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Wild-type and innate immune-deficient mice are not susceptible to the Middle East respiratory syndrome coronavirus

Coleman, Christopher M.; Matthews, Krystal L.; Goicochea, Lindsay; Frieman, Matthew B.

Authors

CHRISTOPHER COLEMAN CHRISTOPHER.COLEMAN@NOTTINGHAM.AC.UK
Assistant Professor of Infection Immunology

Krystal L. Matthews

Lindsay Goicochea

Matthew B. Frieman



Abstract

The Middle East respiratory syndrome coronavirus (MERS-CoV) is a newly emerging highly pathogenic virus causing almost 50% lethality in infected individuals. The development of a smallanimal model is critical for the understanding of this virus and to aid in development of countermeasures against MERS-CoV. We found that BALB/c, 129/SvEv and 129/SvEv STAT1 knockout mice are not permissive to MERS-CoV infection. The lack of infection may be due to the low level of mRNA and protein for the MERS-CoV receptor, dipeptidyl peptidase 4 (DPP4), in the lungs of mice. The low level of DPP4 in the lungs likely contributes to the lack of viral replication in these mouse models and suggests that a transgenic mouse model expressing DPP4 to higher levels is necessary to create a mouse model for MERS-CoV. © 2014 SGM.

Citation

Coleman, C. M., Matthews, K. L., Goicochea, L., & Frieman, M. B. (2014). Wild-type and innate immune-deficient mice are not susceptible to the Middle East respiratory syndrome coronavirus. Journal of General Virology, 95(PART 2), 408-412. https://doi.org/10.1099/vir.0.060640-0

Journal Article Type Article
Acceptance Date Nov 5, 2013
Online Publication Date Nov 6, 2013
Publication Date Feb 1, 2014
Deposit Date Dec 17, 2019
Journal Journal of General Virology
Print ISSN 0022-1317
Electronic ISSN 1465-2099
Publisher Microbiology Society
Peer Reviewed Peer Reviewed
Volume 95
Issue PART 2
Pages 408-412
DOI https://doi.org/10.1099/vir.0.060640-0
Keywords Virology
Public URL https://nottingham-repository.worktribe.com/output/3590353