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RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs

Porcine reproductive and respiratory syndrome (PRRS) is an economically devastating viral disease causing heavy losses to the swine industry worldwide. Many studies have shown that transient delivery of small interfering RNA (siRNA) or adenovirus-mediated RNA interfere (RNAi) could potentially inhib...

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Autores principales: Li, Li, Li, Qiuyan, Bao, Yonghua, Li, Jinxiu, Chen, Zhisheng, Yu, Xiuling, Zhao, Yaofeng, Tian, Kegong, Li, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127135/
https://www.ncbi.nlm.nih.gov/pubmed/24333125
http://dx.doi.org/10.1016/j.jbiotec.2013.11.022
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author Li, Li
Li, Qiuyan
Bao, Yonghua
Li, Jinxiu
Chen, Zhisheng
Yu, Xiuling
Zhao, Yaofeng
Tian, Kegong
Li, Ning
author_facet Li, Li
Li, Qiuyan
Bao, Yonghua
Li, Jinxiu
Chen, Zhisheng
Yu, Xiuling
Zhao, Yaofeng
Tian, Kegong
Li, Ning
author_sort Li, Li
collection PubMed
description Porcine reproductive and respiratory syndrome (PRRS) is an economically devastating viral disease causing heavy losses to the swine industry worldwide. Many studies have shown that transient delivery of small interfering RNA (siRNA) or adenovirus-mediated RNA interfere (RNAi) could potentially inhibit porcine reproductive and respiratory syndrome virus (PRRSV) replication in vivo and in vitro. Here, we applied RNAi to produce transgenic (TG) pigs that constitutively expressed PRRSV-specific siRNA derived from small hairpin RNA (shRNA). First, we evaluated siRNA expression in the founding and F1 generation pigs and confirmed stable transmission. Then, we detected the expression of IFN-β and protein kinase R (PKR) and found no difference among TG, non-transgenic (NTG), and wild-type pigs. Lastly, the F1 generation pigs, including TG and NTG piglets, were challenged with 3 × 10(4.5) TCID(50) of JXA1, a highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV). Our results showed that the in vivo siRNA expression substantially reduced the serum HP-PRRSV titers and increased survival time by 3 days when TG pigs were compared with the NTG controls. These data suggested that RNAi-based genetic modification might be used to breed viral-resistant livestock with stable siRNA expression with no complications of siRNA toxicity.
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spelling pubmed-71271352020-04-08 RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs Li, Li Li, Qiuyan Bao, Yonghua Li, Jinxiu Chen, Zhisheng Yu, Xiuling Zhao, Yaofeng Tian, Kegong Li, Ning J Biotechnol Article Porcine reproductive and respiratory syndrome (PRRS) is an economically devastating viral disease causing heavy losses to the swine industry worldwide. Many studies have shown that transient delivery of small interfering RNA (siRNA) or adenovirus-mediated RNA interfere (RNAi) could potentially inhibit porcine reproductive and respiratory syndrome virus (PRRSV) replication in vivo and in vitro. Here, we applied RNAi to produce transgenic (TG) pigs that constitutively expressed PRRSV-specific siRNA derived from small hairpin RNA (shRNA). First, we evaluated siRNA expression in the founding and F1 generation pigs and confirmed stable transmission. Then, we detected the expression of IFN-β and protein kinase R (PKR) and found no difference among TG, non-transgenic (NTG), and wild-type pigs. Lastly, the F1 generation pigs, including TG and NTG piglets, were challenged with 3 × 10(4.5) TCID(50) of JXA1, a highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV). Our results showed that the in vivo siRNA expression substantially reduced the serum HP-PRRSV titers and increased survival time by 3 days when TG pigs were compared with the NTG controls. These data suggested that RNAi-based genetic modification might be used to breed viral-resistant livestock with stable siRNA expression with no complications of siRNA toxicity. Published by Elsevier B.V. 2014-02-10 2013-12-11 /pmc/articles/PMC7127135/ /pubmed/24333125 http://dx.doi.org/10.1016/j.jbiotec.2013.11.022 Text en Copyright © 2013 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Li, Li
Li, Qiuyan
Bao, Yonghua
Li, Jinxiu
Chen, Zhisheng
Yu, Xiuling
Zhao, Yaofeng
Tian, Kegong
Li, Ning
RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
title RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
title_full RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
title_fullStr RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
title_full_unstemmed RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
title_short RNAi-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
title_sort rnai-based inhibition of porcine reproductive and respiratory syndrome virus replication in transgenic pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127135/
https://www.ncbi.nlm.nih.gov/pubmed/24333125
http://dx.doi.org/10.1016/j.jbiotec.2013.11.022
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