Middle East respiratory syndrome coronavirus (MERS-CoV) causes transient lower respiratory tract infection in rhesus macaques

Emmie de Wit(State Key Laboratory of Virology), Angela L. Rasmussen(University of Washington), Darryl Falzarano(State Key Laboratory of Virology), Trenton Bushmaker(State Key Laboratory of Virology), Friederike Feldmann, Douglas Brining, Elizabeth R. Fischer(National Institute of Allergy and Infectious Diseases), Cynthia Martellaro(State Key Laboratory of Virology), Atsushi Okumura(University of Washington), Jean Chang(University of Washington), Dana Scott, Arndt Benecke(University of Washington), Michael G. Katze(University of Washington), Heinz Feldmann(State Key Laboratory of Virology), Vincent J. Munster(State Key Laboratory of Virology)
Proceedings of the National Academy of Sciences
September 23, 2013
Cited by 322Open Access
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Abstract

In 2012, a novel betacoronavirus, designated Middle East respiratory syndrome coronavirus or MERS-CoV and associated with severe respiratory disease in humans, emerged in the Arabian Peninsula. To date, 108 human cases have been reported, including cases of human-to-human transmission. The availability of an animal disease model is essential for understanding pathogenesis and developing effective countermeasures. Upon a combination of intratracheal, ocular, oral, and intranasal inoculation with 7 × 10(6) 50% tissue culture infectious dose of the MERS-CoV isolate HCoV-EMC/2012, rhesus macaques developed a transient lower respiratory tract infection. Clinical signs, virus shedding, virus replication in respiratory tissues, gene expression, and cytokine and chemokine profiles peaked early in infection and decreased over time. MERS-CoV caused a multifocal, mild to marked interstitial pneumonia, with virus replication occurring mainly in alveolar pneumocytes. This tropism of MERS-CoV for the lower respiratory tract may explain the severity of the disease observed in humans and the, up to now, limited human-to-human transmission.


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