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Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells

During 2020, understanding the molecular mechanism of SARS-CoV-2 infection (the cause of COVID-19) became a scientific priority due to the devastating effects of the COVID-19. Many researchers have studied the effect of this viral infection on lung epithelial transcriptomes and deposited data in pub...

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Autores principales: Chandrashekar, Darshan S., Athar, Mohammad, Manne, Upender, Varambally, Sooryanarayana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8355180/
https://www.ncbi.nlm.nih.gov/pubmed/34376762
http://dx.doi.org/10.1038/s41598-021-95733-w
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author Chandrashekar, Darshan S.
Athar, Mohammad
Manne, Upender
Varambally, Sooryanarayana
author_facet Chandrashekar, Darshan S.
Athar, Mohammad
Manne, Upender
Varambally, Sooryanarayana
author_sort Chandrashekar, Darshan S.
collection PubMed
description During 2020, understanding the molecular mechanism of SARS-CoV-2 infection (the cause of COVID-19) became a scientific priority due to the devastating effects of the COVID-19. Many researchers have studied the effect of this viral infection on lung epithelial transcriptomes and deposited data in public repositories. Comprehensive analysis of such data could pave the way for development of efficient vaccines and effective drugs. In the current study, we obtained high-throughput gene expression data associated with human lung epithelial cells infected with respiratory viruses such as SARS-CoV-2, SARS, H1N1, avian influenza, rhinovirus and Dhori, then performed comparative transcriptome analysis to identify SARS-CoV-2 exclusive genes. The analysis yielded seven SARS-CoV-2 specific genes including CSF2 [GM-CSF] (colony-stimulating factor 2) and calcium-binding proteins (such as S100A8 and S100A9), which are known to be involved in respiratory diseases. The analyses showed that genes involved in inflammation are commonly altered by infection of SARS-CoV-2 and influenza viruses. Furthermore, results of protein–protein interaction analyses were consistent with a functional role of CSF2 and S100A9 in COVID-19 disease. In conclusion, our analysis revealed cellular genes associated with SARS-CoV-2 infection of the human lung epithelium; these are potential therapeutic targets.
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spelling pubmed-83551802021-08-11 Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells Chandrashekar, Darshan S. Athar, Mohammad Manne, Upender Varambally, Sooryanarayana Sci Rep Article During 2020, understanding the molecular mechanism of SARS-CoV-2 infection (the cause of COVID-19) became a scientific priority due to the devastating effects of the COVID-19. Many researchers have studied the effect of this viral infection on lung epithelial transcriptomes and deposited data in public repositories. Comprehensive analysis of such data could pave the way for development of efficient vaccines and effective drugs. In the current study, we obtained high-throughput gene expression data associated with human lung epithelial cells infected with respiratory viruses such as SARS-CoV-2, SARS, H1N1, avian influenza, rhinovirus and Dhori, then performed comparative transcriptome analysis to identify SARS-CoV-2 exclusive genes. The analysis yielded seven SARS-CoV-2 specific genes including CSF2 [GM-CSF] (colony-stimulating factor 2) and calcium-binding proteins (such as S100A8 and S100A9), which are known to be involved in respiratory diseases. The analyses showed that genes involved in inflammation are commonly altered by infection of SARS-CoV-2 and influenza viruses. Furthermore, results of protein–protein interaction analyses were consistent with a functional role of CSF2 and S100A9 in COVID-19 disease. In conclusion, our analysis revealed cellular genes associated with SARS-CoV-2 infection of the human lung epithelium; these are potential therapeutic targets. Nature Publishing Group UK 2021-08-10 /pmc/articles/PMC8355180/ /pubmed/34376762 http://dx.doi.org/10.1038/s41598-021-95733-w 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chandrashekar, Darshan S.
Athar, Mohammad
Manne, Upender
Varambally, Sooryanarayana
Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells
title Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells
title_full Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells
title_fullStr Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells
title_full_unstemmed Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells
title_short Comparative transcriptome analyses reveal genes associated with SARS-CoV-2 infection of human lung epithelial cells
title_sort comparative transcriptome analyses reveal genes associated with sars-cov-2 infection of human lung epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8355180/
https://www.ncbi.nlm.nih.gov/pubmed/34376762
http://dx.doi.org/10.1038/s41598-021-95733-w
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