Sarathi M, Simon Martin C, Ahmed V P Ishaq, Kumar S Rajesh, Hameed A S Sahul
Aquaculture Biotechnology Division, Department of Zoology, C. Abdul Hakeem College, Melvisharam-632, 509, Tamil Nadu, India.
Mar Biotechnol (NY). 2008 Mar-Apr;10(2):198-206. doi: 10.1007/s10126-007-9052-y. Epub 2007 Oct 27.
An in vivo expression system to produce large amounts of virus-derived dsRNAs in bacteria to provide a practical control of white spot syndrome virus (WSSV) in shrimp was developed. The bacterially synthesized dsRNA specific to VP28 gene of WSSV promoted gene-specific interference with the WSSV infection in shrimp. Virus infectivity was significantly reduced in WSSV-challenged shrimp injected with VP28-dsRNA and 100% survival was recorded. The inhibition of the expression of WSSV VP28 gene in experimentally challenged animals by VP28-dsRNA was confirmed by RT-PCR and Western blot analyses. Furthermore, we have demonstrated the efficacy of bacterially expressed VP28-dsRNA to silence VP28 gene expression in SISK cell line transfected with eukaryotic expression vector (pcDNA3.1) inserted with VP28 gene of WSSV. The expression level of VP28 gene in SISK cells was determined by fluorescent microscopy and ELISA. The results showed that the expression was significantly reduced in cells transfected with VP28dsRNA, whereas the cells transected with pcDNA-VP28 alone showed higher expression. The in vivo production of dsRNA using prokaryotic expression system could be an alternative to in vitro method for large-scale production of dsRNA corresponding to VP28 gene of WSSV for practical application to control the WSSV in shrimp farming.
开发了一种体内表达系统,用于在细菌中大量生产病毒衍生的双链RNA,以实现对虾白斑综合征病毒(WSSV)的实际控制。针对WSSV VP28基因的细菌合成双链RNA促进了对虾中WSSV感染的基因特异性干扰。在注射了VP28-dsRNA的WSSV攻击虾中,病毒感染性显著降低,记录到100%的存活率。通过RT-PCR和蛋白质印迹分析证实了VP28-dsRNA在实验攻击动物中对WSSV VP28基因表达的抑制作用。此外,我们已经证明了细菌表达的VP28-dsRNA在转染了插入WSSV VP28基因的真核表达载体(pcDNA3.1)的SISK细胞系中沉默VP28基因表达的功效。通过荧光显微镜和ELISA测定SISK细胞中VP28基因的表达水平。结果表明,用VP28dsRNA转染的细胞中表达显著降低,而单独用pcDNA-VP28转染的细胞显示出更高的表达。使用原核表达系统在体内生产双链RNA可能是体外方法的一种替代方案,用于大规模生产与WSSV VP28基因对应的双链RNA,以便在对虾养殖中实际应用来控制WSSV。