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吡丙醚激活褐飞虱 Nilaparvata lugens 的 TRPV 通道。

Pymetrozine activates TRPV channels of brown planthopper Nilaparvata lugens.

机构信息

College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, China.

BASF Corporation, 26 Davis Drive, Research Triangle Park, NC 27709, USA.

出版信息

Pestic Biochem Physiol. 2019 Jan;153:77-86. doi: 10.1016/j.pestbp.2018.11.005. Epub 2018 Nov 5.

Abstract

The commercial insecticide pymetrozine has been extensively used for brown planthopper control in East Asia. The transient receptor potential vanilloid (TRPV) channel, which consists of two proteins, Nanchung (Nan) and Inactive (Iav), has recently been shown to be the molecular target of pymetrozine in the fruit fly (Drosophila melanogaster) and pea aphid (Acyrthosiphon pisum). In this study, we characterized the Nan and Iav TRPV channel subunits of N. lugens and measured the action of pymetrozine on them. NlNan and NlIav are structurally similar to homologs from other insects. The expression pattern analysis of various body parts showed that NlNan and NlIav were both more abundantly expressed in antennae. When NlNan and NlIav were co-expressed in Xenopus laevis oocytes, they formed channels with high sensitivity to pymetrozine (EC = 5.5 × 10 M). Behavioral observation revealed that the gravitaxis defect in the fruit fly nan mutant was rescued by ectopically expressed NlNan and the rescued behavior could be abolished by pymetrozine. Our results confirm that NlNan and NlIav co-expressed complexes can be activated by pymetrozine both in vitro and in vivo and provide useful information for future resistance mechanism studies.

摘要

商业杀虫剂吡虫啉在东亚地区被广泛用于防治褐飞虱。瞬时受体电位香草酸 (TRPV) 通道由两种蛋白质,Nanchung(Nan)和Inactive(Iav)组成,最近已被证明是吡虫啉在果蝇(Drosophila melanogaster)和豌豆蚜(Acyrthosiphon pisum)中的分子靶标。在这项研究中,我们对 N. lugens 的 Nan 和 Iav TRPV 通道亚基进行了表征,并测量了吡虫啉对它们的作用。NlNan 和 NlIav 与其他昆虫的同源物在结构上相似。对各种身体部位的表达模式分析表明,NlNan 和 NlIav 在触角中表达更为丰富。当 NlNan 和 NlIav 在非洲爪蟾卵母细胞中共同表达时,它们形成对吡虫啉高度敏感的通道(EC = 5.5 × 10 M)。行为观察表明,果蝇 nan 突变体的趋地性缺陷可以通过异位表达 NlNan 得到挽救,而挽救的行为可以被吡虫啉消除。我们的结果证实,NlNan 和 NlIav 共表达复合物既可以在体外又可以在体内被吡虫啉激活,并为未来的抗性机制研究提供了有用的信息。

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