Emerging role of D-Amino acid metabolism in the innate defense

Jumpei Sasabe, Masataka Suzuki

Research output: Contribution to journalShort survey

11 Citations (Scopus)

Abstract

Mammalian innate and adaptive immune systems use the pattern recognition receptors, such as toll-like receptors, to detect conserved bacterial and viral components. Bacteria synthesize diverse D-amino acids while eukaryotes and archaea generally produce two D-amino acids, raising the possibility that many of bacterial D-amino acids are bacteria-specific metabolites. Although D-amino acids have not been identified to bind to any known pattern recognition receptors, D-amino acids are enantioselectively recognized by some other receptors and enzymes including a flavoenzyme D-amino acid oxidase (DAO) in mammals. At host-microbe interfaces in the neutrophils and intestinal mucosa, DAO catalyzes oxidation of bacterial D-amino acids, such as D-alanine, and generates H2O2, which is linked to antimicrobial activity. Intestinal DAO also modifies the composition of microbiota through modulation of growth for some bacteria that are dependent on host nutrition. Furthermore, regulation and recognition of D-amino acids in mammals have additional meanings at various host-microbe interfaces; D-phenylalanine and D-tryptophan regulate chemotaxis of neutrophils through a G-coupled protein receptor, D-serine has a bacteriostatic role in the urinary tract, D-phenylalanine and D-leucine inhibit innate immunity through the sweet taste receptor in the upper airway, and D-tryptophan modulates immune tolerance in the lower airway. This mini-review highlights recent evidence supporting the hypothesis that D-amino acids are utilized as inter-kingdom communication at host-microbe interface to modulate bacterial colonization and host defense.

Original languageEnglish
Article number933
JournalFrontiers in Microbiology
Volume9
Issue numberMAY
DOIs
Publication statusPublished - 2018 May 9

Keywords

  • D-amino acid
  • D-amino acid oxidase
  • Host-microbe interaction
  • Hydrogen peroxide
  • Innate immunity
  • Mucosal immunity
  • Neutrophil
  • Small intestine

ASJC Scopus subject areas

  • Microbiology
  • Microbiology (medical)

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