MersV1, Ncbi, Merge, bibRecord, 001247

Genome-Wide Screen Reveals Valosin-Containing Protein Requirement for Coronavirus Exit from Endosomes.

Identifieur interne : 001247 ( Ncbi/Merge ); précédent : 001246; suivant : 001248

Genome-Wide Screen Reveals Valosin-Containing Protein Requirement for Coronavirus Exit from Endosomes.

Auteurs : Hui Hui Wong [Singapour] ; Pankaj Kumar [Singapour] ; Felicia Pei Ling Tay [Singapour] ; Dimitri Moreau [Singapour] ; Ding Xiang Liu [Singapour] ; Frédéric Bard [Singapour]

Source :

Journal of virology [ 1098-5514 ] ; 2015.

RBID : pubmed:26311884

Descripteurs français

KwdFr :
- Adenosine triphosphatases (génétique), Adenosine triphosphatases (métabolisme), Animaux, Annotation de séquence moléculaire, Cellules Vero, Endosomes (virologie), Humains, Infections à coronavirus (transmission), Libération de particules virales (physiologie), Lignée cellulaire, Petit ARN interférent (génétique), Protéines du cycle cellulaire (génétique), Protéines du cycle cellulaire (métabolisme), Technique d'immunofluorescence, Technique de Western, Virus de la bronchite infectieuse (physiologie), Étude d'association pangénomique.
MESH :
- génétique : Adenosine triphosphatases, Petit ARN interférent, Protéines du cycle cellulaire.
- métabolisme : Adenosine triphosphatases, Protéines du cycle cellulaire.
- physiologie : Libération de particules virales, Virus de la bronchite infectieuse.
- virologie : Endosomes.
- transmission : Animaux, Annotation de séquence moléculaire, Cellules Vero, Humains, Infections à coronavirus, Lignée cellulaire, Technique d'immunofluorescence, Technique de Western, Étude d'association pangénomique.

English descriptors

KwdEn :
- Adenosine Triphosphatases (genetics), Adenosine Triphosphatases (metabolism), Animals, Blotting, Western, Cell Cycle Proteins (genetics), Cell Cycle Proteins (metabolism), Cell Line, Chlorocebus aethiops, Coronavirus Infections (transmission), Endosomes (virology), Fluorescent Antibody Technique, Genome-Wide Association Study, Humans, Infectious bronchitis virus (physiology), Molecular Sequence Annotation, RNA, Small Interfering (genetics), Valosin Containing Protein, Vero Cells, Virus Release (physiology).
MESH :
- chemical , genetics : Adenosine Triphosphatases, Cell Cycle Proteins, RNA, Small Interfering.
- chemical , metabolism : Adenosine Triphosphatases, Cell Cycle Proteins.
- physiology : Infectious bronchitis virus, Virus Release.
- transmission : Coronavirus Infections.
- virology : Endosomes.
- Animals, Blotting, Western, Cell Line, Chlorocebus aethiops, Fluorescent Antibody Technique, Genome-Wide Association Study, Humans, Molecular Sequence Annotation, Valosin Containing Protein, Vero Cells.

Abstract

Coronaviruses are RNA viruses with a large zoonotic reservoir and propensity for host switching, representing a real threat for public health, as evidenced by severe acute respiratory syndrome (SARS) and the emerging Middle East respiratory syndrome (MERS). Cellular factors required for their replication are poorly understood. Using genome-wide small interfering RNA (siRNA) screening, we identified 83 novel genes supporting infectious bronchitis virus (IBV) replication in human cells. Thirty of these hits can be placed in a network of interactions with viral proteins and are involved in RNA splicing, membrane trafficking, and ubiquitin conjugation. In addition, our screen reveals an unexpected role for valosin-containing protein (VCP/p97) in early steps of infection. Loss of VCP inhibits a previously uncharacterized degradation of the nucleocapsid N protein. This inhibition derives from virus accumulation in early endosomes, suggesting a role for VCP in the maturation of virus-loaded endosomes. The several host factors identified in this study may provide avenues for targeted therapeutics.

DOI: 10.1128/JVI.01360-15
PubMed: 26311884

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 001491
to stream PubMed, to step Curation: 001491
to stream PubMed, to step Checkpoint: 001541

Links to Exploration step

pubmed:26311884

Le document en format XML

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<term>Blotting, Western</term>
<term>Cell Cycle Proteins (genetics)</term>
<term>Cell Cycle Proteins (metabolism)</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
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<term>Humans</term>
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<term>Adenosine triphosphatases (métabolisme)</term>
<term>Animaux</term>
<term>Annotation de séquence moléculaire</term>
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<term>Humains</term>
<term>Infections à coronavirus (transmission)</term>
<term>Libération de particules virales (physiologie)</term>
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<term>Protéines du cycle cellulaire</term>
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<term>Virus de la bronchite infectieuse</term>
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<front><div type="abstract" xml:lang="en">Coronaviruses are RNA viruses with a large zoonotic reservoir and propensity for host switching, representing a real threat for public health, as evidenced by severe acute respiratory syndrome (SARS) and the emerging Middle East respiratory syndrome (MERS). Cellular factors required for their replication are poorly understood. Using genome-wide small interfering RNA (siRNA) screening, we identified 83 novel genes supporting infectious bronchitis virus (IBV) replication in human cells. Thirty of these hits can be placed in a network of interactions with viral proteins and are involved in RNA splicing, membrane trafficking, and ubiquitin conjugation. In addition, our screen reveals an unexpected role for valosin-containing protein (VCP/p97) in early steps of infection. Loss of VCP inhibits a previously uncharacterized degradation of the nucleocapsid N protein. This inhibition derives from virus accumulation in early endosomes, suggesting a role for VCP in the maturation of virus-loaded endosomes. The several host factors identified in this study may provide avenues for targeted therapeutics.</div>
</front>
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<Abstract><AbstractText Label="UNLABELLED">Coronaviruses are RNA viruses with a large zoonotic reservoir and propensity for host switching, representing a real threat for public health, as evidenced by severe acute respiratory syndrome (SARS) and the emerging Middle East respiratory syndrome (MERS). Cellular factors required for their replication are poorly understood. Using genome-wide small interfering RNA (siRNA) screening, we identified 83 novel genes supporting infectious bronchitis virus (IBV) replication in human cells. Thirty of these hits can be placed in a network of interactions with viral proteins and are involved in RNA splicing, membrane trafficking, and ubiquitin conjugation. In addition, our screen reveals an unexpected role for valosin-containing protein (VCP/p97) in early steps of infection. Loss of VCP inhibits a previously uncharacterized degradation of the nucleocapsid N protein. This inhibition derives from virus accumulation in early endosomes, suggesting a role for VCP in the maturation of virus-loaded endosomes. The several host factors identified in this study may provide avenues for targeted therapeutics.</AbstractText>
<AbstractText Label="IMPORTANCE" NlmCategory="OBJECTIVE">Coronaviruses are RNA viruses representing a real threat for public health, as evidenced by SARS and the emerging MERS. However, cellular factors required for their replication are poorly understood. Using genome-wide siRNA screening, we identified novel genes supporting infectious bronchitis virus (IBV) replication in human cells. The several host factors identified in this study may provide directions for future research on targeted therapeutics.</AbstractText>
<CopyrightInformation>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</CopyrightInformation>
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<ForeName>Ding Xiang</ForeName>
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Genome-Wide Screen Reveals Valosin-Containing Protein Requirement for Coronavirus Exit from Endosomes.

Genome-Wide Screen Reveals Valosin-Containing Protein Requirement for Coronavirus Exit from Endosomes.

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