期刊论文详细信息
eLife
Selection for infectivity profiles in slow and fast epidemics, and the rise of SARS-CoV-2 variants
Florence Débarre1  François Blanquart2  Simon Cauchemez3  Nathanaël Hozé4  Benjamin John Cowling5 
[1] Laboratory of Data Discovery for Health, Hong Kong Science and Technology Park New Territories, Hong Kong Special Administrative Region, Hong Kong, China;Centre for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS INSERM, PSL Research University, Paris, France;Institute of Ecology and Environmental Sciences of Paris (iEES-Paris, UMR 7618) CNRS, Sorbonne Université, UPEC, IRD, INRAE, Paris, France;Mathematical Modelling of Infectious Diseases Unit, Institut Pasteur, Université de Paris, UMR2000, CNRS, Paris, France;WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong Pokfulam, Hong Kong Special Administrative Region, Hong Kong, China;
关键词: SARS-CoV-2;    adaptation;    variants of concern;   
DOI  :  10.7554/eLife.75791
来源: DOAJ
【 摘 要 】

Evaluating the characteristics of emerging SARS-CoV-2 variants of concern is essential to inform pandemic risk assessment. A variant may grow faster if it produces a larger number of secondary infections (“R advantage”) or if the timing of secondary infections (generation time) is better. So far, assessments have largely focused on deriving the R advantage assuming the generation time was unchanged. Yet, knowledge of both is needed to anticipate the impact. Here, we develop an analytical framework to investigate the contribution of both the R advantage and generation time to the growth advantage of a variant. It is known that selection on a variant with larger R increases with levels of transmission in the community. We additionally show that variants conferring earlier transmission are more strongly favored when the historical strains have fast epidemic growth, while variants conferring later transmission are more strongly favored when historical strains have slow or negative growth. We develop these conceptual insights into a new statistical framework to infer both the R advantage and generation time of a variant. On simulated data, our framework correctly estimates both parameters when it covers time periods characterized by different epidemiological contexts. Applied to data for the Alpha and Delta variants in England and in Europe, we find that Alpha confers a+54% [95% CI, 45–63%] R advantage compared to previous strains, and Delta +140% [98–182%] compared to Alpha, and mean generation times are similar to historical strains for both variants. This work helps interpret variant frequency dynamics and will strengthen risk assessment for future variants of concern.

【 授权许可】

Unknown   

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