IKKβ regulates antimicrobial innate immune responses in the yellow mealworm, Tenebrio molitor

Dev Comp Immunol. 2023 Oct:147:104761. doi: 10.1016/j.dci.2023.104761. Epub 2023 Jun 16.

Abstract

Toll and IMD pathways regulate antimicrobial innate immune responses in insect model systems. The transcriptional activation of antimicrobial peptides (AMPs) confers humoral immunity in the host against invaded pathogens. The IKK kinase complex (IKKα, IKKβ, and the regulatory subunit IKKγ/NEMO) centrally regulates the NF-κB response to various stimuli. It triggers an appropriate antimicrobial immune response in the host. In this study, a TmIKKβ (or TmIrd5) homolog was screened from the RNA-seq database of the coleopteran beetle, Tenebrio molitor. A single exon characterizes the TmIKKβ gene, and the open reading frame (ORF) comprises of 2112 bp that putatively encodes a polypeptide of 703 amino acid residues. TmIKKβ contains a serine/threonine kinase domain and is phylogenetically close to Tribolium castaneum IKKβ homolog (TcIKKβ). TmIKKβ transcripts were highly expressed in the early pupal (P1) and adult (A5) stages. Among the tissues, TmIKKβ showed higher expression in the integument of the last instar larvae and the fat body and hemocytes of 5-day-old adults. TmIKKβ mRNA was upregulated post-E. coli challenge to the host. Moreover, RNAi-based TmIKKβ mRNA silencing increased host larvae' susceptibility against E. coli, S. aureus and C. albicans. TmIKKβ RNAi in the fat body led to a downregulation in mRNA expression of ten out of fourteen AMP genes, including TmTenecin1, -2, and -4; TmDefensin, and -like; TmColeoptericinA, and -B; and TmAttacin1a, -1b, and -2, suggesting the requirement of the gene in antimicrobial innate immune responses. Further, a decrease in the mRNA expression of NF-κB factors such as TmRelish, TmDorsal1, and TmDorsal2 in the fat body of T. molitor larvae was observed post-microorganisms challenge. Thus, TmIKKβ regulates antimicrobial innate immune responses in T. molitor.

Keywords: Antimicrobial peptides; IKK; Imd pathway; Innate immunity; RNAi; Tenebrio molitor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anti-Infective Agents* / metabolism
  • Escherichia coli
  • I-kappa B Kinase / genetics
  • I-kappa B Kinase / metabolism
  • Immunity, Innate
  • NF-kappa B / metabolism
  • Protein Serine-Threonine Kinases / metabolism
  • RNA, Messenger / metabolism
  • Staphylococcus aureus
  • Tenebrio*

Substances

  • I-kappa B Kinase
  • NF-kappa B
  • Anti-Infective Agents
  • Protein Serine-Threonine Kinases
  • RNA, Messenger