Cargando…

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

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, teste...

Descripción completa

Detalles Bibliográficos
Autores principales: Walker, A Sarah, Pritchard, Emma, House, Thomas, Robotham, Julie V, Birrell, Paul J, Bell, Iain, Bell, John I, Newton, John N, Farrar, Jeremy, Diamond, Ian, Studley, Ruth, Hay, Jodie, Vihta, Karina-Doris, Peto, Timothy EA, Stoesser, Nicole, Matthews, Philippa C, Eyre, David W, Pouwels, Koen B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282332/
https://www.ncbi.nlm.nih.gov/pubmed/34250907
http://dx.doi.org/10.7554/eLife.64683
_version_ 1783722988966772736
author Walker, A Sarah
Pritchard, Emma
House, Thomas
Robotham, Julie V
Birrell, Paul J
Bell, Iain
Bell, John I
Newton, John N
Farrar, Jeremy
Diamond, Ian
Studley, Ruth
Hay, Jodie
Vihta, Karina-Doris
Peto, Timothy EA
Stoesser, Nicole
Matthews, Philippa C
Eyre, David W
Pouwels, Koen B
author_facet Walker, A Sarah
Pritchard, Emma
House, Thomas
Robotham, Julie V
Birrell, Paul J
Bell, Iain
Bell, John I
Newton, John N
Farrar, Jeremy
Diamond, Ian
Studley, Ruth
Hay, Jodie
Vihta, Karina-Doris
Peto, Timothy EA
Stoesser, Nicole
Matthews, Philippa C
Eyre, David W
Pouwels, Koen B
author_sort Walker, A Sarah
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8282332
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-82823322021-07-19 Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time Walker, A Sarah Pritchard, Emma House, Thomas Robotham, Julie V Birrell, Paul J Bell, Iain Bell, John I Newton, John N Farrar, Jeremy Diamond, Ian Studley, Ruth Hay, Jodie Vihta, Karina-Doris Peto, Timothy EA Stoesser, Nicole Matthews, Philippa C Eyre, David W Pouwels, Koen B eLife Medicine 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. eLife Sciences Publications, Ltd 2021-07-12 /pmc/articles/PMC8282332/ /pubmed/34250907 http://dx.doi.org/10.7554/eLife.64683 Text en © 2021, Walker et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Medicine
Walker, A Sarah
Pritchard, Emma
House, Thomas
Robotham, Julie V
Birrell, Paul J
Bell, Iain
Bell, John I
Newton, John N
Farrar, Jeremy
Diamond, Ian
Studley, Ruth
Hay, Jodie
Vihta, Karina-Doris
Peto, Timothy EA
Stoesser, Nicole
Matthews, Philippa C
Eyre, David W
Pouwels, Koen B
Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time
title Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time
title_full Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time
title_fullStr Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time
title_full_unstemmed Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time
title_short Ct threshold values, a proxy for viral load in community SARS-CoV-2 cases, demonstrate wide variation across populations and over time
title_sort ct threshold values, a proxy for viral load in community sars-cov-2 cases, demonstrate wide variation across populations and over time
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282332/
https://www.ncbi.nlm.nih.gov/pubmed/34250907
http://dx.doi.org/10.7554/eLife.64683
work_keys_str_mv AT walkerasarah ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT pritchardemma ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT housethomas ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT robothamjuliev ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT birrellpaulj ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT belliain ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT belljohni ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT newtonjohnn ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT farrarjeremy ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT diamondian ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT studleyruth ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT hayjodie ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT vihtakarinadoris ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT petotimothyea ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT stoessernicole ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT matthewsphilippac ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT eyredavidw ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT pouwelskoenb ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime
AT ctthresholdvaluesaproxyforviralloadincommunitysarscov2casesdemonstratewidevariationacrosspopulationsandovertime