Estimating SARS-CoV-2 seroprevalence and epidemiological parameters with uncertainty from serological surveys

Author:

Larremore Daniel B12ORCID,Fosdick Bailey K3,Bubar Kate M45,Zhang Sam4,Kissler Stephen M6ORCID,Metcalf C Jessica E7ORCID,Buckee Caroline O89ORCID,Grad Yonatan H6ORCID

Affiliation:

1. Department of Computer Science, University of Colorado Boulder, Boulder, United States

2. BioFrontiers Institute, University of Colorado Boulder, Boulder, United States

3. Department of Statistics, Colorado State University, Fort Collins, United States

4. Department of Applied Mathematics, University of Colorado Boulder, Boulder, United States

5. IQ Biology Program, University of Colorado Boulder, Boulder, United States

6. Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, United States

7. Department of Ecology and Evolutionary Biology and the Woodrow Wilson School, Princeton University, Princeton, United States

8. Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, United States

9. Center for Communicable Disease Dynamics, Harvard T.H. Chan School of Public Health, Boston, United States

Abstract

Establishing how many people have been infected by SARS-CoV-2 remains an urgent priority for controlling the COVID-19 pandemic. Serological tests that identify past infection can be used to estimate cumulative incidence, but the relative accuracy and robustness of various sampling strategies have been unclear. We developed a flexible framework that integrates uncertainty from test characteristics, sample size, and heterogeneity in seroprevalence across subpopulations to compare estimates from sampling schemes. Using the same framework and making the assumption that seropositivity indicates immune protection, we propagated estimates and uncertainty through dynamical models to assess uncertainty in the epidemiological parameters needed to evaluate public health interventions and found that sampling schemes informed by demographics and contact networks outperform uniform sampling. The framework can be adapted to optimize serosurvey design given test characteristics and capacity, population demography, sampling strategy, and modeling approach, and can be tailored to support decision-making around introducing or removing interventions.

Funder

Morris-Singer Fund for the Center for Communicable Disease Dynamics

National Cancer Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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