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dc.contributor.authorKissler, Stephen
dc.contributor.authorFauver, Joseph R.
dc.contributor.authorMack, Christina
dc.contributor.authorTai, Caroline G.
dc.contributor.authorBreban, Mallery I.
dc.contributor.authorWatkins, Anne E.
dc.contributor.authorSamant, Radhika M.
dc.contributor.authorAnderson, Deverick J.
dc.contributor.authorHo, David D.
dc.contributor.authorGrubaugh, Nathan D.
dc.contributor.authorGrad, Yonatan
dc.date.accessioned2021-02-16T16:07:32Z
dc.date.issued2021-02-16
dc.identifier.citationKissler, Stephen, Joseph R. Fauver, Christina Mack, Caroline G. Tai, Mallery I. Breban, et al. "Densely sampled viral trajectories suggest longer duration of acute infection with B.1.1.7 variant relative to non-B.1.1.7 SARS-CoV-2." Preprint, 2021.en_US
dc.identifier.urihttps://nrs.harvard.edu/URN-3:HUL.INSTREPOS:37366884*
dc.description.abstractTo test whether acute infection with B.1.1.7 is associated with higher or more sustained nasopharyngeal viral concentrations, we assessed longitudinal PCR tests performed in a cohort of 65 individuals infected with SARS-CoV-2 undergoing daily surveillance testing, including seven in fected with B.1.1.7. For individuals infected with B.1.1.7, the mean duration of the proliferation phase was 5.3 days (90% credible interval [2.7, 7.8]), the mean duration of the clearance phase was 8.0 days [6.1, 9.9], and the mean overall duration of infection (proliferation plus clearance) was 13.3 days [10.1, 16.5]. These compare to a mean proliferation phase of 2.0 days [0.7, 3.3], a mean clearance phase of 6.2 days [5.1, 7.1], and a mean duration of infection of 8.2 days [6.5, 9.7] for non-B.1.1.7 virus. The peak viral concentration for B.1.1.7 was 19.0 Ct [15.8, 22.0] compared to 20.2 Ct [19.0, 21.4] for non-B.1.1.7. This converts to 8.5 log10 RNA copies/ml [7.6, 9.4] for B.1.1.7 and 8.2 log10 RNA copies/ml [7.8, 8.5] for non-B.1.1.7. These data offer evidence that SARS-CoV-2 variant B.1.1.7 may cause longer infections with similar peak viral concentration compared to non-B.1.1.7 SARS-CoV-2. This extended duration may contribute to B.1.1.7 SARS CoV-2’s increased transmissibility.en_US
dc.language.isoen_USen_US
dash.licenseLAA
dc.titleDensely sampled viral trajectories suggest longer duration of acute infection with B.1.1.7 variant relative to non-B.1.1.7 SARS-CoV-2en_US
dc.typeJournal Articleen_US
dc.description.versionAuthor's Originalen_US
dash.depositing.authorGrad, Yonatan
dc.date.available2021-02-16T16:07:32Z
dash.affiliation.otherHarvard T.H. Chan School of Public Healthen_US
dash.contributor.affiliatedGrad, Yonatan
dash.contributor.affiliatedKissler, Stephen


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