Epidemiology of a Novel Recombinant Middle East Respiratory Syndrome Coronavirus in Humans in Saudi Arabia
Supporting Files
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9 01 2016
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File Language:
English
Details
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Alternative Title:J Infect Dis
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Personal Author:Assiri, Abdullah M. ; Midgley, Claire M. ; Abedi, Glen R. ; Saeed, Abdulaziz Bin ; Almasri, Malak M. ; Lu, Xiaoyan ; Al-Abdely, Hail M. ; Abdalla, Osman ; Mohammed, Mutaz ; Algarni, Homoud S. ; Alhakeem, Raafat F. ; Sakthivel, Senthilkumar K. ; Nooh, Randa ; Alshayab, Zainab ; Alessa, Mohammad ; Srinivasamoorthy, Ganesh ; AlQahtani, Saeed Yahya ; Kheyami, Ali ; HajOmar, Waleed Husein ; Banaser, Talib M. ; Esmaeel, Ahmad ; Hall, Aron J. ; Curns, Aaron T. ; Tamin, Azaibi ; Alsharef, Ali Abraheem ; Erdman, Dean ; Watson, John T. ; Gerber, Susan I.
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Description:Background
Middle East respiratory syndrome coronavirus (MERS-CoV) causes severe respiratory illness in humans. Fundamental questions about circulating viruses and transmission routes remain.
Methods
We assessed routinely collected epidemiologic data for MERS-CoV cases reported in Saudi Arabia during 1 January– 30 June 2015 and conducted a more detailed investigation of cases reported during February 2015. Available respiratory specimens were obtained for sequencing.
Results
During the study period, 216 MERS-CoV cases were reported. Full genome (n = 17) or spike gene sequences (n = 82) were obtained from 99 individuals. Most sequences (72 of 99 [73%]) formed a discrete, novel recombinant subclade (NRC-2015), which was detected in 6 regions and became predominant by June 2015. No clinical differences were noted between clades. Among 87 cases reported during February 2015, 13 had no recognized risks for secondary acquisition; 12 of these 13 also denied camel contact. Most viruses (8 of 9) from these 13 individuals belonged to NRC-2015.
Discussions
Our findings document the spread and eventual predominance of NRC-2015 in humans in Saudi Arabia during the first half of 2015. Our identification of cases without recognized risk factors but with similar virus sequences indicates the need for better understanding of risk factors for MERS-CoV transmission.
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Subjects:
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Source:J Infect Dis. 214(5):712-721
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Pubmed ID:27302191
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Pubmed Central ID:PMC5712457
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Document Type:
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Funding:
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Volume:214
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Issue:5
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Collection(s):
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Main Document Checksum:urn:sha256:164c86eba9ee5f8d25ba61da4eb945dc159d6b2995553b8ac57636503556489f
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Download URL:
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File Type:
Supporting Files
File Language:
English
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