The Dipterose of Black Soldier Fly (Hermetia illucens) Induces Innate Immune Response through Toll-Like Receptor Pathway in Mouse Macrophage RAW264.7 Cells

Biomolecules. 2019 Oct 31;9(11):677. doi: 10.3390/biom9110677.

Abstract

In our study, a novel bioactive polysaccharide was identified in the larvae of the black soldier fly (BSF) (Hermetia illucens) as a molecule that activates the mammalian innate immune response. We attempted to isolate this molecule, which was named dipterose-BSF, by gel-filtration and anion-exchange chromatography, followed by nitric oxide (NO) production in mouse RAW264.7 macrophage cells as a marker of immunomodulatory activity. Dipterose-BSF had an average molecular weight of 1.47 × 105 and consisted of ten monosaccharides. Furthermore, in vitro assays demonstrated that dipterose-BSF enhanced the expression of proinflammatory cytokines and interferon β (IFNβ) in RAW264.7 cells. The inhibition of Toll-like receptor 2 (TLR2) and 4 (TLR4) significantly attenuated NO production by dipterose-BSF, indicating that dipterose-BSF stimulates the induction of various cytokines in macrophages via the TLR signaling pathway. This observation was analogous with the activation of nuclear factor kappa B in RAW264.7 cells after exposure to dipterose-BSF. Our results suggest that dipterose-BSF has immunomodulatory potential through activating the host innate immune system, which allows it to be a novel immunomodulator for implementation as a functional food supplement in poultry, livestock, and farmed fish.

Keywords: Toll-like receptor; innate immunity; insect; macrophage; polysaccharide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Immunity, Innate / drug effects*
  • Immunologic Factors / chemistry
  • Immunologic Factors / pharmacology*
  • Larva / chemistry
  • Mice
  • Monosaccharides / analysis
  • Polysaccharides / chemistry
  • Polysaccharides / pharmacology*
  • RAW 264.7 Cells
  • Signal Transduction / drug effects*
  • Simuliidae / chemistry*
  • Toll-Like Receptors / metabolism*

Substances

  • Immunologic Factors
  • Monosaccharides
  • Polysaccharides
  • Toll-Like Receptors