Biosurfactants Induce Antimicrobial Peptide Production through the Activation of Tm Spatzles in Tenebrio molitor

Int J Mol Sci. 2020 Aug 24;21(17):6090. doi: 10.3390/ijms21176090.

Abstract

Biosurfactant immunomodulatory activities in mammals, nematodes, and plants have been investigated. However, the immune activation property of biosurfactants in insects has not been reported. Therefore, here, we studied the defense response triggered by lipopeptides (fengycin and iturin A), glycolipids (rhamnolipid), and cyclic polypeptides (bacitracin) in the coleopteran insect, mealworm Tenebrio molitor. The in vitro antimicrobial activities against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria and fungi (Candida albicans) were assessed by mixing these pathogens with the hemolymph of biosurfactant-immune-activated larvae. E. coli growth was remarkably inhibited by this hemolymph. The antimicrobial peptide (AMP) induction results also revealed that all biosurfactants tested induced several AMPs, exclusively in hemocytes. The survivability analysis of T. molitor larvae challenged by E. coli (106 CFU/µL) at 24 h post biosurfactant-immune activation showed that fengycin, iturin A, and rhamnopid significantly increased survivability against E. coli. Biosurfactant-induced TmSpatzles activation was also monitored, and the results showed that TmSpz3 and TmSpz-like were upregulated in the hemocytes of iturin A-injected larvae, while TmSpz4 and TmSpz6 were upregulated in the fat bodies of the fengycin-, iturin A-, and rhamnolipid-injected larvae. Overall, these results suggest that lipopeptide and glycolipid biosurfactants induce the expression of AMPs in T. molitor via the activation of spätzle genes, thereby increasing the survivability of T. molitor against E. coli.

Keywords: TmSpatzle; antimicrobial peptides; biosurfactants; glycolipids; immunity; lipopeptides; mealworm.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Antimicrobial Cationic Peptides / metabolism*
  • Gene Expression Regulation / drug effects
  • Gene Silencing / physiology
  • Genes, Insect
  • Hemocytes / metabolism
  • Immunity, Innate / drug effects
  • Immunity, Innate / genetics
  • Insect Proteins / genetics*
  • Insect Proteins / metabolism
  • Surface-Active Agents / pharmacology*
  • Tenebrio* / genetics
  • Tenebrio* / immunology
  • Tenebrio* / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Insect Proteins
  • Surface-Active Agents