Link of a ubiquitous human coronavirus to dromedary camels
Significance
Our results raise a scenario for the natural history of a ubiquitous respiratory coronavirus (CoV) that has established itself in humans after it was likely acquired from camels. This scenario reminds us of the pandemic potential of the Middle East respiratory syndrome CoV, an agent that is thought to be acquired from camels without presently causing sustained human-to-human transmission.
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Abstract
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-CoVinfected 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.
full article
http://www.pnas.org/content/early/20...604472113.full
- Victor M. Cormana,b,1,
- Isabella Eckerlea,1,
- Ziad A. Memishc,
- Anne M. Liljanderd,
- Ronald Dijkmane,f,
- Hulda Jonsdottire,f,
- Kisi J. Z. Juma Ngeiywag,
- Esther Kamaug,
- Mario Younanh,
- Malakita Al Masrii,
- Abdullah Assirii,
- Ilona Gluecksj,
- Bakri E. Musak,
- Benjamin Meyera,
- Marcel A. M?llera,
- Mosaad Hilalil,
- Set Bornsteinm,
- Ulrich Werneryn,
- Volker Thiele,f,
- Joerg Joresd,o,
- Jan Felix Drexlera,b,2, and
- Christian Drostena,b,2
Significance
Our results raise a scenario for the natural history of a ubiquitous respiratory coronavirus (CoV) that has established itself in humans after it was likely acquired from camels. This scenario reminds us of the pandemic potential of the Middle East respiratory syndrome CoV, an agent that is thought to be acquired from camels without presently causing sustained human-to-human transmission.
Next Section
Abstract
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-CoVinfected 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.
full article
http://www.pnas.org/content/early/20...604472113.full