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Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats

ORF3 is a supplemental open reading frame coding for an accessory glycoprotein gp3 of unknown function, only present in genotype I canine strain (CCoV-I) and some atypical feline FCoV strains. In these latter hosts, the ORF3 gene systematically displays one or two identical deletions leading to the...

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Autores principales: Pham-Hung d’Alexandry d’Orengiani, Anne-Laure, Duarte, Lidia, Pavio, Nicole, Le Poder, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114440/
https://www.ncbi.nlm.nih.gov/pubmed/25665789
http://dx.doi.org/10.1016/j.virusres.2015.01.027
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author Pham-Hung d’Alexandry d’Orengiani, Anne-Laure
Duarte, Lidia
Pavio, Nicole
Le Poder, Sophie
author_facet Pham-Hung d’Alexandry d’Orengiani, Anne-Laure
Duarte, Lidia
Pavio, Nicole
Le Poder, Sophie
author_sort Pham-Hung d’Alexandry d’Orengiani, Anne-Laure
collection PubMed
description ORF3 is a supplemental open reading frame coding for an accessory glycoprotein gp3 of unknown function, only present in genotype I canine strain (CCoV-I) and some atypical feline FCoV strains. In these latter hosts, the ORF3 gene systematically displays one or two identical deletions leading to the synthesis of truncated proteins gp3-Δ1 and gp3-Δ2. As deletions in CoV accessory proteins have already been involved in tissue or host switch, studies of these different gp3 proteins were conducted in canine and feline cell. All proteins oligomerise through covalent bonds, are N-glycosylated and are maintained in the ER in non-infected but also in CCoV-II infected cells, without any specific retention signal. However, deletions influence their level of expression. In canine cells, all proteins are expressed with similar level whereas in feline cells, the expression of gp3-Δ1 is higher than the two other forms of gp3. None of the gp3 proteins modulate the viral replication cycle of heterologous genotype II CCoV in canine cell line, leading to the conclusion that the gp3 proteins are probably advantageous only for CCoV-I and atypical FCoV strains.
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spelling pubmed-71144402020-04-02 Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats Pham-Hung d’Alexandry d’Orengiani, Anne-Laure Duarte, Lidia Pavio, Nicole Le Poder, Sophie Virus Res Article ORF3 is a supplemental open reading frame coding for an accessory glycoprotein gp3 of unknown function, only present in genotype I canine strain (CCoV-I) and some atypical feline FCoV strains. In these latter hosts, the ORF3 gene systematically displays one or two identical deletions leading to the synthesis of truncated proteins gp3-Δ1 and gp3-Δ2. As deletions in CoV accessory proteins have already been involved in tissue or host switch, studies of these different gp3 proteins were conducted in canine and feline cell. All proteins oligomerise through covalent bonds, are N-glycosylated and are maintained in the ER in non-infected but also in CCoV-II infected cells, without any specific retention signal. However, deletions influence their level of expression. In canine cells, all proteins are expressed with similar level whereas in feline cells, the expression of gp3-Δ1 is higher than the two other forms of gp3. None of the gp3 proteins modulate the viral replication cycle of heterologous genotype II CCoV in canine cell line, leading to the conclusion that the gp3 proteins are probably advantageous only for CCoV-I and atypical FCoV strains. Elsevier B.V. 2015-04-16 2015-02-07 /pmc/articles/PMC7114440/ /pubmed/25665789 http://dx.doi.org/10.1016/j.virusres.2015.01.027 Text en Copyright © 2015 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
Pham-Hung d’Alexandry d’Orengiani, Anne-Laure
Duarte, Lidia
Pavio, Nicole
Le Poder, Sophie
Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats
title Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats
title_full Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats
title_fullStr Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats
title_full_unstemmed Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats
title_short Characterisation of different forms of the accessory gp3 canine coronavirus type I protein identified in cats
title_sort characterisation of different forms of the accessory gp3 canine coronavirus type i protein identified in cats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114440/
https://www.ncbi.nlm.nih.gov/pubmed/25665789
http://dx.doi.org/10.1016/j.virusres.2015.01.027
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