| Literature DB >> 32902372 |
Arinjay Banerjee1,2, Andrew C Doxey3,4, Benjamin J-M Tremblay3, Michael J Mansfield5, Sonu Subudhi6, Jeremy A Hirota4,1, Matthew S Miller7,1, Andrew G McArthur7,1, Samira Mubareka8,9, Karen Mossman2,1.
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) recently emerged to cause widespread infections in humans. SARS-CoV-2 infections have been reported in the Kingdom of Saudi Arabia, where Middle East respiratory syndrome coronavirus (MERS-CoV) causes seasonal outbreaks with a case fatality rate of ~37 %. Here we show that there exists a theoretical possibility of future recombination events between SARS-CoV-2 and MERS-CoV RNA. Through computational analyses, we have identified homologous genomic regions within the ORF1ab and S genes that could facilitate recombination, and have analysed co-expression patterns of the cellular receptors for SARS-CoV-2 and MERS-CoV, ACE2 and DPP4, respectively, to identify human anatomical sites that could facilitate co-infection. Furthermore, we have investigated the likely susceptibility of various animal species to MERS-CoV and SARS-CoV-2 infection by comparing known virus spike protein-receptor interacting residues. In conclusion, we suggest that a recombination between SARS-CoV-2 and MERS-CoV RNA is possible and urge public health laboratories in high-risk areas to develop diagnostic capability for the detection of recombined coronaviruses in patient samples.Entities:
Keywords: MERS-CoV; SARS-CoV-2; coronavirus; emergence; predictions; recombination
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Year: 2020 PMID: 32902372 DOI: 10.1099/jgv.0.001491
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891