dc.contributor.author | Granerud, Beathe Kiland | |
dc.contributor.author | Ueland, Thor | |
dc.contributor.author | Lind, Andreas | |
dc.contributor.author | Søraas, Arne Vasli | |
dc.contributor.author | Fevang, Børre | |
dc.contributor.author | Steffensen, Anne Katrine | |
dc.contributor.author | Al-Baldawi, Huda | |
dc.contributor.author | Lund-Johansen, Fridtjof | |
dc.contributor.author | Aukrust, Pål | |
dc.contributor.author | Halvorsen, Bente Evy | |
dc.contributor.author | Dahl, Tuva Børresdatter | |
dc.contributor.author | Dudman, Susanne | |
dc.contributor.author | Müller, Fredrik | |
dc.contributor.author | Holter, Jan Cato | |
dc.date.accessioned | 2023-01-11T12:27:08Z | |
dc.date.available | 2023-01-11T12:27:08Z | |
dc.date.issued | 2022-10-31 | |
dc.description.abstract | The Omicron variant of SARS-CoV-2 spreads more easily than earlier variants, possibly as a result of a higher viral load in the upper respiratory tract and oral cavity. Hence, we investigated whether the Omicron variant generates a higher viral load than that of the Delta variant in saliva and nasopharynx. Both specimens were collected from 52 Omicron and 17 Delta cases at two time points one week apart and analyzed by qRT-PCR. Viral load was measured as 10 log RNA genome copies per 1000 human cells according to the WHO reference standard. We found that Omicron cases carried a higher viral load and had more sustained viral shedding compared to the Delta cases, especially in the nasopharynx. | en_US |
dc.identifier.citation | Granerud, Ueland, Lind, Søraas, Fevang, Steffensen, Al-Baldawi, Lund-Johansen, Aukrust, Halvorsen, Dahl, Dudman, Müller, Holter. Omicron Variant Generates a Higher and More Sustained Viral Load in Nasopharynx and Saliva Than the Delta Variant of SARS-CoV-2. Viruses. 2022;14(11) | en_US |
dc.identifier.cristinID | FRIDAID 2074735 | |
dc.identifier.doi | 10.3390/v14112420 | |
dc.identifier.issn | 1999-4915 | |
dc.identifier.uri | https://hdl.handle.net/10037/28156 | |
dc.language.iso | eng | en_US |
dc.publisher | MDPI | en_US |
dc.relation.journal | Viruses | |
dc.relation.projectID | Oslo universitetssykehus HF: Fredrik Müller | en_US |
dc.relation.projectID | Vivaldi Invest: Jan Cato Holter | en_US |
dc.relation.projectID | Norges forskningsråd: 312780 | en_US |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2022 The Author(s) | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | en_US |
dc.rights | Attribution 4.0 International (CC BY 4.0) | en_US |
dc.subject | VDP::Medisinske fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk mikrobiologi : 715 | en_US |
dc.subject | VDP::Midical sciences: 700::Basic medical, dental and veterinary sciences: 710::Medical microbiology: 715 | en_US |
dc.subject | SARS-CoV-2 / SARS-CoV-2 | en_US |
dc.title | Omicron Variant Generates a Higher and More Sustained Viral Load in Nasopharynx and Saliva Than the Delta Variant of SARS-CoV-2 | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |