Cargando…

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

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 cas...

Descripción completa

Detalles Bibliográficos
Autores principales: ZHANG, XIAOXI, ZHENG, HAIXUE, XU, MINJUN, ZHOU, YU, LI, XIANGPING, YANG, FAN, LIU, QINGYOU, SHI, DESHUN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626173/
https://www.ncbi.nlm.nih.gov/pubmed/26323462
http://dx.doi.org/10.3892/mmr.2015.4246
_version_ 1782398093468106752
author ZHANG, XIAOXI
ZHENG, HAIXUE
XU, MINJUN
ZHOU, YU
LI, XIANGPING
YANG, FAN
LIU, QINGYOU
SHI, DESHUN
author_facet ZHANG, XIAOXI
ZHENG, HAIXUE
XU, MINJUN
ZHOU, YU
LI, XIANGPING
YANG, FAN
LIU, QINGYOU
SHI, DESHUN
author_sort ZHANG, XIAOXI
collection PubMed
description 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 (TCID(50))/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 (LD(50)). 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.
format Online
Article
Text
id pubmed-4626173
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-46261732016-02-23 Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo ZHANG, XIAOXI ZHENG, HAIXUE XU, MINJUN ZHOU, YU LI, XIANGPING YANG, FAN LIU, QINGYOU SHI, DESHUN Mol Med Rep Articles 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 (TCID(50))/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 (LD(50)). 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. D.A. Spandidos 2015-11 2015-08-25 /pmc/articles/PMC4626173/ /pubmed/26323462 http://dx.doi.org/10.3892/mmr.2015.4246 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
ZHANG, XIAOXI
ZHENG, HAIXUE
XU, MINJUN
ZHOU, YU
LI, XIANGPING
YANG, FAN
LIU, QINGYOU
SHI, DESHUN
Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
title Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
title_full Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
title_fullStr Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
title_full_unstemmed Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
title_short Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
title_sort evaluation of a combinatorial rnai lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626173/
https://www.ncbi.nlm.nih.gov/pubmed/26323462
http://dx.doi.org/10.3892/mmr.2015.4246
work_keys_str_mv AT zhangxiaoxi evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT zhenghaixue evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT xuminjun evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT zhouyu evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT lixiangping evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT yangfan evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT liuqingyou evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo
AT shideshun evaluationofacombinatorialrnailentivirusvectortargetingfootandmouthdiseasevirusinvitroandinvivo