Proteome response of Tribolium castaneum larvae to Bacillus thuringiensis toxin producing strains

PLoS One. 2013;8(1):e55330. doi: 10.1371/journal.pone.0055330. Epub 2013 Jan 25.

Abstract

Susceptibility of Tribolium castaneum (Tc) larvae was determined against spore-crystal mixtures of five coleopteran specific and one lepidopteran specific Bacillus thuringiensis Cry toxin producing strains and those containing the structurally unrelated Cry3Ba and Cry23Aa/Cry37Aa proteins were found toxic (LC(50) values 13.53 and 6.30 µg spore-crystal mixture/µL flour disc, respectively). Using iTRAQ combined with LC-MS/MS allowed the discovery of seven novel differentially expressed proteins in early response of Tc larvae to the two active spore-crystal mixtures. Proteins showing a statistically significant change in treated larvae compared to non-intoxicated larvae fell into two major categories; up-regulated proteins were involved in host defense (odorant binding protein C12, apolipophorin-III and chemosensory protein 18) and down-regulated proteins were linked to metabolic pathways affecting larval metabolism and development (pyruvate dehydrogenase Eα subunit, cuticular protein, ribosomal protein L13a and apolipoprotein LI-II). Among increased proteins, Odorant binding protein C12 showed the highest change, 4-fold increase in both toxin treatments. The protein displayed amino acid sequence and structural homology to Tenebrio molitor 12 kDa hemolymph protein b precursor, a non-olfactory odorant binding protein. Analysis of mRNA expression and mortality assays in Odorant binding protein C12 silenced larvae were consistent with a general immune defense function of non-olfactory odorant binding proteins. Regarding down-regulated proteins, at the transcriptional level, pyruvate dehydrogenase and cuticular genes were decreased in Tc larvae exposed to the Cry3Ba producing strain compared to the Cry23Aa/Cry37Aa producing strain, which may contribute to the developmental arrest that we observed with larvae fed the Cry3Ba producing strain. Results demonstrated a distinct host transcriptional regulation depending upon the Cry toxin treatment. Knowledge on how insects respond to Bt intoxication will allow designing more effective management strategies for pest control.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bacillus thuringiensis / metabolism*
  • Bacterial Proteins / metabolism
  • Bacterial Proteins / toxicity
  • Bacterial Toxins / biosynthesis*
  • Bacterial Toxins / toxicity
  • Host-Pathogen Interactions
  • Insect Proteins / chemistry
  • Insect Proteins / classification
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Larva
  • Models, Molecular
  • Molecular Sequence Data
  • Phylogeny
  • Protein Conformation
  • Proteome*
  • Proteomics
  • Receptors, Odorant / chemistry
  • Receptors, Odorant / classification
  • Receptors, Odorant / genetics
  • Receptors, Odorant / metabolism
  • Sequence Alignment
  • Transcription, Genetic
  • Tribolium / drug effects
  • Tribolium / metabolism*
  • Tribolium / microbiology*

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • Insect Proteins
  • Proteome
  • Receptors, Odorant
  • odorant-binding protein

Grants and funding

This work was supported by “Ministerio de Ciencia e Innovación” (BIO 2007-67860, AGL2010-22300-C03-03) and E. Contreras was awarded with a grant from the Conselleria Valenciana d'Educació i Ciència. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.