SrasV1, Ncbi, Merge, bibRecord, 001683

Role for nonstructural protein 1 of severe acute respiratory syndrome coronavirus in chemokine dysregulation.

Identifieur interne : 001683 ( Ncbi/Merge ); précédent : 001682; suivant : 001684

Role for nonstructural protein 1 of severe acute respiratory syndrome coronavirus in chemokine dysregulation.

Auteurs : Anna H Y. Law [République populaire de Chine] ; Davy C W. Lee ; Benny K W. Cheung ; Howard C H. Yim ; Allan S Y. Lau

Source :

Journal of virology [ 0022-538X ] ; 2007.

RBID : pubmed:17035307

Descripteurs français

KwdFr :
- Chimiokine CCL3, Chimiokine CCL5, Chimiokine CXCL10, Chimiokines (génétique), Chimiokines (métabolisme), Chimiokines CC (génétique), Chimiokines CC (métabolisme), Chimiokines CXC (génétique), Chimiokines CXC (métabolisme), Facteur de transcription NF-kappa B (génétique), Facteur de transcription NF-kappa B (métabolisme), Muqueuse respiratoire (cytologie), Muqueuse respiratoire (virologie), Protéines de l'enveloppe virale (physiologie), Protéines de la matrice virale (physiologie), Protéines virales non structurales (métabolisme), Régulation de l'expression des gènes, Virus du SRAS (métabolisme), Virus du SRAS (pathogénicité).
MESH :
- cytologie : Muqueuse respiratoire.
- génétique : Chimiokines, Chimiokines CC, Chimiokines CXC, Facteur de transcription NF-kappa B.
- métabolisme : Chimiokines, Chimiokines CC, Chimiokines CXC, Facteur de transcription NF-kappa B, Protéines virales non structurales, Virus du SRAS.
- pathogénicité : Virus du SRAS.
- physiologie : Protéines de l'enveloppe virale, Protéines de la matrice virale.
- virologie : Muqueuse respiratoire.
- Chimiokine CCL3, Chimiokine CCL5, Chimiokine CXCL10, Régulation de l'expression des gènes.

English descriptors

KwdEn :
- Chemokine CCL3, Chemokine CCL5, Chemokine CXCL10, Chemokines (genetics), Chemokines (metabolism), Chemokines, CC (genetics), Chemokines, CC (metabolism), Chemokines, CXC (genetics), Chemokines, CXC (metabolism), Gene Expression Regulation, NF-kappa B (genetics), NF-kappa B (metabolism), Respiratory Mucosa (cytology), Respiratory Mucosa (virology), SARS Virus (metabolism), SARS Virus (pathogenicity), Viral Envelope Proteins (physiology), Viral Matrix Proteins (physiology), Viral Nonstructural Proteins (metabolism).
MESH :
- chemical , genetics : Chemokines, Chemokines, CC, Chemokines, CXC, NF-kappa B.
- chemical , metabolism : Chemokines, Chemokines, CC, Chemokines, CXC, NF-kappa B, Viral Nonstructural Proteins.
- chemical , physiology : Viral Envelope Proteins, Viral Matrix Proteins.
- chemical : Chemokine CCL3, Chemokine CCL5, Chemokine CXCL10.
- cytology : Respiratory Mucosa.
- metabolism : SARS Virus.
- pathogenicity : SARS Virus.
- virology : Respiratory Mucosa.
- Gene Expression Regulation.

Abstract

Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus. Since its associated morbidity and mortality have been postulated to be due to immune dysregulation, we investigated which of the viral proteins is responsible for chemokine overexpression. To delineate the viral and cellular factor interactions, the role of four SARS coronavirus proteins, including nonstructural protein 1 (nsp-1), nsp-5, envelope, and membrane, were examined in terms of cytokine induction. Our results showed that the SARS coronavirus nsp-1 plays an important role in CCL5, CXCL10, and CCL3 expression in human lung epithelial cells via the activation of NF-kappaB.

DOI: 10.1128/JVI.02336-05
PubMed: 17035307

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

to stream PubMed, to step Corpus: 002067
to stream PubMed, to step Curation: 002067
to stream PubMed, to step Checkpoint: 001D12

Links to Exploration step

pubmed:17035307

Le document en format XML

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<term>Chemokines (metabolism)</term>
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<term>Chemokines, CXC (metabolism)</term>
<term>Gene Expression Regulation</term>
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<term>NF-kappa B (metabolism)</term>
<term>Respiratory Mucosa (cytology)</term>
<term>Respiratory Mucosa (virology)</term>
<term>SARS Virus (metabolism)</term>
<term>SARS Virus (pathogenicity)</term>
<term>Viral Envelope Proteins (physiology)</term>
<term>Viral Matrix Proteins (physiology)</term>
<term>Viral Nonstructural Proteins (metabolism)</term>
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<term>Chimiokine CXCL10</term>
<term>Chimiokines (génétique)</term>
<term>Chimiokines (métabolisme)</term>
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<term>Facteur de transcription NF-kappa B (génétique)</term>
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<term>Muqueuse respiratoire (virologie)</term>
<term>Protéines de l'enveloppe virale (physiologie)</term>
<term>Protéines de la matrice virale (physiologie)</term>
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<term>Chemokines, CXC</term>
<term>NF-kappa B</term>
<term>Viral Nonstructural Proteins</term>
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<term>Chemokine CXCL10</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Chimiokines</term>
<term>Chimiokines CC</term>
<term>Chimiokines CXC</term>
<term>Facteur de transcription NF-kappa B</term>
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<term>Chimiokines CC</term>
<term>Chimiokines CXC</term>
<term>Facteur de transcription NF-kappa B</term>
<term>Protéines virales non structurales</term>
<term>Virus du SRAS</term>
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<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>SARS Virus</term>
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus. Since its associated morbidity and mortality have been postulated to be due to immune dysregulation, we investigated which of the viral proteins is responsible for chemokine overexpression. To delineate the viral and cellular factor interactions, the role of four SARS coronavirus proteins, including nonstructural protein 1 (nsp-1), nsp-5, envelope, and membrane, were examined in terms of cytokine induction. Our results showed that the SARS coronavirus nsp-1 plays an important role in CCL5, CXCL10, and CCL3 expression in human lung epithelial cells via the activation of NF-kappaB.</div>
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<Abstract><AbstractText>Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus. Since its associated morbidity and mortality have been postulated to be due to immune dysregulation, we investigated which of the viral proteins is responsible for chemokine overexpression. To delineate the viral and cellular factor interactions, the role of four SARS coronavirus proteins, including nonstructural protein 1 (nsp-1), nsp-5, envelope, and membrane, were examined in terms of cytokine induction. Our results showed that the SARS coronavirus nsp-1 plays an important role in CCL5, CXCL10, and CCL3 expression in human lung epithelial cells via the activation of NF-kappaB.</AbstractText>
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<affiliations><list><country><li>République populaire de Chine</li>
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<name sortKey="Lee, Davy C W" sort="Lee, Davy C W" uniqKey="Lee D" first="Davy C W" last="Lee">Davy C W. Lee</name>
<name sortKey="Yim, Howard C H" sort="Yim, Howard C H" uniqKey="Yim H" first="Howard C H" last="Yim">Howard C H. Yim</name>
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   |texte=   Role for nonstructural protein 1 of severe acute respiratory syndrome coronavirus in chemokine dysregulation.
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Role for nonstructural protein 1 of severe acute respiratory syndrome coronavirus in chemokine dysregulation.

Role for nonstructural protein 1 of severe acute respiratory syndrome coronavirus in chemokine dysregulation.

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