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Article: MERS coronaviruses from camels in Africa exhibit region-dependent genetic diversity
Title | MERS coronaviruses from camels in Africa exhibit region-dependent genetic diversity |
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Authors | |
Keywords | Africa Coronavirus Evolution MERS Zoonosis |
Issue Date | 2018 |
Publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org |
Citation | Proceedings of the National Academy of Sciences, 2018, v. 115 n. 12, p. 3144-3149 How to Cite? |
Abstract | Middle East respiratory syndrome coronavirus (MERS-CoV) causes a zoonotic respiratory disease of global public health concern, and dromedary camels are the only proven source of zoonotic infection. Although MERS-CoV infection is ubiquitous in dromedaries across Africa as well as in the Arabian Peninsula, zoonotic disease appears confined to the Arabian Peninsula. MERS-CoVs from Africa have hitherto been poorly studied. We genetically and phenotypically characterized MERS-CoV from dromedaries sampled in Morocco, Burkina Faso, Nigeria, and Ethiopia. Viruses from Africa (clade C) are phylogenetically distinct from contemporary viruses from the Arabian Peninsula (clades A and B) but remain antigenically similar in microneutralization tests. Viruses from West (Nigeria, Burkina Faso) and North (Morocco) Africa form a subclade, C1, that shares clade-defining genetic signatures including deletions in the accessory gene ORF4b Compared with human and camel MERS-CoV from Saudi Arabia, virus isolates from Burkina Faso (BF785) and Nigeria (Nig1657) had lower virus replication competence in Calu-3 cells and in ex vivo cultures of human bronchus and lung. BF785 replicated to lower titer in lungs of human DPP4-transduced mice. A reverse genetics-derived recombinant MERS-CoV (EMC) lacking ORF4b elicited higher type I and III IFN responses than the isogenic EMC virus in Calu-3 cells. However, ORF4b deletions may not be the major determinant of the reduced replication competence of BF785 and Nig1657. Genetic and phenotypic differences in West African viruses may be relevant to zoonotic potential. There is an urgent need for studies of MERS-CoV at the animal-human interface. |
Persistent Identifier | http://hdl.handle.net/10722/258334 |
ISSN | 2023 Impact Factor: 9.4 2023 SCImago Journal Rankings: 3.737 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chu, KW | - |
dc.contributor.author | Hui, PY | - |
dc.contributor.author | Perera, RAPM | - |
dc.contributor.author | Miguel, E | - |
dc.contributor.author | Niemeyer, D | - |
dc.contributor.author | Zhao, J | - |
dc.contributor.author | Channappanavar, R | - |
dc.contributor.author | Dudas, G | - |
dc.contributor.author | Oladipo, JO | - |
dc.contributor.author | Traoré, A | - |
dc.contributor.author | Fassi-Fihri, O | - |
dc.contributor.author | Ali, A | - |
dc.contributor.author | Demissié, GF | - |
dc.contributor.author | Muth, D | - |
dc.contributor.author | Chan, MCW | - |
dc.contributor.author | Nicholls, JM | - |
dc.contributor.author | Meyerholz, DK | - |
dc.contributor.author | Kuranga, SA | - |
dc.contributor.author | Mamo, G | - |
dc.contributor.author | ZHOU, Z | - |
dc.contributor.author | SO, TY | - |
dc.contributor.author | Hemida, MG | - |
dc.contributor.author | Webby, RJ | - |
dc.contributor.author | Roger, F | - |
dc.contributor.author | Rambaut, A | - |
dc.contributor.author | Poon, LML | - |
dc.contributor.author | Perlman, S | - |
dc.contributor.author | Drosten, C | - |
dc.contributor.author | Chevalier, V | - |
dc.contributor.author | Peiris, JSM | - |
dc.date.accessioned | 2018-08-22T01:36:49Z | - |
dc.date.available | 2018-08-22T01:36:49Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Proceedings of the National Academy of Sciences, 2018, v. 115 n. 12, p. 3144-3149 | - |
dc.identifier.issn | 0027-8424 | - |
dc.identifier.uri | http://hdl.handle.net/10722/258334 | - |
dc.description.abstract | Middle East respiratory syndrome coronavirus (MERS-CoV) causes a zoonotic respiratory disease of global public health concern, and dromedary camels are the only proven source of zoonotic infection. Although MERS-CoV infection is ubiquitous in dromedaries across Africa as well as in the Arabian Peninsula, zoonotic disease appears confined to the Arabian Peninsula. MERS-CoVs from Africa have hitherto been poorly studied. We genetically and phenotypically characterized MERS-CoV from dromedaries sampled in Morocco, Burkina Faso, Nigeria, and Ethiopia. Viruses from Africa (clade C) are phylogenetically distinct from contemporary viruses from the Arabian Peninsula (clades A and B) but remain antigenically similar in microneutralization tests. Viruses from West (Nigeria, Burkina Faso) and North (Morocco) Africa form a subclade, C1, that shares clade-defining genetic signatures including deletions in the accessory gene ORF4b Compared with human and camel MERS-CoV from Saudi Arabia, virus isolates from Burkina Faso (BF785) and Nigeria (Nig1657) had lower virus replication competence in Calu-3 cells and in ex vivo cultures of human bronchus and lung. BF785 replicated to lower titer in lungs of human DPP4-transduced mice. A reverse genetics-derived recombinant MERS-CoV (EMC) lacking ORF4b elicited higher type I and III IFN responses than the isogenic EMC virus in Calu-3 cells. However, ORF4b deletions may not be the major determinant of the reduced replication competence of BF785 and Nig1657. Genetic and phenotypic differences in West African viruses may be relevant to zoonotic potential. There is an urgent need for studies of MERS-CoV at the animal-human interface. | - |
dc.language | eng | - |
dc.publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org | - |
dc.relation.ispartof | Proceedings of the National Academy of Sciences | - |
dc.rights | Proceedings of the National Academy of Sciences. Copyright © National Academy of Sciences. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Africa | - |
dc.subject | Coronavirus | - |
dc.subject | Evolution | - |
dc.subject | MERS | - |
dc.subject | Zoonosis | - |
dc.title | MERS coronaviruses from camels in Africa exhibit region-dependent genetic diversity | - |
dc.type | Article | - |
dc.identifier.email | Chu, KW: dkwchu@hku.hk | - |
dc.identifier.email | Hui, PY: kenrie@hku.hk | - |
dc.identifier.email | Perera, RAPM: mahenp@hku.hk | - |
dc.identifier.email | Chan, MCW: mchan@hku.hk | - |
dc.identifier.email | Nicholls, JM: jmnichol@hkucc.hku.hk | - |
dc.identifier.email | Poon, LML: llmpoon@hkucc.hku.hk | - |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | - |
dc.identifier.authority | Hui, PY=rp02149 | - |
dc.identifier.authority | Chan, MCW=rp00420 | - |
dc.identifier.authority | Nicholls, JM=rp00364 | - |
dc.identifier.authority | Poon, LML=rp00484 | - |
dc.identifier.authority | Peiris, JSM=rp00410 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1073/pnas.1718769115 | - |
dc.identifier.pmid | 29507189 | - |
dc.identifier.pmcid | PMC5866576 | - |
dc.identifier.scopus | eid_2-s2.0-85044278309 | - |
dc.identifier.hkuros | 286573 | - |
dc.identifier.volume | 115 | - |
dc.identifier.issue | 12 | - |
dc.identifier.spage | 3144 | - |
dc.identifier.epage | 3149 | - |
dc.identifier.isi | WOS:000427829500085 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0027-8424 | - |