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dc.contributor.authorDavies, M
dc.contributor.authorBramwell, LR
dc.contributor.authorJeffery, N
dc.contributor.authorBunce, B
dc.contributor.authorLee, BP
dc.contributor.authorKnight, B
dc.contributor.authorAuckland, C
dc.contributor.authorMasoli, JA
dc.contributor.authorHarries, LW
dc.date.accessioned2022-05-12T14:00:44Z
dc.date.issued2021-12-07
dc.date.updated2022-05-12T13:17:30Z
dc.description.abstractOBJECTIVES: This study aimed to evaluate the associations between COVID-19 severity and active viral load, and to characterize the dynamics of active SARS-CoV-2 clearance in a series of archival samples taken from patients in the first wave of COVID-19 infection in the South West of the UK. METHODS: Subgenomic RNA (sgRNA) and E-gene genomic sequences were measured in a retrospective collection of PCR-confirmed SARS-CoV-2-positive samples from 176 individuals, and related to disease severity. Viral clearance dynamics were then assessed in relation to symptom onset and last positive test. RESULTS: Whilst E-gene sgRNAs declined before E-gene genomic sequences, some individuals retained sgRNA positivity for up to 68 days. 13% of sgRNA-positive cases still exhibited clinically relevant levels of virus after 10 days, with no clinical features previously associated with prolonged viral clearance times. CONCLUSIONS: Our results suggest that potentially active virus can sometimes persist beyond a 10-day period, and could pose a potential risk of onward transmission. Where this would pose a serious public health threat, additional mitigation strategies may be necessary to reduce the risk of secondary cases in vulnerable settings.en_GB
dc.description.sponsorshipNational Institute for Health Research (NIHR)en_GB
dc.format.extent418-425
dc.format.mediumPrint-Electronic
dc.identifier.citationVol. 116, pp. 418-425en_GB
dc.identifier.doihttps://doi.org/10.1016/j.ijid.2021.12.312
dc.identifier.urihttp://hdl.handle.net/10871/129599
dc.identifierORCID: 0000-0001-7791-8061 (Harries, Lorna W)
dc.identifierScopusID: 13805289700 (Harries, Lorna W)
dc.identifierResearcherID: D-2241-2014 | E-2369-2011 (Harries, Lorna W)
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/34890790en_GB
dc.rights© 2022 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)en_GB
dc.subjectSARS-COV-2en_GB
dc.subjectpersistenceen_GB
dc.subjectsgRNAen_GB
dc.subjecttransmissionen_GB
dc.titlePersistence of clinically relevant levels of SARS-CoV2 envelope gene subgenomic RNAs in non-immunocompromised individualsen_GB
dc.typeArticleen_GB
dc.date.available2022-05-12T14:00:44Z
dc.identifier.issn1201-9712
exeter.place-of-publicationCanada
dc.descriptionThis is the final version. Available on open access from Elsevier via the DOI in this recorden_GB
dc.identifier.eissn1878-3511
dc.identifier.journalInternational Journal of Infectious Diseasesen_GB
dc.relation.ispartofInt J Infect Dis, 116
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2021-12-02
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2021-12-07
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-05-12T13:58:53Z
refterms.versionFCDVoR
refterms.dateFOA2022-05-12T14:00:50Z
refterms.panelAen_GB


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© 2022 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
This is an open access article under the CC BY-NC-ND license
(http://creativecommons.org/licenses/by-nc-nd/4.0/)
Except where otherwise noted, this item's licence is described as © 2022 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)