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靶向VP1和VP2双拷贝shRNA重组表达质粒抑制传染性法氏囊病病毒复制的研究
引用本文:欧阳伟,王永山,马金荣,张海彬.靶向VP1和VP2双拷贝shRNA重组表达质粒抑制传染性法氏囊病病毒复制的研究[J].中国预防兽医学报,2011,33(10).
作者姓名:欧阳伟  王永山  马金荣  张海彬
作者单位:1. 江苏省农业科学院兽医研究所/国家兽用生物制品工程技术研究中心,江苏南京,210014
2. 江苏省农业科学院兽医研究所/国家兽用生物制品工程技术研究中心,江苏南京210014;南京农业大学动物医学院,江苏南京210095
3. 南京农业大学动物医学院,江苏南京,210095
基金项目:江苏省自然科学基金(BK2008352、BK2010471)
摘    要:为抑制传染性法氏囊病病毒(IBDV)的复制,本研究构建了靶向IBDV VP1和VP2基因的鸡双向U6启动子(chU6)双拷贝shRNA重组表达质粒pchU6-shRNA12,将其转染鸡胚成纤维细胞(CEF),再接种IBDV,72 h后,未出现细胞病变(CPE),病毒滴度小于101 TCID50/0.1mL;而转染空质粒和未转染两个对照组均出现明显的CPE,病毒滴度均达到108.75 TCID50/0.1 mL.此外,将pchU6-shRNA12与IBDV混合,接种于10日龄SPF鸡胚尿囊腔,96 h后,鸡胚发育正常,病毒滴度小于101 ELD5,0/0.1 mL,实时荧光定量RT-PCR检测VP1和VP2基因,比单纯接种IBDV组分别降低92%和95%;而含有空质粒和不含质粒两个对照组鸡胚则全部死亡,病毒滴度均达到107.00 ELD50/0.1mL.本研究结果表明,chU6启动子在双拷贝shRNA表达质粒pchU6-shRNA12中能高效驱动双拷贝shRNA的转录,生成的siRNA在CEF(in vitro)和鸡胚体内(in vivo)均能有效抑制IBDV的复制.

关 键 词:传染性法氏囊病病毒  RNA干扰  小发夹RNA  鸡U6启动子

Inhibition of infectious bursal disease virus replication by duplex shRNAs targeting the VP1 and VP2 genes driven by chicken U6 promoter
OUYANG Wei,WANG Yong-shan,MA Jin-rong,ZHANG Hai-bin.Inhibition of infectious bursal disease virus replication by duplex shRNAs targeting the VP1 and VP2 genes driven by chicken U6 promoter[J].Chinese Journal of Preventive Veterinary Medicine,2011,33(10).
Authors:OUYANG Wei  WANG Yong-shan  MA Jin-rong  ZHANG Hai-bin
Institution:OUYANG Wei 1,WANG Yong-shan 1,MA Jin-rong 1,2,ZHANG Hai-bin 2 (1.National Center for Engineering Research of Veterinary Bio-products,Institute of Veterinary Medicine,Jiangsu Academy of Agricutural Sciences,Nanjing 210014,China,2.College of Veterinary Medicine,Nanjing Agricultural University,Nanjing 210095,China)
Abstract:To inhibit the replication of infectious bursal disease virus(IBDV),two short hairpin RNAs(shRNAs) targeting VP1 and VP2 genes of IBDV were designed and synthesized.The recombinant plasmid pchU6-shRNA12 containing chicken U6 promoters on each side of the shRNAs based on pSilencer2.1-U6 vector was constructed.In the IBDV inhibition test(in vitro) of the chicken embryo fibroblasts(CEF) infected with IBDV at 24 hours post transfecting with pchU6-shRNA12,the virus titer was less than 10 TCID 50 /0.1 mL,in the c...
Keywords:infectious bursal disease virus  RNA interference  short hairpin RNA  chicken U6 promoter  
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