Systematic surveillance of SARS-CoV-2 reveals dynamics of variant mutagenesis and transmission in a large urban population

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.

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Journal
Nature Communications
Published
2024-12-30
DOI
https://doi.org/10.1038/s41467-024-55031-1
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Systematic surveillance of SARS-CoV-2 reveals dynamics of variant mutagenesis and transmission in a large urban population

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Nature Communications
SARS-CoV-2 and COVID-19 Research
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Systematic surveillance of SARS-CoV-2 reveals dynamics of variant mutagenesis and transmission in a large urban population

Jared T. Simpson, Tony Mazzulli, Seda Barutcu, Min Jin, Abiodun A. Ogunjimi, Lucy Zhang, Bradly G. Wouters, James M. Rini, Shyam Ajay Patel, Marie-Ming Aynaud, Paul M. Krzyzanowski, Analiza Aquino, Laurence Pelletier, Jeffrey L. Wrana, Kathleen-Rose Zakoor, John Bartlett, Andreea Obersterescu, Lauren Caldwell, Susan M. Poutanen, Ilinca M. Lungu, Khalid N. Al‐Zahrani, Mark Jen, Filiam Yonathan, Amelia Ayson-Fortunato, Nursrin Dewsi, Princess Mae Veniegas, Michael Gekas, Ron Padilla, Kin Chan
article en

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.

Nature CommunicationsVol. 15(1)
Ontario Institute for Cancer Research (CA), Mount Sinai Hospital (CA), University Health Network (CA), University of Toronto (CA), Lunenfeld-Tanenbaum Research Institute (CA), Toronto General Hospital (CA), Princess Margaret Cancer Centre (CA)
Government of Ontario, Krembil Foundation, Canadian Institutes of Health Research
Sustainable cities and communities
Openalex Percentile: Top 70%
SARS-CoV-2 and COVID-19 Research
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