody response towards virus matrix or membrane protein(3,4). Matrix protein has not been detected in brain cells(5) and infectious virus is not present. The absence of this virus structural polypeptide is thought to account for the apparent restriction in virus maturation both in vivo and in vitro. SSPE viruses can only rarely be rescued from brain tissue by co-cultivation or cell fusion techniques using tissue culture cell lines susceptible to measles virus infection(6). Often this procedure fails to yield a lytic budding virus but produces instead a carrier cell line in which the agent is cell associated. These lines (known as SSPE cell lines) also do not contain matrix protein(7,8). However, the reason for this deficiency is unknown. We have therefore now examined an SSPE cell line which does not yield infectious virus in order to define this process further. We found that although messenger RNA for membrane protein was present, it was unable to form normal matrix protein in translation reactions. |
format | Online Article Text |
id | pubmed-7094927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1983 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70949272020-03-26 Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line Carter, Michael J. Willcocks, Margaret M. ter Meulen, Volker Nature Article Subacute sclerosing panencephalitis (SSPE) is a slowly progressing fatal human disease of the central nervous system (CNS) that is associated with measles virus persistence. Virus nucleocapsids are present in the brain(1,2) and the patient is in a state of hyperimmunization towards this agent. However, although all other structural polypeptides are recognized by the immune system, there is a markedly decreased antibody response towards virus matrix or membrane protein(3,4). Matrix protein has not been detected in brain cells(5) and infectious virus is not present. The absence of this virus structural polypeptide is thought to account for the apparent restriction in virus maturation both in vivo and in vitro. SSPE viruses can only rarely be rescued from brain tissue by co-cultivation or cell fusion techniques using tissue culture cell lines susceptible to measles virus infection(6). Often this procedure fails to yield a lytic budding virus but produces instead a carrier cell line in which the agent is cell associated. These lines (known as SSPE cell lines) also do not contain matrix protein(7,8). However, the reason for this deficiency is unknown. We have therefore now examined an SSPE cell line which does not yield infectious virus in order to define this process further. We found that although messenger RNA for membrane protein was present, it was unable to form normal matrix protein in translation reactions. Nature Publishing Group UK 1983 /pmc/articles/PMC7094927/ /pubmed/6888557 http://dx.doi.org/10.1038/305153a0 Text en © Nature Publishing Group 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 | Article Carter, Michael J. Willcocks, Margaret M. ter Meulen, Volker Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
title | Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
title_full | Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
title_fullStr | Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
title_full_unstemmed | Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
title_short | Defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
title_sort | defective translation of measles virus matrix protein in a subacute sclerosing panencephalitis cell line |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094927/ https://www.ncbi.nlm.nih.gov/pubmed/6888557 http://dx.doi.org/10.1038/305153a0 |
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