Abstract

The insecticidal Cry toxins produced by Bacillus thuringiensis (Bt) are increasingly important in the biological control of insect pests and vectors of human disease. Markets for Bt products and transgenic plants expressing their toxins are driven by their specificity, safety and the move away from chemical control agents. However, the high specificity of Cry toxins can also prove to be a limitation when there is no known Cry toxin active against a particular target. Novel activities can be discovered by screening natural Bt isolates or through modifications of the Cry proteins. Here we demonstrate the use of λ-phage displaying Cry1Aa13 toxin variants modified in domain II loop 2 (Crybodies) to select retargeted toxins. Through biopanning using gut tissue from larvae of the non-target insect Aedes aegypti, we isolated a number of phage for further testing. Two of the overexpressed Cry toxin variants showed significant activity against A. aegypti larvae while another induced mortality at the pupal stage. We present the first report of the use of phage display to identify novel activities toward insects from distant taxonomic Orders and establish this technology based on the use of Crybodies as a powerful tool for developing tailor-made insecticides against new target insects.

Highlights

  • Bacillus thuringiensis (Bt), is characterized by its ability to produce proteins with insecticidal activity

  • A series of biopanning experiments was performed in order to select and enrich those phage from the library with enhanced affinity to targets present in the A. aegypti guts compared to the wild-type toxin

  • The pool of the phage obtained was considered as the sub-library 1. These phage were amplified and used for a new round of selection using fresh A. aegypti guts and this procedure was used in two further steps, each using the enriched phage from the previous round

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Summary

Introduction

Bacillus thuringiensis (Bt), is characterized by its ability to produce proteins with insecticidal activity. 302 holotypes of Cry toxins are described (http://www.btnomenclature.info/) as a result of a huge international effort to isolate and characterize novel Bt strains Each of these toxins is reported to be active against a limited number of targets (mostly insects and nematodes, molluscs and, in a few cases, human cancer cells9) and this specificity is one of the most remarkable characteristics of Cry toxins. These loops differ in sequence and conformation, and in length This variability, together with domain II’s similarity to the complementarity-determining region of immunoglobulins[15] led researchers to associate this domain with the role of receptor binding and with specificity. Binding to the receptor is not the only requirement for toxicity, it is an essential requirement and it seems that natural evolution of Cry toxins has adapted them to recognize different proteins as receptors to be used in their mechanism of action

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