Kotze Andrew C, Bagnall Neil H
CSIRO Livestock Industries, Queensland Bioscience Precinct, St. Lucia, Qld 4067, Australia.
Mol Biochem Parasitol. 2006 Jan;145(1):101-10. doi: 10.1016/j.molbiopara.2005.09.012. Epub 2005 Oct 10.
We have used RNAi to target two beta-tubulin genes in the parasitic stages of Haemonchus contortus in vitro. Soaking exsheathed-L3, L4 and adult worms in medium containing dsRNA resulted in a significant decrease (greater than 1000-fold in some cases) in the expression of the specific beta-tubulin transcript, as measured by quantitative PCR. During the initial 24h exposure to the dsRNA, the gene suppression effect was quite specific to the targeted gene. Six days after initial exposure to dsRNA, treated L3 worms were less able to migrate through a filter mesh, indicating decreased motility, and showed less development to the L4 stage than control larvae. The gene suppression effect occurs in exsheathed L3 larvae despite the fact that this life stage does not have functioning mouthparts, indicating that uptake of dsRNA does not depend on its ingestion. Suppression occurred with dsRNA presented in 'naked' or liposome-encapsulated forms, indicating that a liposome formulation was not necessary for uptake to occur. Adult worms also showed significant gene suppression, however, they did not show any reduced motility compared to controls over a 3-day period. Adult worms treated with ivermectin to paralyse their pharynx, still showed significant gene suppression, again suggesting that uptake of dsRNA does not require ingestion. We have shown that soaking in dsRNA is an effective method for RNAi with the parasitic stages of H. contortus, and, hence, may offer significant potential as a tool for studying gene function in this parasite species.
我们已利用RNA干扰技术在体外针对捻转血矛线虫寄生阶段的两个β-微管蛋白基因进行靶向作用。将脱鞘的L3期、L4期幼虫及成虫浸泡在含有双链RNA(dsRNA)的培养基中,通过定量PCR检测发现,特定β-微管蛋白转录本的表达显著下降(在某些情况下下降超过1000倍)。在最初暴露于dsRNA的24小时内,基因抑制效应对靶向基因具有高度特异性。初次暴露于dsRNA六天后,经处理的L3期幼虫穿过滤网的能力下降,表明其运动性降低,且与对照幼虫相比,发育至L4期的比例更低。尽管该生命阶段没有功能性口器,但在脱鞘的L3期幼虫中仍发生了基因抑制效应,这表明dsRNA的摄取并不依赖于摄入。无论是“裸露”形式还是脂质体包裹形式的dsRNA均能产生抑制作用,这表明摄取dsRNA并不需要脂质体制剂。成虫也表现出显著的基因抑制,但在三天时间内,与对照相比它们并未表现出任何运动性降低。用伊维菌素使成虫咽部麻痹后进行处理,仍显示出显著的基因抑制,这再次表明dsRNA的摄取不需要摄入。我们已经证明,浸泡在dsRNA中是对捻转血矛线虫寄生阶段进行RNA干扰的有效方法,因此,作为研究该寄生虫物种基因功能的工具,可能具有巨大潜力。