Jiang Yiguo, Loker Eric S, Zhang Si-Ming
Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.
Dev Comp Immunol. 2006;30(10):855-66. doi: 10.1016/j.dci.2005.12.004. Epub 2006 Jan 10.
RNA interference (RNAi) is reported here for the first time for Biomphalaria glabrata, the snail intermediate host for the human parasite Schistosoma mansoni. The fibrinogen-related protein 2 (FREP2) gene, normally expressed at increased levels following exposure to digenetic trematode parasites, such as S. mansoni or Echinostoma paraensei, was targeted for knockdown. Double-stranded RNA (dsRNA) corresponding to specific regions of the FREP2 gene was introduced into snails by direct injection into the hemolymph, 2 days prior to exposure to trematodes, or added to co-cultures of B. glabrata embryonic (Bge) cells and E. paraensei sporocysts. After introduction of FREP2 dsRNA, expression levels of FREP2 were significantly reduced, to 20-30% of control values. In addition, we were able to disrupt expression of the house-keeping myoglobin gene, further confirming the feasibility of RNAi for B. glabrata. Cross-reactivity in RNAi has not been observed either among four FREP gene subfamilies or between FREP2 and myoglobin. Establishment of RNAi techniques in B. glabrata provides an important tool for clarifying the function of genes believed to play a role in host-parasite interactions, specifically between B. glabrata and its trematode parasites, including S. mansoni.
本文首次报道了对光滑双脐螺(Biomphalaria glabrata)的RNA干扰(RNAi),该螺是人类寄生虫曼氏血吸虫(Schistosoma mansoni)的中间宿主。纤维蛋白原相关蛋白2(FREP2)基因通常在暴露于复殖吸虫寄生虫(如曼氏血吸虫或副睾棘口吸虫)后表达水平会升高,该基因被作为敲低的靶点。与FREP2基因特定区域对应的双链RNA(dsRNA)在暴露于吸虫前两天通过直接注射到血淋巴中引入螺体,或添加到光滑双脐螺胚胎(Bge)细胞与副睾棘口吸虫包囊的共培养物中。引入FREP2 dsRNA后,FREP2的表达水平显著降低,降至对照值的20%-30%。此外,我们能够干扰持家基因肌红蛋白的表达,进一步证实了RNAi对光滑双脐螺的可行性。在四个FREP基因亚家族之间或FREP2与肌红蛋白之间均未观察到RNAi的交叉反应。在光滑双脐螺中建立RNAi技术为阐明被认为在宿主-寄生虫相互作用(特别是光滑双脐螺与其吸虫寄生虫,包括曼氏血吸虫之间的相互作用)中起作用的基因功能提供了重要工具。