Microbial Transplantation With Human Gut Commensals Containing CutC Is Sufficient to Transmit Enhanced Platelet Reactivity and Thrombosis Potential

Circ Res. 2018 Oct 26;123(10):1164-1176. doi: 10.1161/CIRCRESAHA.118.313142.

Abstract

Rationale: Gut microbes influence cardiovascular disease and thrombosis risks through the production of trimethylamine N-oxide (TMAO). Microbiota-dependent generation of trimethylamine (TMA)-the precursor to TMAO-is rate limiting in the metaorganismal TMAO pathway in most humans and is catalyzed by several distinct microbial choline TMA-lyases, including the proteins encoded by the cutC/D (choline utilization C/D) genes in multiple human commensals.

Objective: Direct demonstration that the gut microbial cutC gene is sufficient to transmit enhanced platelet reactivity and thrombosis potential in a host via TMA/TMAO generation has not yet been reported.

Methods and results: Herein, we use gnotobiotic mice and a series of microbial colonization studies to show that microbial cutC-dependent TMA/TMAO production is sufficient to transmit heightened platelet reactivity and thrombosis potential in a host. Specifically, we examine in vivo thrombosis potential employing germ-free mice colonized with either high TMA-producing stable human fecal polymcrobial communities or a defined CutC-deficient background microbial community coupled with a CutC-expressing human commensal±genetic disruption of its cutC gene (ie, Clostridium sporogenes Δ cutC).

Conclusions: Collectively, these studies point to the microbial choline TMA-lyase pathway as a rational molecular target for the treatment of atherothrombotic heart disease.

Keywords: cardiovascular diseases; gastrointestinal microbiome; humans; metabolism; thrombosis.

Publication types

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

MeSH terms

  • Adult
  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Choline / metabolism
  • Clostridium / enzymology
  • Clostridium / genetics
  • Fecal Microbiota Transplantation*
  • Female
  • Gastrointestinal Microbiome
  • Humans
  • Lyases / genetics
  • Lyases / metabolism*
  • Male
  • Methylamines / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Platelet Activation*
  • Thrombosis / blood
  • Thrombosis / microbiology*

Substances

  • Bacterial Proteins
  • Methylamines
  • Lyases
  • trimethyloxamine
  • trimethylamine
  • Choline