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基于壳聚糖的口服 dsRNA 递送系统通过诱导 G 蛋白偶联受体激酶 2 基因沉默来控制龟纹瓢虫。

An oral dsRNA delivery system based on chitosan induces G protein-coupled receptor kinase 2 gene silencing for Apolygus lucorum control.

机构信息

Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China; College of Forestry, Nanjing Forestry University, Nanjing, China.

Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.

出版信息

Pestic Biochem Physiol. 2023 Aug;194:105481. doi: 10.1016/j.pestbp.2023.105481. Epub 2023 Jun 5.

Abstract

RNA interference (RNAi) is recognized as a new and environmentally friendly pest control strategy due to its high specificity. However, the RNAi efficiency is relatively low in many sucking insect pests, such as Apolygus lucorum. Therefore, there is an urgent need to develop new and effective ways of dsRNA delivery. Bacterially expressed or T7 synthesized dsRNA targeting a G Protein-Coupled Receptor Kinase 2 gene was mixed with chitosan in a 1:2 ratio by mass. The size of the chitosan/dsRNA nanoparticles was 69 ± 12 nm, and the TEM and AFM images showed typical spherical or ellipsoidal structures. The chitosan nanoparticles protected the dsRNA from nuclease activity, and pH and temperature-dependent degradation, and the fluorescently-tagged nanoparticles were found to be stable on the surface of green bean plants (48 h) (Phaseolus vulgaris) and were absorbed by midgut epithelial cells and transported to hemolymph. Once fed to the A. lucorum nymph, chitosan/dsRNA could effectively inhibit the expression of the G protein-coupled receptor kinase 2 gene (70%), and led to significantly increase mortality (50%), reduced weight (26.54%) and a prolonged developmental period (8.04%). The feeding-based and chitosan-mediated dsRNA delivery method could be a new strategy for A. lucorum management, providing an effective tool for gene silencing of piercing-sucking insects.

摘要

RNA 干扰 (RNAi) 因其高度特异性而被认为是一种新的、环保的害虫防治策略。然而,在许多刺吸式害虫中,如桃小食心虫,RNAi 的效率相对较低。因此,迫切需要开发新的、有效的 dsRNA 递送方法。将细菌表达或 T7 合成的靶向 G 蛋白偶联受体激酶 2 基因的 dsRNA 与壳聚糖以质量比 1:2 混合。壳聚糖/dsRNA 纳米颗粒的大小为 69±12nm,TEM 和 AFM 图像显示出典型的球形或椭圆形结构。壳聚糖纳米颗粒保护 dsRNA 免受核酸酶活性、pH 值和温度依赖性降解的影响,并且荧光标记的纳米颗粒在绿豆植株(48h)(Phaseolus vulgaris)表面稳定,被肠上皮细胞吸收并运输到血液中。一旦喂食桃小食心虫若虫,壳聚糖/dsRNA 可以有效抑制 G 蛋白偶联受体激酶 2 基因的表达(70%),并导致死亡率显著增加(50%)、体重减轻(26.54%)和发育期延长(8.04%)。基于喂食和壳聚糖介导的 dsRNA 递送方法可能成为桃小食心虫管理的一种新策略,为刺吸式昆虫的基因沉默提供了一种有效工具。

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