論文

査読有り 国際誌
2022年2月1日

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

Annals of the rheumatic diseases
  • Yoshihiko Tomofuji
  • Toshihiro Kishikawa
  • Yuichi Maeda
  • Kotaro Ogawa
  • Takuro Nii
  • Tatsusada Okuno
  • Eri Oguro-Igashira
  • Makoto Kinoshita
  • Kenichi Yamamoto
  • Kyuto Sonehara
  • Mayu Yagita
  • Akiko Hosokawa
  • Daisuke Motooka
  • Yuki Matsumoto
  • Hidetoshi Matsuoka
  • Maiko Yoshimura
  • Shiro Ohshima
  • Shota Nakamura
  • Hidenori Inohara
  • Hideki Mochizuki
  • Kiyoshi Takeda
  • Atsushi Kumanogoh
  • Yukinori Okada
  • 全て表示

81
2
開始ページ
278
終了ページ
288
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1136/annrheumdis-2021-221267

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.

リンク情報
DOI
https://doi.org/10.1136/annrheumdis-2021-221267
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/34880054
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761997
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123651187&origin=inward 本文へのリンクあり
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85123651187&origin=inward
ID情報
  • DOI : 10.1136/annrheumdis-2021-221267
  • eISSN : 1468-2060
  • PubMed ID : 34880054
  • PubMed Central 記事ID : PMC8761997
  • SCOPUS ID : 85123651187

エクスポート
BibTeX RIS