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Mucin O-glycans facilitate symbiosynthesis to maintain gut immune homeostasisResearch in context

Authors :
Takahiro Yamada
Shingo Hino
Hideki Iijima
Tomomi Genda
Ryo Aoki
Ryuji Nagata
Kyu-Ho Han
Masato Hirota
Yusuke Kinashi
Hiroyuki Oguchi
Wataru Suda
Yukihiro Furusawa
Yumiko Fujimura
Jun Kunisawa
Masahira Hattori
Michihiro Fukushima
Tatsuya Morita
Koji Hase
Source :
EBioMedicine, Vol 48, Iss , Pp 513-525 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Background: The dysbiosis of gut microbiota has been implicated in the pathogenesis of inflammatory bowel diseases; however, the underlying mechanisms have not yet been elucidated. Heavily glycosylated mucin establishes a first-line barrier against pathogens and serves as a niche for microbial growth. Methods: To elucidate relationships among dysbiosis, abnormal mucin utilisation, and microbial metabolic dysfunction, we analysed short-chain fatty acids (SCFAs) and mucin components in stool samples of 40 healthy subjects, 49 ulcerative colitis (UC) patients, and 44 Crohn's disease (CD) patients from Japan. Findings: Levels of n-butyrate were significantly lower in stools of both CD and UC patients than in stools of healthy subjects. Correlation analysis identified seven bacterial species positively correlated with n-butyrate levels; the major n-butyrate producer, Faecalibacterium prausnitzii, was particularly underrepresented in CD patients, but not in UC patients. In UC patients, there were inverse correlations between mucin O-glycan levels and the production of SCFAs, such as n-butyrate, suggesting that mucin O-glycans serve as an endogenous fermentation substrate for n-butyrate production. Indeed, mucin-fed rodents exhibited enhanced n-butyrate production, leading to the expansion of RORgt+Treg cells and IgA-producing cells in colonic lamina propria. Microbial utilisation of mucin-associated O-glycans was significantly reduced in n-butyrate-deficient UC patients. Interpretation: Mucin O-glycans facilitate symbiosynthesis of n-butyrate by gut microbiota. Abnormal mucin utilisation may lead to reduced n-butyrate production in UC patients. Fund: Japan Society for the Promotion of Science, Health Labour Sciences Research Grant, AMED-Crest, AMED, Yakult Foundation, Keio Gijuku Academic Development Funds, The Aashi Grass Foundation, and The Canon Foundation. Keywords: Microbiota, Butyrate, Mucin, Inflammatory bowel disease

Subjects

Subjects :
Medicine
Medicine (General)
R5-920

Details

Language :
English
ISSN :
23523964
Volume :
48
Issue :
513-525
Database :
Directory of Open Access Journals
Journal :
EBioMedicine
Publication Type :
Academic Journal
Accession number :
edsdoj.1fc34f92344d45ba8b53d2df0d0c350d
Document Type :
article
Full Text :
https://doi.org/10.1016/j.ebiom.2019.09.008