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The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host

Host-pathogen interactions are central components of ecological networks where the MAPK signaling pathways act as central hubs of these complex interactions. We have previously shown that an insect hormone modulated MAPK signaling cascade participates as a general switch to trans-regulate differenti...

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Autores principales: Guo, Zhaojiang, Kang, Shi, Wu, Qingjun, Wang, Shaoli, Crickmore, Neil, Zhou, Xuguo, Bravo, Alejandra, Soberón, Mario, Zhang, Youjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452011/
https://www.ncbi.nlm.nih.gov/pubmed/34495986
http://dx.doi.org/10.1371/journal.ppat.1009917
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author Guo, Zhaojiang
Kang, Shi
Wu, Qingjun
Wang, Shaoli
Crickmore, Neil
Zhou, Xuguo
Bravo, Alejandra
Soberón, Mario
Zhang, Youjun
author_facet Guo, Zhaojiang
Kang, Shi
Wu, Qingjun
Wang, Shaoli
Crickmore, Neil
Zhou, Xuguo
Bravo, Alejandra
Soberón, Mario
Zhang, Youjun
author_sort Guo, Zhaojiang
collection PubMed
description Host-pathogen interactions are central components of ecological networks where the MAPK signaling pathways act as central hubs of these complex interactions. We have previously shown that an insect hormone modulated MAPK signaling cascade participates as a general switch to trans-regulate differential expression of diverse midgut genes in the diamondback moth, Plutella xylostella (L.) to cope with the insecticidal action of Cry1Ac toxin, produced by the entomopathogenic bacterium Bacillus thuringiensis (Bt). The relationship between topology and functions of this four-tiered phosphorylation signaling cascade, however, is an uncharted territory. Here, we carried out a genome-wide characterization of all the MAPK orthologs in P. xylostella to define their phylogenetic relationships and to confirm their evolutionary conserved modules. Results from quantitative phosphoproteomic analyses, combined with functional validations studies using specific inhibitors and dsRNAs lead us to establish a MAPK “road map”, where p38 and ERK MAPK signaling pathways, in large part, mount a resistance response against Bt toxins through regulating the differential expression of multiple Cry toxin receptors and their non-receptor paralogs in P. xylostella midgut. These data not only advance our understanding of host-pathogen interactions in agricultural pests, but also inform the future development of biopesticides that could suppress Cry resistance phenotypes.
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spelling pubmed-84520112021-09-21 The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host Guo, Zhaojiang Kang, Shi Wu, Qingjun Wang, Shaoli Crickmore, Neil Zhou, Xuguo Bravo, Alejandra Soberón, Mario Zhang, Youjun PLoS Pathog Research Article Host-pathogen interactions are central components of ecological networks where the MAPK signaling pathways act as central hubs of these complex interactions. We have previously shown that an insect hormone modulated MAPK signaling cascade participates as a general switch to trans-regulate differential expression of diverse midgut genes in the diamondback moth, Plutella xylostella (L.) to cope with the insecticidal action of Cry1Ac toxin, produced by the entomopathogenic bacterium Bacillus thuringiensis (Bt). The relationship between topology and functions of this four-tiered phosphorylation signaling cascade, however, is an uncharted territory. Here, we carried out a genome-wide characterization of all the MAPK orthologs in P. xylostella to define their phylogenetic relationships and to confirm their evolutionary conserved modules. Results from quantitative phosphoproteomic analyses, combined with functional validations studies using specific inhibitors and dsRNAs lead us to establish a MAPK “road map”, where p38 and ERK MAPK signaling pathways, in large part, mount a resistance response against Bt toxins through regulating the differential expression of multiple Cry toxin receptors and their non-receptor paralogs in P. xylostella midgut. These data not only advance our understanding of host-pathogen interactions in agricultural pests, but also inform the future development of biopesticides that could suppress Cry resistance phenotypes. Public Library of Science 2021-09-08 /pmc/articles/PMC8452011/ /pubmed/34495986 http://dx.doi.org/10.1371/journal.ppat.1009917 Text en © 2021 Guo et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Guo, Zhaojiang
Kang, Shi
Wu, Qingjun
Wang, Shaoli
Crickmore, Neil
Zhou, Xuguo
Bravo, Alejandra
Soberón, Mario
Zhang, Youjun
The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host
title The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host
title_full The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host
title_fullStr The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host
title_full_unstemmed The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host
title_short The regulation landscape of MAPK signaling cascade for thwarting Bacillus thuringiensis infection in an insect host
title_sort regulation landscape of mapk signaling cascade for thwarting bacillus thuringiensis infection in an insect host
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452011/
https://www.ncbi.nlm.nih.gov/pubmed/34495986
http://dx.doi.org/10.1371/journal.ppat.1009917
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