MersV1, PubMed, Curation, bibRecord, 000A49

Coronaviruses and arteriviruses display striking differences in their cyclophilin A-dependence during replication in cell culture.

Identifieur interne : 000A49 ( PubMed/Curation ); précédent : 000A48; suivant : 000A50

Coronaviruses and arteriviruses display striking differences in their cyclophilin A-dependence during replication in cell culture.

Auteurs : Adriaan H. De Wilde [Pays-Bas] ; Jessika C. Zevenhoven-Dobbe [Pays-Bas] ; Corrine Beugeling [Pays-Bas] ; Udayan Chatterji [États-Unis] ; Danielle De Jong [Pays-Bas] ; Philippe Gallay [États-Unis] ; Karoly Szuhai [Pays-Bas] ; Clara C. Posthuma [Pays-Bas] ; Eric J. Snijder [Pays-Bas]

Source :

Virology [ 1096-0341 ] ; 2018.

RBID : pubmed:29249267

Descripteurs français

KwdFr :
- Animaux, Arterivirus (physiologie), Coronavirus (physiologie), Cricetinae, Culture virale, Cyclophiline A (métabolisme), Humains, Lignée cellulaire, Réplication virale (physiologie).
MESH :
- métabolisme : Cyclophiline A.
- physiologie : Arterivirus, Coronavirus, Réplication virale.
- Animaux, Cricetinae, Culture virale, Humains, Lignée cellulaire.

English descriptors

KwdEn :
- Animals, Arterivirus (physiology), Cell Line, Coronavirus (physiology), Cricetinae, Cyclophilin A (metabolism), Humans, Virus Cultivation, Virus Replication (physiology).
MESH :
- chemical , metabolism : Cyclophilin A.
- physiology : Arterivirus, Coronavirus, Virus Replication.
- Animals, Cell Line, Cricetinae, Humans, Virus Cultivation.

Abstract

Cyclophilin A (CypA) is an important host factor in the replication of a variety of RNA viruses. Also the replication of several nidoviruses was reported to depend on CypA, although possibly not to the same extent. These prior studies are difficult to compare, since different nidoviruses, cell lines and experimental set-ups were used. Here, we investigated the CypA dependence of three distantly related nidoviruses that can all replicate in Huh7 cells: the arterivirus equine arteritis virus (EAV), the alphacoronavirus human coronavirus 229E (HCoV-229E), and the betacoronavirus Middle East respiratory syndrome coronavirus (MERS-CoV). The replication of these viruses was compared in the same parental Huh7 cells and in CypA-knockout Huh7 cells generated using CRISPR/Cas9-technology. CypA depletion reduced EAV yields by ~ 3-log, whereas MERS-CoV progeny titers were modestly reduced (3-fold) and HCoV-229E replication was unchanged. This study reveals that the replication of nidoviruses can differ strikingly in its dependence on cellular CypA.

DOI: 10.1016/j.virol.2017.11.022
PubMed: 29249267

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<term>Cyclophilin A (metabolism)</term>
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<front><div type="abstract" xml:lang="en">Cyclophilin A (CypA) is an important host factor in the replication of a variety of RNA viruses. Also the replication of several nidoviruses was reported to depend on CypA, although possibly not to the same extent. These prior studies are difficult to compare, since different nidoviruses, cell lines and experimental set-ups were used. Here, we investigated the CypA dependence of three distantly related nidoviruses that can all replicate in Huh7 cells: the arterivirus equine arteritis virus (EAV), the alphacoronavirus human coronavirus 229E (HCoV-229E), and the betacoronavirus Middle East respiratory syndrome coronavirus (MERS-CoV). The replication of these viruses was compared in the same parental Huh7 cells and in CypA-knockout Huh7 cells generated using CRISPR/Cas9-technology. CypA depletion reduced EAV yields by ~ 3-log, whereas MERS-CoV progeny titers were modestly reduced (3-fold) and HCoV-229E replication was unchanged. This study reveals that the replication of nidoviruses can differ strikingly in its dependence on cellular CypA.</div>
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<Abstract><AbstractText>Cyclophilin A (CypA) is an important host factor in the replication of a variety of RNA viruses. Also the replication of several nidoviruses was reported to depend on CypA, although possibly not to the same extent. These prior studies are difficult to compare, since different nidoviruses, cell lines and experimental set-ups were used. Here, we investigated the CypA dependence of three distantly related nidoviruses that can all replicate in Huh7 cells: the arterivirus equine arteritis virus (EAV), the alphacoronavirus human coronavirus 229E (HCoV-229E), and the betacoronavirus Middle East respiratory syndrome coronavirus (MERS-CoV). The replication of these viruses was compared in the same parental Huh7 cells and in CypA-knockout Huh7 cells generated using CRISPR/Cas9-technology. CypA depletion reduced EAV yields by ~ 3-log, whereas MERS-CoV progeny titers were modestly reduced (3-fold) and HCoV-229E replication was unchanged. This study reveals that the replication of nidoviruses can differ strikingly in its dependence on cellular CypA.</AbstractText>
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Coronaviruses and arteriviruses display striking differences in their cyclophilin A-dependence during replication in cell culture.

Coronaviruses and arteriviruses display striking differences in their cyclophilin A-dependence during replication in cell culture.

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