Identification and characterization of a novel non-structural protein of bluetongue virus.

Bluetongue virus (BTV) is the causative agent of a major disease of livestock (bluetongue). For over two decades, it has been widely accepted that the 10 segments of the dsRNA genome of BTV encode for 7 structural and 3 non-structural proteins. The non-structural proteins (NS1, NS2, NS3/NS3a) play d...

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Main Authors: Maxime Ratinier, Marco Caporale, Matthew Golder, Giulia Franzoni, Kathryn Allan, Sandro Filipe Nunes, Alessia Armezzani, Amr Bayoumy, Frazer Rixon, Andrew Shaw, Massimo Palmarini
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-12-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC3248566?pdf=render
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spelling doaj-fbfb63572adb41878d8da0495d644a1a2020-11-25T01:25:45ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-12-01712e100247710.1371/journal.ppat.1002477Identification and characterization of a novel non-structural protein of bluetongue virus.Maxime RatinierMarco CaporaleMatthew GolderGiulia FranzoniKathryn AllanSandro Filipe NunesAlessia ArmezzaniAmr BayoumyFrazer RixonAndrew ShawMassimo PalmariniBluetongue virus (BTV) is the causative agent of a major disease of livestock (bluetongue). For over two decades, it has been widely accepted that the 10 segments of the dsRNA genome of BTV encode for 7 structural and 3 non-structural proteins. The non-structural proteins (NS1, NS2, NS3/NS3a) play different key roles during the viral replication cycle. In this study we show that BTV expresses a fourth non-structural protein (that we designated NS4) encoded by an open reading frame in segment 9 overlapping the open reading frame encoding VP6. NS4 is 77-79 amino acid residues in length and highly conserved among several BTV serotypes/strains. NS4 was expressed early post-infection and localized in the nucleoli of BTV infected cells. By reverse genetics, we showed that NS4 is dispensable for BTV replication in vitro, both in mammalian and insect cells, and does not affect viral virulence in murine models of bluetongue infection. Interestingly, NS4 conferred a replication advantage to BTV-8, but not to BTV-1, in cells in an interferon (IFN)-induced antiviral state. However, the BTV-1 NS4 conferred a replication advantage both to a BTV-8 reassortant containing the entire segment 9 of BTV-1 and to a BTV-8 mutant with the NS4 identical to the homologous BTV-1 protein. Collectively, this study suggests that NS4 plays an important role in virus-host interaction and is one of the mechanisms played, at least by BTV-8, to counteract the antiviral response of the host. In addition, the distinct nucleolar localization of NS4, being expressed by a virus that replicates exclusively in the cytoplasm, offers new avenues to investigate the multiple roles played by the nucleolus in the biology of the cell.http://europepmc.org/articles/PMC3248566?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Maxime Ratinier
Marco Caporale
Matthew Golder
Giulia Franzoni
Kathryn Allan
Sandro Filipe Nunes
Alessia Armezzani
Amr Bayoumy
Frazer Rixon
Andrew Shaw
Massimo Palmarini
spellingShingle Maxime Ratinier
Marco Caporale
Matthew Golder
Giulia Franzoni
Kathryn Allan
Sandro Filipe Nunes
Alessia Armezzani
Amr Bayoumy
Frazer Rixon
Andrew Shaw
Massimo Palmarini
Identification and characterization of a novel non-structural protein of bluetongue virus.
PLoS Pathogens
author_facet Maxime Ratinier
Marco Caporale
Matthew Golder
Giulia Franzoni
Kathryn Allan
Sandro Filipe Nunes
Alessia Armezzani
Amr Bayoumy
Frazer Rixon
Andrew Shaw
Massimo Palmarini
author_sort Maxime Ratinier
title Identification and characterization of a novel non-structural protein of bluetongue virus.
title_short Identification and characterization of a novel non-structural protein of bluetongue virus.
title_full Identification and characterization of a novel non-structural protein of bluetongue virus.
title_fullStr Identification and characterization of a novel non-structural protein of bluetongue virus.
title_full_unstemmed Identification and characterization of a novel non-structural protein of bluetongue virus.
title_sort identification and characterization of a novel non-structural protein of bluetongue virus.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2011-12-01
description Bluetongue virus (BTV) is the causative agent of a major disease of livestock (bluetongue). For over two decades, it has been widely accepted that the 10 segments of the dsRNA genome of BTV encode for 7 structural and 3 non-structural proteins. The non-structural proteins (NS1, NS2, NS3/NS3a) play different key roles during the viral replication cycle. In this study we show that BTV expresses a fourth non-structural protein (that we designated NS4) encoded by an open reading frame in segment 9 overlapping the open reading frame encoding VP6. NS4 is 77-79 amino acid residues in length and highly conserved among several BTV serotypes/strains. NS4 was expressed early post-infection and localized in the nucleoli of BTV infected cells. By reverse genetics, we showed that NS4 is dispensable for BTV replication in vitro, both in mammalian and insect cells, and does not affect viral virulence in murine models of bluetongue infection. Interestingly, NS4 conferred a replication advantage to BTV-8, but not to BTV-1, in cells in an interferon (IFN)-induced antiviral state. However, the BTV-1 NS4 conferred a replication advantage both to a BTV-8 reassortant containing the entire segment 9 of BTV-1 and to a BTV-8 mutant with the NS4 identical to the homologous BTV-1 protein. Collectively, this study suggests that NS4 plays an important role in virus-host interaction and is one of the mechanisms played, at least by BTV-8, to counteract the antiviral response of the host. In addition, the distinct nucleolar localization of NS4, being expressed by a virus that replicates exclusively in the cytoplasm, offers new avenues to investigate the multiple roles played by the nucleolus in the biology of the cell.
url http://europepmc.org/articles/PMC3248566?pdf=render
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