Predicting the recombination potential of severe acute respiratory syndrome coronavirus 2 and Middle East respiratory syndrome coronavirus

Author:

Banerjee Arinjay12ORCID,Doxey Andrew C.34ORCID,Tremblay Benjamin J.-M.3ORCID,Mansfield Michael J.5,Subudhi Sonu6ORCID,Hirota Jeremy A.41,Miller Matthew S.71ORCID,McArthur Andrew G.71ORCID,Mubareka Samira89,Mossman Karen21ORCID

Affiliation:

1. Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4K1, Canada

2. Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, L8S 4K1, Canada

3. Department of Biology, University of Waterloo, Waterloo, Ontario, N2L 3G1, Canada

4. Division of Respirology, Department of Medicine, McMaster University, Hamilton, Ontario, L8S 4K1, Canada

5. Genomics and Regulatory Systems Unit, Okinawa Institute of Science and Technology Graduate University, Onna, Okinawa 904-0495, Japan

6. Gastrointestinal Unit and Liver Center, Massachusetts General Hospital, Harvard Medical School, Harvard University, Boston, MA 02114, USA

7. Department of Biochemistry and Biomedical Science, McMaster University, Hamilton, Ontario, L8S 4K1, Canada

8. Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, M5S 1A8, Canada

9. Sunnybrook Health Sciences Centre, Toronto, Ontario, M4N 3M5, Canada

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.

Funder

Natural Sciences and Engineering Research Council

Canadian Institutes for Health Research

Publisher

Microbiology Society

Subject

Virology

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