TmToll-7 Plays a Crucial Role in Innate Immune Responses Against Gram-Negative Bacteria by Regulating 5 AMP Genes in Tenebrio molitor

Front Immunol. 2019 Mar 12:10:310. doi: 10.3389/fimmu.2019.00310. eCollection 2019.

Abstract

Although it is known that the Drosophila Toll-7 receptor plays a critical role in antiviral autophagy, its function in other insects has not yet been reported. Here, we have identified a Toll-like receptor 7 gene, TmToll-7, in the coleopteran insect T. molitor and examined its potential role in antibacterial and antifungal immunity. We showed that TmToll-7 expression was significantly induced in larvae 6 h after infection with Escherichia coli and Staphylococcus aureus and 9 h after infection with Candida albicans. However, even though TmToll-7 was induced by all three pathogens, we found that TmToll-7 knockdown significantly reduced larval survival to E. coli, but not to S. aureus, and C. albicans infections. To understand the reasons for this difference, we examined the effects of TmToll-7 knockdown on antimicrobial peptide (AMP) gene expression and found a significant reduction of E. coli-induced expression of AMP genes such as TmTenecin-1, TmDefensin-1, TmDefensin-2, TmColeoptericin-1, and TmAttacin-2. Furthermore, TmToll-7 knockdown larvae infected with E. coli showed significantly higher bacterial growth in the hemolymph compared to control larvae treated with Vermilion dsRNA. Taken together, our results suggest that TmToll-7 plays an important role in regulating the immune response of T. molitor to E. coli.

Keywords: AMP assay; RNAi; Tenebrio molitor; Toll-7; antimicrobial peptides; microbial infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Candida albicans / immunology
  • Escherichia coli / immunology
  • Gene Expression / immunology
  • Gram-Negative Bacteria / immunology*
  • Immunity, Innate / genetics*
  • Immunity, Innate / immunology*
  • Insect Proteins / immunology*
  • Larva / immunology
  • Larva / microbiology
  • Staphylococcus aureus / immunology
  • Tenebrio / immunology*
  • Tenebrio / microbiology*
  • Toll-Like Receptor 7 / genetics
  • Toll-Like Receptor 7 / immunology*

Substances

  • Insect Proteins
  • Toll-Like Receptor 7