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SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant

Objectives: High viral load in upper respiratory tract specimens observed for Delta cases might contribute to its increased infectivity compared to the other variant. However, it is not yet documented if the Omicron variant’s enhanced infectivity is also related to a higher viral load. Our aim was t...

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Autores principales: Sentis, Célia, Billaud, Geneviève, Bal, Antonin, Frobert, Emilie, Bouscambert, Maude, Destras, Gregory, Josset, Laurence, Lina, Bruno, Morfin, Florence, Gaymard, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144383/
https://www.ncbi.nlm.nih.gov/pubmed/35632661
http://dx.doi.org/10.3390/v14050919
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author Sentis, Célia
Billaud, Geneviève
Bal, Antonin
Frobert, Emilie
Bouscambert, Maude
Destras, Gregory
Josset, Laurence
Lina, Bruno
Morfin, Florence
Gaymard, Alexandre
author_facet Sentis, Célia
Billaud, Geneviève
Bal, Antonin
Frobert, Emilie
Bouscambert, Maude
Destras, Gregory
Josset, Laurence
Lina, Bruno
Morfin, Florence
Gaymard, Alexandre
author_sort Sentis, Célia
collection PubMed
description Objectives: High viral load in upper respiratory tract specimens observed for Delta cases might contribute to its increased infectivity compared to the other variant. However, it is not yet documented if the Omicron variant’s enhanced infectivity is also related to a higher viral load. Our aim was to determine if the Omicron variant’s spread is also related to higher viral loads compared to the Delta variant. Methods: Nasopharyngeal swabs, 129 (Omicron) and 85 (Delta), from Health Care Workers were collected during December 2021 at the University Hospital of Lyon, France. Cycle threshold (Ct) for the RdRp target of cobas(®) 6800 SARS-CoV-2 assay was used as a proxy to evaluate SARS-CoV-2 viral load. Variant identification was performed using a screening panel and confirmed by whole genome sequencing. Results: Herein, we showed that the RT-PCR Ct values in Health Care Workers sampled within 5 days after symptom onset were significantly higher for Omicron cases than Delta cases (21.7 for Delta variant and 23.8 for Omicron variant, p = 0.008). This difference was also observed regarding patient with complete vaccination. Conclusions: This result supports the studies showing that the increased transmissibility of Omicron is related to other mechanisms than higher virus excretion.
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spelling pubmed-91443832022-05-29 SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant Sentis, Célia Billaud, Geneviève Bal, Antonin Frobert, Emilie Bouscambert, Maude Destras, Gregory Josset, Laurence Lina, Bruno Morfin, Florence Gaymard, Alexandre Viruses Article Objectives: High viral load in upper respiratory tract specimens observed for Delta cases might contribute to its increased infectivity compared to the other variant. However, it is not yet documented if the Omicron variant’s enhanced infectivity is also related to a higher viral load. Our aim was to determine if the Omicron variant’s spread is also related to higher viral loads compared to the Delta variant. Methods: Nasopharyngeal swabs, 129 (Omicron) and 85 (Delta), from Health Care Workers were collected during December 2021 at the University Hospital of Lyon, France. Cycle threshold (Ct) for the RdRp target of cobas(®) 6800 SARS-CoV-2 assay was used as a proxy to evaluate SARS-CoV-2 viral load. Variant identification was performed using a screening panel and confirmed by whole genome sequencing. Results: Herein, we showed that the RT-PCR Ct values in Health Care Workers sampled within 5 days after symptom onset were significantly higher for Omicron cases than Delta cases (21.7 for Delta variant and 23.8 for Omicron variant, p = 0.008). This difference was also observed regarding patient with complete vaccination. Conclusions: This result supports the studies showing that the increased transmissibility of Omicron is related to other mechanisms than higher virus excretion. MDPI 2022-04-28 /pmc/articles/PMC9144383/ /pubmed/35632661 http://dx.doi.org/10.3390/v14050919 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sentis, Célia
Billaud, Geneviève
Bal, Antonin
Frobert, Emilie
Bouscambert, Maude
Destras, Gregory
Josset, Laurence
Lina, Bruno
Morfin, Florence
Gaymard, Alexandre
SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant
title SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant
title_full SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant
title_fullStr SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant
title_full_unstemmed SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant
title_short SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant
title_sort sars-cov-2 omicron variant, lineage ba.1, is associated with lower viral load in nasopharyngeal samples compared to delta variant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144383/
https://www.ncbi.nlm.nih.gov/pubmed/35632661
http://dx.doi.org/10.3390/v14050919
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