Middle East respiratory syndrome coronavirus and bat coronavirus HKU9 both can utilize GRP78 for attachment onto host cells
Identifieur interne : 000894 ( Main/Exploration ); précédent : 000893; suivant : 000895Middle East respiratory syndrome coronavirus and bat coronavirus HKU9 both can utilize GRP78 for attachment onto host cells
Auteurs : Hin Chu ; Che-Man Chan ; Xi Zhang ; Yixin Wang ; Shuofeng Yuan ; Jie Zhou ; Rex Kwok-Him Au-Yeung ; Kong-Hung Sze ; Dong Yang ; Huiping Shuai ; Yuxin Hou ; Cun Li ; Xiaoyu Zhao ; Vincent Kwok-Man Poon ; Sze Pui Leung ; Man-Lung Yeung ; Jinghua Yan ; Guangwen Lu ; Dong-Yan Jin ; George Fu Gao ; Jasper Fuk-Woo Chan ; Kwok-Yung YuenSource :
- The Journal of Biological Chemistry [ 0021-9258 ] ; 2018.
Descripteurs français
- KwdFr :
- Animaux, Attachement viral, Cartes d'interactions protéiques, Cellules Vero, Coronavirus (physiologie), Coronavirus du syndrome respiratoire du Moyen-Orient (physiologie), Dipeptidyl peptidase 4 (métabolisme), Glycoprotéine de spicule des coronavirus (métabolisme), Humains, Infections à coronavirus (métabolisme), Interactions hôte-pathogène, Lignée cellulaire, Protéines du choc thermique (métabolisme), Récepteurs viraux (métabolisme).
- MESH :
- métabolisme : Dipeptidyl peptidase 4, Glycoprotéine de spicule des coronavirus, Infections à coronavirus, Protéines du choc thermique, Récepteurs viraux.
- physiologie : Coronavirus, Coronavirus du syndrome respiratoire du Moyen-Orient.
- Animaux, Attachement viral, Cartes d'interactions protéiques, Cellules Vero, Humains, Interactions hôte-pathogène, Lignée cellulaire.
English descriptors
- KwdEn :
- Animals, Betacoronavirus (physiology), Cell Line, Chlorocebus aethiops, Coronavirus (physiology), Coronavirus Infections (metabolism), Dipeptidyl Peptidase 4 (metabolism), Heat-Shock Proteins (metabolism), Host-Pathogen Interactions, Humans, Middle East Respiratory Syndrome Coronavirus (physiology), Protein Interaction Maps, Receptors, Virus (metabolism), Spike Glycoprotein, Coronavirus (metabolism), Vero Cells, Virus Attachment.
- MESH :
- chemical , metabolism : Dipeptidyl Peptidase 4, Heat-Shock Proteins, Receptors, Virus, Spike Glycoprotein, Coronavirus.
- metabolism : Coronavirus Infections.
- physiology : Betacoronavirus, Coronavirus, Middle East Respiratory Syndrome Coronavirus.
- Animals, Cell Line, Chlorocebus aethiops, Host-Pathogen Interactions, Humans, Protein Interaction Maps, Vero Cells, Virus Attachment.
Abstract
Coronavirus tropism is predominantly determined by the interaction between
coronavirus spikes and the host receptors. In this regard, coronaviruses have
evolved a complicated receptor-recognition system through their spike proteins.
Spikes from highly related coronaviruses can recognize distinct receptors,
whereas spikes of distant coronaviruses can employ the same cell-surface
molecule for entry. Moreover, coronavirus spikes can recognize a broad range of
cell-surface molecules in addition to the receptors and thereby can augment
coronavirus attachment or entry. The receptor of Middle East respiratory
syndrome coronavirus (MERS-CoV) is dipeptidyl peptidase 4 (DPP4). In this study,
we identified membrane-associated 78-kDa glucose-regulated protein (GRP78) as an
additional binding target of the MERS-CoV spike. Further analyses indicated that
GRP78 could not independently render nonpermissive cells susceptible to MERS-CoV
infection but could facilitate MERS-CoV entry into permissive cells by
augmenting virus attachment. More importantly, by exploring potential
interactions between GRP78 and spikes of other coronaviruses, we discovered that
the highly conserved human GRP78 could interact with the spike protein of bat
coronavirus HKU9 (bCoV-HKU9) and facilitate its attachment to the host cell
surface. Taken together, our study has identified GRP78 as a host factor that
can interact with the spike proteins of two
Url:
DOI: 10.1074/jbc.RA118.001897
PubMed: 29887526
PubMed Central: 6066311
Affiliations:
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Le document en format XML
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<term>Betacoronavirus (physiology)</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
<term>Coronavirus (physiology)</term>
<term>Coronavirus Infections (metabolism)</term>
<term>Dipeptidyl Peptidase 4 (metabolism)</term>
<term>Heat-Shock Proteins (metabolism)</term>
<term>Host-Pathogen Interactions</term>
<term>Humans</term>
<term>Middle East Respiratory Syndrome Coronavirus (physiology)</term>
<term>Protein Interaction Maps</term>
<term>Receptors, Virus (metabolism)</term>
<term>Spike Glycoprotein, Coronavirus (metabolism)</term>
<term>Vero Cells</term>
<term>Virus Attachment</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Attachement viral</term>
<term>Cartes d'interactions protéiques</term>
<term>Cellules Vero</term>
<term>Coronavirus (physiologie)</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient (physiologie)</term>
<term>Dipeptidyl peptidase 4 (métabolisme)</term>
<term>Glycoprotéine de spicule des coronavirus (métabolisme)</term>
<term>Humains</term>
<term>Infections à coronavirus (métabolisme)</term>
<term>Interactions hôte-pathogène</term>
<term>Lignée cellulaire</term>
<term>Protéines du choc thermique (métabolisme)</term>
<term>Récepteurs viraux (métabolisme)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Dipeptidyl Peptidase 4</term>
<term>Heat-Shock Proteins</term>
<term>Receptors, Virus</term>
<term>Spike Glycoprotein, Coronavirus</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Coronavirus Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Dipeptidyl peptidase 4</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Infections à coronavirus</term>
<term>Protéines du choc thermique</term>
<term>Récepteurs viraux</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Coronavirus</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Betacoronavirus</term>
<term>Coronavirus</term>
<term>Middle East Respiratory Syndrome Coronavirus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
<term>Host-Pathogen Interactions</term>
<term>Humans</term>
<term>Protein Interaction Maps</term>
<term>Vero Cells</term>
<term>Virus Attachment</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Animaux</term>
<term>Attachement viral</term>
<term>Cartes d'interactions protéiques</term>
<term>Cellules Vero</term>
<term>Humains</term>
<term>Interactions hôte-pathogène</term>
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<front><div type="abstract" xml:lang="en"><p>Coronavirus tropism is predominantly determined by the interaction between
coronavirus spikes and the host receptors. In this regard, coronaviruses have
evolved a complicated receptor-recognition system through their spike proteins.
Spikes from highly related coronaviruses can recognize distinct receptors,
whereas spikes of distant coronaviruses can employ the same cell-surface
molecule for entry. Moreover, coronavirus spikes can recognize a broad range of
cell-surface molecules in addition to the receptors and thereby can augment
coronavirus attachment or entry. The receptor of Middle East respiratory
syndrome coronavirus (MERS-CoV) is dipeptidyl peptidase 4 (DPP4). In this study,
we identified membrane-associated 78-kDa glucose-regulated protein (GRP78) as an
additional binding target of the MERS-CoV spike. Further analyses indicated that
GRP78 could not independently render nonpermissive cells susceptible to MERS-CoV
infection but could facilitate MERS-CoV entry into permissive cells by
augmenting virus attachment. More importantly, by exploring potential
interactions between GRP78 and spikes of other coronaviruses, we discovered that
the highly conserved human GRP78 could interact with the spike protein of bat
coronavirus HKU9 (bCoV-HKU9) and facilitate its attachment to the host cell
surface. Taken together, our study has identified GRP78 as a host factor that
can interact with the spike proteins of two <italic>Betacoronaviruses</italic>
,
the lineage C MERS-CoV and the lineage D bCoV-HKU9. The capacity of GRP78 to
facilitate surface attachment of both a human coronavirus and a phylogenetically
related bat coronavirus exemplifies the need for continuous surveillance of the
evolution of animal coronaviruses to monitor their potential for human
adaptations.</p>
</div>
</front>
<back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Peck, K X0a M" uniqKey="Peck K">K.
M. Peck</name>
</author>
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</record>
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