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A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States

COVID-19 vaccines were first administered on 15 December 2020, marking an important transition point for the spread of SARS-CoV-2 in the United States (U.S.). Prior to this point in time, the virus spread to an almost completely immunologically naïve population, whereas subsequently, vaccine-induced...

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Autores principales: Capoferri, Adam A., Shao, Wei, Spindler, Jon, Coffin, John M., Rausch, Jason W., Kearney, Mary F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778900/
https://www.ncbi.nlm.nih.gov/pubmed/35062308
http://dx.doi.org/10.3390/v14010104
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author Capoferri, Adam A.
Shao, Wei
Spindler, Jon
Coffin, John M.
Rausch, Jason W.
Kearney, Mary F.
author_facet Capoferri, Adam A.
Shao, Wei
Spindler, Jon
Coffin, John M.
Rausch, Jason W.
Kearney, Mary F.
author_sort Capoferri, Adam A.
collection PubMed
description COVID-19 vaccines were first administered on 15 December 2020, marking an important transition point for the spread of SARS-CoV-2 in the United States (U.S.). Prior to this point in time, the virus spread to an almost completely immunologically naïve population, whereas subsequently, vaccine-induced immune pressure and prior infections might be expected to influence viral evolution. Accordingly, we conducted a study to characterize the spread of SARS-CoV-2 in the U.S. pre-vaccination, investigate the depth and uniformity of genetic surveillance during this period, and measure and otherwise characterize changing viral genetic diversity, including by comparison with more recently emergent variants of concern (VOCs). In 2020, SARS-CoV-2 spread across the U.S. in three phases distinguishable by peaks in the numbers of infections and shifting geographical distributions. Virus was genetically sampled during this period at an overall rate of ~1.2%, though there was a substantial mismatch between case rates and genetic sampling nationwide. Viral genetic diversity tripled over this period but remained low in comparison to other widespread RNA virus pathogens, and although 54 amino acid changes were detected at frequencies exceeding 5%, linkage among them was not observed. Based on our collective observations, our analysis supports a targeted strategy for worldwide genetic surveillance as perhaps the most sensitive and efficient means of detecting new VOCs.
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spelling pubmed-87789002022-01-22 A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States Capoferri, Adam A. Shao, Wei Spindler, Jon Coffin, John M. Rausch, Jason W. Kearney, Mary F. Viruses Article COVID-19 vaccines were first administered on 15 December 2020, marking an important transition point for the spread of SARS-CoV-2 in the United States (U.S.). Prior to this point in time, the virus spread to an almost completely immunologically naïve population, whereas subsequently, vaccine-induced immune pressure and prior infections might be expected to influence viral evolution. Accordingly, we conducted a study to characterize the spread of SARS-CoV-2 in the U.S. pre-vaccination, investigate the depth and uniformity of genetic surveillance during this period, and measure and otherwise characterize changing viral genetic diversity, including by comparison with more recently emergent variants of concern (VOCs). In 2020, SARS-CoV-2 spread across the U.S. in three phases distinguishable by peaks in the numbers of infections and shifting geographical distributions. Virus was genetically sampled during this period at an overall rate of ~1.2%, though there was a substantial mismatch between case rates and genetic sampling nationwide. Viral genetic diversity tripled over this period but remained low in comparison to other widespread RNA virus pathogens, and although 54 amino acid changes were detected at frequencies exceeding 5%, linkage among them was not observed. Based on our collective observations, our analysis supports a targeted strategy for worldwide genetic surveillance as perhaps the most sensitive and efficient means of detecting new VOCs. MDPI 2022-01-07 /pmc/articles/PMC8778900/ /pubmed/35062308 http://dx.doi.org/10.3390/v14010104 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Capoferri, Adam A.
Shao, Wei
Spindler, Jon
Coffin, John M.
Rausch, Jason W.
Kearney, Mary F.
A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States
title A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States
title_full A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States
title_fullStr A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States
title_full_unstemmed A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States
title_short A Pre-Vaccination Baseline of SARS-CoV-2 Genetic Surveillance and Diversity in the United States
title_sort pre-vaccination baseline of sars-cov-2 genetic surveillance and diversity in the united states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778900/
https://www.ncbi.nlm.nih.gov/pubmed/35062308
http://dx.doi.org/10.3390/v14010104
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