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Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)

Aphis craccivora (Koch) is an economically important pest that affects legumes in worldwide. Chemical control is still the primary efficient method for A. craccivora management. However, the mechanism underlying insecticide resistance in A. craccivora has not been elucidated. A previous study observ...

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Autores principales: Yang, Yuan-Xue, Lin, Rong-Hua, Li, Zhuo, Wang, Ai-Yu, Xue, Chao, Duan, Ai-Ling, Zhao, Ming, Zhang, Jian-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854575/
https://www.ncbi.nlm.nih.gov/pubmed/33551847
http://dx.doi.org/10.3389/fphys.2020.624287
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author Yang, Yuan-Xue
Lin, Rong-Hua
Li, Zhuo
Wang, Ai-Yu
Xue, Chao
Duan, Ai-Ling
Zhao, Ming
Zhang, Jian-Hua
author_facet Yang, Yuan-Xue
Lin, Rong-Hua
Li, Zhuo
Wang, Ai-Yu
Xue, Chao
Duan, Ai-Ling
Zhao, Ming
Zhang, Jian-Hua
author_sort Yang, Yuan-Xue
collection PubMed
description Aphis craccivora (Koch) is an economically important pest that affects legumes in worldwide. Chemical control is still the primary efficient method for A. craccivora management. However, the mechanism underlying insecticide resistance in A. craccivora has not been elucidated. A previous study observed that piperonyl butoxide (PBO) and diethyl maleate (DEM) significantly synergized imidacloprid in A. craccivora field populations, indicating that cytochrome P450 (P450) and glutathione S-transferase (GST) genes may play pivotal roles in imidacloprid resistance. In this study, 38 P450 genes and 10 GST genes were identified in A. craccivora through transcriptomic analysis. The expression levels of these P450 and GST genes were measured in susceptible (SUS) strains of A. craccivora under imidacloprid treatment with LC(15), LC(50), and LC(85) doses. The expression levels of CYP18A1, CYP6CY21, CYP6DA1, CYP6DA2, CYP4CJ1, CYP4CJ2, and CYP380C6 were up-regulated in the three treatments. Most of these genes belong to CYP3 and CYP4 Clans. In addition, the expression levels of all P450 and GST genes in A. craccivora were also measured in the Juye (JY) and Linqing (LQ) field populations. The expression levels of CYP6DA2, CYP4CJ1, and CYP380C6 were up-regulated in the SUS strain after imidacloprid treatment at three doses, and these genes were overexpressed in the JY population. Furthermore, the sensitivity of A. craccivora to imidacloprid was significantly increased after knockdown of CYP380C6 and CYP6DA2 through RNA interference. These results may help to elucidate the mechanisms underlying of imidacloprid resistance in A. craccivora.
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spelling pubmed-78545752021-02-04 Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch) Yang, Yuan-Xue Lin, Rong-Hua Li, Zhuo Wang, Ai-Yu Xue, Chao Duan, Ai-Ling Zhao, Ming Zhang, Jian-Hua Front Physiol Physiology Aphis craccivora (Koch) is an economically important pest that affects legumes in worldwide. Chemical control is still the primary efficient method for A. craccivora management. However, the mechanism underlying insecticide resistance in A. craccivora has not been elucidated. A previous study observed that piperonyl butoxide (PBO) and diethyl maleate (DEM) significantly synergized imidacloprid in A. craccivora field populations, indicating that cytochrome P450 (P450) and glutathione S-transferase (GST) genes may play pivotal roles in imidacloprid resistance. In this study, 38 P450 genes and 10 GST genes were identified in A. craccivora through transcriptomic analysis. The expression levels of these P450 and GST genes were measured in susceptible (SUS) strains of A. craccivora under imidacloprid treatment with LC(15), LC(50), and LC(85) doses. The expression levels of CYP18A1, CYP6CY21, CYP6DA1, CYP6DA2, CYP4CJ1, CYP4CJ2, and CYP380C6 were up-regulated in the three treatments. Most of these genes belong to CYP3 and CYP4 Clans. In addition, the expression levels of all P450 and GST genes in A. craccivora were also measured in the Juye (JY) and Linqing (LQ) field populations. The expression levels of CYP6DA2, CYP4CJ1, and CYP380C6 were up-regulated in the SUS strain after imidacloprid treatment at three doses, and these genes were overexpressed in the JY population. Furthermore, the sensitivity of A. craccivora to imidacloprid was significantly increased after knockdown of CYP380C6 and CYP6DA2 through RNA interference. These results may help to elucidate the mechanisms underlying of imidacloprid resistance in A. craccivora. Frontiers Media S.A. 2021-01-20 /pmc/articles/PMC7854575/ /pubmed/33551847 http://dx.doi.org/10.3389/fphys.2020.624287 Text en Copyright © 2021 Yang, Lin, Li, Wang, Xue, Duan, Zhao and Zhang. 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 Physiology
Yang, Yuan-Xue
Lin, Rong-Hua
Li, Zhuo
Wang, Ai-Yu
Xue, Chao
Duan, Ai-Ling
Zhao, Ming
Zhang, Jian-Hua
Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)
title Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)
title_full Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)
title_fullStr Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)
title_full_unstemmed Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)
title_short Function Analysis of P450 and GST Genes to Imidacloprid in Aphis craccivora (Koch)
title_sort function analysis of p450 and gst genes to imidacloprid in aphis craccivora (koch)
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854575/
https://www.ncbi.nlm.nih.gov/pubmed/33551847
http://dx.doi.org/10.3389/fphys.2020.624287
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