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COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts

The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading across the world despite vast global vaccination efforts. Consequently, many studies have looked for potential human host factors and immune mechanisms associated with the...

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Autores principales: Välikangas, Tommi, Junttila, Sini, Rytkönen, Kalle T., Kukkonen-Macchi, Anu, Suomi, Tomi, Elo, Laura L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388772/
https://www.ncbi.nlm.nih.gov/pubmed/35991542
http://dx.doi.org/10.3389/fgene.2022.929887
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author Välikangas, Tommi
Junttila, Sini
Rytkönen, Kalle T.
Kukkonen-Macchi, Anu
Suomi, Tomi
Elo, Laura L.
author_facet Välikangas, Tommi
Junttila, Sini
Rytkönen, Kalle T.
Kukkonen-Macchi, Anu
Suomi, Tomi
Elo, Laura L.
author_sort Välikangas, Tommi
collection PubMed
description The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading across the world despite vast global vaccination efforts. Consequently, many studies have looked for potential human host factors and immune mechanisms associated with the disease. However, most studies have focused on comparing COVID-19 patients to healthy controls, while fewer have elucidated the specific host factors distinguishing COVID-19 from other infections. To discover genes specifically related to COVID-19, we reanalyzed transcriptome data from nine independent cohort studies, covering multiple infections, including COVID-19, influenza, seasonal coronaviruses, and bacterial pneumonia. The identified COVID-19-specific signature consisted of 149 genes, involving many signals previously associated with the disease, such as induction of a strong immunoglobulin response and hemostasis, as well as dysregulation of cell cycle-related processes. Additionally, potential new gene candidates related to COVID-19 were discovered. To facilitate exploration of the signature with respect to disease severity, disease progression, and different cell types, we also offer an online tool for easy visualization of the selected genes across multiple datasets at both bulk and single-cell levels.
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spelling pubmed-93887722022-08-20 COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts Välikangas, Tommi Junttila, Sini Rytkönen, Kalle T. Kukkonen-Macchi, Anu Suomi, Tomi Elo, Laura L. Front Genet Genetics The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading across the world despite vast global vaccination efforts. Consequently, many studies have looked for potential human host factors and immune mechanisms associated with the disease. However, most studies have focused on comparing COVID-19 patients to healthy controls, while fewer have elucidated the specific host factors distinguishing COVID-19 from other infections. To discover genes specifically related to COVID-19, we reanalyzed transcriptome data from nine independent cohort studies, covering multiple infections, including COVID-19, influenza, seasonal coronaviruses, and bacterial pneumonia. The identified COVID-19-specific signature consisted of 149 genes, involving many signals previously associated with the disease, such as induction of a strong immunoglobulin response and hemostasis, as well as dysregulation of cell cycle-related processes. Additionally, potential new gene candidates related to COVID-19 were discovered. To facilitate exploration of the signature with respect to disease severity, disease progression, and different cell types, we also offer an online tool for easy visualization of the selected genes across multiple datasets at both bulk and single-cell levels. Frontiers Media S.A. 2022-08-05 /pmc/articles/PMC9388772/ /pubmed/35991542 http://dx.doi.org/10.3389/fgene.2022.929887 Text en Copyright © 2022 Välikangas, Junttila, Rytkönen, Kukkonen-Macchi, Suomi and Elo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Välikangas, Tommi
Junttila, Sini
Rytkönen, Kalle T.
Kukkonen-Macchi, Anu
Suomi, Tomi
Elo, Laura L.
COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts
title COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts
title_full COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts
title_fullStr COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts
title_full_unstemmed COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts
title_short COVID-19-specific transcriptomic signature detectable in blood across multiple cohorts
title_sort covid-19-specific transcriptomic signature detectable in blood across multiple cohorts
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388772/
https://www.ncbi.nlm.nih.gov/pubmed/35991542
http://dx.doi.org/10.3389/fgene.2022.929887
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