基于微生物的双链RNA生产开发具有成本效益的RNA干扰应用于害虫管理。

International journal of insect science Pub Date : 2019-04-24 eCollection Date: 2019-01-01 DOI:10.1177/1179543319840323
Seung-Joon Ahn, Kelly Donahue, Youngho Koh, Robert R Martin, Man-Yeon Choi
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引用次数: 31

摘要

RNA干扰(RNAi)是一种方便的识别和表征生物功能的工具。近年来,它已成为化学杀虫剂的替代品,成为一种基于生物的防治剂。这项有前途的技术有可能避免与传统化学杀虫剂相关的许多问题。为了使RNAi应用于实际的现场使用,一个主要的障碍是开发一种具有成本效益的双链RNA (dsRNA)生产系统,用于大量的dsRNA。一些研究报告已经证明了利用L4440载体和HT115 (DE3)大肠杆菌生产基于微生物的dsRNA可应用于脊椎动物和无脊椎动物系统。然而,该体外系统的dsRNA产率、生产效率和生物纯度尚不清楚。因此,我们的研究详细介绍了利用微生物系统大规模生产dsRNA的生化和分子工具,并研究了粗dsRNA和纯化dsRNA的生产效率和产量。利用不相关的昆虫基因绿色荧光蛋白(GFP)和昆虫神经肽基因火激肽(PK),构建了重组蛋白L4440,并在HT115 (DE3)细胞中表达。通过超声波破坏和苯酚萃取,分离出19.5µg/mL的dsRNA。进一步评价了超声法提取粗dsRNA而不需要额外的苯酚提取和核酸酶处理,同时也降低了潜在的细菌活力。结果表明,超声法在没有大肠杆菌污染的情况下直接从大量细胞培养物中分离粗dsRNA,节省了时间和成本。我们调查了PK dsRNA注射果蝇是否会导致成虫死亡率增加,但在95%的置信水平下没有统计学意义。在本研究中,基于微生物的dsRNA生产具有应用RNAi技术补充当前害虫管理实践的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Microbial-Based Double-Stranded RNA Production to Develop Cost-Effective RNA Interference Application for Insect Pest Management.

RNA interference (RNAi) is a convenient tool to identify and characterize biological functions in organisms. Recently, it has become an alternative to chemical insecticides as a biologically based control agent. This promising technology has the potential to avoid many problems associated with conventional chemical insecticides. In order for RNAi application to be practical for field use, a major hurdle is the development of a cost-effective system of double-stranded RNA (dsRNA) production for a large quantity of dsRNA. A handful of research reports has demonstrated microbial-based dsRNA production using L4440 vector and HT115 (DE3) Escherichia coli for application to vertebrate and invertebrate systems. However, the dsRNA yield, production efficiency, and biological purity from this in vitro system is still unclear. Thus, our study detailed biochemical and molecular tools for large-scale dsRNA production using the microbial system and investigated the production efficiency and yield of crude and purified dsRNAs. An unrelated insect gene, green fluorescent protein (GFP), and an insect neuropeptide gene, pyrokinin (PK) identified from Drosophila suzukii, were used to construct the recombinant L4440 to be expressed in the HT115 (DE3) cell. A considerable amount of dsRNA, 19.5 µg/mL of liquid culture, was isolated using ultrasonic disruption followed by phenol extraction. The sonication method was further evaluated to extract crude dsRNA without the additional phenol extraction and nuclease treatments and also to reduce potential bacterial viability. The results suggest that the ultrasonic method saved time and costs to isolate crude dsRNA directly from large volumes of cell culture without E coli contamination. We investigated whether the injection of PK dsRNA into flies resulted in increased adult mortality, but it was not statistically significant at 95% confidence level. In this study, the microbial-based dsRNA production has potential for applied RNAi technology to complement current insect pest management practices.

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