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Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera

Insect resistance to Bacillus thuringiensis (Bt) insecticidal proteins has rapidly evolved with the expansion of the planting area of transgenic Bt crops. Pyramiding RNA interference (RNAi) and Bt in crops is urgently needed to counter the rapid increase in pest resistance. The ideal “pyramid” strat...

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Autores principales: Wei, Jizhen, Yao, Xue, Yang, Shuo, Liu, Shaokai, Zhou, Shuai, Cen, Junjuan, Liu, Xiaoguang, Du, Mengfang, Tang, Qingbo, An, Shiheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904703/
https://www.ncbi.nlm.nih.gov/pubmed/33643268
http://dx.doi.org/10.3389/fmicb.2021.634619
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author Wei, Jizhen
Yao, Xue
Yang, Shuo
Liu, Shaokai
Zhou, Shuai
Cen, Junjuan
Liu, Xiaoguang
Du, Mengfang
Tang, Qingbo
An, Shiheng
author_facet Wei, Jizhen
Yao, Xue
Yang, Shuo
Liu, Shaokai
Zhou, Shuai
Cen, Junjuan
Liu, Xiaoguang
Du, Mengfang
Tang, Qingbo
An, Shiheng
author_sort Wei, Jizhen
collection PubMed
description Insect resistance to Bacillus thuringiensis (Bt) insecticidal proteins has rapidly evolved with the expansion of the planting area of transgenic Bt crops. Pyramiding RNA interference (RNAi) and Bt in crops is urgently needed to counter the rapid increase in pest resistance. The ideal “pyramid” strategy simultaneously targets different action pathways that exert synergetic effects on each other. Here, we identified a dephosphatase, namely, Helicoverpa armigera calcineurin (HaCAN), which might enhance the insecticidal activity of Cry1Ac against Helicoverpa armigera by regulating immune gene expression via dephosphatase activity, but not by acting as a receptor. Notably, blocking enzyme activity or knocking down endogenous HaCAN significantly promoted the enhancement in Cry1Ac toxicity to insect larvae and cells. Correspondingly, the increase in HaCAN activity reduced the cytotoxicity of Cry1Ac as shown by the heterologous expression of HaCAN. Our results provide a probable that HaCAN is an important candidate gene for pyramiding RNAi and Cry1Ac crops to control cotton bollworm.
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spelling pubmed-79047032021-02-26 Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera Wei, Jizhen Yao, Xue Yang, Shuo Liu, Shaokai Zhou, Shuai Cen, Junjuan Liu, Xiaoguang Du, Mengfang Tang, Qingbo An, Shiheng Front Microbiol Microbiology Insect resistance to Bacillus thuringiensis (Bt) insecticidal proteins has rapidly evolved with the expansion of the planting area of transgenic Bt crops. Pyramiding RNA interference (RNAi) and Bt in crops is urgently needed to counter the rapid increase in pest resistance. The ideal “pyramid” strategy simultaneously targets different action pathways that exert synergetic effects on each other. Here, we identified a dephosphatase, namely, Helicoverpa armigera calcineurin (HaCAN), which might enhance the insecticidal activity of Cry1Ac against Helicoverpa armigera by regulating immune gene expression via dephosphatase activity, but not by acting as a receptor. Notably, blocking enzyme activity or knocking down endogenous HaCAN significantly promoted the enhancement in Cry1Ac toxicity to insect larvae and cells. Correspondingly, the increase in HaCAN activity reduced the cytotoxicity of Cry1Ac as shown by the heterologous expression of HaCAN. Our results provide a probable that HaCAN is an important candidate gene for pyramiding RNAi and Cry1Ac crops to control cotton bollworm. Frontiers Media S.A. 2021-02-11 /pmc/articles/PMC7904703/ /pubmed/33643268 http://dx.doi.org/10.3389/fmicb.2021.634619 Text en Copyright © 2021 Wei, Yao, Yang, Liu, Zhou, Cen, Liu, Du, Tang and An. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wei, Jizhen
Yao, Xue
Yang, Shuo
Liu, Shaokai
Zhou, Shuai
Cen, Junjuan
Liu, Xiaoguang
Du, Mengfang
Tang, Qingbo
An, Shiheng
Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera
title Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera
title_full Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera
title_fullStr Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera
title_full_unstemmed Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera
title_short Suppression of Calcineurin Enhances the Toxicity of Cry1Ac to Helicoverpa armigera
title_sort suppression of calcineurin enhances the toxicity of cry1ac to helicoverpa armigera
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904703/
https://www.ncbi.nlm.nih.gov/pubmed/33643268
http://dx.doi.org/10.3389/fmicb.2021.634619
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