Almeida Garcia Rayssa, Lima Pepino Macedo Leonardo, Cabral do Nascimento Danila, Gillet François-Xavier, Moreira-Pinto Clidia Eduarda, Faheem Muhammad, Moreschi Basso Angelina Maria, Mattar Silva Maria Cristina, Grossi-de-Sa Maria Fatima
Brasilia Federal University (UnB), Brasília - CEP, Brasília, Federal District, Brazil.
Embrapa Genetic Resources and Biotechnology, Brasília, Federal District, Brazil.
PLoS One. 2017 Dec 20;12(12):e0189600. doi: 10.1371/journal.pone.0189600. eCollection 2017.
RNA interference (RNAi) approaches have been applied as a biotechnological tool for controlling plant insect pests via selective gene down regulation. However, the inefficiency of RNAi mechanism in insects is associated with several barriers, including dsRNA delivery and uptake by the cell, dsRNA interaction with the cellular membrane receptor and dsRNA exposure to insect gut nucleases during feeding. The cotton boll weevil (Anthonomus grandis) is a coleopteran in which RNAi-mediated gene silencing does not function efficiently through dsRNA feeding, and the factors involved in the mechanism remain unknown. Herein, we identified three nucleases in the cotton boll weevil transcriptome denoted AgraNuc1, AgraNuc2, and AgraNuc3, and the influences of these nucleases on the gene silencing of A. grandis chitin synthase II (AgraChSII) were evaluated through oral dsRNA feeding trials. A phylogenetic analysis showed that all three nucleases share high similarity with the DNA/RNA non-specific endonuclease family of other insects. These nucleases were found to be mainly expressed in the posterior midgut region of the insect. Two days after nuclease RNAi-mediated gene silencing, dsRNA degradation by the gut juice was substantially reduced. Notably, after nucleases gene silencing, the orally delivered dsRNA against the AgraChSII gene resulted in improved gene silencing efficiency when compared to the control (non-silenced nucleases). The data presented here demonstrates that A. grandis midgut nucleases are effectively one of the main barriers to dsRNA delivery and emphasize the need to develop novel RNAi delivery strategies focusing on protecting the dsRNA from gut nucleases and enhancing its oral delivery and uptake to crop insect pests.
RNA干扰(RNAi)方法已作为一种生物技术工具,通过选择性下调基因来控制植物害虫。然而,RNAi机制在昆虫中的低效性与几个障碍有关,包括dsRNA被细胞递送和摄取、dsRNA与细胞膜受体的相互作用以及喂食期间dsRNA暴露于昆虫肠道核酸酶。棉铃象甲(Anthonomus grandis)是一种鞘翅目昆虫,在其中通过dsRNA喂食,RNAi介导的基因沉默不能有效发挥作用,且该机制涉及的因素仍不清楚。在此,我们在棉铃象甲转录组中鉴定出三种核酸酶,分别命名为AgraNuc1、AgraNuc2和AgraNuc3,并通过口服dsRNA喂食试验评估了这些核酸酶对棉铃象甲几丁质合酶II(AgraChSII)基因沉默的影响。系统发育分析表明,所有这三种核酸酶与其他昆虫的DNA/RNA非特异性核酸内切酶家族具有高度相似性。发现这些核酸酶主要在昆虫中肠后部区域表达。在核酸酶RNAi介导的基因沉默两天后,肠液对dsRNA的降解显著减少。值得注意的是,在核酸酶基因沉默后,与对照(未沉默核酸酶)相比,口服针对AgraChSII基因的dsRNA导致基因沉默效率提高。此处呈现的数据表明,棉铃象甲中肠核酸酶实际上是dsRNA递送的主要障碍之一,并强调需要开发新的RNAi递送策略,重点是保护dsRNA免受肠道核酸酶的影响,并增强其对农作物害虫的口服递送和摄取。