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Identification of Cellular Factors Required for SARS-CoV-2 Replication
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the recently emerged virus responsible for the COVID-19 pandemic. Clinical presentation can range from asymptomatic disease and mild respiratory tract infection to severe disease with lung injury, multiorgan failure, and death. SARS-CoV...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622730/ https://www.ncbi.nlm.nih.gov/pubmed/34831382 http://dx.doi.org/10.3390/cells10113159 |
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author | Synowiec, Aleksandra Jedrysik, Malwina Branicki, Wojciech Klajmon, Adrianna Lei, Jing Owczarek, Katarzyna Suo, Chen Szczepanski, Artur Wang, Jingru Zhang, Pengyan Labaj, Pawel P. Pyrc, Krzysztof |
author_facet | Synowiec, Aleksandra Jedrysik, Malwina Branicki, Wojciech Klajmon, Adrianna Lei, Jing Owczarek, Katarzyna Suo, Chen Szczepanski, Artur Wang, Jingru Zhang, Pengyan Labaj, Pawel P. Pyrc, Krzysztof |
author_sort | Synowiec, Aleksandra |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the recently emerged virus responsible for the COVID-19 pandemic. Clinical presentation can range from asymptomatic disease and mild respiratory tract infection to severe disease with lung injury, multiorgan failure, and death. SARS-CoV-2 is the third animal coronavirus to emerge in humans in the 21st century, and coronaviruses appear to possess a unique ability to cross borders between species and infect a wide range of organisms. This is somewhat surprising as, except for the requirement of host cell receptors, cell–pathogen interactions are usually species-specific. Insights into these host–virus interactions will provide a deeper understanding of the process of SARS-CoV-2 infection and provide a means for the design and development of antiviral agents. In this study, we describe a complex analysis of SARS-CoV-2 infection using a genome-wide CRISPR-Cas9 knock-out system in HeLa cells overexpressing entry receptor angiotensin-converting enzyme 2 (ACE2). This platform allows for the identification of factors required for viral replication. This study was designed to include a high number of replicates (48 replicates; 16 biological repeats with 3 technical replicates each) to prevent data instability, remove sources of bias, and allow multifactorial bioinformatic analyses in order to study the resulting interaction network. The results obtained provide an interesting insight into the replication mechanisms of SARS-CoV-2. |
format | Online Article Text |
id | pubmed-8622730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86227302021-11-27 Identification of Cellular Factors Required for SARS-CoV-2 Replication Synowiec, Aleksandra Jedrysik, Malwina Branicki, Wojciech Klajmon, Adrianna Lei, Jing Owczarek, Katarzyna Suo, Chen Szczepanski, Artur Wang, Jingru Zhang, Pengyan Labaj, Pawel P. Pyrc, Krzysztof Cells Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the recently emerged virus responsible for the COVID-19 pandemic. Clinical presentation can range from asymptomatic disease and mild respiratory tract infection to severe disease with lung injury, multiorgan failure, and death. SARS-CoV-2 is the third animal coronavirus to emerge in humans in the 21st century, and coronaviruses appear to possess a unique ability to cross borders between species and infect a wide range of organisms. This is somewhat surprising as, except for the requirement of host cell receptors, cell–pathogen interactions are usually species-specific. Insights into these host–virus interactions will provide a deeper understanding of the process of SARS-CoV-2 infection and provide a means for the design and development of antiviral agents. In this study, we describe a complex analysis of SARS-CoV-2 infection using a genome-wide CRISPR-Cas9 knock-out system in HeLa cells overexpressing entry receptor angiotensin-converting enzyme 2 (ACE2). This platform allows for the identification of factors required for viral replication. This study was designed to include a high number of replicates (48 replicates; 16 biological repeats with 3 technical replicates each) to prevent data instability, remove sources of bias, and allow multifactorial bioinformatic analyses in order to study the resulting interaction network. The results obtained provide an interesting insight into the replication mechanisms of SARS-CoV-2. MDPI 2021-11-13 /pmc/articles/PMC8622730/ /pubmed/34831382 http://dx.doi.org/10.3390/cells10113159 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Synowiec, Aleksandra Jedrysik, Malwina Branicki, Wojciech Klajmon, Adrianna Lei, Jing Owczarek, Katarzyna Suo, Chen Szczepanski, Artur Wang, Jingru Zhang, Pengyan Labaj, Pawel P. Pyrc, Krzysztof Identification of Cellular Factors Required for SARS-CoV-2 Replication |
title | Identification of Cellular Factors Required for SARS-CoV-2 Replication |
title_full | Identification of Cellular Factors Required for SARS-CoV-2 Replication |
title_fullStr | Identification of Cellular Factors Required for SARS-CoV-2 Replication |
title_full_unstemmed | Identification of Cellular Factors Required for SARS-CoV-2 Replication |
title_short | Identification of Cellular Factors Required for SARS-CoV-2 Replication |
title_sort | identification of cellular factors required for sars-cov-2 replication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622730/ https://www.ncbi.nlm.nih.gov/pubmed/34831382 http://dx.doi.org/10.3390/cells10113159 |
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