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靶向口蹄疫病毒的组合RNA干扰慢病毒载体的体内外评价

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

作者信息

Zhang Xiaoxi, Zheng Haixue, Xu Minjun, Zhou Yu, Li Xiangping, Yang Fan, Liu Qingyou, Shi Deshun

机构信息

State Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.

State Key Laboratory of Veterinary Etiological Biology, National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, P.R. China.

出版信息

Mol Med Rep. 2015 Nov;12(5):6672-8. doi: 10.3892/mmr.2015.4246. Epub 2015 Aug 25.

DOI:10.3892/mmr.2015.4246
PMID:26323462
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4626173/
Abstract

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 107‑times the tissue culture infective dose (TCID50)/ml of O 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.

摘要

口蹄疫病毒(FMDV)可引发偶蹄动物的一种高度传染性疾病,会导致严重的经济损失。接种疫苗或采取生物安全措施无法充分控制FMDV。为了培育出转基因抗FMDV动物,利用慢病毒(LV)载体LV-3shRNA构建了一个产生三种短发夹(sh)RNA的组合表达盒。这三种shRNA在源自水牛和牛的DNA聚合酶III启动子的调控下表达,其中一种靶向非结构蛋白3B,另外两种分别靶向FMDV的病毒聚合酶蛋白3D。在BHK-21细胞和乳鼠中确定了LV-3shRNA在抑制FMDV复制中的作用。结果显示,当用107倍组织培养感染剂量(TCID50)/毫升的O型口蹄疫病毒攻击细胞时,LV-3shRNA在感染后24小时使病毒生长减少了3倍。用LV-3shRNA预处理的乳鼠在给予5倍剂量的FMDV(否则足以杀死50%的实验动物,即LD50)后得到了完全保护。这些结果表明,LV介导的三种FMDV特异性shRNA的双重表达为对抗FMDV提供了一种新策略,这将有助于未来将新的抗病性状永久引入水牛和牛的基因组中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/15a1b3b6d6ec/MMR-12-05-6672-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/bcb159d61882/MMR-12-05-6672-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/de9886e2e68f/MMR-12-05-6672-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/887259a29dfa/MMR-12-05-6672-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/15a1b3b6d6ec/MMR-12-05-6672-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/bcb159d61882/MMR-12-05-6672-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/de9886e2e68f/MMR-12-05-6672-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/887259a29dfa/MMR-12-05-6672-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/665d/4626173/15a1b3b6d6ec/MMR-12-05-6672-g03.jpg

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