Rhodnius prolixus: Identification of missing components of the IMD immune signaling pathway and functional characterization of its role in eliminating bacteria

PLoS One. 2019 Apr 3;14(4):e0214794. doi: 10.1371/journal.pone.0214794. eCollection 2019.

Abstract

The innate immune system in insects is regulated by specific signalling pathways. Most immune related pathways were identified and characterized in holometabolous insects such as Drosophila melanogaster, and it was assumed they would be highly conserved in all insects. The hemimetabolous insect, Rhodnius prolixus, has served as a model to study basic insect physiology, but also is a major vector of the human parasite, Trypanosoma cruzi, that causes 10,000 deaths annually. The publication of the R. prolixus genome revealed that one of the main immune pathways, the Immune-deficiency pathway (IMD), was incomplete and probably non-functional, an observation shared with other hemimetabolous insects including the pea aphid (Acyrthosiphon pisum) and the bedbug (Cimex lectularius). It was proposed that the IMD pathway is inactive in R. prolixus as an adaptation to prevent eliminating beneficial symbiont gut bacteria. We used bioinformatic analyses based on reciprocal BLAST and HMM-profile searches to find orthologs for most of the "missing" elements of the IMD pathway and provide data that these are regulated in response to infection with Gram-negative bacteria. We used RNAi strategies to demonstrate the role of the IMD pathway in regulating the expression of specific antimicrobial peptides (AMPs) in the fat body of R. prolixus. The data indicate that the IMD pathway is present and active in R. prolixus, which opens up new avenues of research on R. prolixus-T. cruzi interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / immunology
  • Genome, Insect
  • Gram-Negative Bacteria
  • Host-Parasite Interactions
  • Immunity, Innate*
  • Insect Vectors
  • Muramidase / immunology*
  • Rhodnius / genetics
  • Rhodnius / immunology*
  • Rhodnius / microbiology*
  • Rhodnius / parasitology
  • Signal Transduction* / immunology
  • Trypanosoma cruzi

Substances

  • Antimicrobial Cationic Peptides
  • Muramidase

Grants and funding

This work was supported by NSERC Discovery grant to CL (RGPIN261940), www.nserc-crsng.gc.ca; MITACS Globalink Research Award to NSP (IT08650), https://www.mitacs.ca/en/programs/globalink/globalink-research-award. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.