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Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?

During the COVID-19 pandemic, several generic variants emerged, including the Alpha variant, with increased transmissibility compared to historical strains. We aimed to compare the evolution of the viral load between patients infected with the Alpha variant and those infected with the historical SAR...

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Autores principales: Bonnet, Camille, Masse, Shirley, Benamar, Hayat, Vilcu, Ana-Maria, Swital, Morgane, Hanslik, Thomas, van der Werf, Sylvie, Duval, Xavier, Carrat, Fabrice, Falchi, Alessandra, Blanchon, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879902/
https://www.ncbi.nlm.nih.gov/pubmed/35207451
http://dx.doi.org/10.3390/life12020163
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author Bonnet, Camille
Masse, Shirley
Benamar, Hayat
Vilcu, Ana-Maria
Swital, Morgane
Hanslik, Thomas
van der Werf, Sylvie
Duval, Xavier
Carrat, Fabrice
Falchi, Alessandra
Blanchon, Thierry
author_facet Bonnet, Camille
Masse, Shirley
Benamar, Hayat
Vilcu, Ana-Maria
Swital, Morgane
Hanslik, Thomas
van der Werf, Sylvie
Duval, Xavier
Carrat, Fabrice
Falchi, Alessandra
Blanchon, Thierry
author_sort Bonnet, Camille
collection PubMed
description During the COVID-19 pandemic, several generic variants emerged, including the Alpha variant, with increased transmissibility compared to historical strains. We aimed to compare the evolution of the viral load between patients infected with the Alpha variant and those infected with the historical SARS-CoV-2 strains, while taking into account the time interval between the onset of symptoms and samples. We used data collected from patients with an acute respiratory infection (mild to moderate symptoms) and seen in consultation in primary care, included in a prospective longitudinal study, COVID-A. Patients performed four salivary samples during the follow-up. All patients who had at least one of the saliva samples test positive for SARS-CoV-2 were included in the analysis. Overall, 118 patients were included: 89 infected by the historical strain and 29 infected by the Alpha variant. Even though we tended to observe a higher viral load in the Alpha variant group, we found no significant difference in the evolution of the viral load in saliva samples between patients infected with the Alpha variant of the SARS-CoV-2 and those infected by historical strains when controlling for the time interval between the onset of symptoms and sampling.
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spelling pubmed-88799022022-02-26 Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms? Bonnet, Camille Masse, Shirley Benamar, Hayat Vilcu, Ana-Maria Swital, Morgane Hanslik, Thomas van der Werf, Sylvie Duval, Xavier Carrat, Fabrice Falchi, Alessandra Blanchon, Thierry Life (Basel) Article During the COVID-19 pandemic, several generic variants emerged, including the Alpha variant, with increased transmissibility compared to historical strains. We aimed to compare the evolution of the viral load between patients infected with the Alpha variant and those infected with the historical SARS-CoV-2 strains, while taking into account the time interval between the onset of symptoms and samples. We used data collected from patients with an acute respiratory infection (mild to moderate symptoms) and seen in consultation in primary care, included in a prospective longitudinal study, COVID-A. Patients performed four salivary samples during the follow-up. All patients who had at least one of the saliva samples test positive for SARS-CoV-2 were included in the analysis. Overall, 118 patients were included: 89 infected by the historical strain and 29 infected by the Alpha variant. Even though we tended to observe a higher viral load in the Alpha variant group, we found no significant difference in the evolution of the viral load in saliva samples between patients infected with the Alpha variant of the SARS-CoV-2 and those infected by historical strains when controlling for the time interval between the onset of symptoms and sampling. MDPI 2022-01-21 /pmc/articles/PMC8879902/ /pubmed/35207451 http://dx.doi.org/10.3390/life12020163 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
Bonnet, Camille
Masse, Shirley
Benamar, Hayat
Vilcu, Ana-Maria
Swital, Morgane
Hanslik, Thomas
van der Werf, Sylvie
Duval, Xavier
Carrat, Fabrice
Falchi, Alessandra
Blanchon, Thierry
Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?
title Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?
title_full Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?
title_fullStr Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?
title_full_unstemmed Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?
title_short Is the Alpha Variant of SARS-CoV-2 Associated with a Higher Viral Load than the Historical Strain in Saliva Samples in Patients with Mild to Moderate Symptoms?
title_sort is the alpha variant of sars-cov-2 associated with a higher viral load than the historical strain in saliva samples in patients with mild to moderate symptoms?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879902/
https://www.ncbi.nlm.nih.gov/pubmed/35207451
http://dx.doi.org/10.3390/life12020163
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