Author:
Menachery Vineet D.,Yount Boyd L.,Sims Amy C.,Debbink Kari,Agnihothram Sudhakar S.,Gralinski Lisa E.,Graham Rachel L.,Scobey Trevor,Plante Jessica A.,Royal Scott R.,Swanstrom Jesica,Sheahan Timothy P.,Pickles Raymond J.,Corti Davide,Randell Scott H.,Lanzavecchia Antonio,Marasco Wayne A.,Baric Ralph S.
Abstract
Outbreaks from zoonotic sources represent a threat to both human disease as well as the global economy. Despite a wealth of metagenomics studies, methods to leverage these datasets to identify future threats are underdeveloped. In this study, we describe an approach that combines existing metagenomics data with reverse genetics to engineer reagents to evaluate emergence and pathogenic potential of circulating zoonotic viruses. Focusing on the severe acute respiratory syndrome (SARS)-like viruses, the results indicate that the WIV1-coronavirus (CoV) cluster has the ability to directly infect and may undergo limited transmission in human populations. However, in vivo attenuation suggests additional adaptation is required for epidemic disease. Importantly, available SARS monoclonal antibodies offered success in limiting viral infection absent from available vaccine approaches. Together, the data highlight the utility of a platform to identify and prioritize prepandemic strains harbored in animal reservoirs and document the threat posed by WIV1-CoV for emergence in human populations.
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
Division of Intramural Research, National Institute of Allergy and Infectious Diseases
HHS | NIH | National Institute on Aging
HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
Proceedings of the National Academy of Sciences
Cited by
387 articles.
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