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Genomic reconstruction of the SARS-CoV-2 epidemic in England

Author

Listed:
  • Harald S. Vöhringer

    (European Bioinformatics Institute EMBL-EBI)

  • Theo Sanderson

    (Wellcome Sanger Institute
    The Francis Crick Institute)

  • Matthew Sinnott

    (Wellcome Sanger Institute)

  • Nicola Maio

    (European Bioinformatics Institute EMBL-EBI)

  • Thuy Nguyen

    (Wellcome Sanger Institute)

  • Richard Goater

    (Wellcome Sanger Institute)

  • Frank Schwach

    (Wellcome Sanger Institute
    Public Health England)

  • Ian Harrison

    (Public Health England)

  • Joel Hellewell

    (London School of Hygiene & Tropical Medicine)

  • Cristina V. Ariani

    (Wellcome Sanger Institute)

  • Sonia Gonçalves

    (Wellcome Sanger Institute)

  • David K. Jackson

    (Wellcome Sanger Institute)

  • Ian Johnston

    (Wellcome Sanger Institute)

  • Alexander W. Jung

    (European Bioinformatics Institute EMBL-EBI)

  • Callum Saint

    (Wellcome Sanger Institute)

  • John Sillitoe

    (Wellcome Sanger Institute)

  • Maria Suciu

    (Wellcome Sanger Institute)

  • Nick Goldman

    (European Bioinformatics Institute EMBL-EBI)

  • Jasmina Panovska-Griffiths

    (University of Oxford)

  • Ewan Birney

    (European Bioinformatics Institute EMBL-EBI)

  • Erik Volz

    (Imperial College London)

  • Sebastian Funk

    (London School of Hygiene & Tropical Medicine)

  • Dominic Kwiatkowski

    (Wellcome Sanger Institute)

  • Meera Chand

    (Public Health England
    Guy’s and St Thomas’ NHS Foundation Trust)

  • Inigo Martincorena

    (Wellcome Sanger Institute)

  • Jeffrey C. Barrett

    (Wellcome Sanger Institute)

  • Moritz Gerstung

    (European Bioinformatics Institute EMBL-EBI
    German Cancer Research Centre DKFZ)

Abstract

The evolution of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus leads to new variants that warrant timely epidemiological characterization. Here we use the dense genomic surveillance data generated by the COVID-19 Genomics UK Consortium to reconstruct the dynamics of 71 different lineages in each of 315 English local authorities between September 2020 and June 2021. This analysis reveals a series of subepidemics that peaked in early autumn 2020, followed by a jump in transmissibility of the B.1.1.7/Alpha lineage. The Alpha variant grew when other lineages declined during the second national lockdown and regionally tiered restrictions between November and December 2020. A third more stringent national lockdown suppressed the Alpha variant and eliminated nearly all other lineages in early 2021. Yet a series of variants (most of which contained the spike E484K mutation) defied these trends and persisted at moderately increasing proportions. However, by accounting for sustained introductions, we found that the transmissibility of these variants is unlikely to have exceeded the transmissibility of the Alpha variant. Finally, B.1.617.2/Delta was repeatedly introduced in England and grew rapidly in early summer 2021, constituting approximately 98% of sampled SARS-CoV-2 genomes on 26 June 2021.

Suggested Citation

  • Harald S. Vöhringer & Theo Sanderson & Matthew Sinnott & Nicola Maio & Thuy Nguyen & Richard Goater & Frank Schwach & Ian Harrison & Joel Hellewell & Cristina V. Ariani & Sonia Gonçalves & David K. Ja, 2021. "Genomic reconstruction of the SARS-CoV-2 epidemic in England," Nature, Nature, vol. 600(7889), pages 506-511, December.
  • Handle: RePEc:nat:nature:v:600:y:2021:i:7889:d:10.1038_s41586-021-04069-y
    DOI: 10.1038/s41586-021-04069-y
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