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Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization
BACKGROUND: The variant of concern, Omicron, has become the sole circulating SARS-CoV-2 variant for the past several months. Omicron subvariants BA.1, BA.2, BA.3, BA.4, and BA.5 evolved over the time, with BA.1 causing the largest wave of infections globally in December 2021– January 2022. In this s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516865/ https://www.ncbi.nlm.nih.gov/pubmed/36172137 http://dx.doi.org/10.1101/2022.09.20.22280154 |
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author | Morris, C. Paul Eldesouki, Raghda E. Sachithanandham, Jaiprasath Fall, Amary Norton, Julie M. Abdullah, Omar Gallagher, Nicholas Li, Maggie Pekosz, Andrew Klein, Eili Y. Mostafa, Heba H. |
author_facet | Morris, C. Paul Eldesouki, Raghda E. Sachithanandham, Jaiprasath Fall, Amary Norton, Julie M. Abdullah, Omar Gallagher, Nicholas Li, Maggie Pekosz, Andrew Klein, Eili Y. Mostafa, Heba H. |
author_sort | Morris, C. Paul |
collection | PubMed |
description | BACKGROUND: The variant of concern, Omicron, has become the sole circulating SARS-CoV-2 variant for the past several months. Omicron subvariants BA.1, BA.2, BA.3, BA.4, and BA.5 evolved over the time, with BA.1 causing the largest wave of infections globally in December 2021– January 2022. In this study, we compare the clinical outcomes in patients infected with different Omicron subvariants and compare the relative viral loads, and recovery of infectious virus from upper respiratory specimens. METHODS: SARS-CoV-2 positive remnant clinical specimens, diagnosed at the Johns Hopkins Microbiology Laboratory between December 2021 and July 2022, were used for whole genome sequencing. The clinical outcomes of infections with Omicron subvariants were compared to infections with BA.1. Cycle threshold values (Ct) and the recovery of infectious virus on VeroTMPRSS2 cell line from clinical specimens were compared. RESULTS: The BA.1 was associated with the largest increase in SARS-CoV-2 positivity rate and COVID-19 related hospitalizations at the Johns Hopkins system. After a peak in January cases fell in the spring, but the emergence of BA.2.12.1 followed by BA.5 in May 2022 led to an increase in case positivity and admissions. BA.1 infections had a lower mean Ct when compared to other Omicron subvariants. BA.5 samples had a greater likelihood of having infectious virus at Ct values less than 20. CONCLUSIONS: Omicron subvariants continue to associate with a relatively high positivity and admissions. The BA.5 infections are more while BA.2 infections are less likely to have infectious virus, suggesting potential differences in infectibility during the Omicron waves. |
format | Online Article Text |
id | pubmed-9516865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-95168652022-09-29 Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization Morris, C. Paul Eldesouki, Raghda E. Sachithanandham, Jaiprasath Fall, Amary Norton, Julie M. Abdullah, Omar Gallagher, Nicholas Li, Maggie Pekosz, Andrew Klein, Eili Y. Mostafa, Heba H. medRxiv Article BACKGROUND: The variant of concern, Omicron, has become the sole circulating SARS-CoV-2 variant for the past several months. Omicron subvariants BA.1, BA.2, BA.3, BA.4, and BA.5 evolved over the time, with BA.1 causing the largest wave of infections globally in December 2021– January 2022. In this study, we compare the clinical outcomes in patients infected with different Omicron subvariants and compare the relative viral loads, and recovery of infectious virus from upper respiratory specimens. METHODS: SARS-CoV-2 positive remnant clinical specimens, diagnosed at the Johns Hopkins Microbiology Laboratory between December 2021 and July 2022, were used for whole genome sequencing. The clinical outcomes of infections with Omicron subvariants were compared to infections with BA.1. Cycle threshold values (Ct) and the recovery of infectious virus on VeroTMPRSS2 cell line from clinical specimens were compared. RESULTS: The BA.1 was associated with the largest increase in SARS-CoV-2 positivity rate and COVID-19 related hospitalizations at the Johns Hopkins system. After a peak in January cases fell in the spring, but the emergence of BA.2.12.1 followed by BA.5 in May 2022 led to an increase in case positivity and admissions. BA.1 infections had a lower mean Ct when compared to other Omicron subvariants. BA.5 samples had a greater likelihood of having infectious virus at Ct values less than 20. CONCLUSIONS: Omicron subvariants continue to associate with a relatively high positivity and admissions. The BA.5 infections are more while BA.2 infections are less likely to have infectious virus, suggesting potential differences in infectibility during the Omicron waves. Cold Spring Harbor Laboratory 2022-09-23 /pmc/articles/PMC9516865/ /pubmed/36172137 http://dx.doi.org/10.1101/2022.09.20.22280154 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Morris, C. Paul Eldesouki, Raghda E. Sachithanandham, Jaiprasath Fall, Amary Norton, Julie M. Abdullah, Omar Gallagher, Nicholas Li, Maggie Pekosz, Andrew Klein, Eili Y. Mostafa, Heba H. Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization |
title | Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization |
title_full | Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization |
title_fullStr | Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization |
title_full_unstemmed | Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization |
title_short | Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization |
title_sort | omicron subvariants: clinical, laboratory, and cell culture characterization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516865/ https://www.ncbi.nlm.nih.gov/pubmed/36172137 http://dx.doi.org/10.1101/2022.09.20.22280154 |
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