Relationship between the gut microbiota and bile acid composition in the ileal mucosa of Crohn's disease

被引:16
作者
Bamba, Shigeki [1 ]
Inatomi, Osamu [1 ]
Nishida, Atsushi [1 ]
Ohno, Masashi [1 ]
Imai, Takayuki [1 ]
Takahashi, Kenichiro [1 ]
Naito, Yuji [2 ]
Iwamoto, Junichi [3 ]
Honda, Akira [4 ]
Inohara, Naohiro [5 ]
Andoh, Akira [1 ]
机构
[1] Shiga Univ Med Sci, Div Gastroenterol, Otsu, Shiga, Japan
[2] Kyoto Prefectural Univ Med, Dept Gastroenterol & Hepatol, Kyoto, Japan
[3] Tokyo Med Univ, Ibaraki Med Ctr, Dept Gastroenterol & Hepatol, Ibaraki, Japan
[4] Tokyo Med Univ, Ibaraki Med Ctr, Joint Res Ctr, Ibaraki, Japan
[5] Univ Michigan, Med Sch, Dept Pathol, Ann Arbor, MI 48109 USA
关键词
Single-balloon enteroscopy; Crohn disease; Mucosa associated microbiota; DYSBIOSIS; COMMUNITY; BACTERIA;
D O I
10.5217/ir.2021.00054
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Crosstalk between the gut microbiota and bile acid plays an important role in the pathogenesis of gastrointestinal disorders. We investigated the relationship between microbial structure and bile acid metabolism in the ileal mucosa of Crohn's disease (CD). Methods: Twelve non-CD controls and 38 CD patients in clinical remission were enrolled. Samples were collected from the distal ileum under balloon-assisted enteroscopy. Bile acid composition was analyzed by liquid chromatography-mass spectrometry. The gut microbiota was analyzed by 16S rRNA gene sequencing. Results: The Shannon evenness index was significantly lower in endoscopically active lesions than in non-CD controls. beta-Diversity, evaluated by the UniFrac metric, revealed a significant difference between the active lesions and non-CD controls (P=0.039). The relative abundance of Escherichia was significantly higher and that of Faecalibacterium and Roseburia was significantly lower in CD samples than in non-CD controls. The increased abundance of Escherichia was more prominent in active lesions than in inactive lesions. The proportion of conjugated bile acids was significantly higher in CD patients than in non-CD controls, but there was no difference in the proportion of primary or secondary bile acids. The genera Escherichia and Lactobacillus were positively correlated with the proportion of conjugated bile acids. On the other hand, Roseburia, Intestinibacter, and Faecalibacterium were negatively correlated with the proportion of conjugated bile acids. Conclusions: Mucosa-associated dysbiosis and the alteration of bile acid composition were identified in the ileum of CD patients. These may play a role in the pathophysiology of ileal lesions in CD patients.
引用
收藏
页码:370 / +
页数:13
相关论文
共 30 条
  • [1] Epidemiology and risk factors for IBD
    Ananthakrishnan, Ashwin N.
    [J]. NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2015, 12 (04) : 205 - 217
  • [2] Gastroenterology 2 - Inflammatory bowel disease: clinical aspects and established and evolving therapies
    Baumgart, Daniel C.
    Sandborn, William J.
    [J]. LANCET, 2007, 369 (9573) : 1641 - 1657
  • [3] The interaction between bacteria and bile
    Begley, M
    Gahan, CGM
    Hill, C
    [J]. FEMS MICROBIOLOGY REVIEWS, 2005, 29 (04) : 625 - 651
  • [4] BEST WR, 1976, GASTROENTEROLOGY, V70, P439
  • [5] Bacterial Community Variation in Human Body Habitats Across Space and Time
    Costello, Elizabeth K.
    Lauber, Christian L.
    Hamady, Micah
    Fierer, Noah
    Gordon, Jeffrey I.
    Knight, Rob
    [J]. SCIENCE, 2009, 326 (5960) : 1694 - 1697
  • [6] Connecting dysbiosis, bile-acid dysmetabolism and gut inflammation in inflammatory bowel diseases
    Duboc, Henri
    Rajca, Sylvie
    Rainteau, Dominique
    Benarous, David
    Maubert, Marie-Anne
    Quervain, Elodie
    Thomas, Ginette
    Barbu, Veronique
    Humbert, Lydie
    Despras, Guillaume
    Bridonneau, Chantal
    Dumetz, Fabien
    Grill, Jean-Pierre
    Masliah, Joelle
    Beaugerie, Laurent
    Cosnes, Jacques
    Chazouilleres, Olivier
    Poupon, Raoul
    Wolf, Claude
    Mallet, Jean-Maurice
    Langella, Philippe
    Trugnan, Germain
    Sokol, Harry
    Seksik, Philippe
    [J]. GUT, 2013, 62 (04) : 531 - 539
  • [7] Disease Phenotype and Genotype Are Associated with Shifts in Intestinal-associated Microbiota in Inflammatory Bowel Diseases
    Frank, Daniel N.
    Robertson, Charles E.
    Hamm, Christina M.
    Kpadeh, Zegbeh
    Zhang, Tianyi
    Chen, Hongyan
    Zhu, Wei
    Sartor, R. Balfour
    Boedeker, Edgar C.
    Harpaz, Noam
    Pace, Norman R.
    Li, Ellen
    [J]. INFLAMMATORY BOWEL DISEASES, 2011, 17 (01) : 179 - 184
  • [8] Gut microbiome structure and metabolic activity in inflammatory bowel disease
    Franzosa, Eric A.
    Sirota-Madi, Alexandra
    Avila-Pacheco, Julian
    Fornelos, Nadine
    Haiser, Henryj
    Reinker, Stefan
    Vatanen, Tommi
    Hall, A. Brantley
    Mallick, Himel
    Mclver, Lauren J.
    Sauk, Jenny S.
    Wilson, Robin G.
    Stevens, Betsy W.
    Scott, Justin M.
    Pierce, Kerry
    Deik, Amy A.
    Bullock, Kevin
    Imhann, Floris
    Porter, Jeffrey A.
    Zhernakova, Alexandra
    Fu, Jingyuan
    Weersma, Rinse K.
    Wijmenga, Cisca
    Clish, Clary B.
    Vlamakis, Hera
    Huttenhower, Curtis
    Xavier, Ramnik J.
    [J]. NATURE MICROBIOLOGY, 2019, 4 (02) : 293 - 305
  • [9] The role of diet on intestinal microbiota metabolism: downstream impacts on host immune function and health, and therapeutic implications
    Goldsmith, Jason R.
    Sartor, R. Balfour
    [J]. JOURNAL OF GASTROENTEROLOGY, 2014, 49 (05) : 785 - 798
  • [10] Regulation of the gut microbiota by the mucosal immune system in mice
    Hasegawa, Mizuho
    Inohara, Naohiro
    [J]. INTERNATIONAL IMMUNOLOGY, 2014, 26 (09) : 481 - 487