Prevalence of persistent SARS-CoV-2 in a large community surveillance study

Ghafari, Mahan and Hall, Matthew and Golubchik, Tanya and Ayoubkhani, Daniel and House, Thomas and MacIntyre-Cockett, George and Fryer, Helen R. and Thomson, Laura and Nurtay, Anel and Kemp, Steven A. and Ferretti, Luca and Buck, David and Green, Angie and Trebes, Amy and Piazza, Paolo and Lonie, Lorne J. and Studley, Ruth and Rourke, Emma and Smith, Darren L. and Bashton, Matthew and Nelson, Andrew and Crown, Matthew and McCann, Clare and Young, Gregory R. and Santos, Rui Andre Nunes dos and Richards, Zack and Tariq, Mohammad Adnan and Cahuantzi, Roberto and Barrett, Jeff and Fraser, Christophe and Bonsall, David and Walker, Ann Sarah and Lythgoe, Katrina (2024) Prevalence of persistent SARS-CoV-2 in a large community surveillance study. Nature. ISSN 0028-0836

[thumbnail of s41586-024-07029-4.pdf] Text
s41586-024-07029-4.pdf - Published Version

Download (10MB)

Abstract

Persistent SARS-CoV-2 infections may act as viral reservoirs that could seed future outbreaks give rise to highly divergent lineages and contribute to cases with post-acute COVID-19 sequelae (long COVID)9,10. However, the population prevalence of persistent infections, their viral load kinetics and evolutionary dynamics over the course of infections remain largely unknown. Here, using viral sequence data collected as part of a national infection survey, we identified 381 individuals with SARS-CoV-2 RNA at high titre persisting for at least 30 days, of which 54 had viral RNA persisting at least 60 days. We refer to these as ‘persistent infections’ as available evidence suggests that they represent ongoing viral replication, although the persistence of non-replicating RNA cannot be ruled out in all. Individuals with persistent infection had more than 50% higher odds of self-reporting long COVID than individuals with non-persistent infection. We estimate that 0.1–0.5% of infections may become persistent with typically rebounding high viral loads and last for at least 60 days. In some individuals, we identified many viral amino acid substitutions, indicating periods of strong positive selection, whereas others had no consensus change in the sequences for prolonged periods, consistent with weak selection. Substitutions included mutations that are lineage defining for SARS-CoV-2 variants, at target sites for monoclonal antibodies and/or are commonly found in immunocompromised people11,12,13,14. This work has profound implications for understanding and characterizing SARS-CoV-2 infection, epidemiology and evolution.

Item Type: Article
Subjects: Archive Paper Guardians > Multidisciplinary
Depositing User: Unnamed user with email support@archive.paperguardians.com
Date Deposited: 22 Feb 2024 05:24
Last Modified: 22 Feb 2024 05:24
URI: http://archives.articleproms.com/id/eprint/2668

Actions (login required)

View Item
View Item