TY - JOUR
T1 - Quantifying asymptomatic infection and transmission of COVID-19 in New York City using observed cases, serology, and testing capacity
AU - Subramanian, Rahul
AU - He, Qixin
AU - Pascual, Mercedes
N1 - Funding Information:
R.S. was supported by an NSF Research Trainee-ship (1735359: NRT-INFEWS: Computational data science to advance research at the energy environment nexus). We thank Aaron King for his insightful discussions. This work was completed with resources and support provided by the University of Chicago's Research Computing Center.
Funding Information:
ACKNOWLEDGMENTS. R.S. was supported by an NSF Research Traineeship (1735359: NRT-INFEWS: Computational data science to advance research at the energy environment nexus). We thank Aaron King for his insightful discussions. This work was completed with resources and support provided by the University of Chicago’s Research Computing Center.
Publisher Copyright:
© 2021 National Academy of Sciences. All rights reserved.
PY - 2021/3/2
Y1 - 2021/3/2
N2 - The contributions of asymptomatic infections to herd immunity and community transmission are key to the resurgence and control of COVID-19, but are difficult to estimate using current models that ignore changes in testing capacity. Using a model that incorporates daily testing information fit to the case and serology data from New York City, we show that the proportion of symptomatic cases is low, ranging from 13 to 18%, and that the reproductive number may be larger than often assumed. Asymptomatic infections contribute substantially to herd immunity, and to community transmission together with presymptomatic ones. If asymptomatic infections transmit at similar rates as symptomatic ones, the overall reproductive number across all classes is larger than often assumed, with estimates ranging from 3.2 to 4.4. If they transmit poorly, then symptomatic cases have a larger reproductive number ranging from 3.9 to 8.1. Even in this regime, presymptomatic and asymptomatic cases together comprise at least 50% of the force of infection at the outbreak peak. We find no regimes in which all infection subpopulations have reproductive numbers lower than three. These findings elucidate the uncertainty that current case and serology data cannot resolve, despite consideration of different model structures. They also emphasize how temporal data on testing can reduce and better define this uncertainty, as we move forward through longer surveillance and second epidemic waves. Complementary information is required to determine the transmissibility of asymptomatic cases, which we discuss. Regardless, current assumptions about the basic reproductive number of severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) should be reconsidered.
AB - The contributions of asymptomatic infections to herd immunity and community transmission are key to the resurgence and control of COVID-19, but are difficult to estimate using current models that ignore changes in testing capacity. Using a model that incorporates daily testing information fit to the case and serology data from New York City, we show that the proportion of symptomatic cases is low, ranging from 13 to 18%, and that the reproductive number may be larger than often assumed. Asymptomatic infections contribute substantially to herd immunity, and to community transmission together with presymptomatic ones. If asymptomatic infections transmit at similar rates as symptomatic ones, the overall reproductive number across all classes is larger than often assumed, with estimates ranging from 3.2 to 4.4. If they transmit poorly, then symptomatic cases have a larger reproductive number ranging from 3.9 to 8.1. Even in this regime, presymptomatic and asymptomatic cases together comprise at least 50% of the force of infection at the outbreak peak. We find no regimes in which all infection subpopulations have reproductive numbers lower than three. These findings elucidate the uncertainty that current case and serology data cannot resolve, despite consideration of different model structures. They also emphasize how temporal data on testing can reduce and better define this uncertainty, as we move forward through longer surveillance and second epidemic waves. Complementary information is required to determine the transmissibility of asymptomatic cases, which we discuss. Regardless, current assumptions about the basic reproductive number of severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) should be reconsidered.
KW - Asymptomatic transmission
KW - COVID-19
KW - Epidemiological model
KW - Epidemiological parameter estimates
KW - Testing submodel
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U2 - 10.1073/pnas.2019716118
DO - 10.1073/pnas.2019716118
M3 - Article
C2 - 33571106
AN - SCOPUS:85101443089
SN - 0027-8424
VL - 118
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 9
M1 - e2019716118
ER -