TY - JOUR
T1 - Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
AU - Tomofuji, Yoshihiko
AU - Kishikawa, Toshihiro
AU - Maeda, Yuichi
AU - Ogawa, Kotaro
AU - Nii, Takuro
AU - Okuno, Tatsusada
AU - Oguro-Igashira, Eri
AU - Kinoshita, Makoto
AU - Yamamoto, Kenichi
AU - Sonehara, Kyuto
AU - Yagita, Mayu
AU - Hosokawa, Akiko
AU - Motooka, Daisuke
AU - Matsumoto, Yuki
AU - Matsuoka, Hidetoshi
AU - Yoshimura, Maiko
AU - Ohshima, Shiro
AU - Nakamura, Shota
AU - Inohara, Hidenori
AU - Mochizuki, Hideki
AU - Takeda, Kiyoshi
AU - Kumanogoh, Atsushi
AU - Okada, Yukinori
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2022.
PY - 2022/2
Y1 - 2022/2
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85123651187&partnerID=8YFLogxK
U2 - 10.1136/annrheumdis-2021-221267
DO - 10.1136/annrheumdis-2021-221267
M3 - Article
C2 - 34880054
AN - SCOPUS:85123651187
SN - 0003-4967
VL - 81
SP - 278
EP - 288
JO - Annals of the Rheumatic Diseases
JF - Annals of the Rheumatic Diseases
IS - 2
ER -