Cargando…

A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics

The study of insect adaptation to the defensive metabolites of host plants and various kinds of insecticides in order to acquire resistance is a hot topic in the pest-control field, but the mechanism is still unclear. In our study, we found that a general signal pathway exists in H. armigera which c...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lei, Lv, Shenglan, Li, Mingjian, Gu, Meng, Gao, Xiwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788003/
https://www.ncbi.nlm.nih.gov/pubmed/36555764
http://dx.doi.org/10.3390/ijms232416126
_version_ 1784858648927797248
author Zhang, Lei
Lv, Shenglan
Li, Mingjian
Gu, Meng
Gao, Xiwu
author_facet Zhang, Lei
Lv, Shenglan
Li, Mingjian
Gu, Meng
Gao, Xiwu
author_sort Zhang, Lei
collection PubMed
description The study of insect adaptation to the defensive metabolites of host plants and various kinds of insecticides in order to acquire resistance is a hot topic in the pest-control field, but the mechanism is still unclear. In our study, we found that a general signal pathway exists in H. armigera which can regulate multiple P450s, GSTs and UGTs genes to help insects decrease their susceptibility to xenobiotics. Knockdown of HaNrf2 and HaAhR expression could significantly increase the toxicity of xenobiotics to H. armigera, and simultaneously decrease the gene expression of P450s, GSTs and UGTs which are related to the xenobiotic metabolism and synthesis of insect hormone pathways. Then, we used EMSA and dual luciferase assay to verify that a crosstalk exists between AhR and Nrf2 to regulate multiple P450s, GSTs and UGTs genes to mediate H. armigera susceptibility to plant allelochemicals and insecticides. The detoxification genes’ expression network which can be regulated by Nrf2 and AhR is still unknown, and there were also no reports about the crosstalk between AhR and Nrf2 that exist in insects and can regulate multiple detoxification genes’ expression. Our results provide a new general signaling pathway to reveal the adaptive mechanism of insects to xenobiotics and provides further insight into designing effective pest-management strategies to avoid the overuse of insecticides.
format Online
Article
Text
id pubmed-9788003
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97880032022-12-24 A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics Zhang, Lei Lv, Shenglan Li, Mingjian Gu, Meng Gao, Xiwu Int J Mol Sci Article The study of insect adaptation to the defensive metabolites of host plants and various kinds of insecticides in order to acquire resistance is a hot topic in the pest-control field, but the mechanism is still unclear. In our study, we found that a general signal pathway exists in H. armigera which can regulate multiple P450s, GSTs and UGTs genes to help insects decrease their susceptibility to xenobiotics. Knockdown of HaNrf2 and HaAhR expression could significantly increase the toxicity of xenobiotics to H. armigera, and simultaneously decrease the gene expression of P450s, GSTs and UGTs which are related to the xenobiotic metabolism and synthesis of insect hormone pathways. Then, we used EMSA and dual luciferase assay to verify that a crosstalk exists between AhR and Nrf2 to regulate multiple P450s, GSTs and UGTs genes to mediate H. armigera susceptibility to plant allelochemicals and insecticides. The detoxification genes’ expression network which can be regulated by Nrf2 and AhR is still unknown, and there were also no reports about the crosstalk between AhR and Nrf2 that exist in insects and can regulate multiple detoxification genes’ expression. Our results provide a new general signaling pathway to reveal the adaptive mechanism of insects to xenobiotics and provides further insight into designing effective pest-management strategies to avoid the overuse of insecticides. MDPI 2022-12-17 /pmc/articles/PMC9788003/ /pubmed/36555764 http://dx.doi.org/10.3390/ijms232416126 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Lei
Lv, Shenglan
Li, Mingjian
Gu, Meng
Gao, Xiwu
A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics
title A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics
title_full A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics
title_fullStr A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics
title_full_unstemmed A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics
title_short A General Signal Pathway to Regulate Multiple Detoxification Genes Drives the Evolution of Helicoverpa armigera Adaptation to Xenobiotics
title_sort general signal pathway to regulate multiple detoxification genes drives the evolution of helicoverpa armigera adaptation to xenobiotics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788003/
https://www.ncbi.nlm.nih.gov/pubmed/36555764
http://dx.doi.org/10.3390/ijms232416126
work_keys_str_mv AT zhanglei ageneralsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT lvshenglan ageneralsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT limingjian ageneralsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT gumeng ageneralsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT gaoxiwu ageneralsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT zhanglei generalsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT lvshenglan generalsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT limingjian generalsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT gumeng generalsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics
AT gaoxiwu generalsignalpathwaytoregulatemultipledetoxificationgenesdrivestheevolutionofhelicoverpaarmigeraadaptationtoxenobiotics