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Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate
The mortality rates of COVID-19 vary widely across countries, but the underlying mechanisms remain unelucidated. We aimed at the elucidation of relationship between gut microbiota and the mortality rates of COVID-19 across countries. Raw sequencing data of 16S rRNA V3-V5 regions of gut microbiota in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610263/ https://www.ncbi.nlm.nih.gov/pubmed/34813629 http://dx.doi.org/10.1371/journal.pone.0260451 |
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author | Hirayama, Masaaki Nishiwaki, Hiroshi Hamaguchi, Tomonari Ito, Mikako Ueyama, Jun Maeda, Tetsuya Kashihara, Kenichi Tsuboi, Yoshio Ohno, Kinji |
author_facet | Hirayama, Masaaki Nishiwaki, Hiroshi Hamaguchi, Tomonari Ito, Mikako Ueyama, Jun Maeda, Tetsuya Kashihara, Kenichi Tsuboi, Yoshio Ohno, Kinji |
author_sort | Hirayama, Masaaki |
collection | PubMed |
description | The mortality rates of COVID-19 vary widely across countries, but the underlying mechanisms remain unelucidated. We aimed at the elucidation of relationship between gut microbiota and the mortality rates of COVID-19 across countries. Raw sequencing data of 16S rRNA V3-V5 regions of gut microbiota in 953 healthy subjects in ten countries were obtained from the public database. We made a generalized linear model (GLM) to predict the COVID-19 mortality rates using gut microbiota. GLM revealed that low genus Collinsella predicted high COVID-19 mortality rates with a markedly low p-value. Unsupervised clustering of gut microbiota in 953 subjects yielded five enterotypes. The mortality rates were increased from enterotypes 1 to 5, whereas the abundances of Collinsella were decreased from enterotypes 1 to 5 except for enterotype 2. Collinsella produces ursodeoxycholate. Ursodeoxycholate was previously reported to inhibit binding of SARS-CoV-2 to angiotensin-converting enzyme 2; suppress pro-inflammatory cytokines like TNF-α, IL-1β, IL-2, IL-4, and IL-6; have antioxidant and anti-apoptotic effects; and increase alveolar fluid clearance in acute respiratory distress syndrome. Ursodeoxycholate produced by Collinsella may prevent COVID-19 infection and ameliorate acute respiratory distress syndrome in COVID-19 by suppressing cytokine storm syndrome. |
format | Online Article Text |
id | pubmed-8610263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-86102632021-11-24 Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate Hirayama, Masaaki Nishiwaki, Hiroshi Hamaguchi, Tomonari Ito, Mikako Ueyama, Jun Maeda, Tetsuya Kashihara, Kenichi Tsuboi, Yoshio Ohno, Kinji PLoS One Research Article The mortality rates of COVID-19 vary widely across countries, but the underlying mechanisms remain unelucidated. We aimed at the elucidation of relationship between gut microbiota and the mortality rates of COVID-19 across countries. Raw sequencing data of 16S rRNA V3-V5 regions of gut microbiota in 953 healthy subjects in ten countries were obtained from the public database. We made a generalized linear model (GLM) to predict the COVID-19 mortality rates using gut microbiota. GLM revealed that low genus Collinsella predicted high COVID-19 mortality rates with a markedly low p-value. Unsupervised clustering of gut microbiota in 953 subjects yielded five enterotypes. The mortality rates were increased from enterotypes 1 to 5, whereas the abundances of Collinsella were decreased from enterotypes 1 to 5 except for enterotype 2. Collinsella produces ursodeoxycholate. Ursodeoxycholate was previously reported to inhibit binding of SARS-CoV-2 to angiotensin-converting enzyme 2; suppress pro-inflammatory cytokines like TNF-α, IL-1β, IL-2, IL-4, and IL-6; have antioxidant and anti-apoptotic effects; and increase alveolar fluid clearance in acute respiratory distress syndrome. Ursodeoxycholate produced by Collinsella may prevent COVID-19 infection and ameliorate acute respiratory distress syndrome in COVID-19 by suppressing cytokine storm syndrome. Public Library of Science 2021-11-23 /pmc/articles/PMC8610263/ /pubmed/34813629 http://dx.doi.org/10.1371/journal.pone.0260451 Text en © 2021 Hirayama et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hirayama, Masaaki Nishiwaki, Hiroshi Hamaguchi, Tomonari Ito, Mikako Ueyama, Jun Maeda, Tetsuya Kashihara, Kenichi Tsuboi, Yoshio Ohno, Kinji Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate |
title | Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate |
title_full | Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate |
title_fullStr | Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate |
title_full_unstemmed | Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate |
title_short | Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate |
title_sort | intestinal collinsella may mitigate infection and exacerbation of covid-19 by producing ursodeoxycholate |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610263/ https://www.ncbi.nlm.nih.gov/pubmed/34813629 http://dx.doi.org/10.1371/journal.pone.0260451 |
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