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评估 SARS-CoV-2 谱系 B.1.1.7 在英国的传播能力。

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

机构信息

MRC Centre for Global Infectious Disease Analysis, Jameel Institute for Disease and Emergency Analytics, Imperial College London, London, UK.

Public Health England, London, UK.

出版信息

Nature. 2021 May;593(7858):266-269. doi: 10.1038/s41586-021-03470-x. Epub 2021 Mar 25.

Abstract

The SARS-CoV-2 lineage B.1.1.7, designated variant of concern (VOC) 202012/01 by Public Health England, was first identified in the UK in late summer to early autumn 2020. 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.

摘要

新冠病毒 2019 年冠状病毒病(COVID-19)大流行期间,SARS-CoV-2 的 B.1.1.7 谱系于 2020 年夏末至初秋在英国首次被发现。从基于社区的 COVID-19 诊断检测中收集的全基因组 SARS-CoV-2 序列数据显示,B.1.1.7 谱系在 2020 年秋季迅速扩张,表明其具有选择优势。在这里,我们发现从遗传数据推断的 VOC 频率变化与基于社区的诊断 PCR 检测中 S 基因靶标失败(SGTF)推断的变化非常吻合。对英格兰各地社区诊断 PCR 检测中非 SGTF 和 SGTF 病例数量变化趋势的分析表明,B.1.1.7 的传染性高于非 VOC 谱系,即使其潜伏期或代时不同。SGTF 数据表明报告病例的年龄构成发生了短暂变化,B.1.1.7 病例中 20 岁以下病例的比例高于非 VOC 病例。我们使用 SGTF 和基因组数据估计了 B.1.1.7 和共循环谱系的时变繁殖数。最佳支持模型并未表明不同年龄组的 VOC 传染性有实质性差异,但所有分析均表明 B.1.1.7 与其他谱系相比具有实质性的传播优势,繁殖数高出 50%至 100%。

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