» Articles » PMID: 27659481

Expression of the Aryl Hydrocarbon Receptor Contributes to the Establishment of Intestinal Microbial Community Structure in Mice

Overview
Journal Sci Rep
Specialty Science
Date 2016 Sep 24
PMID 27659481
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

Environmental and genetic factors represent key components in the establishment/maintenance of the intestinal microbiota. The aryl hydrocarbon receptor (AHR) is emerging as a pleiotropic factor, modulating pathways beyond its established role as a xenobiotic sensor. The AHR is known to regulate immune surveillance within the intestine through retention of intraepithelial lymphocytes, functional redistribution of Th17/Treg balance. Consequently, environmental/genetic manipulation of AHR activity likely influences host-microbe homeostasis. Utilizing C57BL6/J Ahr and Ahr co-housed littermates followed by 18 days of genotypic segregation, we examined the influence of AHR expression upon intestinal microbe composition/functionality and host physiology. 16S sequencing/quantitative PCR (qPCR) revealed significant changes in phyla abundance, particularly Verrucomicrobia together with segmented filamentous bacteria, and an increase in species diversity in Ahr mice following genotypic segregation. Metagenomics/metabolomics indicate microbial composition is associated with functional shifts in bacterial metabolism. Analysis identified Ahr-dependent increases in ileal gene expression, indicating increased inflammatory tone. Transfer of Ahr microbiota to wild-type germ-free mice recapitulated the increase Verrucomicrobia and inflammatory tone, indicating Ahr-microbial dependence. These data suggest a role for the AHR in influencing the community structure of the intestinal microbiota.

Citing Articles

Environmental and population influences on mummichog () gut microbiomes.

Ma L, Hahn M, Karchner S, Nacci D, Clark B, Apprill A Microbiol Spectr. 2025; 13(3):e0094724.

PMID: 39868785 PMC: 11878049. DOI: 10.1128/spectrum.00947-24.


as a potential drug in the treatment of ulcerative colitis: a comprehensive review of current evidence.

Hu Y, Chen L, Ye Z, Li L, Qian H, Wu M Pharm Biol. 2024; 62(1):818-832.

PMID: 39475104 PMC: 11533244. DOI: 10.1080/13880209.2024.2415652.


Vertical Transfer of Maternal Gut Microbes to Offspring of Western Diet-Fed Dams Drives Reduced Levels of Tryptophan Metabolites and Postnatal Innate Immune Response.

Sugino K, Janssen R, McMahan R, Zimmerman C, Friedman J, Jonscher K Nutrients. 2024; 16(12).

PMID: 38931163 PMC: 11206590. DOI: 10.3390/nu16121808.


Novel Insights into Psychosis and Antipsychotic Interventions: From Managing Symptoms to Improving Outcomes.

Sfera A, Imran H, Sfera D, Anton J, Kozlakidis Z, Hazan S Int J Mol Sci. 2024; 25(11).

PMID: 38892092 PMC: 11173215. DOI: 10.3390/ijms25115904.


Aryl hydrocarbon receptor activity in intestinal epithelial cells in the formation of colonic tertiary lymphoid tissues.

Garcia-Villatoro E, Ufondu A, Callaway E, Allred K, Safe S, Chapkin R Am J Physiol Gastrointest Liver Physiol. 2024; 327(2):G154-G174.

PMID: 38563893 PMC: 11427098. DOI: 10.1152/ajpgi.00274.2023.


References
1.
Canfora E, Jocken J, Blaak E . Short-chain fatty acids in control of body weight and insulin sensitivity. Nat Rev Endocrinol. 2015; 11(10):577-91. DOI: 10.1038/nrendo.2015.128. View

2.
OMahony S, Marchesi J, Scully P, Codling C, Ceolho A, Quigley E . Early life stress alters behavior, immunity, and microbiota in rats: implications for irritable bowel syndrome and psychiatric illnesses. Biol Psychiatry. 2008; 65(3):263-7. DOI: 10.1016/j.biopsych.2008.06.026. View

3.
Reigstad C, Lunden G, Felin J, Backhed F . Regulation of serum amyloid A3 (SAA3) in mouse colonic epithelium and adipose tissue by the intestinal microbiota. PLoS One. 2009; 4(6):e5842. PMC: 2688757. DOI: 10.1371/journal.pone.0005842. View

4.
Monteleone I, Rizzo A, Sarra M, Sica G, Sileri P, Biancone L . Aryl hydrocarbon receptor-induced signals up-regulate IL-22 production and inhibit inflammation in the gastrointestinal tract. Gastroenterology. 2011; 141(1):237-48, 248.e1. DOI: 10.1053/j.gastro.2011.04.007. View

5.
Maurice C, Haiser H, Turnbaugh P . Xenobiotics shape the physiology and gene expression of the active human gut microbiome. Cell. 2013; 152(1-2):39-50. PMC: 3552296. DOI: 10.1016/j.cell.2012.10.052. View