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The 3a protein of severe acute respiratory syndrome-associated coronavirus induces apoptosis in Vero E6 cells.

Identifieur interne : 002443 ( PubMed/Checkpoint ); précédent : 002442; suivant : 002444

The 3a protein of severe acute respiratory syndrome-associated coronavirus induces apoptosis in Vero E6 cells.

Auteurs : Patrick T W. Law [République populaire de Chine] ; Chi-Hang Wong [République populaire de Chine] ; Thomas C C. Au [République populaire de Chine] ; Chi-Pang Chuck [République populaire de Chine] ; Siu-Kai Kong [République populaire de Chine] ; Paul K S. Chan [République populaire de Chine] ; Ka-Fai To [République populaire de Chine] ; Anthony W I. Lo [République populaire de Chine] ; Judy Y W. Chan [République populaire de Chine] ; Yick-Keung Suen [République populaire de Chine] ; H Y Edwin Chan [République populaire de Chine] ; Kwok-Pui Fung [République populaire de Chine] ; Mary M Y. Waye [République populaire de Chine] ; Joseph J Y. Sung [République populaire de Chine] ; Y M Dennis Lo [République populaire de Chine] ; Stephen K W. Tsui [République populaire de Chine]

Source :

RBID : pubmed:15958670

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English descriptors

Abstract

An outbreak of severe acute respiratory syndrome (SARS) occurred in China and the first case emerged in mid-November 2002. The aetiological agent of this disease was found to be a previously unknown coronavirus, SARS-associated coronavirus (SARS-CoV). The detailed pathology of SARS-CoV infection and the host response to the viral infection are still not known. The 3a gene encodes a non-structural viral protein, which is predicted to be a transmembrane protein. In this study, it was shown that the 3a protein was expressed in the lungs and intestinal tissues of SARS patients and that the protein localized to the endoplasmic reticulum in 3a-transfected monkey kidney Vero E6 cells. In vitro experiments of chromatin condensation and DNA fragmentation suggested that the 3a protein may trigger apoptosis. These data showed that overexpression of a single SARS-CoV protein can induce apoptosis in vitro.

DOI: 10.1099/vir.0.80813-0
PubMed: 15958670


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pubmed:15958670

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<name sortKey="Waye, Mary M Y" sort="Waye, Mary M Y" uniqKey="Waye M" first="Mary M Y" last="Waye">Mary M Y. Waye</name>
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<title level="j">The Journal of general virology</title>
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<term>Animals</term>
<term>Apoptosis</term>
<term>Chlorocebus aethiops</term>
<term>Endoplasmic Reticulum (metabolism)</term>
<term>Endoplasmic Reticulum (virology)</term>
<term>Humans</term>
<term>Intestinal Mucosa (metabolism)</term>
<term>Intestines (virology)</term>
<term>Lung (metabolism)</term>
<term>Lung (virology)</term>
<term>SARS Virus (metabolism)</term>
<term>SARS Virus (pathogenicity)</term>
<term>Severe Acute Respiratory Syndrome (virology)</term>
<term>Vero Cells</term>
<term>Viral Proteins (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Apoptose</term>
<term>Cellules Vero</term>
<term>Humains</term>
<term>Intestins (virologie)</term>
<term>Muqueuse intestinale (métabolisme)</term>
<term>Poumon (métabolisme)</term>
<term>Poumon (virologie)</term>
<term>Protéines virales (métabolisme)</term>
<term>Réticulum endoplasmique (métabolisme)</term>
<term>Réticulum endoplasmique (virologie)</term>
<term>Syndrome respiratoire aigu sévère (virologie)</term>
<term>Virus du SRAS (métabolisme)</term>
<term>Virus du SRAS (pathogénicité)</term>
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<term>Viral Proteins</term>
</keywords>
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<term>Endoplasmic Reticulum</term>
<term>Intestinal Mucosa</term>
<term>Lung</term>
<term>SARS Virus</term>
</keywords>
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<term>Muqueuse intestinale</term>
<term>Poumon</term>
<term>Protéines virales</term>
<term>Réticulum endoplasmique</term>
<term>Virus du SRAS</term>
</keywords>
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<term>Endoplasmic Reticulum</term>
<term>Intestines</term>
<term>Lung</term>
<term>Severe Acute Respiratory Syndrome</term>
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<term>Apoptosis</term>
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<term>Vero Cells</term>
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<div type="abstract" xml:lang="en">An outbreak of severe acute respiratory syndrome (SARS) occurred in China and the first case emerged in mid-November 2002. The aetiological agent of this disease was found to be a previously unknown coronavirus, SARS-associated coronavirus (SARS-CoV). The detailed pathology of SARS-CoV infection and the host response to the viral infection are still not known. The 3a gene encodes a non-structural viral protein, which is predicted to be a transmembrane protein. In this study, it was shown that the 3a protein was expressed in the lungs and intestinal tissues of SARS patients and that the protein localized to the endoplasmic reticulum in 3a-transfected monkey kidney Vero E6 cells. In vitro experiments of chromatin condensation and DNA fragmentation suggested that the 3a protein may trigger apoptosis. These data showed that overexpression of a single SARS-CoV protein can induce apoptosis in vitro.</div>
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<Day>28</Day>
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<Day>06</Day>
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<Volume>86</Volume>
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<Year>2005</Year>
<Month>Jul</Month>
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<Title>The Journal of general virology</Title>
<ISOAbbreviation>J. Gen. Virol.</ISOAbbreviation>
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<ArticleTitle>The 3a protein of severe acute respiratory syndrome-associated coronavirus induces apoptosis in Vero E6 cells.</ArticleTitle>
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<MedlinePgn>1921-1930</MedlinePgn>
</Pagination>
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<AbstractText>An outbreak of severe acute respiratory syndrome (SARS) occurred in China and the first case emerged in mid-November 2002. The aetiological agent of this disease was found to be a previously unknown coronavirus, SARS-associated coronavirus (SARS-CoV). The detailed pathology of SARS-CoV infection and the host response to the viral infection are still not known. The 3a gene encodes a non-structural viral protein, which is predicted to be a transmembrane protein. In this study, it was shown that the 3a protein was expressed in the lungs and intestinal tissues of SARS patients and that the protein localized to the endoplasmic reticulum in 3a-transfected monkey kidney Vero E6 cells. In vitro experiments of chromatin condensation and DNA fragmentation suggested that the 3a protein may trigger apoptosis. These data showed that overexpression of a single SARS-CoV protein can induce apoptosis in vitro.</AbstractText>
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<LastName>Law</LastName>
<ForeName>Patrick T W</ForeName>
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<Affiliation>Department of Biochemistry, The Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Centre for Emerging Infectious Diseases, The Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.</Affiliation>
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</AffiliationInfo>
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<Affiliation>Department of Biochemistry, The Chinese University of Hong Kong, Shatin, NT, Hong Kong SAR, China.</Affiliation>
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<name sortKey="Lo, Anthony W I" sort="Lo, Anthony W I" uniqKey="Lo A" first="Anthony W I" last="Lo">Anthony W I. Lo</name>
<name sortKey="Lo, Y M Dennis" sort="Lo, Y M Dennis" uniqKey="Lo Y" first="Y M Dennis" last="Lo">Y M Dennis Lo</name>
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