Modification of Cry4Aa toward Improved Toxin Processing in the Gut of the Pea Aphid, Acyrthosiphon pisum

PLoS One. 2016 May 12;11(5):e0155466. doi: 10.1371/journal.pone.0155466. eCollection 2016.

Abstract

Aphids are sap-sucking insects (order: Hemiptera) that cause extensive damage to a wide range of agricultural crops. Our goal was to optimize a naturally occurring insecticidal crystalline (Cry) toxins produced by the soil-dwelling bacterium Bacillus thuringiensis for use against the pea aphid, Acyrthosiphon pisum. On the basis that activation of the Cry4Aa toxin is a rate-limiting factor contributing to the relatively low aphicidal activity of this toxin, we introduced cathepsin L and cathepsin B cleavage sites into Cry4Aa for rapid activation in the aphid gut environment. Incubation of modified Cry4Aa and aphid proteases in vitro demonstrated enhanced processing of the toxin into the active form for some of the modified constructs relative to non-modified Cry4Aa. Aphids fed artificial diet with toxin at a final concentration of 125 μg/ml showed enhanced mortality after two days for one of the four modified constructs. Although only modest toxin improvement was achieved by use of this strategy, such specific toxin modifications designed to overcome factors that limit aphid toxicity could be applied toward managing aphid populations via transgenic plant resistance.

MeSH terms

  • Animals
  • Aphids / drug effects
  • Aphids / metabolism*
  • Bacillus thuringiensis Toxins
  • Bacterial Proteins / toxicity*
  • Cathepsin B / metabolism
  • Cathepsin L / metabolism
  • Endotoxins / toxicity*
  • Gastrointestinal Tract / drug effects
  • Gastrointestinal Tract / metabolism*
  • Hemolysin Proteins / toxicity*
  • Pisum sativum / parasitology*
  • Protein Engineering
  • Protein Processing, Post-Translational* / drug effects
  • Toxicity Tests
  • Trypsin / metabolism

Substances

  • Bacillus thuringiensis Toxins
  • Bacterial Proteins
  • Endotoxins
  • Hemolysin Proteins
  • insecticidal crystal protein, Bacillus Thuringiensis
  • Trypsin
  • Cathepsin B
  • Cathepsin L

Grants and funding

This work was funded by the Iowa Soybean Association (http://www.iasoybeans.com/) to BCB, as well as Hatch Act and State of Iowa funds. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.