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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Main Authors: Masaaki Hirayama, Hiroshi Nishiwaki, Tomonari Hamaguchi, Mikako Ito, Jun Ueyama, Tetsuya Maeda, Kenichi Kashihara, Yoshio Tsuboi, Kinji Ohno
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
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.
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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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