Mouse Dipeptidyl Peptidase 4 Is Not a Functional Receptor for Middle East Respiratory Syndrome Coronavirus Infection

被引:75
作者
Cockrell, Adam S. [1 ]
Peck, Kayla M. [4 ]
Yount, Boyd L. [2 ]
Agnihothram, Sudhakar S. [2 ]
Scobey, Trevor [2 ]
Curnes, Nicole R. [1 ]
Baric, Ralph S. [2 ,3 ]
Heise, Mark T. [1 ,3 ]
机构
[1] Univ N Carolina, Dept Genet, Chapel Hill, NC 27523 USA
[2] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC USA
[3] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC USA
[4] Univ N Carolina, Dept Biol, Chapel Hill, NC USA
关键词
MERS-COV; BINDING;
D O I
10.1128/JVI.03764-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:5195 / 5199
页数:5
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