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Using phage display technology to obtain Crybodies active against non-target insects
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668233/ https://www.ncbi.nlm.nih.gov/pubmed/29097681 http://dx.doi.org/10.1038/s41598-017-09384-x |
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author | Domínguez-Flores, Tania Romero-Bosquet, María Dolores Gantiva-Díaz, Diana Marcela Luque-Navas, María José Berry, Colin Osuna, Antonio Vílchez, Susana |
author_facet | Domínguez-Flores, Tania Romero-Bosquet, María Dolores Gantiva-Díaz, Diana Marcela Luque-Navas, María José Berry, Colin Osuna, Antonio Vílchez, Susana |
author_sort | Domínguez-Flores, Tania |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5668233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56682332017-11-08 Using phage display technology to obtain Crybodies active against non-target insects Domínguez-Flores, Tania Romero-Bosquet, María Dolores Gantiva-Díaz, Diana Marcela Luque-Navas, María José Berry, Colin Osuna, Antonio Vílchez, Susana Sci Rep Article 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. Nature Publishing Group UK 2017-11-02 /pmc/articles/PMC5668233/ /pubmed/29097681 http://dx.doi.org/10.1038/s41598-017-09384-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Domínguez-Flores, Tania Romero-Bosquet, María Dolores Gantiva-Díaz, Diana Marcela Luque-Navas, María José Berry, Colin Osuna, Antonio Vílchez, Susana Using phage display technology to obtain Crybodies active against non-target insects |
title | Using phage display technology to obtain Crybodies active against non-target insects |
title_full | Using phage display technology to obtain Crybodies active against non-target insects |
title_fullStr | Using phage display technology to obtain Crybodies active against non-target insects |
title_full_unstemmed | Using phage display technology to obtain Crybodies active against non-target insects |
title_short | Using phage display technology to obtain Crybodies active against non-target insects |
title_sort | using phage display technology to obtain crybodies active against non-target insects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668233/ https://www.ncbi.nlm.nih.gov/pubmed/29097681 http://dx.doi.org/10.1038/s41598-017-09384-x |
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