Dynamics of viral shedding during ancestral or Omicron BA.1 SARS-CoV-2 infection and enhancement of pre-existing immunity during breakthrough infections. Issue 1 (31st December 2022)
- Record Type:
- Journal Article
- Title:
- Dynamics of viral shedding during ancestral or Omicron BA.1 SARS-CoV-2 infection and enhancement of pre-existing immunity during breakthrough infections. Issue 1 (31st December 2022)
- Main Title:
- Dynamics of viral shedding during ancestral or Omicron BA.1 SARS-CoV-2 infection and enhancement of pre-existing immunity during breakthrough infections
- Authors:
- Saade, Carla
Brengel-Pesce, Karen
Gaymard, Alexandre
Trabaud, Mary-Anne
Destras, Gregory
Oriol, Guy
Cheynet, Valérie
Debombourg, Marion
Mokdad, Bouchra
Billaud, Geneviève
Oblette, Antoine
Créhalet, Hervé
Giannoli, Jean-Marc
Garrigou, Christine
Generenaz, Laurence
Compagnon, Christelle
Boibieux, André
Lina, Bruno
Morfin, Florence
Pozzetto, Bruno
Josset, Laurence
Touillet-Assant, Sophie
Bal, Antonin - Abstract:
- ABSTRACT: Omicron variant is circulating in the presence of a globally acquired immunity unlike the ancestral SARS-CoV-2 isolate. Herein, we investigated the normalized viral load dynamics and viral culture status in 44 fully vaccinated healthcare workers (HCWs) infected with the Omicron BA.1 variant. Viral load dynamics of 38 unvaccinated HCWs infected with the 20A variant during the first pandemic wave was also studied. We then explored the impact of Omicron infection on pre-existing immunity assessing anti-RBD IgG levels, neutralizing antibody titres against 19A, Delta and Omicron isolates, as well as IFN-γ release following cell stimulation with SARS-CoV-2 peptides. We reported that two weeks after diagnosis a greater proportion of HCWs infected with 20A (78.9%, 15/19) than with Omicron BA.1 (44.7%, 17/38; p = 0.02) were still positive by RT-qPCR. We found that Omicron breakthrough infections led to an overall enhancement of vaccine-induced humoral and cellular immunity as soon as a median [interquartile range] of 8 [7–9] days post symptom onset. Among samples with similar high viral loads, non-culturable samples exhibited higher neutralizing antibody titres and anti-RBD IgG levels than culturable samples. Additionally, Omicron infection led to an enhancement of antibodies neutralization capacity against other SARS-CoV-2 isolates. Taken together, the results suggest that Omicron BA.1 vaccine breakthrough infection is associated with a faster viral clearance than that ofABSTRACT: Omicron variant is circulating in the presence of a globally acquired immunity unlike the ancestral SARS-CoV-2 isolate. Herein, we investigated the normalized viral load dynamics and viral culture status in 44 fully vaccinated healthcare workers (HCWs) infected with the Omicron BA.1 variant. Viral load dynamics of 38 unvaccinated HCWs infected with the 20A variant during the first pandemic wave was also studied. We then explored the impact of Omicron infection on pre-existing immunity assessing anti-RBD IgG levels, neutralizing antibody titres against 19A, Delta and Omicron isolates, as well as IFN-γ release following cell stimulation with SARS-CoV-2 peptides. We reported that two weeks after diagnosis a greater proportion of HCWs infected with 20A (78.9%, 15/19) than with Omicron BA.1 (44.7%, 17/38; p = 0.02) were still positive by RT-qPCR. We found that Omicron breakthrough infections led to an overall enhancement of vaccine-induced humoral and cellular immunity as soon as a median [interquartile range] of 8 [7–9] days post symptom onset. Among samples with similar high viral loads, non-culturable samples exhibited higher neutralizing antibody titres and anti-RBD IgG levels than culturable samples. Additionally, Omicron infection led to an enhancement of antibodies neutralization capacity against other SARS-CoV-2 isolates. Taken together, the results suggest that Omicron BA.1 vaccine breakthrough infection is associated with a faster viral clearance than that of the ancestral SARS-CoV-2, in addition this new variant leads to a rapid enhancement of the humoral response against multiple SARS-CoV-2 variants, and of the cellular response. … (more)
- Is Part Of:
- Emerging microbes & infections. Volume 11:Issue 1(2022)
- Journal:
- Emerging microbes & infections
- Issue:
- Volume 11:Issue 1(2022)
- Issue Display:
- Volume 11, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 11
- Issue:
- 1
- Issue Sort Value:
- 2022-0011-0001-0000
- Page Start:
- 2423
- Page End:
- 2432
- Publication Date:
- 2022-12-31
- Subjects:
- SARS-CoV-2 -- viral shedding -- Omicron -- viral culture -- infectiousness -- vaccine-immunity
Medical microbiology -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
616.9041 - Journal URLs:
- http://www.nature.com/ ↗
https://www.nature.com/emi/ ↗ - DOI:
- 10.1080/22221751.2022.2122578 ↗
- Languages:
- English
- ISSNs:
- 2222-1751
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24190.xml