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...
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Format: | Article |
Language: | English |
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Public Library of Science (PLoS)
2021-01-01
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Series: | PLoS ONE |
Online Access: | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0260451&type=printable |
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author | Masaaki Hirayama Hiroshi Nishiwaki Tomonari Hamaguchi Mikako Ito Jun Ueyama Tetsuya Maeda Kenichi Kashihara Yoshio Tsuboi Kinji Ohno |
author_facet | Masaaki Hirayama Hiroshi Nishiwaki Tomonari Hamaguchi Mikako Ito Jun Ueyama Tetsuya Maeda Kenichi Kashihara Yoshio Tsuboi Kinji Ohno |
author_sort | Masaaki Hirayama |
collection | DOAJ |
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. |
first_indexed | 2024-04-11T20:17:15Z |
format | Article |
id | doaj.art-a4427b6e874647a68ff3451e2dcb739f |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2025-03-14T07:45:05Z |
publishDate | 2021-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-a4427b6e874647a68ff3451e2dcb739f2025-03-03T05:33:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-011611e026045110.1371/journal.pone.0260451Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate.Masaaki HirayamaHiroshi NishiwakiTomonari HamaguchiMikako ItoJun UeyamaTetsuya MaedaKenichi KashiharaYoshio TsuboiKinji OhnoThe 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.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0260451&type=printable |
spellingShingle | Masaaki Hirayama Hiroshi Nishiwaki Tomonari Hamaguchi Mikako Ito Jun Ueyama Tetsuya Maeda Kenichi Kashihara Yoshio Tsuboi Kinji Ohno Intestinal Collinsella may mitigate infection and exacerbation of COVID-19 by producing ursodeoxycholate. PLoS ONE |
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 |
url | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0260451&type=printable |
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