COVID-19 in non-hospitalised adults caused by either SARS-CoV-2 sub-variants Omicron BA.1, BA.2, BA.5 or Delta associates with similar illness duration, symptom severity and viral kinetics, irrespective of vaccination history
Author:
Townsley Hermaleigh, Gahir Joshua, Russell Timothy WORCID, Carr Edward J, Dyke Matala, Adams Lorin, Miah Murad, Clayton Bobbi, Smith Callie, Miranda Mauro, Mears Harriet V, Bailey Chris, Black James RM, Fowler Ashley S, Crawford Margaret, Wilkinson Katalin, Hutchinson Matthew, Harvey Ruth, O’Reilly Nicola, Kelly Gavin, Goldstone Robert, Beale Rupert, Papineni Padmasayee, Corrah Tumena, Gilson Richard, Caidan Simon, Nicod JeromeORCID, Gamblin Steve, Kassiotis GeorgeORCID, Libri Vincenzo, Williams Bryan, Gandhi Sonia, Kucharski Adam J, Swanton Charles, Bauer David LVORCID, Wall Emma CORCID
Abstract
AbstractBackgroundSARS-CoV-2 variant Omicron rapidly evolved over 2022, causing three waves of infection due to sub-variants BA.1, BA.2 and BA.4/5. We sought to characterise symptoms and viral loads over the course of COVID-19 infection with these sub-variants in otherwise-healthy, vaccinated, non-hospitalised adults, and compared data to infections with the preceding Delta variant of concern (VOC).MethodsIn a prospective, observational cohort study, healthy vaccinated UK adults who reported a positive PCR or lateral flow test, self-swabbed on alternate days until day 10. We compared symptoms and viral load trajectories between infections caused by VOCs Delta and Omicron (sub-variants BA.1, BA.2 and BA.4/5), and tested for relationships between vaccine dose, symptoms and PCR Ct value as a proxy for viral load.Results555 infection episodes were reported among 483 participants. Across VOCs, symptom burden and duration were similar, however symptom profiles differed among infections caused by Delta compared to Omicron sub-variants; symptoms of all Omicron sub-variants BA.1, BA.2 and BA.4/5 were very similar. Anosmia was reported in 7-13% of participants with Omicron sub-variants, compared to 25/60 (42%) with Delta infection (P= 1.31e-08 or 1.03e-05 or 5.63e-05; χ2test d2+Delta vs. Omicron BA.1 or vs. BA.2, or BA.5, respectively), fever was more common with Omicron BA.5 (30/55, 55%) than Delta (20/60, 33%) (p 0.03). Amongst infections with all Omicron sub-variants, symptoms of coryza, fatigue, cough and myalgia predominated. Viral load trajectories and peaks did not differ between Delta, and Omicron, irrespective of symptom severity (including asymptomatic participants), VOC or vaccination status. Ct values were negatively associated with time since vaccination in participants infected with BA.1; however, this trend was not observed in BA.2/BA.4/5 infections.ConclusionOur study emphasises both the changing symptom profile of COVID-19 infections in the Omicron era, and ongoing transmission risk of Omicron sub-variants in vaccinated adults.Trial registrationNCT04750356
Publisher
Cold Spring Harbor Laboratory
Reference60 articles.
1. Prevention CfDCa. Ending Isolation and Precautions for People with COVID-19: Interim Guidance: CDC; 2022 [updated 14/1/2022. Available from: https://www.cdc.gov/coronavirus/2019-ncov/hcp/duration-isolation.html. 2. Evolution of enhanced innate immune evasion by SARS-CoV-2;Nature,2022 3. Peacock TP , Brown JC , Zhou J , Thakur N , Sukhova K , Newman J , et al. The altered entry pathway and antigenic distance of the SARS-CoV-2 Omicron variant map to separate domains of spike protein. bioRxiv. 2022:2021.12.31.474653. 4. Willett BJ , Grove J , MacLean O , Wilkie C , Logan N , De Lorenzo G , et al. The hyper-transmissible SARS-CoV-2 Omicron variant exhibits significant antigenic change, vaccine escape and a switch in cell entry mechanism. medRxiv. 2022:2022.01.03.21268111. 5. Neutralising antibody activity against SARS-CoV-2 VOCs B.1.617.2 and B.1.351 by BNT162b2 vaccination;Lancet,2021
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
|
|