Plant Molecular Biology and Genetic Engineering Department, CSIR-National Botanical Research Institute, Council of Scientific and Industrial Research, Lucknow, India.
Department of Botany, Lucknow University, Lucknow, Uttar Pradesh, 226007, India.
Pest Manag Sci. 2021 Apr;77(4):1796-1805. doi: 10.1002/ps.6204. Epub 2020 Dec 16.
Cotton is a cash crop majorly affected by many hemipteran pests, among them the cotton mealybug, Phenacoccus solenopsis. Cotton mealybug attack has a devastating effect on cotton production and causes huge yield losses.
In this study, 25 potential RNA interference (RNAi) target genes were selected from the iBeetle database and a transcriptome data set for P. solenopsis. To assess the effectiveness of the selected target genes, three methods were utilized to deliver double-stranded (ds)RNA (ingestion, artificial diet bioassay and transient gene silencing). dsRNA molecules at different concentrations were fed to insects and insect mortality was recorded for each target gene. Based on the mortality data, three genes, Krüppel homologue-1, ADP-ATP/Translocase and IDGF-1, were selected for further gene expression studies using a reduced concentration of dsRNA (5 μg/ml). Of the three genes, Krüppel homologue-1 showed significantly downregulated expression (by 70.81% and 84.33%) at two different time points (8 and 14 days). An RNAi silencing construct was designed for Krüppel homologue-1 under control of the double enhancer CamV35S promoter in the plant binary vector. Significant downregulation of gene expression, by 66.69% and 81.80%, was found for Krüppel homologue-1 using transient gene silencing at the same time intervals.
This work provides the first evidence for targeting the Krüppel homologue-1 gene in a hemipteran pest, P. solenopsis, using RNAi technology through oral delivery and in planta-based transient gene silencing methods. © 2020 Society of Chemical Industry.
棉花是一种主要受多种半翅目害虫影响的经济作物,其中包括棉红铃虫(Phenacoccus solenopsis)。棉红铃虫的攻击对棉花生产具有破坏性影响,并导致巨大的产量损失。
在这项研究中,从 iBeetle 数据库和 P. solenopsis 的转录组数据集选择了 25 个潜在的 RNA 干扰(RNAi)靶基因。为了评估所选靶基因的有效性,使用三种方法(摄食、人工饲料生物测定和瞬时基因沉默)递送双链(ds)RNA。将不同浓度的 dsRNA 喂食给昆虫,并记录每个靶基因的昆虫死亡率。根据死亡率数据,选择三个基因(Krüppel 同源物-1、ADP-ATP/Translocase 和 IDGF-1)进行进一步的基因表达研究,使用浓度较低的 dsRNA(5μg/ml)。在这三个基因中,Krüppel 同源物-1 在两个不同时间点(8 天和 14 天)的表达显著下调(分别为 70.81%和 84.33%)。Krüppel 同源物-1 的 RNAi 沉默构建体在植物双元载体中受双增强子 CamV35S 启动子的控制。在相同的时间间隔内,通过瞬时基因沉默,发现 Krüppel 同源物-1 的基因表达显著下调,下调率分别为 66.69%和 81.80%。
这项工作首次提供了使用 RNAi 技术通过口服和基于植物的瞬时基因沉默方法靶向半翅目害虫 P. solenopsis 中的 Krüppel 同源物-1 基因的证据。© 2020 化学工业协会。