4.7 Article

Dietary vitamin K is remodeled by gut microbiota and influences community composition

Journal

GUT MICROBES
Volume 13, Issue 1, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/19490976.2021.1887721

Keywords

Gut microbiota; micronutrient; vitamin K; menaquinone; stable isotope; metabolism

Funding

  1. USDA Agricultural Research Service [58-1950-7-707]
  2. NIH/NIDDK [T32 DK062032]
  3. Iowa Pork Producers Association/National Pork Board [17-003]
  4. U.S. Defense Healthy Agency Joint Program Committee-5/Military Operational Medicine Research Program [58-8050-9-004]

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The experiment revealed that dietary vitamin K deficiency can alter the gut microbial composition, and further studies are needed to determine if menadione generated by host metabolism serves as an intermediate in dietary vitamin K remodeling in vivo.
Vitamins have well-established roles in bacterial metabolism. Menaquinones (MKn, n = prenyl units in sidechain) are bacterially produced forms of vitamin K produced by the gut microbiota and consumed in the diet. Little is known about the influence of dietary vitamin K quinones on gut microbial composition and MKn production. Here, male and female C57BL6 mice were fed a vitamin K deficient diet or vitamin K sufficient diets containing phylloquinone (PK, plant-based vitamin K form), MK4, and/or MK9. DNA was extracted from cecal contents and 16S sequencing conducted to assess microbial composition. Cecal microbial community composition was significantly different in vitamin K deficient female mice compared to females on vitamin K sufficient diets (all p < .007). Parallel trends were seen in male mice, but were not statistically significant (all p > .05 but <0.1). Next, stable isotope-labeled vitamin K quinones were supplemented to male and female C57BL6 mice ((H7PK)-H-2, (13)C(11)MK4, (2)H(7)MK7, (2)H(7)MK9) and to an in vitro fermentation model inoculated with human stool ((H7PK)-H-2, (2)H(7)MK4, (2)H(7)MK9, or vitamin K precursor H-2(8)-menadione). Vitamin K quinones in feces and culture aliquots were measured using LC-MS. In vivo, supplemented vitamin K quinones were remodeled to other MKn (H-2(7)- or C-13(6)-labeled MK4, MK10, MK11, and MK12), but in vitro only the precursor H-2(8)-menadione was remodeled to (2)H(7)MK4, (2)H(7)MK9, (2)H(7)MK10, and (2)H(7)MK11. These results suggest that dietary vitamin K deficiency alters the gut microbial community composition. Further studies are needed to determine if menadione generated by host metabolism may serve as an intermediate in dietary vitamin K remodeling in vivo.

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