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烟碱型乙酰胆碱受体亚基对三氟甲吡醚和新烟碱类药物敏感性的贡献。

Contribution of Nicotinic Acetylcholine Receptor Subunits Toward Triflumezopyrim and Neonicotinoid Susceptibility.

作者信息

Zhang Yan-Chao, Zhuang Zi-Xin, Zhang Fan, Song Xiao-Yan, Ye Wen-Nan, Wu Shun-Fan, Bass Chris, O'Reilly Andrias O, Gao Congfen

机构信息

College of Plant Protection, Nanjing Agricultural University/State & Local Joint Engineering Research Center of Green Pesticide-Invention and Application, Nanjing 210095 Jiangsu, China.

Centre for Ecology and Conservation, University of Exeter, Penryn Campus, Penryn, Cornwall TR10 9FE, U.K.

出版信息

Environ Sci Technol. 2025 Apr 15;59(14):7054-7065. doi: 10.1021/acs.est.5c02110. Epub 2025 Apr 4.

Abstract

Nicotinic acetylcholine receptors (nAChRs) are the molecular targets of some important insecticides including triflumezopyrim and neonicotinoids. However, our understanding of insect nAChR pharmacology and the specific nAChR subunits targeted by these insecticides remains limited. Here, we cloned 11 nAChR subunit genes, comprising to , , and , from , a highly damaging insect pest of rice crops worldwide. Analysis of the expression of these genes in different tissues of by qPCR analysis identified the brain as the primary site of expression. Knock down of the expression of , , and using RNAi reduced sensitivity to triflumezopyrim, suggesting these genes encode potential target subunits for triflumezopyrim. Knock out of and nAChR subunits by CRISPR/Cas9 genome editing showed that their deletion significantly reduced the toxicity of triflumezopyrim toward . Furthermore, the deletion of also increased resistance to imidacloprid and dinotefuran. However, numerous attempts revealed that the knockout was nonviable. expression of receptors composed of homologous subunits showed that this all-insect nAChR was inhibited by nanomolar concentrations of triflumezopyrim. The present findings identify specific nAChR subunits that are important both as targets for monitoring resistance-associated mutations and as subjects for molecular studies aimed at developing novel insecticides targeting these essential ion channels.

摘要

烟碱型乙酰胆碱受体(nAChRs)是包括三氟苯嘧啶和新烟碱类在内的一些重要杀虫剂的分子靶点。然而,我们对昆虫nAChR药理学以及这些杀虫剂所靶向的特定nAChR亚基的了解仍然有限。在此,我们从褐飞虱(一种对全球水稻作物具有高度破坏性的害虫)中克隆了11个nAChR亚基基因,包括α1至α9、β1至β3。通过qPCR分析对这些基因在褐飞虱不同组织中的表达进行分析,确定大脑是主要表达部位。利用RNA干扰敲低α1、α4、α5和β2的表达降低了褐飞虱对三氟苯嘧啶的敏感性,表明这些基因编码三氟苯嘧啶的潜在靶标亚基。通过CRISPR/Cas9基因组编辑敲除α1和β2 nAChR亚基表明,它们的缺失显著降低了三氟苯嘧啶对褐飞虱的毒性。此外,α1的缺失还增加了褐飞虱对吡虫啉和呋虫胺的抗性。然而,大量尝试表明α1敲除是不可行的。由α1同源亚基组成的受体的功能性表达表明,这种全昆虫nAChR受到纳摩尔浓度三氟苯嘧啶的抑制。本研究结果确定了特定的nAChR亚基,这些亚基作为监测抗性相关突变的靶点以及作为旨在开发针对这些必需离子通道的新型杀虫剂的分子研究对象都很重要。

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