SrasV1, Main, Exploration, bibRecord, 002355

The ADP-ribose-1"-monophosphatase domains of severe acute respiratory syndrome coronavirus and human coronavirus 229E mediate resistance to antiviral interferon responses

Identifieur interne : 002355 ( Main/Exploration ); précédent : 002354; suivant : 002356

The ADP-ribose-1"-monophosphatase domains of severe acute respiratory syndrome coronavirus and human coronavirus 229E mediate resistance to antiviral interferon responses

Auteurs : Thomas Kuri [Allemagne] ; Klara K. Eriksson [Suisse] ; Akos Putics [Allemagne] ; Roland Züst [Suisse] ; Eric J. Snijder [Pays-Bas] ; Andrew D. Davidson [Royaume-Uni] ; Stuart G. Siddell [Royaume-Uni] ; Volker Thiel [Suisse] ; John Ziebuhr [Allemagne] ; Friedemann Weber [Allemagne]

Source :

Journal of general virology [ 0022-1317 ] ; 2011.

RBID : Pascal:11-0347288

Descripteurs français

Pascal (Inist)
- Coronavirus, Homme, ADP, Résistance, Antiviral, Interféron, Syndrome respiratoire aigu sévère.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- ADP, Antiviral, Coronavirus, Human, Interferon, Resistance, Severe acute respiratory syndrome.

Abstract

Several plus-strand RNA viruses encode proteins containing macrodomains. These domains possess ADP-ribose-1"-phosphatase (ADRP) activity and/or bind poly(ADP-ribose), poly(A) or poly(G). The relevance of these activities in the viral life cycle has not yet been resolved. Here, we report that genetically engineered mutants of severe acute respiratory syndrome coronavirus (SARS-CoV) and human coronavirus 229E (HCoV-229E) expressing ADRP-deficient macrodomains displayed an increased sensitivity to the antiviral effect of alpha interferon compared with their wild-type counterparts. The data suggest that macrodomain-associated ADRP activities may have a role in viral escape from the innate immune responses of the host.

Affiliations:

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

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Le document en format XML

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<front><div type="abstract" xml:lang="en">Several plus-strand RNA viruses encode proteins containing macrodomains. These domains possess ADP-ribose-1"-phosphatase (ADRP) activity and/or bind poly(ADP-ribose), poly(A) or poly(G). The relevance of these activities in the viral life cycle has not yet been resolved. Here, we report that genetically engineered mutants of severe acute respiratory syndrome coronavirus (SARS-CoV) and human coronavirus 229E (HCoV-229E) expressing ADRP-deficient macrodomains displayed an increased sensitivity to the antiviral effect of alpha interferon compared with their wild-type counterparts. The data suggest that macrodomain-associated ADRP activities may have a role in viral escape from the innate immune responses of the host.</div>
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The ADP-ribose-1"-monophosphatase domains of severe acute respiratory syndrome coronavirus and human coronavirus 229E mediate resistance to antiviral interferon responses

The ADP-ribose-1"-monophosphatase domains of severe acute respiratory syndrome coronavirus and human coronavirus 229E mediate resistance to antiviral interferon responses

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Abstract

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