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author Marques, Andrew D.
Sherrill-Mix, Scott
Everett, John
Reddy, Shantan
Hokama, Pascha
Roche, Aoife M.
Hwang, Young
Glascock, Abigail
Whiteside, Samantha A.
Graham-Wooten, Jevon
Khatib, Layla A.
Fitzgerald, Ayannah S.
Moustafa, Ahmed M.
Bianco, Colleen
Rajagopal, Swetha
Helton, Jenna
Deming, Regan
Denu, Lidiya
Ahmed, Azad
Kitt, Eimear
Coffin, Susan E.
Newbern, Claire
Mell, Josh Chang
Planet, Paul J.
Badjatia, Nitika
Richards, Bonnie
Wang, Zi-Xuan
Cannuscio, Carolyn C.
Strelau, Katherine M.
Jaskowiak-Barr, Anne
Cressman, Leigh
Loughrey, Sean
Ganguly, Arupa
Feldman, Michael D.
Collman, Ronald G.
Rodino, Kyle G.
Kelly, Brendan J.
Bushman, Frederic D.
author_facet Marques, Andrew D.
Sherrill-Mix, Scott
Everett, John
Reddy, Shantan
Hokama, Pascha
Roche, Aoife M.
Hwang, Young
Glascock, Abigail
Whiteside, Samantha A.
Graham-Wooten, Jevon
Khatib, Layla A.
Fitzgerald, Ayannah S.
Moustafa, Ahmed M.
Bianco, Colleen
Rajagopal, Swetha
Helton, Jenna
Deming, Regan
Denu, Lidiya
Ahmed, Azad
Kitt, Eimear
Coffin, Susan E.
Newbern, Claire
Mell, Josh Chang
Planet, Paul J.
Badjatia, Nitika
Richards, Bonnie
Wang, Zi-Xuan
Cannuscio, Carolyn C.
Strelau, Katherine M.
Jaskowiak-Barr, Anne
Cressman, Leigh
Loughrey, Sean
Ganguly, Arupa
Feldman, Michael D.
Collman, Ronald G.
Rodino, Kyle G.
Kelly, Brendan J.
Bushman, Frederic D.
author_sort Marques, Andrew D.
collection PubMed
description The severe acute respiratory coronavirus-2 (SARS-CoV-2) is the cause of the global outbreak of COVID-19. Evidence suggests that the virus is evolving to allow efficient spread through the human population, including vaccinated individuals. Here we report a study of viral variants from surveillance of the Delaware Valley, including the city of Philadelphia, and variants infecting vaccinated subjects. We sequenced and analyzed complete viral genomes from 2621 surveillance samples from March 2020 to September 2021 and compared them to genome sequences from 159 vaccine breakthroughs. In the early spring of 2020, all detected variants were of the B.1 and closely related lineages. A mixture of lineages followed, notably including B.1.243 followed by B.1.1.7 (alpha), with other lineages present at lower levels. Later isolations were dominated by B.1.617.2 (delta) and other delta lineages; delta was the exclusive variant present by the last time sampled. To investigate whether any variants appeared preferentially in vaccine breakthroughs, we devised a model based on Bayesian autoregressive moving average logistic multinomial regression to allow rigorous comparison. This revealed that B.1.617.2 (delta) showed three-fold enrichment in vaccine breakthrough cases (odds ratio of 3; 95% credible interval 0.89–11). Viral point substitutions could also be associated with vaccine breakthroughs, notably the N501Y substitution found in the alpha, beta and gamma variants (odds ratio 2.04; 95% credible interval of 1.25–3.18). This study thus provides a detailed picture of viral evolution in the Delaware Valley and a geographically matched analysis of vaccine breakthroughs; it also introduces a rigorous statistical approach to interrogating enrichment of viral variants.
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spelling pubmed-85475302021-10-27 SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021 Marques, Andrew D. Sherrill-Mix, Scott Everett, John Reddy, Shantan Hokama, Pascha Roche, Aoife M. Hwang, Young Glascock, Abigail Whiteside, Samantha A. Graham-Wooten, Jevon Khatib, Layla A. Fitzgerald, Ayannah S. Moustafa, Ahmed M. Bianco, Colleen Rajagopal, Swetha Helton, Jenna Deming, Regan Denu, Lidiya Ahmed, Azad Kitt, Eimear Coffin, Susan E. Newbern, Claire Mell, Josh Chang Planet, Paul J. Badjatia, Nitika Richards, Bonnie Wang, Zi-Xuan Cannuscio, Carolyn C. Strelau, Katherine M. Jaskowiak-Barr, Anne Cressman, Leigh Loughrey, Sean Ganguly, Arupa Feldman, Michael D. Collman, Ronald G. Rodino, Kyle G. Kelly, Brendan J. Bushman, Frederic D. medRxiv Article The severe acute respiratory coronavirus-2 (SARS-CoV-2) is the cause of the global outbreak of COVID-19. Evidence suggests that the virus is evolving to allow efficient spread through the human population, including vaccinated individuals. Here we report a study of viral variants from surveillance of the Delaware Valley, including the city of Philadelphia, and variants infecting vaccinated subjects. We sequenced and analyzed complete viral genomes from 2621 surveillance samples from March 2020 to September 2021 and compared them to genome sequences from 159 vaccine breakthroughs. In the early spring of 2020, all detected variants were of the B.1 and closely related lineages. A mixture of lineages followed, notably including B.1.243 followed by B.1.1.7 (alpha), with other lineages present at lower levels. Later isolations were dominated by B.1.617.2 (delta) and other delta lineages; delta was the exclusive variant present by the last time sampled. To investigate whether any variants appeared preferentially in vaccine breakthroughs, we devised a model based on Bayesian autoregressive moving average logistic multinomial regression to allow rigorous comparison. This revealed that B.1.617.2 (delta) showed three-fold enrichment in vaccine breakthrough cases (odds ratio of 3; 95% credible interval 0.89–11). Viral point substitutions could also be associated with vaccine breakthroughs, notably the N501Y substitution found in the alpha, beta and gamma variants (odds ratio 2.04; 95% credible interval of 1.25–3.18). This study thus provides a detailed picture of viral evolution in the Delaware Valley and a geographically matched analysis of vaccine breakthroughs; it also introduces a rigorous statistical approach to interrogating enrichment of viral variants. Cold Spring Harbor Laboratory 2021-11-17 /pmc/articles/PMC8547530/ /pubmed/34704098 http://dx.doi.org/10.1101/2021.10.18.21264623 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Marques, Andrew D.
Sherrill-Mix, Scott
Everett, John
Reddy, Shantan
Hokama, Pascha
Roche, Aoife M.
Hwang, Young
Glascock, Abigail
Whiteside, Samantha A.
Graham-Wooten, Jevon
Khatib, Layla A.
Fitzgerald, Ayannah S.
Moustafa, Ahmed M.
Bianco, Colleen
Rajagopal, Swetha
Helton, Jenna
Deming, Regan
Denu, Lidiya
Ahmed, Azad
Kitt, Eimear
Coffin, Susan E.
Newbern, Claire
Mell, Josh Chang
Planet, Paul J.
Badjatia, Nitika
Richards, Bonnie
Wang, Zi-Xuan
Cannuscio, Carolyn C.
Strelau, Katherine M.
Jaskowiak-Barr, Anne
Cressman, Leigh
Loughrey, Sean
Ganguly, Arupa
Feldman, Michael D.
Collman, Ronald G.
Rodino, Kyle G.
Kelly, Brendan J.
Bushman, Frederic D.
SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021
title SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021
title_full SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021
title_fullStr SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021
title_full_unstemmed SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021
title_short SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021
title_sort sars-cov-2 variants associated with vaccine breakthrough in the delaware valley through summer 2021
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547530/
https://www.ncbi.nlm.nih.gov/pubmed/34704098
http://dx.doi.org/10.1101/2021.10.18.21264623
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