PreprintCited by 116SARS-CoV-2 and COVID-19 ResearchCOVID-19 epidemiological studiesCOVID-19 Clinical Research Studies

SARS-CoV-2 variant Delta rapidly displaced variant Alpha in the United States and led to higher viral loads

Open access
Bolze, Alexandre, Cirulli, Elizabeth T, Luo, Shishi, White, Simon, Wyman, Dana, Dei Rossi, Andrew, Machado, Henrique, Cassens, Tyler +14 more·2021·Cell Reports Medicine

Preprint — published as 10.1016/j.xcrm.2022.100564

Abstract

This study reports on the displacement of Alpha (B.1.1.7) by Delta (B.1.617.2 and its substrains AY.1, AY.2, and AY.3) in the United States. By analyzing RT-qPCR testing results and viral sequencing results of samples collected across the United States, we show that the percentage of SARS-CoV-2 positive cases caused by Alpha dropped from 67% in May 2021 to less than 3.0% in just 10 weeks. We also show that the Delta variant has outcompeted the Iota (B.1.526) variant of interest and Gamma (P.1) variant of concern. An analysis of the mean quantification cycles (Cq) values in positive tests over time also reveal that Delta infections lead to a higher viral load on average compared to Alpha infections, but this increase is only 2 to 3x on average for our study design. Our results are consistent with the hypothesis that the Delta variant is more transmissible than the Alpha variant, and that this could be due to the Delta variant's ability to establish a higher viral load earlier in the infection compared to the Alpha variant.

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  • By June 2021, the Gamma variant accounted for a high proportion of infections in several South American and Caribbean countries and 10% of US infections.

    “By June 2021, the Gamma variant accounted for a high proportion of infections in several South American and Caribbean countries 196 and 10% of US infections 33 .”

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  1. Annavajhala, M. K. et al. A Novel and Expanding SARS-CoV-2 Variant, B. 1.526, Identified in New York. medRxiv (2021).

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Authors
Bolze, A., Cirulli, E. T., Luo, S., White, S., Wyman, D., Dei Rossi, A., Machado, H., Cassens, T., Jacobs, S., Schiabor Barrett, K. M., Tsan, K., Nguyen, J., Ramirez, J. M., Sandoval, E., Wang, X., Wong, D., Becker, D., Laurent, M., Lu, J., Isaksson, M., Washington, N. L., & Lee, W.
Affiliations
Helix (United States) (US)
Corresponding author
  • Bolze, Alexandre
  • Lee, William
Venue
Cell Reports Medicine
Publisher
openRxiv
Published
2021-06-21
Volume
3
Issue
3
Pages
100564-100564
ISSN
2666-3791 (ISSN-L)
OpenAlex
W4220894005
Cited by
116
References
6
Citations by year
2026: 6 · 2025: 9 · 2024: 15 · 2023: 23 · 2022: 40 · 2021: 22 · 2020: 1
FWCI
7.92
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Cell Reports Medicine (publishedVersion, cc-by-nc-nd)
  • SSRN Electronic Journal (publishedVersion)
  • medRxiv (acceptedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Funders
  • Public Health England
  • Centers for Disease Control and Prevention
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
  • Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
Keywords
SARS-CoV-2, Alpha variant, viral load, transmissibility, COVID-19 pandemic, United States
MeSH terms
COVID-19, SARS-CoV-2, Humans, United States, Viral Load

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