Depletion of dietary aryl hydrocarbon receptor ligands alters microbiota composition and function

被引:45
作者
Brawner, Kyle M. [1 ]
Yeramilli, Venkata A. [1 ]
Duck, Lennard W. [2 ]
Van der Pol, William [3 ,4 ]
Smythies, Lesley E. [2 ]
Morrow, Casey D. [4 ]
Elson, Charles O. [2 ]
Martin, Colin A. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[3] Univ Alabama, Ctr Clin & Translat Sci, Tuscaloosa, AL 35487 USA
[4] Univ Alabama, Dept Cell Dev & Integrat Biol, Tuscaloosa, AL 35487 USA
基金
美国国家卫生研究院;
关键词
GUT MICROBIOTA; SECRETORY COMPONENT; J-CHAIN; IMMUNOGLOBULIN; IGA; TRYPTOPHAN; TRANSPORT; BINDING; OBESITY; CELLS;
D O I
10.1038/s41598-019-51194-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The intestinal microbiota is critical for maintaining homeostasis. Dysbiosis, an imbalance in the microbial community, contributes to the susceptibility of several diseases. Many factors are known to influence gut microbial composition, including diet. We have previously shown that fecal immunoglobulin (Ig) A levels are decreased in mice fed a diet free of aryl hydrocarbon receptor (AhR) ligands. Here, we hypothesize this IgA decrease is secondary to diet-induced dysbiosis. We assigned mice to a conventional diet, an AhR ligand-free diet, or an AhR ligand-free diet supplemented with the dietary AhR ligand indole-3-carbinol (I3C). We observed a global alteration of fecal microbiota upon dietary AhR ligand deprivation. Compared to mice on the conventional diet, family Erysipelotrichaceae was enriched in the feces of mice on the AhR ligand-free diet but returned to normal levels upon dietary supplementation with I3C. Faecalibaculum rodentium, an Erysipelotrichaceae species, depleted its growth media of AhR ligands. Cultured fecal bacteria from mice on the AhR ligand-free diet, but not the other two diets, were able to alter IgA levels in vitro, as was F. rodentium alone. Our data point to the critical role of AhR dietary ligands in shaping the composition and proper functioning of gut microbiota.
引用
收藏
页数:12
相关论文
共 58 条
[1]   Gut Microbiota Regulation of Tryptophan Metabolism in Health and Disease [J].
Agus, Allison ;
Planchais, Julien ;
Sokol, Harry .
CELL HOST & MICROBE, 2018, 23 (06) :716-724
[2]   Microbiota-Derived Indole Metabolites Promote Human and Murine Intestinal Homeostasis through Regulation of Interleukin-10 Receptor [J].
Alexeev, Erica E. ;
Lanis, Jordi M. ;
Kao, Daniel J. ;
Campbell, Eric L. ;
Kelly, Caleb J. ;
Battista, Kayla D. ;
Gerich, Mark E. ;
Jenkins, Brittany R. ;
Walk, Seth T. ;
Kominsky, Douglas J. ;
Colgan, Sean P. .
AMERICAN JOURNAL OF PATHOLOGY, 2018, 188 (05) :1183-1194
[3]   Pharmacokinetics and tissue disposition of indole-3-carbinol and its acid condensation products after oral administration to mice [J].
Anderton, MJ ;
Manson, MM ;
Verschoyle, RD ;
Gescher, A ;
Lamb, JH ;
Farmer, PB ;
Steward, WP ;
Williams, ML .
CLINICAL CANCER RESEARCH, 2004, 10 (15) :5233-5241
[4]   MONOCLONAL IMMUNOGLOBULIN A ANTIBODIES DIRECTED AGAINST CHOLERA-TOXIN PREVENT THE TOXIN-INDUCED CHLORIDE SECRETORY RESPONSE AND BLOCK TOXIN BINDING TO INTESTINAL EPITHELIAL-CELLS IN-VITRO [J].
APTER, FM ;
LENCER, WI ;
FINKELSTEIN, RA ;
MEKALANOS, JJ ;
NEUTRA, MR .
INFECTION AND IMMUNITY, 1993, 61 (12) :5271-5278
[5]   Lifespan is prolonged in autoimmune-prone (NZB/NZW) F1 mice fed a diet supplemented with indole-3-carbinol [J].
Auborn, KJ ;
Qi, M ;
Yan, XJ ;
Teichberg, S ;
Chen, DZ ;
Madaio, MP ;
Chiorazzi, N .
JOURNAL OF NUTRITION, 2003, 133 (11) :3610-3613
[6]   AROMATIC HYDROCARBON RESPONSIVENESS-RECEPTOR AGONISTS GENERATED FROM INDOLE-3-CARBINOL INVITRO AND INVIVO - COMPARISONS WITH 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN [J].
BJELDANES, LF ;
KIM, JY ;
GROSE, KR ;
BARTHOLOMEW, JC ;
BRADFIELD, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9543-9547
[7]  
BRANDTZAEG P, 1984, CLIN EXP IMMUNOL, V58, P709
[8]   Gate-keeper function of the intestinal epithelium [J].
Brandtzaeg, P. .
BENEFICIAL MICROBES, 2013, 4 (01) :67-82
[9]   Mucosal Immunity: Induction, Dissemination, and Effector Functions [J].
Brandtzaeg, P. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2009, 70 (06) :505-515
[10]   DIRECT EVIDENCE FOR AN INTEGRATED FUNCTION OF J-CHAIN AND SECRETORY COMPONENT IN EPITHELIAL TRANSPORT OF IMMUNOGLOBULINS [J].
BRANDTZAEG, P ;
PRYDZ, H .
NATURE, 1984, 311 (5981) :71-74