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Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England

  • The COVID-19 Genomics UK (COG-UK) Consortium
  • Department of Medicine
  • Imperial College London
  • UK Health Security Agency
  • Wellcome Sanger Institute
  • EaStCHEM School of Chemistry, University of Edinburgh
  • Liverpool Clinical Laboratories
  • University of Birmingham
  • Barking, Havering and Redbridge University Hospitals NHS Trust
  • Basingstoke Hospital
  • Belfast Health & Social Care Trust
  • Betsi Cadwaladr University Health Board
  • Nuffield Department of Medicine
  • University Hospitals Sussex NHS Foundation Trust
  • University of Cambridge
  • Cambridge University Hospitals NHS Foundation Trust
  • Cardiff & Vale University Health Board
  • Cardiff University
  • St Thomas’ Hospital and Kings College London
  • Guy’s and St Thomas’ NHS Foundation Trust
  • University of Portsmouth
  • University of Oxford
  • Queens Medical Centre
  • University Hospitals of Leicester NHS Trust
  • County Durham and Darlington NHS Foundation Trust
  • University of Nottingham
  • London School of Hygiene & Tropical Medicine
  • King's College London
  • Kettering General Hospital
  • East Kent Hospitals University NHS Foundation Trust
  • East Suffolk and North Essex NHS Foundation Trust
  • Gateshead Health NHS Foundation Trust
  • Gloucestershire Hospitals NHS Foundation Trust
  • Great Ormond Street Hospital for Children NHS Foundation Trust
  • Hampshire Hospitals NHS Foundation Trust
  • Health Data Research UK
  • Health Services Laboratories
  • Heartlands Hospital
  • Northumbria University
  • Imperial College Healthcare NHS Trust
  • University of Glasgow
  • Maidstone and Tunbridge Wells NHS Trust
  • Manchester University NHS Foundation Trust
  • Wye valley NHS Trust
  • MRC Biostatistics Unit
  • MRC-University of Glasgow Centre for Virus Research
  • Leeds Teaching Hospitals NHS Trust
  • Newcastle upon Tyne Hospitals NHS Foundation Trust
  • Newcastle University
  • NHS Greater Glasgow and Clyde
  • NHS Lothian
  • Norwich University Hospital
  • Norfolk County Council
  • North Cumbria Integrated Care NHS Foundation Trust
  • North Tees and Hartlepool NHS Foundation Trust
  • Oxford University Hospitals NHS Foundation Trust
  • Northern Lincolnshire & Goole NHS Foundation Trust
  • Portsmouth Hospitals University NHS Trust
  • The Princess Alexandra Hospital NHS Trust
  • Public Health Agency
  • Public Health Scotland
  • Public Health Wales
  • Quadram Institute
  • University Hospitals Birmingham NHS Foundation Trust
  • Queen's University Belfast
  • Royal Devon and Exeter NHS Foundation Trust
  • Royal Free NHS Trust
  • Sandwell and West Birmingham Hospitals NHS Trust
  • Sheffield Teaching Hospitals NHS Foundation Trust
  • South Tees Hospitals NHS Foundation Trust
  • Swansea University
  • University Hospital Southampton NHS Foundation Trust
  • University College London
  • University Hospitals Coventry and Warwickshire NHS Trust
  • University of Brighton
  • University of East Anglia
  • University of Exeter
  • University of Liverpool
  • University of Sheffield
  • University of Warwick
  • Viapath
  • King’s College Hospital NHS Foundation Trust
  • University of Copenhagen

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

850 Citas (Scopus)

Resumen

The SARS-CoV-2 lineage B.1.1.7, designated variant of concern (VOC) 202012/01 by Public Health England1, was first identified in the UK in late summer to early autumn 20202. Whole-genome SARS-CoV-2 sequence data collected from community-based diagnostic testing for COVID-19 show an extremely rapid expansion of the B.1.1.7 lineage during autumn 2020, suggesting that it has a selective advantage. Here we show that changes in VOC frequency inferred from genetic data correspond closely to changes inferred by S gene target failures (SGTF) in community-based diagnostic PCR testing. Analysis of trends in SGTF and non-SGTF case numbers in local areas across England shows that B.1.1.7 has higher transmissibility than non-VOC lineages, even if it has a different latent period or generation time. The SGTF data indicate a transient shift in the age composition of reported cases, with cases of B.1.1.7 including a larger share of under 20-year-olds than non-VOC cases. We estimated time-varying reproduction numbers for B.1.1.7 and co-circulating lineages using SGTF and genomic data. The best-supported models did not indicate a substantial difference in VOC transmissibility among different age groups, but all analyses agreed that B.1.1.7 has a substantial transmission advantage over other lineages, with a 50% to 100% higher reproduction number.

Idioma originalInglés
Páginas (desde-hasta)266-269
Número de páginas4
PublicaciónNature
Volumen593
N.º7858
DOI
EstadoPublicada - 13 may. 2021
Publicado de forma externa

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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