Variant-Specific Viral Kinetics in Acute COVID-19

Author:

Ribeiro Ruy M1,Choudhary Manish C2,Deo Rinki2,Giganti Mark J3ORCID,Moser Carlee3ORCID,Ritz Justin3,Greninger Alexander L4,Regan James2,Flynn James P2,Wohl David A5,Currier Judith S6,Eron Joseph J5,Hughes Michael D3,Smith Davey M7,Chew Kara W6,Daar Eric S8,Perelson Alan S1,Li Jonathan Z2ORCID,Hosey Lara,Roa Jhoanna,Patel Nilam,Aldrovandi Grace,Murtaugh William,Science Frontier,Cooper Marlene,Gutzman Howard,Knowles Kevin,Bowman Rachel,Erhardt Bill,Adams Stacey,

Affiliation:

1. Theoretical Biology and Biophysics Group, Los Alamos National Laboratory , New Mexico

2. Division of Infectious Diseases, Brigham & Women's Hospital, Harvard Medical School , Cambridge, Massachusetts

3. Center for Biostatistics in AIDS Research, Harvard T. H. Chan School of Public Health , Boston, Massachusetts

4. Department of Laboratory Medicine and Pathology, University of Washington , Seattle

5. Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill

6. Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles

7. Division of Infectious Diseases and Global Public Health, University of California , San Diego, La Jolla, California

8. Lundquist Institute, Harbor-UCLA Medical Center , Torrance, California

Abstract

Abstract Understanding variant-specific differences in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral kinetics may explain differences in transmission efficiency and provide insights on pathogenesis and prevention. We evaluated SARS-CoV-2 kinetics from nasal swabs across multiple variants (Alpha, Delta, Epsilon, Gamma) in placebo recipients of the ACTIV-2/A5401 trial. Delta variant infection led to the highest maximum viral load and shortest time from symptom onset to viral load peak. There were no significant differences in time to viral clearance across the variants. Viral decline was biphasic with first- and second-phase decays having half-lives of 11 hours and 2.5 days, respectively, with differences among variants, especially in the second phase. These results suggest that while variant-specific differences in viral kinetics exist, post–peak viral load all variants appeared to be efficiently cleared by the host. Clinical Trials Registration. NCT04518410.

Funder

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference30 articles.

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