The effect of combined knockdowns of Attacins on survival and bacterial load in Tenebrio molitor

Front Immunol. 2023 Mar 28:14:1140627. doi: 10.3389/fimmu.2023.1140627. eCollection 2023.

Abstract

Introduction: Upon infection, insect hosts simultaneously express a cocktail of antimicrobial peptides (AMPs) which can impede pathogen colonization and increase host fitness. It has been proposed that such a cocktail might be adaptive if the effects of co-expressed AMPs are greater than the sum of individual activities. This could potentially prevent the evolution of bacterial resistance. However, in vivo studies on AMPs in combination are scarce. Attacins are one of the relatively large AMP families, which show anti-Gram-negative activity in vitro.

Material and methods: Here, we used RNA interference (RNAi) to silence three members of the Attacin family genes in the mealworm beetle, Tenebrio molitor: (TmAttacin1a (TmAtt1a), TmAttacin1b (TmAtt1b), and TmAttacin2 (TmAtt2) both individually and in combination. We then infected T. molitor with the Gram negative entomopathogen Pseudomonas entomophila.

Results: We found that survival of the beetles was only affected by the knockdown of TmAttacin1b, TmAttacin2 and the knockdown of all three Attacins together. Triple knockdown, rather than individual or double knockdowns of AMPs, changes the temporal dynamics of their efficiency in controlling the colonization of P. entomophila in the insect body.

Discussion: More precisely, AMP gene expression influences P. entomophila load early in the infection process, resulting in differences in host survival. Our results highlight the importance of studying AMP-interactions in vivo.

Keywords: Attacin; Pseudomonas entomophila; RNA interference; Tenebrio molitor; antimicrobial peptides (AMPs); host survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / genetics
  • Antimicrobial Peptides
  • Bacterial Load
  • Coleoptera*
  • Tenebrio* / genetics
  • Tenebrio* / microbiology

Substances

  • attacin antibacterial protein, insect
  • Antimicrobial Cationic Peptides
  • Antimicrobial Peptides

Grants and funding

This research was supported by the Rising star junior fellowship awarded by the Department of Biology, Chemistry and Pharmacy at FU Berlin and Alexander von Humboldt Foundation to MK. JR and CZ were funded by Deutsche Forschungsgemeinschaft (DFG) (FOR5026).