Glycosylation of mouse DPP4 plays a role in inhibiting Middle East respiratory syndrome coronavirus infection.

نویسندگان

  • Kayla M Peck
  • Adam S Cockrell
  • Boyd L Yount
  • Trevor Scobey
  • Ralph S Baric
  • Mark T Heise
چکیده

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.

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عنوان ژورنال:
  • Journal of virology

دوره 89 8  شماره 

صفحات  -

تاریخ انتشار 2015