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Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs

BACKGROUND: Highly pathogenic porcine reproductive and respiratory syndrome (HP-PRRS) has caused large economic losses in swine industry in recent years. However, current antiviral strategy could not effectively prevent and control this disease. In this research, five artificial microRNAs (amiRNAs)...

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Autores principales: Xiao, Shuqi, Wang, Qiwei, Gao, Jintao, Wang, Liangliang, He, Zuyong, Mo, Delin, Liu, Xiaohong, Chen, Yaosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215188/
https://www.ncbi.nlm.nih.gov/pubmed/22040357
http://dx.doi.org/10.1186/1743-422X-8-491
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author Xiao, Shuqi
Wang, Qiwei
Gao, Jintao
Wang, Liangliang
He, Zuyong
Mo, Delin
Liu, Xiaohong
Chen, Yaosheng
author_facet Xiao, Shuqi
Wang, Qiwei
Gao, Jintao
Wang, Liangliang
He, Zuyong
Mo, Delin
Liu, Xiaohong
Chen, Yaosheng
author_sort Xiao, Shuqi
collection PubMed
description BACKGROUND: Highly pathogenic porcine reproductive and respiratory syndrome (HP-PRRS) has caused large economic losses in swine industry in recent years. However, current antiviral strategy could not effectively prevent and control this disease. In this research, five artificial microRNAs (amiRNAs) respectively targeted towards ORF5 (amirGP5-243, -370) and ORF6 (amirM-82, -217,-263) were designed and incorporated into a miRNA-based vector that mimics the backbone of murine miR-155 and permits high expression of amiRNAs in a GFP fused form mediated by RNA Pol II promoter CMV. RESULTS: It was found that amirGP5-370 could effectively inhibit H-PRRSV replication. The amirM-263-M-263, which was a dual pre-amiRNA expression cassette where two amirM-263s were chained, showed stronger virus inhibitory effects than single amirM-263. H-PRRSV replication was inhibited up to 120 hours in the MARC-145 cells which were stably transduced by recombinant lentiviruses (Lenti-amirGP5-370, -amirM-263-M-263). Additionally, efficacious dose of amirGP5-370 and amirM-263 expression did not trigger the innate interferon response. CONCLUSIONS: Our study is the first attempt to suppress H-PRRSV replication in MARC-145 cells through vector-based and lentiviral mediated amiRNAs targeting GP5 or M proteins coding sequences of PRRSV, which indicated that artificial microRNAs and recombinant lentiviruses might be applied to be a new potent anti-PRRSV strategy.
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spelling pubmed-32151882011-11-15 Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs Xiao, Shuqi Wang, Qiwei Gao, Jintao Wang, Liangliang He, Zuyong Mo, Delin Liu, Xiaohong Chen, Yaosheng Virol J Research BACKGROUND: Highly pathogenic porcine reproductive and respiratory syndrome (HP-PRRS) has caused large economic losses in swine industry in recent years. However, current antiviral strategy could not effectively prevent and control this disease. In this research, five artificial microRNAs (amiRNAs) respectively targeted towards ORF5 (amirGP5-243, -370) and ORF6 (amirM-82, -217,-263) were designed and incorporated into a miRNA-based vector that mimics the backbone of murine miR-155 and permits high expression of amiRNAs in a GFP fused form mediated by RNA Pol II promoter CMV. RESULTS: It was found that amirGP5-370 could effectively inhibit H-PRRSV replication. The amirM-263-M-263, which was a dual pre-amiRNA expression cassette where two amirM-263s were chained, showed stronger virus inhibitory effects than single amirM-263. H-PRRSV replication was inhibited up to 120 hours in the MARC-145 cells which were stably transduced by recombinant lentiviruses (Lenti-amirGP5-370, -amirM-263-M-263). Additionally, efficacious dose of amirGP5-370 and amirM-263 expression did not trigger the innate interferon response. CONCLUSIONS: Our study is the first attempt to suppress H-PRRSV replication in MARC-145 cells through vector-based and lentiviral mediated amiRNAs targeting GP5 or M proteins coding sequences of PRRSV, which indicated that artificial microRNAs and recombinant lentiviruses might be applied to be a new potent anti-PRRSV strategy. BioMed Central 2011-11-01 /pmc/articles/PMC3215188/ /pubmed/22040357 http://dx.doi.org/10.1186/1743-422X-8-491 Text en Copyright ©2011 Xiao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xiao, Shuqi
Wang, Qiwei
Gao, Jintao
Wang, Liangliang
He, Zuyong
Mo, Delin
Liu, Xiaohong
Chen, Yaosheng
Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs
title Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs
title_full Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs
title_fullStr Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs
title_full_unstemmed Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs
title_short Inhibition of highly pathogenic PRRSV replication in MARC-145 cells by artificial microRNAs
title_sort inhibition of highly pathogenic prrsv replication in marc-145 cells by artificial micrornas
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215188/
https://www.ncbi.nlm.nih.gov/pubmed/22040357
http://dx.doi.org/10.1186/1743-422X-8-491
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