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An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses

Recombinant canine coronaviruses, resembling the transmissible gastroenteritis virus of swine (TGEV) in a 5′ fragment of the S glycoprotein, have been detected recently and showed to be present in canine populations. The 5′ fragment of the S protein (S′) of a TGEV-like canine coronavirus (CCoV), str...

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Autores principales: Elia, Gabriella, Decaro, Nicola, Martella, Vito, Lorusso, Eleonora, Mari, Viviana, Maria, Stella Lucente, Cordioli, Paolo, Buonavoglia, Canio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112913/
https://www.ncbi.nlm.nih.gov/pubmed/19878695
http://dx.doi.org/10.1016/j.jviromet.2009.10.015
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author Elia, Gabriella
Decaro, Nicola
Martella, Vito
Lorusso, Eleonora
Mari, Viviana
Maria, Stella Lucente
Cordioli, Paolo
Buonavoglia, Canio
author_facet Elia, Gabriella
Decaro, Nicola
Martella, Vito
Lorusso, Eleonora
Mari, Viviana
Maria, Stella Lucente
Cordioli, Paolo
Buonavoglia, Canio
author_sort Elia, Gabriella
collection PubMed
description Recombinant canine coronaviruses, resembling the transmissible gastroenteritis virus of swine (TGEV) in a 5′ fragment of the S glycoprotein, have been detected recently and showed to be present in canine populations. The 5′ fragment of the S protein (S′) of a TGEV-like canine coronavirus (CCoV), strain 174/06, was expressed in an Escherichia coli cell-free system. The purified recombinant polypeptide was employed to develop an ELISA test for the detection of TGEV-like CCoV-specific antibodies in dog sera. Four canine sera positive for TGEV-like CCoV, six sera positive to classical CCoV-II strains and 10 negative control sera were examined. The recombinant S′ was not recognized by antibodies to classical CCoV-II, as only sera from dogs infected experimentally with TGEV-like CCoV reacted strongly with the recombinant S′ polypeptide whereas dog sera with antibodies to classical CCoV-II did not react. As classical CCoV-II and TEGV-like CCoVs are related antigenically, the recombinant S′ ELISA is a useful method to investigate serologically the prevalence of TGEV-like CCoVs in dogs.
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spelling pubmed-71129132020-04-02 An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses Elia, Gabriella Decaro, Nicola Martella, Vito Lorusso, Eleonora Mari, Viviana Maria, Stella Lucente Cordioli, Paolo Buonavoglia, Canio J Virol Methods Article Recombinant canine coronaviruses, resembling the transmissible gastroenteritis virus of swine (TGEV) in a 5′ fragment of the S glycoprotein, have been detected recently and showed to be present in canine populations. The 5′ fragment of the S protein (S′) of a TGEV-like canine coronavirus (CCoV), strain 174/06, was expressed in an Escherichia coli cell-free system. The purified recombinant polypeptide was employed to develop an ELISA test for the detection of TGEV-like CCoV-specific antibodies in dog sera. Four canine sera positive for TGEV-like CCoV, six sera positive to classical CCoV-II strains and 10 negative control sera were examined. The recombinant S′ was not recognized by antibodies to classical CCoV-II, as only sera from dogs infected experimentally with TGEV-like CCoV reacted strongly with the recombinant S′ polypeptide whereas dog sera with antibodies to classical CCoV-II did not react. As classical CCoV-II and TEGV-like CCoVs are related antigenically, the recombinant S′ ELISA is a useful method to investigate serologically the prevalence of TGEV-like CCoVs in dogs. Elsevier B.V. 2010-02 2009-10-28 /pmc/articles/PMC7112913/ /pubmed/19878695 http://dx.doi.org/10.1016/j.jviromet.2009.10.015 Text en Copyright © 2009 Elsevier B.V. All rights reserved. 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
Elia, Gabriella
Decaro, Nicola
Martella, Vito
Lorusso, Eleonora
Mari, Viviana
Maria, Stella Lucente
Cordioli, Paolo
Buonavoglia, Canio
An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
title An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
title_full An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
title_fullStr An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
title_full_unstemmed An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
title_short An ELISA based on recombinant spike protein S for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
title_sort elisa based on recombinant spike protein s for the detection of antibodies to transmissible gastroenteritis virus of swine-like canine coronaviruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112913/
https://www.ncbi.nlm.nih.gov/pubmed/19878695
http://dx.doi.org/10.1016/j.jviromet.2009.10.015
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