Expression of cry2Ah1 and two domain II mutants in transgenic tobacco confers high resistance to susceptible and Cry1Ac-resistant cotton bollworm

Sci Rep. 2018 Jan 11;8(1):508. doi: 10.1038/s41598-017-19064-5.

Abstract

To improve the novel Bacillus thuringiensis insecticidal gene cry2Ah1 toxicity, two mutants cry2Ah1-vp (V354VP) and cry2Ah1-sp (V354SP) were performed. SWISS-MODEL analysis showed two mutants had a longer loop located between β-4 and β-5 of domain II, resulting in higher binding affinity with brush border membrane vesicles (BBMV) of Helicoverpa armigera comparing with Cry2Ah1. The cry2Ah1, cry2Ah1-vp, and cry2Ah1-sp were optimized codon usage according to plant codon bias, and named mcry2Ah1, mcry2Ah1-vp, and mcry2Ah1-sp. They were transformed into tobacco via Agrobacterium-mediated transformation and a total of 4, 8, and 24 transgenic tobacco plants were obtained, respectively. The molecular detection showed the exogenous gene was integrated into tobacco genome, and successfully expressed at the transcript and translation levels. Cry2Ah1 protein in transgenic tobacco plants varied from 4.41 to 40.28 μg g-1 fresh weight. Insect bioassays indicated that all transgenic tobacco plants were highly toxic to both susceptible and Cry1Ac-resistant cotton bollworm larvae, and the insect resistance efficiency to Cry1Ac-resistant cotton bollworm was highest in mcry2Ah1-sp transgenic tobacco plants. The results demonstrated that cry2Ah1 was a useful Bt insecticidal gene to susceptible and Cry1Ac-resistant cotton bollworm and had potential application for insect biocontrol and as a candidate for pyramid strategy in Bt crops.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacillus thuringiensis / genetics
  • Bacillus thuringiensis Toxins
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Bacterial Proteins / pharmacology
  • Cryptochromes / genetics*
  • Cryptochromes / metabolism
  • Endotoxins / pharmacology
  • Extracellular Vesicles / metabolism
  • Hemolysin Proteins / pharmacology
  • Insect Control
  • Insecticide Resistance / genetics*
  • Larva / drug effects
  • Larva / growth & development
  • Moths / drug effects
  • Moths / growth & development*
  • Mutagenesis
  • Nicotiana / metabolism
  • Plants, Genetically Modified / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary
  • Recombinant Proteins / analysis
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / pharmacology

Substances

  • Bacillus thuringiensis Toxins
  • Bacterial Proteins
  • Cryptochromes
  • Endotoxins
  • Hemolysin Proteins
  • Recombinant Proteins
  • insecticidal crystal protein, Bacillus Thuringiensis