Publication:
Link of a ubiquitous human coronavirus to dromedary camels.

cris.virtual.author-orcid0000-0003-0320-2743
cris.virtual.author-orcid0000-0003-3790-5746
cris.virtualsource.author-orcide7ed3985-2317-4692-9977-138458c0c638
cris.virtualsource.author-orcid2fd87396-be69-4e98-823f-358e8e40ce91
cris.virtualsource.author-orcid54c32983-0197-4cba-b58f-e62b74b28281
cris.virtualsource.author-orcid34538ef3-18b4-458d-8bfa-db9ed491c6bf
dc.contributor.authorCorman, Victor M
dc.contributor.authorEckerle, Isabella
dc.contributor.authorMemish, Ziad A
dc.contributor.authorLiljander, Anne M
dc.contributor.authorDijkman, Ronald
dc.contributor.authorJonsdottir, Hulda Run
dc.contributor.authorJuma Ngeiywa, Kisi J Z
dc.contributor.authorKamau, Esther
dc.contributor.authorYounan, Mario
dc.contributor.authorAl Masri, Malakita
dc.contributor.authorAssiri, Abdullah
dc.contributor.authorGluecks, Ilona
dc.contributor.authorMusa, Bakri E
dc.contributor.authorMeyer, Benjamin
dc.contributor.authorMüller, Marcel A
dc.contributor.authorHilali, Mosaad
dc.contributor.authorBornstein, Set
dc.contributor.authorWernery, Ulrich
dc.contributor.authorThiel, Volker Earl
dc.contributor.authorJores, Jörg
dc.contributor.authorDrexler, Jan Felix
dc.contributor.authorDrosten, Christian
dc.date.accessioned2025-01-08T20:11:09Z
dc.date.available2025-01-08T20:11:09Z
dc.date.issued2016-08-30
dc.description.abstractThe 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.
dc.description.numberOfPages6
dc.description.sponsorshipInstitut für Virologie und Immunologie (IVI)
dc.description.sponsorshipInstitut für Veterinärbakteriologie (IVB)
dc.identifier.doi10.7892/boris.95441
dc.identifier.pmid27528677
dc.identifier.publisherDOI10.1073/pnas.1604472113
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/198902
dc.language.isoen
dc.publisherNational Academy of Sciences NAS
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America - PNAS
dc.relation.issn0027-8424
dc.relation.organizationDCD5A442C0BAE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C208E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C1CCE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C494E17DE0405C82790C4DE2
dc.subjectcoronavirus ecology evolution livestock zoonotic diseases
dc.subject.ddc600 - Technology::630 - Agriculture
dc.titleLink of a ubiquitous human coronavirus to dromedary camels.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage9869
oaire.citation.issue35
oaire.citation.startPage9864
oaire.citation.volume113
oairecerif.author.affiliationInstitut für Virologie und Immunologie (IVI)
oairecerif.author.affiliationInstitut für Virologie und Immunologie (IVI)
oairecerif.author.affiliationInstitut für Virologie und Immunologie (IVI)
oairecerif.author.affiliationInstitut für Veterinärbakteriologie (IVB)
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unibe.date.licenseChanged2019-10-22 17:51:40
unibe.description.ispublishedpub
unibe.eprints.legacyId95441
unibe.journal.abbrevTitleP NATL ACAD SCI USA
unibe.refereedTRUE
unibe.subtype.articlejournal

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