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Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers
Porcine reproductive and respiratory syndrome virus (PRRSV) is the causative agent of a contagious disease characterized by reproductive failure in sows and respiratory disease in piglets. This infectious disease results in significant losses in the swine industry and specific anti-PRRSV drugs are n...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117520/ https://www.ncbi.nlm.nih.gov/pubmed/16839712 http://dx.doi.org/10.1016/j.vetmic.2006.06.006 |
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author | Zhang, Yan-Jin Stein, David A. Fan, Su-Min Wang, Kai-Yu Kroeker, Andrew D. Meng, Xiang-Jin Iversen, Patrick L. Matson, David O. |
author_facet | Zhang, Yan-Jin Stein, David A. Fan, Su-Min Wang, Kai-Yu Kroeker, Andrew D. Meng, Xiang-Jin Iversen, Patrick L. Matson, David O. |
author_sort | Zhang, Yan-Jin |
collection | PubMed |
description | Porcine reproductive and respiratory syndrome virus (PRRSV) is the causative agent of a contagious disease characterized by reproductive failure in sows and respiratory disease in piglets. This infectious disease results in significant losses in the swine industry and specific anti-PRRSV drugs are needed. In this study, we evaluated a novel class of antisense compounds, peptide-conjugated phosphorodiamidate morpholino oligomers (P-PMOs), for their ability to suppress PRRSV replication in cell culture. P-PMOs are analogs of single-stranded DNA and contain a modified backbone that confers highly specific binding to RNA and resistance to nucleases. Of six P-PMOs tested, one (‘5UP1’), with sequence complementary to the 5′-terminal 21 nucleotides of the PRRSV genome, was found to be highly effective at reducing PRRSV replication in a specific and dose-dependent manner in CRL11171 cells in culture. 5UP1 treatment generated up to a 4.5 log reduction in infectious PRRSV yield, while a control P-PMO had no effect on viral titer. Immunofluorescence assay with an anti-PRRSV monoclonal antibody confirmed the titer observations. The sequence-specificity of 5UP1 effect was confirmed in part by a cell-free luciferase reporter assay system, which showed that 5UP1-mediated inhibition of translation decreased if the target-RNA contained mispairings in relation to the 5UP1 P-PMO. Real-time RT-PCR showed that the production of PRRSV negative-sense RNA was reduced if 5UP1 was added to cells at up to 6 h post-virus inoculation. Cell viability assays detected no cytotoxicity of 5UP1 within the concentration-range of this study. These results indicate that P-PMO 5UP1 has potential as an anti-PRRSV agent. |
format | Online Article Text |
id | pubmed-7117520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71175202020-04-02 Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers Zhang, Yan-Jin Stein, David A. Fan, Su-Min Wang, Kai-Yu Kroeker, Andrew D. Meng, Xiang-Jin Iversen, Patrick L. Matson, David O. Vet Microbiol Article Porcine reproductive and respiratory syndrome virus (PRRSV) is the causative agent of a contagious disease characterized by reproductive failure in sows and respiratory disease in piglets. This infectious disease results in significant losses in the swine industry and specific anti-PRRSV drugs are needed. In this study, we evaluated a novel class of antisense compounds, peptide-conjugated phosphorodiamidate morpholino oligomers (P-PMOs), for their ability to suppress PRRSV replication in cell culture. P-PMOs are analogs of single-stranded DNA and contain a modified backbone that confers highly specific binding to RNA and resistance to nucleases. Of six P-PMOs tested, one (‘5UP1’), with sequence complementary to the 5′-terminal 21 nucleotides of the PRRSV genome, was found to be highly effective at reducing PRRSV replication in a specific and dose-dependent manner in CRL11171 cells in culture. 5UP1 treatment generated up to a 4.5 log reduction in infectious PRRSV yield, while a control P-PMO had no effect on viral titer. Immunofluorescence assay with an anti-PRRSV monoclonal antibody confirmed the titer observations. The sequence-specificity of 5UP1 effect was confirmed in part by a cell-free luciferase reporter assay system, which showed that 5UP1-mediated inhibition of translation decreased if the target-RNA contained mispairings in relation to the 5UP1 P-PMO. Real-time RT-PCR showed that the production of PRRSV negative-sense RNA was reduced if 5UP1 was added to cells at up to 6 h post-virus inoculation. Cell viability assays detected no cytotoxicity of 5UP1 within the concentration-range of this study. These results indicate that P-PMO 5UP1 has potential as an anti-PRRSV agent. Elsevier B.V. 2006-10-31 2006-07-12 /pmc/articles/PMC7117520/ /pubmed/16839712 http://dx.doi.org/10.1016/j.vetmic.2006.06.006 Text en Copyright © 2006 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 Zhang, Yan-Jin Stein, David A. Fan, Su-Min Wang, Kai-Yu Kroeker, Andrew D. Meng, Xiang-Jin Iversen, Patrick L. Matson, David O. Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
title | Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
title_full | Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
title_fullStr | Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
title_full_unstemmed | Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
title_short | Suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
title_sort | suppression of porcine reproductive and respiratory syndrome virus replication by morpholino antisense oligomers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117520/ https://www.ncbi.nlm.nih.gov/pubmed/16839712 http://dx.doi.org/10.1016/j.vetmic.2006.06.006 |
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