Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2022
Materias:
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
_version_ 1784798796254806016
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
work_keys_str_mv AT morriscpaul omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT eldesoukiraghdae omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT sachithanandhamjaiprasath omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT fallamary omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT nortonjuliem omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT abdullahomar omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT gallaghernicholas omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT limaggie omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT pekoszandrew omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT kleineiliy omicronsubvariantsclinicallaboratoryandcellculturecharacterization
AT mostafahebah omicronsubvariantsclinicallaboratoryandcellculturecharacterization