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Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo

机译:体外和体内针对口蹄疫病毒的组合RNAi慢病毒载体的评估

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Foot-and-mouth disease virus (FMDV) causes a highly contagious disease of cloven-hoofed animals, which leads to serious economical losses. FMDV is not adequately controlled by vaccination or biosecurity measures. To generate genetically modified FMDV-resistant animals, a combinatorial expression cassette producing three short hairpin (sh) RNAs was constructed using the lentivirus (LV) vector, LV-3shRNA. The three shRNAs were expressed under the regulation of DNA polymerase III promoters from a buffalo and a bovine source, with one targeted to the non-structural protein 3B, and the other two targeted to the viral polymerase protein 3D of FMDV, respectively. The role of LV-3shRNA in the inhibition of the replication of FMDV was determined in BHK-21 cells and in suckling mice. The results revealed that LV-3shRNA reduced viral growth 3-fold (24 h post-infection) when the cells were challenged with 10(7)-times the tissue culture infective dose (TCID50)/ml of 0 serotype FMDV. The suckling mice pretreated with LV-3shRNA were completely protected on administration of 5-times the dose of FMDV otherwise sufficient to kill 50% of the experimental animals (LD50). These results demonstrated that the LV-mediated dual expression of three FMDV-specific shRNAs provided a novel strategy towards combating FMDV, which facilitates the permanent introduction of novel disease-resistance traits into the buffalo and bovine genomes in the future.
机译:口蹄疫病毒(FMDV)引起丁香蹄类动物的高度传染性疾病,导致严重的经济损失。 FMDV没有通过疫苗接种或生物安全措施得到充分控制。为了产生抗FMDV的基因改造动物,使用慢病毒(LV)载体LV-3shRNA构建了产生三个短发夹(sh)RNA的组合表达盒。在来自水牛和牛的DNA聚合酶III启动子的调控下表达了三个shRNA,一个针对非结构蛋白3B,另一个针对FMDV病毒聚合酶3D。在BHK-21细胞和哺乳小鼠中确定了LV-3shRNA在抑制FMDV复制中的作用。结果表明,当用10(7)倍组织培养感染剂量(TCID50)/ ml的0血清型FMDV攻击细胞时,LV-3shRNA将病毒生长降低了3倍(感染后24小时)。用LV-3shRNA预处理的乳鼠在施用5倍FMDV剂量后受到完全保护,否则足以杀死50%的实验动物(LD50)。这些结果表明,LV介导的三个FMDV特异性shRNA的双重表达提供了对抗FMDV的新策略,这有助于将来将新的抗病性状永久引入水牛和牛基因组。

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