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Coronavirus humains (HCoV)

Identifieur interne : 003143 ( Main/Exploration ); précédent : 003142; suivant : 003144

Coronavirus humains (HCoV)

Auteurs : A. Vabret [France] ; J. Dina [France] ; E. Brison [France] ; J. Brouard [France] ; F. Freymuth [France]

Source :

RBID : PMC:7125620

Descripteurs français

English descriptors

Abstract

Résumé

Les coronavirus forment un grand groupe de virus infectant les mammifères et les oiseaux ; cinq d’entre eux infectent l’homme : HCoV 229E et OC43, connus depuis les années 1960, SARS-CoV identifié en mars 2003 lors de l’épidémie de syndrome de détresse respiratoire aigu sévère, NL63 et HKU1, identifiés respectivement en 2004 et 2005. Ce sont des virus enveloppés dont le génome est une molécule d’ARN de polarité positive de très grande taille. Leur mode évolutif fait intervenir plusieurs paramètres : la génération de nombreux mutants lors de la réplication, responsable d’une distribution en quasi-espèces de la population virale, la capacité à établir des infections persistantes, la possibilité de délétions importantes, la grande flexibilité du génome due à un fort taux de recombinaisons homologues et hétérologues, la capacité à franchir les barrières d’espèces et à s’adapter au nouvel environnement. Les coronavirus (hors SARS-CoV) sont ubiquitaires et circulent sous forme épidémique. Les différents HCoV co-circulent avec une distribution entre les types qui est variable selon les années et les régions géographiques. Ce sont essentiellement des virus responsables d’infections respiratoires hautes et basses. Le SARS-CoV est, lui, un virus émergent responsable de l’épidémie de pneumopathies atypiques entre novembre 2002 et juillet 2003. Sa circulation a été interrompue grâce à la mise en place de mesures sanitaires drastiques. L’implication des HCoV dans des pathologies digestives et neurologiques reste à préciser. La détection des coronavirus est difficile, et fait appel surtout à des techniques moléculaires. Il n’existe actuellement aucun traitement spécifique des infections à HCoV.


Url:
DOI: 10.1016/j.patbio.2008.02.018
PubMed: 18456429
PubMed Central: 7125620


Affiliations:


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


Le document en format XML

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<author>
<name sortKey="Talbot, P J" uniqKey="Talbot P">P.J. Talbot</name>
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<li>France</li>
</country>
<region>
<li>Basse-Normandie</li>
<li>Région Normandie</li>
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<li>Caen</li>
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<country name="France">
<region name="Région Normandie">
<name sortKey="Vabret, A" sort="Vabret, A" uniqKey="Vabret A" first="A." last="Vabret">A. Vabret</name>
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<name sortKey="Brison, E" sort="Brison, E" uniqKey="Brison E" first="E." last="Brison">E. Brison</name>
<name sortKey="Brouard, J" sort="Brouard, J" uniqKey="Brouard J" first="J." last="Brouard">J. Brouard</name>
<name sortKey="Dina, J" sort="Dina, J" uniqKey="Dina J" first="J." last="Dina">J. Dina</name>
<name sortKey="Freymuth, F" sort="Freymuth, F" uniqKey="Freymuth F" first="F." last="Freymuth">F. Freymuth</name>
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