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Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients
OBJECTIVES: We aimed to characterize and compare the viral loads (VL) of the Omicron BA.1 and BA.2 lineages and the Delta variant in nasopharyngeal samples from newly diagnosed COVID-19 patients and their kinetics over time. PATIENTS AND METHODS: The kinetics of the VL were measured on the CT data f...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Masson SAS.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618294/ https://www.ncbi.nlm.nih.gov/pubmed/36323397 http://dx.doi.org/10.1016/j.idnow.2022.10.001 |
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author | Teyssou, Elisa Marot, Stéphane Cocherie, Théophile Fauchois, Antoine Abdi, Basma Todesco, Eve Akhavan, Sepideh Pourcher, Valérie Calvez, Vincent Marcelin, Anne-Geneviève Soulie, Cathia |
author_facet | Teyssou, Elisa Marot, Stéphane Cocherie, Théophile Fauchois, Antoine Abdi, Basma Todesco, Eve Akhavan, Sepideh Pourcher, Valérie Calvez, Vincent Marcelin, Anne-Geneviève Soulie, Cathia |
author_sort | Teyssou, Elisa |
collection | PubMed |
description | OBJECTIVES: We aimed to characterize and compare the viral loads (VL) of the Omicron BA.1 and BA.2 lineages and the Delta variant in nasopharyngeal samples from newly diagnosed COVID-19 patients and their kinetics over time. PATIENTS AND METHODS: The kinetics of the VL were measured on the CT data from 215 SARS-CoV-2 positive patients who presented at least two positive PCRs a day apart and were screened for SARS-CoV-2 viral lineages. RESULTS: We observed no significant difference in median CT value during the first diagnostic test between the Delta variant and the two Omicron lineages. However, the kinetics of CT decreases for the BA.1 and BA.2 lineage were significantly lengthier in time than the kinetics for the Delta variant. The BA.2 lineage presented lower median CT value (-2 CT) (inversely proportional to the VL) than the BA.1 lineage. CONCLUSIONS: BA.2 Omicron lineage presented higher VL than BA.1 Omicron lineage at diagnostic. Omicron BA.1 and BA.2 lineages have more prolonged replication than the Delta variant. |
format | Online Article Text |
id | pubmed-9618294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier Masson SAS. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96182942022-10-31 Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients Teyssou, Elisa Marot, Stéphane Cocherie, Théophile Fauchois, Antoine Abdi, Basma Todesco, Eve Akhavan, Sepideh Pourcher, Valérie Calvez, Vincent Marcelin, Anne-Geneviève Soulie, Cathia Infect Dis Now Short Communication OBJECTIVES: We aimed to characterize and compare the viral loads (VL) of the Omicron BA.1 and BA.2 lineages and the Delta variant in nasopharyngeal samples from newly diagnosed COVID-19 patients and their kinetics over time. PATIENTS AND METHODS: The kinetics of the VL were measured on the CT data from 215 SARS-CoV-2 positive patients who presented at least two positive PCRs a day apart and were screened for SARS-CoV-2 viral lineages. RESULTS: We observed no significant difference in median CT value during the first diagnostic test between the Delta variant and the two Omicron lineages. However, the kinetics of CT decreases for the BA.1 and BA.2 lineage were significantly lengthier in time than the kinetics for the Delta variant. The BA.2 lineage presented lower median CT value (-2 CT) (inversely proportional to the VL) than the BA.1 lineage. CONCLUSIONS: BA.2 Omicron lineage presented higher VL than BA.1 Omicron lineage at diagnostic. Omicron BA.1 and BA.2 lineages have more prolonged replication than the Delta variant. Elsevier Masson SAS. 2023-02 2022-10-30 /pmc/articles/PMC9618294/ /pubmed/36323397 http://dx.doi.org/10.1016/j.idnow.2022.10.001 Text en © 2022 Elsevier Masson SAS. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Short Communication Teyssou, Elisa Marot, Stéphane Cocherie, Théophile Fauchois, Antoine Abdi, Basma Todesco, Eve Akhavan, Sepideh Pourcher, Valérie Calvez, Vincent Marcelin, Anne-Geneviève Soulie, Cathia Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients |
title | Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients |
title_full | Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients |
title_fullStr | Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients |
title_full_unstemmed | Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients |
title_short | Prolonged replication of BA.1 and BA.2 Omicron lineages compared to Delta variant in nasopharyngeal samples from COVID-19 patients |
title_sort | prolonged replication of ba.1 and ba.2 omicron lineages compared to delta variant in nasopharyngeal samples from covid-19 patients |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618294/ https://www.ncbi.nlm.nih.gov/pubmed/36323397 http://dx.doi.org/10.1016/j.idnow.2022.10.001 |
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