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Omicron Subvariants: Clinical, Laboratory, and Cell Culture Characterization
BACKGROUND: The variant of concern Omicron has become the sole circulating severe acute respiratory syndrome coronavirus 2 (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 gl...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069846/ https://www.ncbi.nlm.nih.gov/pubmed/36366857 http://dx.doi.org/10.1093/cid/ciac885 |
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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 severe acute respiratory syndrome coronavirus 2 (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. This study compared the clinical outcomes in patients infected with different Omicron subvariants and 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 with infections with BA.1. Cycle threshold (Ct) values and the recovery of infectious virus on the VeroTMPRSS2 cell line from clinical specimens were compared. RESULTS: BA.1 was associated with the largest increase in SARS-CoV-2 positivity rate and coronavirus disease 2019 (COVID-19)–related hospitalizations at the Johns Hopkins system. After a peak in January, cases decreased 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 value when compared with other Omicron subvariants. BA.5 samples had a greater likelihood of having infectious virus at Ct values <20. CONCLUSIONS: Omicron subvariants continue to be associated with a relatively high rate of polymerase chain reaction (PCR) positivity and hospital 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-10069846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100698462023-04-04 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 Clin Infect Dis Major Article BACKGROUND: The variant of concern Omicron has become the sole circulating severe acute respiratory syndrome coronavirus 2 (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. This study compared the clinical outcomes in patients infected with different Omicron subvariants and 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 with infections with BA.1. Cycle threshold (Ct) values and the recovery of infectious virus on the VeroTMPRSS2 cell line from clinical specimens were compared. RESULTS: BA.1 was associated with the largest increase in SARS-CoV-2 positivity rate and coronavirus disease 2019 (COVID-19)–related hospitalizations at the Johns Hopkins system. After a peak in January, cases decreased 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 value when compared with other Omicron subvariants. BA.5 samples had a greater likelihood of having infectious virus at Ct values <20. CONCLUSIONS: Omicron subvariants continue to be associated with a relatively high rate of polymerase chain reaction (PCR) positivity and hospital 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. Oxford University Press 2022-11-11 /pmc/articles/PMC10069846/ /pubmed/36366857 http://dx.doi.org/10.1093/cid/ciac885 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major 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 | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069846/ https://www.ncbi.nlm.nih.gov/pubmed/36366857 http://dx.doi.org/10.1093/cid/ciac885 |
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