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  3. Link of a ubiquitous human coronavirus to dromedary camels.
 

Link of a ubiquitous human coronavirus to dromedary camels.

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BORIS DOI
10.7892/boris.95441
Date of Publication
August 30, 2016
Publication Type
Article
Division/Institute

Institut für Virologi...

Institut für Veterinä...

Author
Corman, Victor M
Eckerle, Isabella
Memish, Ziad A
Liljander, Anne M
Dijkman, Ronaldorcid-logo
Institut für Virologie und Immunologie (IVI)
Jonsdottir, Hulda Run
Institut für Virologie und Immunologie (IVI)
Juma Ngeiywa, Kisi J Z
Kamau, Esther
Younan, Mario
Al Masri, Malakita
Assiri, Abdullah
Gluecks, Ilona
Musa, Bakri E
Meyer, Benjamin
Müller, Marcel A
Hilali, Mosaad
Bornstein, Set
Wernery, Ulrich
Thiel, Volker Earl
Institut für Virologie und Immunologie (IVI)
Jores, Jörgorcid-logo
Institut für Veterinärbakteriologie (IVB)
Drexler, Jan Felix
Drosten, Christian
Subject(s)

600 - Technology::630...

Series
Proceedings of the National Academy of Sciences of the United States of America - PNAS
ISSN or ISBN (if monograph)
0027-8424
Publisher
National Academy of Sciences NAS
Language
English
Publisher DOI
10.1073/pnas.1604472113
PubMed ID
27528677
Uncontrolled Keywords

coronavirus ecology e...

Description
The four human coronaviruses (HCoVs) are globally endemic respiratory pathogens. The Middle East respiratory syndrome (MERS) coronavirus (CoV) is an emerging CoV with a known zoonotic source in dromedary camels. Little is known about the origins of endemic HCoVs. Studying these viruses' evolutionary history could provide important insight into CoV emergence. In tests of MERS-CoV-infected dromedaries, we found viruses related to an HCoV, known as HCoV-229E, in 5.6% of 1,033 animals. Human- and dromedary-derived viruses are each monophyletic, suggesting ecological isolation. One gene of dromedary viruses exists in two versions in camels, full length and deleted, whereas only the deleted version exists in humans. The deletion increased in size over a succession starting from camelid viruses via old human viruses to contemporary human viruses. Live isolates of dromedary 229E viruses were obtained and studied to assess human infection risks. The viruses used the human entry receptor aminopeptidase N and replicated in human hepatoma cells, suggesting a principal ability to cause human infections. However, inefficient replication in several mucosa-derived cell lines and airway epithelial cultures suggested lack of adaptation to the human host. Dromedary viruses were as sensitive to the human type I interferon response as HCoV-229E. Antibodies in human sera neutralized dromedary-derived viruses, suggesting population immunity against dromedary viruses. Although no current epidemic risk seems to emanate from these viruses, evolutionary inference suggests that the endemic human virus HCoV-229E may constitute a descendant of camelid-associated viruses. HCoV-229E evolution provides a scenario for MERS-CoV emergence.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/198902
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PNAS-2016-Corman-9864-9.pdftextAdobe PDF1.09 MBpublisherpublished restricted
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