Iron supplementation promotes gut microbiota metabolic activity but not colitis markers in human gut microbiota-associated rats

Br J Nutr. 2014 Jun 28;111(12):2135-45. doi: 10.1017/S000711451400021X. Epub 2014 Feb 21.

Abstract

The global prevalence of Fe deficiency is high and a common corrective strategy is oral Fe supplementation, which may affect the commensal gut microbiota and gastrointestinal health. The aim of the present study was to investigate the impact of different dietary Fe concentrations on the gut microbiota and gut health of rats inoculated with human faecal microbiota. Rats (8 weeks old, n 40) were divided into five (n 8 each) groups and fed diets differing only in Fe concentration during an Fe-depletion period (12 weeks) and an Fe-repletion period (4 weeks) as follows: (1) Fe-sufficient diet throughout the study period; (2) Fe-sufficient diet followed by 70 mg Fe/kg diet; (3) Fe-depleted diet throughout the study period; (4) Fe-depleted diet followed by 35 mg Fe/kg diet; (5) Fe-depleted diet followed by 70 mg Fe/kg diet. Faecal and caecal samples were analysed for gut microbiota composition (quantitative PCR and pyrosequencing) and bacterial metabolites (HPLC), and intestinal tissue samples were investigated histologically. Fe depletion did not significantly alter dominant populations of the gut microbiota and did not induce Fe-deficiency anaemia in the studied rats. Provision of the 35 mg Fe/kg diet after feeding an Fe-deficient diet significantly increased the abundance of dominant bacterial groups such as Bacteroides spp. and Clostridium cluster IV members compared with that of an Fe-deficient diet. Fe supplementation increased gut microbial butyrate concentration 6-fold compared with Fe depletion and did not affect histological colitis scores. The present results suggest that Fe supplementation enhances the concentration of beneficial gut microbiota metabolites and thus may contribute to gut health.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteroides / growth & development*
  • Bacteroides / immunology
  • Bacteroides / isolation & purification
  • Bacteroides / metabolism
  • Biomarkers / metabolism
  • Butyric Acid / metabolism
  • Cecum / growth & development
  • Cecum / immunology
  • Cecum / metabolism
  • Cecum / microbiology
  • Child
  • Clostridium / growth & development*
  • Clostridium / immunology
  • Clostridium / isolation & purification
  • Clostridium / metabolism
  • Colitis / immunology
  • Colitis / metabolism
  • Colitis / microbiology
  • Colitis / prevention & control*
  • Colon / growth & development
  • Colon / immunology
  • Colon / metabolism
  • Colon / microbiology*
  • Dietary Supplements* / adverse effects
  • Disease Models, Animal*
  • Feces / chemistry
  • Feces / microbiology
  • Female
  • Germ-Free Life
  • Humans
  • Ileum / growth & development
  • Ileum / immunology
  • Ileum / metabolism
  • Ileum / microbiology
  • Immunity, Mucosal
  • Iron / administration & dosage
  • Iron / analysis
  • Iron Deficiencies
  • Iron, Dietary / adverse effects
  • Iron, Dietary / analysis
  • Iron, Dietary / metabolism
  • Iron, Dietary / therapeutic use*
  • Rats
  • Rats, Inbred F344
  • Weight Gain

Substances

  • Biomarkers
  • Iron, Dietary
  • Butyric Acid
  • Iron