Two-carbon folate cycle of commensal Lactobacillus reuteri 6475 gives rise to immunomodulatory ethionine, a source for histone ethylation

FASEB J. 2019 Mar;33(3):3536-3548. doi: 10.1096/fj.201801848R. Epub 2018 Nov 19.

Abstract

Colonization of the gut by certain probiotic Lactobacillus reuteri strains has been associated with reduced risk of inflammatory diseases and colorectal cancer. Previous studies pointed to a functional link between immunomodulation, histamine production, and folate metabolism, the central 1-carbon pathway for the transfer of methyl groups. Using mass spectrometry and NMR spectroscopy, we analyzed folate metabolites of L. reuteri strain 6475 and discovered that the bacterium produces a 2-carbon-transporting folate in the form of 5,10-ethenyl-tetrahydrofolyl polyglutamate. Isotopic labeling permitted us to trace the source of the 2-carbon unit back to acetate of the culture medium. We show that the 2C folate cycle of L. reuteri is capable of transferring 2 carbon atoms to homocysteine to generate the unconventional amino acid ethionine, a known immunomodulator. When we treated monocytic THP-1 cells with ethionine, their transcription of TNF-α was inhibited and cell proliferation reduced. Mass spectrometry of THP-1 histones revealed incorporation of ethionine instead of methionine into proteins, a reduction of histone-methylation, and ethylation of histone lysine residues. Our findings suggest that the microbiome can expose the host to ethionine through a novel 2-carbon transporting variant of the folate cycle and modify human chromatin via ethylation.-Röth, D., Chiang, A. J., Hu, W., Gugiu, G. B., Morra, C. N., Versalovic, J., Kalkum, M. The two-carbon folate cycle of commensal Lactobacillus reuteri 6475 gives rise to immunomodulatory ethionine, a source for histone ethylation.

Keywords: ethenyltetrahydrofolate; lysine ethylation; microbiome; posttranslational modification; probiotic bacteria.

Publication types

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

MeSH terms

  • Amino Acids / metabolism
  • Carbon / metabolism*
  • Cell Proliferation / physiology
  • Cells, Cultured
  • Culture Media / metabolism
  • Ethionine / metabolism*
  • Folic Acid / metabolism*
  • Histones / metabolism*
  • Homocysteine / metabolism
  • Humans
  • Immunomodulation / physiology*
  • Limosilactobacillus reuteri / metabolism*
  • Methionine / metabolism
  • Methylation
  • Microbiota / physiology
  • Probiotics / metabolism
  • THP-1 Cells / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Amino Acids
  • Culture Media
  • Histones
  • Tumor Necrosis Factor-alpha
  • Homocysteine
  • Carbon
  • Folic Acid
  • Methionine
  • Ethionine