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Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus
A series of recombinant fusion proteins derived from equine arteritis virus (EAV) open reading frame (ORF) 7 have been used to define the immunoreactive region of the viral nucleocapsid (N) protein. Reactivities of recombinant N fusion proteins with post-infection equine sera in immunoblots and ELIS...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133929/ https://www.ncbi.nlm.nih.gov/pubmed/8837890 http://dx.doi.org/10.1016/0168-1702(95)00098-4 |
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author | Chirnside, E.D. Francis, P.M. Mumford, J.A. |
author_facet | Chirnside, E.D. Francis, P.M. Mumford, J.A. |
author_sort | Chirnside, E.D. |
collection | PubMed |
description | A series of recombinant fusion proteins derived from equine arteritis virus (EAV) open reading frame (ORF) 7 have been used to define the immunoreactive region of the viral nucleocapsid (N) protein. Reactivities of recombinant N fusion proteins with post-infection equine sera in immunoblots and ELISAs indicate that the major nucleocapsid protein epitope is located within amino acid residues 1–69. In ELISAs two recombinant nucleocapsid fusion proteins containing residues 1–69 (rN1–69) and 1–28 (rN1–28) discriminated between pre- and post-infection, and pre- and post-vaccination serum samples. Additionally rN1–69 and rN1–28 detected seroconversions following vaccination with a killed virus preparation, even in the absence of a detectable virus neutralising response. Although a good correlation existed between virus neutralising antibody and rN1–69 ELISA positive values in post-infection sera, all the rN proteins failed to induce any virus neutralising response in immunised rabbits. |
format | Online Article Text |
id | pubmed-7133929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71339292020-04-08 Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus Chirnside, E.D. Francis, P.M. Mumford, J.A. Virus Res Article A series of recombinant fusion proteins derived from equine arteritis virus (EAV) open reading frame (ORF) 7 have been used to define the immunoreactive region of the viral nucleocapsid (N) protein. Reactivities of recombinant N fusion proteins with post-infection equine sera in immunoblots and ELISAs indicate that the major nucleocapsid protein epitope is located within amino acid residues 1–69. In ELISAs two recombinant nucleocapsid fusion proteins containing residues 1–69 (rN1–69) and 1–28 (rN1–28) discriminated between pre- and post-infection, and pre- and post-vaccination serum samples. Additionally rN1–69 and rN1–28 detected seroconversions following vaccination with a killed virus preparation, even in the absence of a detectable virus neutralising response. Although a good correlation existed between virus neutralising antibody and rN1–69 ELISA positive values in post-infection sera, all the rN proteins failed to induce any virus neutralising response in immunised rabbits. Published by Elsevier B.V. 1995-12 2000-03-07 /pmc/articles/PMC7133929/ /pubmed/8837890 http://dx.doi.org/10.1016/0168-1702(95)00098-4 Text en Copyright © 1995 Published by Elsevier B.V. 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 Chirnside, E.D. Francis, P.M. Mumford, J.A. Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
title | Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
title_full | Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
title_fullStr | Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
title_full_unstemmed | Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
title_short | Expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
title_sort | expression cloning and antigenic analysis of the nucleocapsid protein of equine arteritis virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133929/ https://www.ncbi.nlm.nih.gov/pubmed/8837890 http://dx.doi.org/10.1016/0168-1702(95)00098-4 |
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