Department of Entomology, University of Kentucky, S-225 Agricultural Science Center North, Lexington, KY 40546-0091, USA.
Int J Mol Sci. 2022 Aug 15;23(16):9167. doi: 10.3390/ijms23169167.
Exogenously applied double-stranded RNA (dsRNA) can induce potent host specific gene knockdown and mortality in insects. The deployment of RNA-interference (RNAi) technologies for pest suppression is gaining traction in both agriculture and horticulture, but its implementation in forest systems is lagging. While numerous forest pests have demonstrated susceptibility to RNAi mediated gene silencing, including the southern pine beetle (SPB), , multiple barriers stand between laboratory screening and real-world deployment. One such barrier is dsRNA delivery. One possible delivery method is through host plants, but an understanding of exogenous dsRNA movement through plant tissues is essential. Therefore, we sought to understand the translocation and persistence of dsRNAs designed for SPB throughout woody plant tissues after hydroponic exposure. Loblolly pine, , seedlings were exposed to dsRNAs as a root soak, followed by destructive sampling. Total RNA was extracted from different tissue types including root, stem, crown, needle, and meristem, after which gel electrophoresis confirmed the recovery of the exogenous dsRNAs, which were further verified using Sanger sequencing. Both techniques confirmed the presence of the exogenously applied target dsRNAs in each tissue type after 1, 3, 5, and 7 d of dsRNA exposure. These findings suggest that root drench applications of exogenous dsRNAs could provide a viable delivery route for RNAi technology designed to combat tree feeding pests.
外源双链 RNA(dsRNA)可诱导昆虫产生强烈的宿主特异性基因敲低和死亡。RNA 干扰 (RNAi) 技术在农业和园艺中的害虫防治方面的应用越来越受到关注,但在森林系统中的应用却滞后。虽然许多森林害虫已经表现出对 RNAi 介导的基因沉默的敏感性,包括南方松甲虫 (SPB),但在实验室筛选和实际应用之间存在许多障碍。其中一个障碍是 dsRNA 的传递。一种可能的传递方法是通过宿主植物,但对外源 dsRNA 在植物组织中的运动的理解是必不可少的。因此,我们试图了解在水培暴露后,dsRNA 设计用于 SPB 在整个木本植物组织中的转运和持久性。火炬松 ,幼苗被暴露在 dsRNA 中作为根浸泡,然后进行破坏性采样。从不同的组织类型(包括根、茎、冠、针叶和分生组织)中提取总 RNA,之后通过凝胶电泳确认回收了外源 dsRNA,进一步使用 Sanger 测序进行验证。两种技术都证实了在 dsRNA 暴露 1、3、5 和 7 天后,外源 dsRNA 存在于每种组织类型中。这些发现表明,外源 dsRNA 的根部浸溃应用可能为针对树木取食害虫的 RNAi 技术提供一种可行的传递途径。