Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time

Author:

Walker A Sarah1234ORCID,Pritchard Emma12,House Thomas56,Robotham Julie V27,Birrell Paul J78ORCID,Bell Iain9,Bell John I10,Newton John N11,Farrar Jeremy12,Diamond Ian9,Studley Ruth9,Hay Jodie1314,Vihta Karina-Doris12,Peto Timothy EA12315,Stoesser Nicole12315ORCID,Matthews Philippa C115ORCID,Eyre David W121416ORCID,Pouwels Koen B1217ORCID,

Affiliation:

1. Nuffield Department of Medicine, University of Oxford

2. The National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford

3. The National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford

4. MRC Clinical Trials Unit at UCL, UCL

5. Department of Mathematics, University of Manchester

6. IBM Research, Hartree Centre

7. National Infection Service, Public Health England

8. MRC Biostatistics Unit, University of Cambridge, Cambridge Institute of Public Health

9. Office for National Statistics

10. Office of the Regius Professor of Medicine, University of Oxford

11. Health Improvement Directorate, Public Health England

12. Wellcome Trust

13. University of Glasgow

14. Lighthouse Laboratory in Glasgow, Queen Elizabeth University Hospital

15. Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital

16. Big Data Institute, Nuffield Department of Population Health, University of Oxford

17. Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford

Abstract

Background:Information on SARS-CoV-2 in representative community surveillance is limited, particularly cycle threshold (Ct) values (a proxy for viral load).Methods:We included all positive nose and throat swabs 26 April 2020 to 13 March 2021 from the UK’s national COVID-19 Infection Survey, tested by RT-PCR for the N, S, and ORF1ab genes. We investigated predictors of median Ct value using quantile regression.Results:Of 3,312,159 nose and throat swabs, 27,902 (0.83%) were RT-PCR-positive, 10,317 (37%), 11,012 (40%), and 6550 (23%) for 3, 2, or 1 of the N, S, and ORF1ab genes, respectively, with median Ct = 29.2 (~215 copies/ml; IQR Ct = 21.9–32.8, 14–56,400 copies/ml). Independent predictors of lower Cts (i.e. higher viral load) included self-reported symptoms and more genes detected, with at most small effects of sex, ethnicity, and age. Single-gene positives almost invariably had Ct > 30, but Cts varied widely in triple-gene positives, including without symptoms. Population-level Cts changed over time, with declining Ct preceding increasing SARS-CoV-2 positivity. Of 6189 participants with IgG S-antibody tests post-first RT-PCR-positive, 4808 (78%) were ever antibody-positive; Cts were significantly higher in those remaining antibody negative.Conclusions:Marked variation in community SARS-CoV-2 Ct values suggests that they could be a useful epidemiological early-warning indicator.Funding:Department of Health and Social Care, National Institutes of Health Research, Huo Family Foundation, Medical Research Council UK; Wellcome Trust.

Funder

Department of Health & Social Care

National Institutes of Health

Huo Family Foundation

Medical Research Council

Wellcome Trust

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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