Glycosylation of mouse DPP4 plays a role in inhibiting Middle East respiratory syndrome coronavirus infection.
Identifieur interne : 001707 ( PubMed/Curation ); précédent : 001706; suivant : 001708Glycosylation of mouse DPP4 plays a role in inhibiting Middle East respiratory syndrome coronavirus infection.
Auteurs : Kayla M. Peck [États-Unis] ; Adam S. Cockrell [États-Unis] ; Boyd L. Yount [États-Unis] ; Trevor Scobey [États-Unis] ; Ralph S. Baric [États-Unis] ; Mark T. Heise [États-Unis]Source :
- Journal of virology [ 1098-5514 ] ; 2015.
Descripteurs français
- KwdFr :
- Animaux, Coronavirus du syndrome respiratoire du Moyen-Orient (métabolisme), Dipeptidyl peptidase 4 (), Dipeptidyl peptidase 4 (génétique), Dipeptidyl peptidase 4 (métabolisme), Données de séquences moléculaires, Glycosylation, Infections à coronavirus (), Modèles moléculaires, Pénétration virale, Souris, Spécificité d'espèce, Séquence d'acides aminés, Technique d'immunofluorescence.
- MESH :
- génétique : Dipeptidyl peptidase 4.
- métabolisme : Coronavirus du syndrome respiratoire du Moyen-Orient, Dipeptidyl peptidase 4.
- Animaux, Dipeptidyl peptidase 4, Données de séquences moléculaires, Glycosylation, Infections à coronavirus, Modèles moléculaires, Pénétration virale, Souris, Spécificité d'espèce, Séquence d'acides aminés, Technique d'immunofluorescence.
English descriptors
- KwdEn :
- Amino Acid Sequence, Animals, Coronavirus Infections (prevention & control), Dipeptidyl Peptidase 4 (chemistry), Dipeptidyl Peptidase 4 (genetics), Dipeptidyl Peptidase 4 (metabolism), Fluorescent Antibody Technique, Glycosylation, Mice, Middle East Respiratory Syndrome Coronavirus (metabolism), Models, Molecular, Molecular Sequence Data, Species Specificity, Virus Internalization.
- MESH :
- chemical , chemistry : Dipeptidyl Peptidase 4.
- chemical , genetics : Dipeptidyl Peptidase 4.
- chemical , metabolism : Dipeptidyl Peptidase 4.
- metabolism : Middle East Respiratory Syndrome Coronavirus.
- prevention & control : Coronavirus Infections.
- Amino Acid Sequence, Animals, Fluorescent Antibody Technique, Glycosylation, Mice, Models, Molecular, Molecular Sequence Data, Species Specificity, Virus Internalization.
Abstract
Middle East respiratory syndrome coronavirus (MERS-CoV) utilizes dipeptidyl peptidase 4 (DPP4) as an entry receptor. Mouse DPP4 (mDPP4) does not support MERS-CoV entry; however, changes at positions 288 and 330 can confer permissivity. Position 330 changes the charge and glycosylation state of mDPP4. We show that glycosylation is a major factor impacting DPP4 receptor function. These results provide insight into DPP4 species-specific differences impacting MERS-CoV host range and may inform MERS-CoV mouse model development.
DOI: 10.1128/JVI.03445-14
PubMed: 25653445
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pubmed:25653445Le document en format XML
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<front><div type="abstract" xml:lang="en">Middle East respiratory syndrome coronavirus (MERS-CoV) utilizes dipeptidyl peptidase 4 (DPP4) as an entry receptor. Mouse DPP4 (mDPP4) does not support MERS-CoV entry; however, changes at positions 288 and 330 can confer permissivity. Position 330 changes the charge and glycosylation state of mDPP4. We show that glycosylation is a major factor impacting DPP4 receptor function. These results provide insight into DPP4 species-specific differences impacting MERS-CoV host range and may inform MERS-CoV mouse model development. </div>
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