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A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s

The adaptation of herbivorous insects to their host plants is hypothesized to be intimately associated with their ubiquitous development of resistance to synthetic pesticides. However, not much is known about the mechanisms underlying the relationship between detoxification of plant toxins and synth...

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Autores principales: Zhu, Fang, Moural, Timothy W., Nelson, David R., Palli, Subba R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748221/
https://www.ncbi.nlm.nih.gov/pubmed/26861263
http://dx.doi.org/10.1038/srep20421
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author Zhu, Fang
Moural, Timothy W.
Nelson, David R.
Palli, Subba R.
author_facet Zhu, Fang
Moural, Timothy W.
Nelson, David R.
Palli, Subba R.
author_sort Zhu, Fang
collection PubMed
description The adaptation of herbivorous insects to their host plants is hypothesized to be intimately associated with their ubiquitous development of resistance to synthetic pesticides. However, not much is known about the mechanisms underlying the relationship between detoxification of plant toxins and synthetic pesticides. To address this knowledge gap, we used specialist pest Colorado potato beetle (CPB) and its host plant, potato, as a model system. Next-generation sequencing (454 pyrosequencing) was performed to reveal the CPB transcriptome. Differential expression patterns of cytochrome P450 complement (CYPome) were analyzed between the susceptible (S) and imidacloprid resistant (R) beetles. We also evaluated the global transcriptome repertoire of CPB CYPome in response to the challenge by potato leaf allelochemicals and imidacloprid. The results showed that more than half (51.2%) of the CBP cytochrome P450 monooxygenases (P450s) that are up-regulated in the R strain are also induced by both host plant toxins and pesticide in a tissue-specific manner. These data suggest that xenobiotic adaptation in this specialist herbivore is through up-regulation of multiple P450s that are potentially involved in detoxifying both pesticide and plant allelochemicals.
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spelling pubmed-47482212016-02-17 A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s Zhu, Fang Moural, Timothy W. Nelson, David R. Palli, Subba R. Sci Rep Article The adaptation of herbivorous insects to their host plants is hypothesized to be intimately associated with their ubiquitous development of resistance to synthetic pesticides. However, not much is known about the mechanisms underlying the relationship between detoxification of plant toxins and synthetic pesticides. To address this knowledge gap, we used specialist pest Colorado potato beetle (CPB) and its host plant, potato, as a model system. Next-generation sequencing (454 pyrosequencing) was performed to reveal the CPB transcriptome. Differential expression patterns of cytochrome P450 complement (CYPome) were analyzed between the susceptible (S) and imidacloprid resistant (R) beetles. We also evaluated the global transcriptome repertoire of CPB CYPome in response to the challenge by potato leaf allelochemicals and imidacloprid. The results showed that more than half (51.2%) of the CBP cytochrome P450 monooxygenases (P450s) that are up-regulated in the R strain are also induced by both host plant toxins and pesticide in a tissue-specific manner. These data suggest that xenobiotic adaptation in this specialist herbivore is through up-regulation of multiple P450s that are potentially involved in detoxifying both pesticide and plant allelochemicals. Nature Publishing Group 2016-02-10 /pmc/articles/PMC4748221/ /pubmed/26861263 http://dx.doi.org/10.1038/srep20421 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhu, Fang
Moural, Timothy W.
Nelson, David R.
Palli, Subba R.
A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s
title A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s
title_full A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s
title_fullStr A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s
title_full_unstemmed A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s
title_short A specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple Cytochrome P450s
title_sort specialist herbivore pest adaptation to xenobiotics through up-regulation of multiple cytochrome p450s
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748221/
https://www.ncbi.nlm.nih.gov/pubmed/26861263
http://dx.doi.org/10.1038/srep20421
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