Cargando…

Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease

OBJECTIVE: The relationship between autoimmune diseases and the gut microbiome has been intensively studied, and several autoimmunity-associated bacterial taxa have been identified. However, much less is known about the roles of the gut virome in autoimmune diseases. METHODS: Here, we performed a wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Tomofuji, Yoshihiko, Kishikawa, Toshihiro, Maeda, Yuichi, Ogawa, Kotaro, Nii, Takuro, Okuno, Tatsusada, Oguro-Igashira, Eri, Kinoshita, Makoto, Yamamoto, Kenichi, Sonehara, Kyuto, Yagita, Mayu, Hosokawa, Akiko, Motooka, Daisuke, Matsumoto, Yuki, Matsuoka, Hidetoshi, Yoshimura, Maiko, Ohshima, Shiro, Nakamura, Shota, Inohara, Hidenori, Mochizuki, Hideki, Takeda, Kiyoshi, Kumanogoh, Atsushi, Okada, Yukinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761997/
https://www.ncbi.nlm.nih.gov/pubmed/34880054
http://dx.doi.org/10.1136/annrheumdis-2021-221267
_version_ 1784633662273224704
author Tomofuji, Yoshihiko
Kishikawa, Toshihiro
Maeda, Yuichi
Ogawa, Kotaro
Nii, Takuro
Okuno, Tatsusada
Oguro-Igashira, Eri
Kinoshita, Makoto
Yamamoto, Kenichi
Sonehara, Kyuto
Yagita, Mayu
Hosokawa, Akiko
Motooka, Daisuke
Matsumoto, Yuki
Matsuoka, Hidetoshi
Yoshimura, Maiko
Ohshima, Shiro
Nakamura, Shota
Inohara, Hidenori
Mochizuki, Hideki
Takeda, Kiyoshi
Kumanogoh, Atsushi
Okada, Yukinori
author_facet Tomofuji, Yoshihiko
Kishikawa, Toshihiro
Maeda, Yuichi
Ogawa, Kotaro
Nii, Takuro
Okuno, Tatsusada
Oguro-Igashira, Eri
Kinoshita, Makoto
Yamamoto, Kenichi
Sonehara, Kyuto
Yagita, Mayu
Hosokawa, Akiko
Motooka, Daisuke
Matsumoto, Yuki
Matsuoka, Hidetoshi
Yoshimura, Maiko
Ohshima, Shiro
Nakamura, Shota
Inohara, Hidenori
Mochizuki, Hideki
Takeda, Kiyoshi
Kumanogoh, Atsushi
Okada, Yukinori
author_sort Tomofuji, Yoshihiko
collection PubMed
description OBJECTIVE: The relationship between autoimmune diseases and the gut microbiome has been intensively studied, and several autoimmunity-associated bacterial taxa have been identified. However, much less is known about the roles of the gut virome in autoimmune diseases. METHODS: Here, we performed a whole gut virome analysis based on the shotgun sequencing of 476 Japanese which included patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), multiple sclerosis and healthy control subjects. RESULTS: Our case–control comparison of the viral abundance revealed that crAss-like phages, which are one of the main components of a healthy gut virome, significantly decreased in the gut of the patients with autoimmune disease, specifically the patients with RA and SLE. In addition, Podoviridae significantly decreased in the gut of the patients with SLE. To understand how these viruses affected the bacteriome, we performed a quantitative virus–bacterium association analysis and clustered regularly interspaced short palindromic repeat-based virus–bacterium interaction analysis. We identified a symbiosis between Podoviridae and Faecalibacterium. In addition, multiple bacterial targets of crAss-like phages were identified (eg, Ruminococcus spp). CONCLUSION: Our data suggest that the gut virome can affect our body either directly or via bacteria. Our analyses have elucidated a previously missing part of the autoimmunity-associated gut microbiome and presented new candidates that contribute to the development of autoimmune diseases.
format Online
Article
Text
id pubmed-8761997
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-87619972022-01-26 Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease Tomofuji, Yoshihiko Kishikawa, Toshihiro Maeda, Yuichi Ogawa, Kotaro Nii, Takuro Okuno, Tatsusada Oguro-Igashira, Eri Kinoshita, Makoto Yamamoto, Kenichi Sonehara, Kyuto Yagita, Mayu Hosokawa, Akiko Motooka, Daisuke Matsumoto, Yuki Matsuoka, Hidetoshi Yoshimura, Maiko Ohshima, Shiro Nakamura, Shota Inohara, Hidenori Mochizuki, Hideki Takeda, Kiyoshi Kumanogoh, Atsushi Okada, Yukinori Ann Rheum Dis Autoimmunity OBJECTIVE: The relationship between autoimmune diseases and the gut microbiome has been intensively studied, and several autoimmunity-associated bacterial taxa have been identified. However, much less is known about the roles of the gut virome in autoimmune diseases. METHODS: Here, we performed a whole gut virome analysis based on the shotgun sequencing of 476 Japanese which included patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), multiple sclerosis and healthy control subjects. RESULTS: Our case–control comparison of the viral abundance revealed that crAss-like phages, which are one of the main components of a healthy gut virome, significantly decreased in the gut of the patients with autoimmune disease, specifically the patients with RA and SLE. In addition, Podoviridae significantly decreased in the gut of the patients with SLE. To understand how these viruses affected the bacteriome, we performed a quantitative virus–bacterium association analysis and clustered regularly interspaced short palindromic repeat-based virus–bacterium interaction analysis. We identified a symbiosis between Podoviridae and Faecalibacterium. In addition, multiple bacterial targets of crAss-like phages were identified (eg, Ruminococcus spp). CONCLUSION: Our data suggest that the gut virome can affect our body either directly or via bacteria. Our analyses have elucidated a previously missing part of the autoimmunity-associated gut microbiome and presented new candidates that contribute to the development of autoimmune diseases. BMJ Publishing Group 2022-02 2021-12-08 /pmc/articles/PMC8761997/ /pubmed/34880054 http://dx.doi.org/10.1136/annrheumdis-2021-221267 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Autoimmunity
Tomofuji, Yoshihiko
Kishikawa, Toshihiro
Maeda, Yuichi
Ogawa, Kotaro
Nii, Takuro
Okuno, Tatsusada
Oguro-Igashira, Eri
Kinoshita, Makoto
Yamamoto, Kenichi
Sonehara, Kyuto
Yagita, Mayu
Hosokawa, Akiko
Motooka, Daisuke
Matsumoto, Yuki
Matsuoka, Hidetoshi
Yoshimura, Maiko
Ohshima, Shiro
Nakamura, Shota
Inohara, Hidenori
Mochizuki, Hideki
Takeda, Kiyoshi
Kumanogoh, Atsushi
Okada, Yukinori
Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
title Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
title_full Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
title_fullStr Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
title_full_unstemmed Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
title_short Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
title_sort whole gut virome analysis of 476 japanese revealed a link between phage and autoimmune disease
topic Autoimmunity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761997/
https://www.ncbi.nlm.nih.gov/pubmed/34880054
http://dx.doi.org/10.1136/annrheumdis-2021-221267
work_keys_str_mv AT tomofujiyoshihiko wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT kishikawatoshihiro wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT maedayuichi wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT ogawakotaro wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT niitakuro wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT okunotatsusada wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT oguroigashiraeri wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT kinoshitamakoto wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT yamamotokenichi wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT soneharakyuto wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT yagitamayu wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT hosokawaakiko wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT motookadaisuke wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT matsumotoyuki wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT matsuokahidetoshi wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT yoshimuramaiko wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT ohshimashiro wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT nakamurashota wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT inoharahidenori wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT mochizukihideki wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT takedakiyoshi wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT kumanogohatsushi wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease
AT okadayukinori wholegutviromeanalysisof476japaneserevealedalinkbetweenphageandautoimmunedisease