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Mouse dipeptidyl peptidase 4 is not a functional receptor for Middle East respiratory syndrome coronavirus infection.

Identifieur interne : 001B38 ( Main/Exploration ); précédent : 001B37; suivant : 001B39

Mouse dipeptidyl peptidase 4 is not a functional receptor for Middle East respiratory syndrome coronavirus infection.

Auteurs : Adam S. Cockrell [États-Unis] ; Kayla M. Peck ; Boyd L. Yount ; Sudhakar S. Agnihothram ; Trevor Scobey ; Nicole R. Curnes ; Ralph S. Baric ; Mark T. Heise

Source :

RBID : pubmed:24574399

Descripteurs français

English descriptors

Abstract

Human dipeptidyl peptidase 4 (hDPP4) was recently identified as the receptor for Middle East respiratory syndrome coronavirus (MERS-CoV) infection, suggesting that other mammalian DPP4 orthologs may also support infection. We demonstrate that mouse DPP4 cannot support MERS-CoV infection. However, employing mouse DPP4 as a scaffold, we identified two critical amino acids (A288L and T330R) that regulate species specificity in the mouse. This knowledge can support the rational design of a mouse-adapted MERS-CoV for rapid assessment of therapeutics.

DOI: 10.1128/JVI.03764-13
PubMed: 24574399


Affiliations:


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Le document en format XML

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<term>DNA Mutational Analysis</term>
<term>Dipeptidyl Peptidase 4 (metabolism)</term>
<term>Host Specificity</term>
<term>Humans</term>
<term>Mice</term>
<term>Models, Molecular</term>
<term>Molecular Sequence Data</term>
<term>Protein Conformation</term>
<term>Receptors, Virus (metabolism)</term>
<term>Species Specificity</term>
<term>Virus Attachment</term>
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<term>Analyse de mutations d'ADN</term>
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<term>Coronavirus (physiologie)</term>
<term>Dipeptidyl peptidase 4 (métabolisme)</term>
<term>Données de séquences moléculaires</term>
<term>Humains</term>
<term>Infections à coronavirus (virologie)</term>
<term>Modèles moléculaires</term>
<term>Récepteurs viraux (métabolisme)</term>
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<term>Séquence d'acides aminés</term>
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<term>Données de séquences moléculaires</term>
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<div type="abstract" xml:lang="en">Human dipeptidyl peptidase 4 (hDPP4) was recently identified as the receptor for Middle East respiratory syndrome coronavirus (MERS-CoV) infection, suggesting that other mammalian DPP4 orthologs may also support infection. We demonstrate that mouse DPP4 cannot support MERS-CoV infection. However, employing mouse DPP4 as a scaffold, we identified two critical amino acids (A288L and T330R) that regulate species specificity in the mouse. This knowledge can support the rational design of a mouse-adapted MERS-CoV for rapid assessment of therapeutics. </div>
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