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Genomic surveillance of SARS-CoV-2 in the Bronx enables clinical and epidemiological inference.

J Maximilian FelsSaad KhanRyan ForsterKarin A SkalinaSurksha SirichandAmy S FoxAviv BergmanWilliam B MitchellLucia R WolgastWendy A SzymczakRobert H BortzM Eugenia DieterleCatalina FlorezDenise HaslwanterRohit K JangraEthan LaudermilchAriel S WirchnianskiJason BarnhillDavid L GoldmanHnin KhineD Yitzchak GoldsteinJohanna P DailyKartik ChandranLibusha Kelly
Published in: medRxiv : the preprint server for health sciences (2021)
The Bronx was an early epicenter of the COVID-19 pandemic in the USA. We conducted temporal genomic surveillance of SARS-CoV-2 genomes across the Bronx from March-October 2020. Although the local structure of SARS-CoV-2 lineages mirrored those of New York City and New York State, temporal sampling revealed a dynamic and changing landscape of SARS- CoV-2 genomic diversity. Mapping the trajectories of variants, we found that while some have become 'endemic' to the Bronx, other, novel variants rose in prevalence in the late summer/early fall. Geographically resolved genomes enabled us to distinguish between a case of reinfection and a case of persistent infection. We propose that limited, targeted, temporal genomic surveillance has clinical and epidemiological utility in managing the ongoing COVID pandemic.
Keyphrases
  • sars cov
  • copy number
  • respiratory syndrome coronavirus
  • public health
  • single cell
  • genome wide
  • risk factors
  • depressive symptoms
  • high resolution
  • dna methylation
  • gene expression
  • heat stress
  • drug delivery