The antiviral effect of interferon-beta against SARS-coronavirus is not mediated by MxA protein
Identifieur interne : 005A54 ( Main/Exploration ); précédent : 005A53; suivant : 005A55The antiviral effect of interferon-beta against SARS-coronavirus is not mediated by MxA protein
Auteurs : Martin Spiegel [Allemagne] ; Andreas Pichlmair [Allemagne] ; Elke Mühlberger [Allemagne] ; Otto Haller [Allemagne] ; Friedemann Weber [Allemagne]Source :
- Journal of clinical virology [ 1386-6532 ] ; 2004.
Descripteurs français
- KwdFr :
- MESH :
- métabolisme : Protéines G.
- pharmacologie : Interféron bêta.
- physiologie : Virus du SRAS.
- virologie : Syndrome respiratoire aigu sévère.
- Pascal (Inist)
English descriptors
- KwdEn :
- Animals, Antiviral, Beta interferon, Chlorocebus aethiops, Coronavirus, GTP-Binding Proteins (metabolism), Humans, Interferon-beta (pharmacology), Microbiology, Myxovirus Resistance Proteins, Protein, SARS Virus (drug effects), SARS Virus (physiology), Severe Acute Respiratory Syndrome (virology), Severe acute respiratory syndrome, Vero Cells, Virology, Virus Replication (drug effects).
- MESH :
- chemical , metabolism : GTP-Binding Proteins.
- chemical , pharmacology : Interferon-beta.
- drug effects : SARS Virus, Virus Replication.
- physiology : SARS Virus.
- virology : Severe Acute Respiratory Syndrome.
- Animals, Chlorocebus aethiops, Humans, Myxovirus Resistance Proteins, Vero Cells.
Abstract
Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus termed SARS-CoV. No antiviral treatment has been established so far. Interferons are cytokines which induce the synthesis of several antivirally active proteins in the cell. In this study, we demonstrated that multiplication of SARS-CoV in cell culture can be strongly inhibited by pretreatment with interferon-beta. Interferon-alpha and interferon-gamma, by contrast, were less effective. The human MxA protein is one of the most prominent proteins induced by interferon-beta. Nevertheless, no interference with SARS-CoV replication was observed in Vero cells stably expressing MxA. Therefore, other interferon-induced proteins must be responsible for the strong inhibitory effect of interferon-beta against SARS-CoV.
Affiliations:
- Allemagne
- Bade-Wurtemberg, District de Fribourg-en-Brisgau, District de Giessen, Hesse (Land)
- Fribourg-en-Brisgau, Marbourg
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Le document en format XML
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<term>GTP-Binding Proteins (metabolism)</term>
<term>Humans</term>
<term>Interferon-beta (pharmacology)</term>
<term>Microbiology</term>
<term>Myxovirus Resistance Proteins</term>
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<term>SARS Virus (drug effects)</term>
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<term>Humains</term>
<term>Interféron bêta (pharmacologie)</term>
<term>Protéines G (métabolisme)</term>
<term>Protéines de résistance aux myxovirus</term>
<term>Réplication virale ()</term>
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus termed SARS-CoV. No antiviral treatment has been established so far. Interferons are cytokines which induce the synthesis of several antivirally active proteins in the cell. In this study, we demonstrated that multiplication of SARS-CoV in cell culture can be strongly inhibited by pretreatment with interferon-beta. Interferon-alpha and interferon-gamma, by contrast, were less effective. The human MxA protein is one of the most prominent proteins induced by interferon-beta. Nevertheless, no interference with SARS-CoV replication was observed in Vero cells stably expressing MxA. Therefore, other interferon-induced proteins must be responsible for the strong inhibitory effect of interferon-beta against SARS-CoV.</div>
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<name sortKey="Haller, Otto" sort="Haller, Otto" uniqKey="Haller O" first="Otto" last="Haller">Otto Haller</name>
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