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SARS coronavirus induces apoptosis in Vero E6 cells.

Identifieur interne : 005131 ( Main/Exploration ); précédent : 005130; suivant : 005132

SARS coronavirus induces apoptosis in Vero E6 cells.

Auteurs : Huimin Yan [République populaire de Chine] ; Gengfu Xiao ; Jiamin Zhang ; Yuanyang Hu ; Fang Yuan ; David K. Cole ; Congyi Zheng ; George F. Gao

Source :

RBID : pubmed:15170624

Descripteurs français

English descriptors

Abstract

Severe acute respiratory syndrome (SARS) is an emerging infectious disease. Its etiological agent has been convincingly identified as a new member of family Coronaviridae (SARS-CoV). It causes serious damage to the respiratory system yet the mechanism is not clear. Infection-induced apoptosis or necrosis is suspected but no direct evidence for this yet exists. To date, Vero E6 cells are the only cell line that could be used to replicate the virus with obvious CPE (cytopathic effect) in vitro. It is known for some viruses (including members of family Coronaviridae) that CPE can be caused either by virus-induced apoptosis (active death) or cell necrosis (passive death). In this study, we examined the apoptosis in the SARS-CoV infected Vero E6 cells. Indeed, the results do show that the CPE was induced by apoptosis rather than necrosis, shown by typical DNA fragmentation, through the existence of apoptotic bodies and swollen mitochondria. This observation has some implications for the SARS-CoV pathogenicity: SARS-CoV does induce apoptosis in cell cultures and might have the same effect in vivo, responsible for the severe damage of the respiratory system.

DOI: 10.1002/jmv.20094
PubMed: 15170624


Affiliations:


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Le document en format XML

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<term>Apoptosis</term>
<term>Cell Nucleus (pathology)</term>
<term>Cell Nucleus (ultrastructure)</term>
<term>Chlorocebus aethiops</term>
<term>Chromatin (ultrastructure)</term>
<term>Cytopathogenic Effect, Viral</term>
<term>DNA Fragmentation</term>
<term>Fluorescence</term>
<term>Immunochemistry</term>
<term>Microscopy, Electron</term>
<term>Mitochondria (pathology)</term>
<term>Mitochondria (ultrastructure)</term>
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<term>SARS Virus (pathogenicity)</term>
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<term>Apoptose</term>
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<term>Chromatine (ultrastructure)</term>
<term>Coloration et marquage</term>
<term>Effet cytopathogène viral</term>
<term>Fluorescence</term>
<term>Fragmentation de l'ADN</term>
<term>Immunochimie</term>
<term>Microscopie électronique</term>
<term>Mitochondries (anatomopathologie)</term>
<term>Mitochondries (ultrastructure)</term>
<term>Noyau de la cellule (anatomopathologie)</term>
<term>Noyau de la cellule (ultrastructure)</term>
<term>Virus du SRAS (croissance et développement)</term>
<term>Virus du SRAS (pathogénicité)</term>
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<term>Noyau de la cellule</term>
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<term>Virus du SRAS</term>
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<div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is an emerging infectious disease. Its etiological agent has been convincingly identified as a new member of family Coronaviridae (SARS-CoV). It causes serious damage to the respiratory system yet the mechanism is not clear. Infection-induced apoptosis or necrosis is suspected but no direct evidence for this yet exists. To date, Vero E6 cells are the only cell line that could be used to replicate the virus with obvious CPE (cytopathic effect) in vitro. It is known for some viruses (including members of family Coronaviridae) that CPE can be caused either by virus-induced apoptosis (active death) or cell necrosis (passive death). In this study, we examined the apoptosis in the SARS-CoV infected Vero E6 cells. Indeed, the results do show that the CPE was induced by apoptosis rather than necrosis, shown by typical DNA fragmentation, through the existence of apoptotic bodies and swollen mitochondria. This observation has some implications for the SARS-CoV pathogenicity: SARS-CoV does induce apoptosis in cell cultures and might have the same effect in vivo, responsible for the severe damage of the respiratory system.</div>
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