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From bedside to bench: regulation of host factors in SARS-CoV-2 infection
The zoonotic coronavirus SARS-CoV-2 (severe acute respiratory syndrome coronavirus-2), which causes COVID-19 (coronavirus disease-2019), has resulted in a pandemic. This has led to an urgent need to understand the molecular determinants of SARS-CoV-2 infection, factors associated with COVID-19 heter...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024942/ https://www.ncbi.nlm.nih.gov/pubmed/33828231 http://dx.doi.org/10.1038/s12276-021-00595-x |
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author | Ong, Samantha Y. Q. Flyamer, Ilya M. Bickmore, Wendy A. Biddie, Simon C. |
author_facet | Ong, Samantha Y. Q. Flyamer, Ilya M. Bickmore, Wendy A. Biddie, Simon C. |
author_sort | Ong, Samantha Y. Q. |
collection | PubMed |
description | The zoonotic coronavirus SARS-CoV-2 (severe acute respiratory syndrome coronavirus-2), which causes COVID-19 (coronavirus disease-2019), has resulted in a pandemic. This has led to an urgent need to understand the molecular determinants of SARS-CoV-2 infection, factors associated with COVID-19 heterogeneity and severity, and therapeutic options for these patients. In this review, we discuss the role of host factors in SARS-CoV-2 infection and describe variations in host factor expression as mechanisms underlying the symptoms and severity of COVID-19. We focus on two host factors, angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2), implicated in SARS-CoV-2 infection. We also discuss genetic variants associated with COVID-19 severity revealed in selected patients and based on genome-wide association studies (GWASs). Furthermore, we highlight important advances in cell and chromatin biology, such as single-cell RNA and chromatin sequencing and chromosomal conformation assays, as methods that may aid in the discovery of viral–host interactions in COVID-19. Understanding how regulation of host factor genes varies in physiological and pathological states might explain the heterogeneity observed in SARS-CoV-2 infection, help identify pathways for therapeutic development, and identify patients most likely to progress to severe COVID-19. |
format | Online Article Text |
id | pubmed-8024942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80249422021-04-07 From bedside to bench: regulation of host factors in SARS-CoV-2 infection Ong, Samantha Y. Q. Flyamer, Ilya M. Bickmore, Wendy A. Biddie, Simon C. Exp Mol Med Review Article The zoonotic coronavirus SARS-CoV-2 (severe acute respiratory syndrome coronavirus-2), which causes COVID-19 (coronavirus disease-2019), has resulted in a pandemic. This has led to an urgent need to understand the molecular determinants of SARS-CoV-2 infection, factors associated with COVID-19 heterogeneity and severity, and therapeutic options for these patients. In this review, we discuss the role of host factors in SARS-CoV-2 infection and describe variations in host factor expression as mechanisms underlying the symptoms and severity of COVID-19. We focus on two host factors, angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2), implicated in SARS-CoV-2 infection. We also discuss genetic variants associated with COVID-19 severity revealed in selected patients and based on genome-wide association studies (GWASs). Furthermore, we highlight important advances in cell and chromatin biology, such as single-cell RNA and chromatin sequencing and chromosomal conformation assays, as methods that may aid in the discovery of viral–host interactions in COVID-19. Understanding how regulation of host factor genes varies in physiological and pathological states might explain the heterogeneity observed in SARS-CoV-2 infection, help identify pathways for therapeutic development, and identify patients most likely to progress to severe COVID-19. Nature Publishing Group UK 2021-04-07 /pmc/articles/PMC8024942/ /pubmed/33828231 http://dx.doi.org/10.1038/s12276-021-00595-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Ong, Samantha Y. Q. Flyamer, Ilya M. Bickmore, Wendy A. Biddie, Simon C. From bedside to bench: regulation of host factors in SARS-CoV-2 infection |
title | From bedside to bench: regulation of host factors in SARS-CoV-2 infection |
title_full | From bedside to bench: regulation of host factors in SARS-CoV-2 infection |
title_fullStr | From bedside to bench: regulation of host factors in SARS-CoV-2 infection |
title_full_unstemmed | From bedside to bench: regulation of host factors in SARS-CoV-2 infection |
title_short | From bedside to bench: regulation of host factors in SARS-CoV-2 infection |
title_sort | from bedside to bench: regulation of host factors in sars-cov-2 infection |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024942/ https://www.ncbi.nlm.nih.gov/pubmed/33828231 http://dx.doi.org/10.1038/s12276-021-00595-x |
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