Nature Communications (Dec 2024)
Systematic surveillance of SARS-CoV-2 reveals dynamics of variant mutagenesis and transmission in a large urban population
- Marie-Ming Aynaud,
- Lauren Caldwell,
- Khalid N. Al-Zahrani,
- Seda Barutcu,
- Kin Chan,
- Andreea Obersterescu,
- Abiodun A. Ogunjimi,
- Min Jin,
- Kathleen-Rose Zakoor,
- Shyam Patel,
- Ron Padilla,
- Mark C. C. Jen,
- Princess Mae Veniegas,
- Nursrin Dewsi,
- Filiam Yonathan,
- Lucy Zhang,
- Amelia Ayson-Fortunato,
- Analiza Aquino,
- Paul Krzyzanowski,
- Jared Simpson,
- John Bartlett,
- Ilinca Lungu,
- Bradly G. Wouters,
- James M. Rini,
- Michael Gekas,
- Susan Poutanen,
- Laurence Pelletier,
- Tony Mazzulli,
- Jeffrey L. Wrana
Affiliations
- Marie-Ming Aynaud
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Lauren Caldwell
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Khalid N. Al-Zahrani
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Seda Barutcu
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Kin Chan
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Andreea Obersterescu
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Abiodun A. Ogunjimi
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Min Jin
- Departments of Molecular Genetics and Biochemistry, University of Toronto, MaRS Center, Toronto
- Kathleen-Rose Zakoor
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Shyam Patel
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Ron Padilla
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Mark C. C. Jen
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Princess Mae Veniegas
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Nursrin Dewsi
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Filiam Yonathan
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Lucy Zhang
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Amelia Ayson-Fortunato
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Analiza Aquino
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Paul Krzyzanowski
- Ontario Institute for Cancer Research, Toronto General Hospital
- Jared Simpson
- Ontario Institute for Cancer Research, Toronto General Hospital
- John Bartlett
- Ontario Institute for Cancer Research, Toronto General Hospital
- Ilinca Lungu
- Ontario Institute for Cancer Research, Toronto General Hospital
- Bradly G. Wouters
- Princess Margaret Cancer Centre and Campbell Family Institute for Cancer Research, University Health Network, Toronto
- James M. Rini
- Departments of Molecular Genetics and Biochemistry, University of Toronto, MaRS Center, Toronto
- Michael Gekas
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Susan Poutanen
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Laurence Pelletier
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- Tony Mazzulli
- Department of Microbiology, Mount Sinai Hospital/University Health Network, Toronto
- Jeffrey L. Wrana
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto
- DOI
- https://doi.org/10.1038/s41467-024-55031-1
- Journal volume & issue
-
Vol. 15,
no. 1
pp. 1 – 16
Abstract
Abstract Highly mutable pathogens generate viral diversity that impacts virulence, transmissibility, treatment, and thwarts acquired immunity. We previously described C19-SPAR-Seq, a high-throughput, next-generation sequencing platform to detect SARS-CoV-2 that we here deployed to systematically profile variant dynamics of SARS-CoV-2 for over 3 years in a large, North American urban environment (Toronto, Canada). Sequencing of the ACE2 receptor binding motif and polybasic furin cleavage site of the Spike gene in over 70,000 patients revealed that population sweeps of canonical variants of concern (VOCs) occurred in repeating wavelets. Furthermore, we found that VOC mutant derivatives and putative quasispecies that targeted functionally important residues and were found in future VOCs arose frequently, but were always extinguished. Systematic screening of functionally relevant domains in pathogens could thus provide a powerful tool for monitoring spread and mutational trajectories, particularly those with zoonotic potential.