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In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference
Classical swine fever (CSF) is a highly contagious viral disease of pigs which causes major economic losses worldwide. No specific drug is currently available for the effective treatment of CSFV infection. RNA interference (RNAi) technology depends on effective delivery systems, for which several ef...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112837/ https://www.ncbi.nlm.nih.gov/pubmed/20691206 http://dx.doi.org/10.1016/j.jviromet.2010.07.036 |
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author | Li, Jiangnan Guo, Huancheng Shi, Zixue Tu, Changchun |
author_facet | Li, Jiangnan Guo, Huancheng Shi, Zixue Tu, Changchun |
author_sort | Li, Jiangnan |
collection | PubMed |
description | Classical swine fever (CSF) is a highly contagious viral disease of pigs which causes major economic losses worldwide. No specific drug is currently available for the effective treatment of CSFV infection. RNA interference (RNAi) technology depends on effective delivery systems, for which several effective vectors have recently been developed. Three retroviral plasmids containing siRNA genes targeting different regions of N(pro) and NS4A have been constructed, and 3 replication-incompetent retroviral vectors have been produced in the human embryo kidney cell line GP2-293 by retroviral plasmid transfection. PK-15 cells were then infected with these replication-incompetent retroviral vectors and screened for siRNA stably expressing PK-15 cell clones. Growth of CSFV in such siRNA stably expressing cell clones resulted in a 186-fold reduction in viral genome copies and, at 72 h post-infection, only a small % of cells showed infection by indirect immunofluorescence microscopy, and effective inhibition of virus replication persisted for up to 120 h. Retroviral vector-mediated RNAi can therefore be used to study the specific function of viral genes associated with CSFV replication and may have potential therapeutic application. |
format | Online Article Text |
id | pubmed-7112837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71128372020-04-02 In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference Li, Jiangnan Guo, Huancheng Shi, Zixue Tu, Changchun J Virol Methods Article Classical swine fever (CSF) is a highly contagious viral disease of pigs which causes major economic losses worldwide. No specific drug is currently available for the effective treatment of CSFV infection. RNA interference (RNAi) technology depends on effective delivery systems, for which several effective vectors have recently been developed. Three retroviral plasmids containing siRNA genes targeting different regions of N(pro) and NS4A have been constructed, and 3 replication-incompetent retroviral vectors have been produced in the human embryo kidney cell line GP2-293 by retroviral plasmid transfection. PK-15 cells were then infected with these replication-incompetent retroviral vectors and screened for siRNA stably expressing PK-15 cell clones. Growth of CSFV in such siRNA stably expressing cell clones resulted in a 186-fold reduction in viral genome copies and, at 72 h post-infection, only a small % of cells showed infection by indirect immunofluorescence microscopy, and effective inhibition of virus replication persisted for up to 120 h. Retroviral vector-mediated RNAi can therefore be used to study the specific function of viral genes associated with CSFV replication and may have potential therapeutic application. Elsevier B.V. 2010-11 2010-08-04 /pmc/articles/PMC7112837/ /pubmed/20691206 http://dx.doi.org/10.1016/j.jviromet.2010.07.036 Text en Copyright © 2010 Elsevier B.V. All rights reserved. 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, Jiangnan Guo, Huancheng Shi, Zixue Tu, Changchun In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference |
title | In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference |
title_full | In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference |
title_fullStr | In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference |
title_full_unstemmed | In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference |
title_short | In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference |
title_sort | in vitro inhibition of csfv replication by retroviral vector-mediated rna interference |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112837/ https://www.ncbi.nlm.nih.gov/pubmed/20691206 http://dx.doi.org/10.1016/j.jviromet.2010.07.036 |
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