Larval midgut modifications associated with Bti resistance in the yellow fever mosquito using proteomic and transcriptomic approaches

BMC Genomics. 2012 Jun 15:13:248. doi: 10.1186/1471-2164-13-248.

Abstract

Background: Bacillus thuringiensis var. israelensis (Bti) is a natural larval mosquito pathogen producing pore-forming toxins targeting the midgut of Diptera larvae. It is used worldwide for mosquito control. Resistance mechanisms of an Aedes aegypti laboratory strain selected for 30 generations with field-collected leaf litter containing Bti toxins were investigated in larval midguts at two levels: 1. gene transcription using DNA microarray and RT-qPCR and 2. differential expression of brush border membrane proteins using DIGE (Differential In Gel Electrophoresis).

Results: Several Bti Cry toxin receptors including alkaline phosphatases and N-aminopeptidases and toxin-binding V-ATPases exhibited altered expression levels in the resistant strain. The under-expression of putative Bti-receptors is consistent with Bt-resistance mechanisms previously described in Lepidoptera. Four soluble metalloproteinases were found under-transcribed together with a drastic decrease of metalloproteinases activity in the resistant strain, suggesting a role in resistance by decreasing the amount of activated Cry toxins in the larval midgut.

Conclusions: By combining transcriptomic and proteomic approaches, we detected expression changes at nearly each step of the ingestion-to-infection process, providing a short list of genes and proteins potentially involved in Bti-resistance whose implication needs to be validated. Collectively, these results open the way to further functional analyses to better characterize Bti-resistance mechanisms in mosquitoes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism
  • Aminopeptidases / genetics
  • Aminopeptidases / metabolism
  • Animals
  • Bacillus thuringiensis / metabolism*
  • Bacillus thuringiensis / pathogenicity*
  • Culicidae / genetics
  • Culicidae / metabolism*
  • Culicidae / microbiology*
  • Larva / genetics
  • Larva / metabolism*
  • Larva / microbiology*
  • Oligonucleotide Array Sequence Analysis
  • Proteomics / methods*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcriptome / genetics*
  • Vacuolar Proton-Translocating ATPases / genetics
  • Vacuolar Proton-Translocating ATPases / metabolism
  • Yellow Fever / transmission*

Substances

  • Alkaline Phosphatase
  • Aminopeptidases
  • Vacuolar Proton-Translocating ATPases