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Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota

COVID-19, an infectious disease caused by a novel coronavirus (SARS-CoV-2) has emerged as global pandemic. Here, we described the changes in microbiota of upper respiratory tract by analyzing the publically available RNA sequencing data of SARS-CoV-2-infected ferrets. The bacterial dysbiosis due to...

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Autores principales: Velmurugan, Ganesan, Vasudevan, Dinakaran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chang Gung University 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912354/
https://www.ncbi.nlm.nih.gov/pubmed/34507920
http://dx.doi.org/10.1016/j.bj.2021.02.008
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author Velmurugan, Ganesan
Vasudevan, Dinakaran
author_facet Velmurugan, Ganesan
Vasudevan, Dinakaran
author_sort Velmurugan, Ganesan
collection PubMed
description COVID-19, an infectious disease caused by a novel coronavirus (SARS-CoV-2) has emerged as global pandemic. Here, we described the changes in microbiota of upper respiratory tract by analyzing the publically available RNA sequencing data of SARS-CoV-2-infected ferrets. The bacterial dysbiosis due to SARS-CoV-2 was largely inversely proportional to the dysbiosis caused by influenza-A virus. The bacterial taxa which are defined as healthy ecostate were significantly reduced during SARS-CoV-2 infection. Altogether, this preliminary study provides a new insight on the possible role of bacterial communities of upper respiratory tract in determining the immunity, susceptibility, and mortality for COVID-19.
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spelling pubmed-79123542021-03-01 Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota Velmurugan, Ganesan Vasudevan, Dinakaran Biomed J Brief Communication COVID-19, an infectious disease caused by a novel coronavirus (SARS-CoV-2) has emerged as global pandemic. Here, we described the changes in microbiota of upper respiratory tract by analyzing the publically available RNA sequencing data of SARS-CoV-2-infected ferrets. The bacterial dysbiosis due to SARS-CoV-2 was largely inversely proportional to the dysbiosis caused by influenza-A virus. The bacterial taxa which are defined as healthy ecostate were significantly reduced during SARS-CoV-2 infection. Altogether, this preliminary study provides a new insight on the possible role of bacterial communities of upper respiratory tract in determining the immunity, susceptibility, and mortality for COVID-19. Chang Gung University 2021-08 2021-02-27 /pmc/articles/PMC7912354/ /pubmed/34507920 http://dx.doi.org/10.1016/j.bj.2021.02.008 Text en © 2021 Chang Gung University. Publishing services provided by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Brief Communication
Velmurugan, Ganesan
Vasudevan, Dinakaran
Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota
title Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota
title_full Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota
title_fullStr Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota
title_full_unstemmed Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota
title_short Metagenomic analysis of RNA sequencing data reveals SARS-CoV-2-mediated progressive dysbiosis of upper respiratory tract microbiota
title_sort metagenomic analysis of rna sequencing data reveals sars-cov-2-mediated progressive dysbiosis of upper respiratory tract microbiota
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912354/
https://www.ncbi.nlm.nih.gov/pubmed/34507920
http://dx.doi.org/10.1016/j.bj.2021.02.008
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