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

机译:基于微生物的双链RNA生产以开发具有成本效益的RNA干扰应用程序进行害虫管理

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摘要

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.
机译:RNA干扰(RNAi)是识别和表征生物体生物学功能的便捷工具。最近,它已成为化学杀虫剂的替代品,成为一种基于生物学的控制剂。这种有前途的技术具有避免与常规化学杀虫剂相关的许多问题的潜力。为了使RNAi应用在现场实际可行,一个主要的障碍是开发一种经济高效的双链RNA(dsRNA)生产系统,以生产大量的dsRNA。少数研究报告证明了使用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。但是,尚不清楚该体外系统的dsRNA产量,生产效率和生物纯度。因此,我们的研究详述了使用微生物系统大规模生产dsRNA的生化和分子工具,并研究了粗制和纯化dsRNA的生产效率和产量。从铃木果蝇鉴定出的无关的昆虫基因绿色荧光蛋白(GFP)和昆虫神经肽基因焦磷酸激酶(PK)用于构建在HT115(DE3)细胞中表达的重组L4440。使用超声破碎然后酚提取分离出大量的dsRNA,液体培养物为19.5μg/ mL。进一步评估了超声处理方法,可在不进行额外的苯酚提取和核酸酶处理的情况下提取粗制dsRNA,并降低潜在的细菌生存力。结果表明,超声方法节省了从大量细胞培养物中直接分离粗dsRNA的时间和成本,而没有受到大肠杆菌的污染。我们调查了果蝇中注射PK dsRNA是否导致成年死亡率增加,但在95%置信度水平上无统计学意义。在这项研究中,基于微生物的dsRNA生产对于应用RNAi技术具有补充当前昆虫有害生物管理实践的潜力。

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