Diversification of host bile acids by members of the gut microbiota

Gut Microbes. 2020;11(2):158-171. doi: 10.1080/19490976.2019.1674124. Epub 2019 Oct 9.

Abstract

Bile acid biotransformation is a collaborative effort by the host and the gut microbiome. Host hepatocytes synthesize primary bile acids from cholesterol. Once these host-derived primary bile acids enter the gastrointestinal tract, the gut microbiota chemically modify them into secondary bile acids. Interest into the gut-bile acid-host axis is expanding in diverse fields including gastroenterology, endocrinology, oncology, and infectious disease. This review aims to 1) describe the physiologic aspects of collaborative bile acid metabolism by the host and gut microbiota; 2) to evaluate how gut microbes influence bile acid pools, and in turn how bile acid pools modulate the gut microbial community structure; 3) to compare species differences in bile acid pools; and lastly, 4) discuss the effects of ursodeoxycholic acid (UDCA) administration, a common therapeutic bile acid, on the gut microbiota-bile acid-host axis.

Keywords: C. difficile; FXR; bile acids; gut microbiota; ursodeoxycholic acid (UDCA).

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Bacteria / metabolism*
  • Bile Acids and Salts* / biosynthesis
  • Bile Acids and Salts* / metabolism
  • Cholesterol / metabolism
  • Clostridioides difficile / pathogenicity
  • Gastrointestinal Microbiome* / drug effects
  • Gastrointestinal Microbiome* / physiology
  • Hepatocytes / metabolism
  • Humans
  • Lipid Metabolism
  • Microbiota / drug effects
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Ursodeoxycholic Acid / pharmacology

Substances

  • Bile Acids and Salts
  • Receptors, Cytoplasmic and Nuclear
  • farnesoid X-activated receptor
  • Ursodeoxycholic Acid
  • Cholesterol