Lustigman Sara, Zhang Jun, Liu Jing, Oksov Yelena, Hashmi Sarwar
Laboratory of Molecular Parasitology, Lindsley F. Kimball Research Institute, New York Blood Center, 310 East 67th Street, New York, NY 10021, USA.
Mol Biochem Parasitol. 2004 Dec;138(2):165-70. doi: 10.1016/j.molbiopara.2004.08.003.
We describe the successful use of RNA interference (RNAi) to investigate gene function in the human filarial parasite Onchocerca volvulus third-stage larvae (L3). We targeted two specific gene products, the O. volvulus cathepsin L (Ov-CPL) and cathepsin Z-like (Ov-CPZ) cysteine proteases, which were proposed to function during O. volvulus L3 molting. We show that fluorescent-labeled Cy3-dsRNA corresponding to cpl or cpz regions encoding the mature enzymes can enter the larvae. The molting rate of larvae treated overnight with 0.5 mg ml(-1) cpl was reduced by 92% and 86% in comparison to normal control worms. It appeared that although the larvae started the molting process the last stage of molting, ecdysis was inhibited. The effect was gene specific, as larvae that did not molt in the presence of cpl or cpz dsRNA expressed the other cysteine protease, CPZ and CPL, respectively. This was confirmed by immunoelectron microscopy using antibodies directed against each enzyme. Our present study validate conclusively that both enzymes are essential for the molting of O. volvulus L3 to fourth-stage larvae. We also confirmed that the activity of the enzymes is specific to the changes that occur during the molting process on days 1-3, when the separation between the cuticles is in progress. The development of RNAi in O. volvulus L3 could further help study many of the abundant L3 and molting L3 genes identified through the filarial genome project, many of which, although have no attributed function, were identified as vaccine candidates or potential drug targets.
我们描述了成功运用RNA干扰(RNAi)技术来研究人体丝虫寄生虫旋盘尾丝虫第三期幼虫(L3)的基因功能。我们针对两种特定的基因产物,即旋盘尾丝虫组织蛋白酶L(Ov-CPL)和组织蛋白酶Z样(Ov-CPZ)半胱氨酸蛋白酶,它们被认为在旋盘尾丝虫L3蜕皮过程中发挥作用。我们发现,与编码成熟酶的cpl或cpz区域相对应的荧光标记Cy3-dsRNA能够进入幼虫体内。与正常对照蠕虫相比,用0.5 mg ml(-1) cpl处理过夜的幼虫蜕皮率降低了92%和86%。虽然幼虫开始了蜕皮过程,但似乎蜕皮的最后阶段,即蜕壳受到了抑制。这种效应具有基因特异性,因为在存在cpl或cpz dsRNA时未蜕皮的幼虫分别表达了另一种半胱氨酸蛋白酶CPZ和CPL。这通过使用针对每种酶的抗体进行免疫电子显微镜检查得到了证实。我们目前的研究最终证实,这两种酶对于旋盘尾丝虫L3蜕皮至第四期幼虫都是必不可少的。我们还证实,这些酶的活性特定于蜕皮过程第1 - 3天发生的变化,此时角质层之间的分离正在进行。旋盘尾丝虫L3中RNAi技术的发展可能进一步有助于研究通过丝虫基因组计划鉴定出的许多丰富的L3和正在蜕皮的L3基因,其中许多基因虽然尚未确定功能,但已被鉴定为疫苗候选物或潜在的药物靶点。