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Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication
Porcine reproductive and respiratory syndrome (PRRS) has been devastating the global swine industry for more than a decade, and current strategies to control PRRS are inadequate. In this study we characterized the inhibition of PRRS virus (PRRSV) replication by antisense phosphorodiamidate morpholin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114306/ https://www.ncbi.nlm.nih.gov/pubmed/17959259 http://dx.doi.org/10.1016/j.antiviral.2007.09.002 |
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author | Patel, Deendayal Opriessnig, Tanja Stein, David A. Halbur, Patrick G. Meng, Xiang-Jin Iversen, Patrick L. Zhang, Yan-Jin |
author_facet | Patel, Deendayal Opriessnig, Tanja Stein, David A. Halbur, Patrick G. Meng, Xiang-Jin Iversen, Patrick L. Zhang, Yan-Jin |
author_sort | Patel, Deendayal |
collection | PubMed |
description | Porcine reproductive and respiratory syndrome (PRRS) has been devastating the global swine industry for more than a decade, and current strategies to control PRRS are inadequate. In this study we characterized the inhibition of PRRS virus (PRRSV) replication by antisense phosphorodiamidate morpholino oligomers (PMO). Of 12 peptide-conjugated PMO (PPMO), four were found to be highly effective at inhibiting PRRSV replication in cell culture in a dose-dependant and sequence-specific manner. PPMO 5UP2 and 5HP are complementary to sequence in the 5′ end of the PRRSV genome, and 6P1 and 7P1 to sequence in the translation initiation regions of ORF6 and ORF7, respectively. Treatment of cells with 5UP2 or 5HP caused a 4.5 log(10) reduction in PRRSV yield, compared to a control PPMO. Combination of 6P1 and 7P1 led to higher level reduction than 6P1 or 7P1 alone. 5UP2, 5HP, and a combination of 6P1 and 7P1 inhibited PRRSV replication in porcine alveolar macrophages and protected the cells from PRRSV-induced cytopathic effect. Northern blot and real-time RT-PCR results demonstrated that the effective PPMO led to a reduction of PRRSV RNA level. 5UP2 and 5HP inhibited virus replication of 10 other strains of PRRSV. Results from this study suggest potential applications of PPMO for PRRS control. |
format | Online Article Text |
id | pubmed-7114306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71143062020-04-02 Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication Patel, Deendayal Opriessnig, Tanja Stein, David A. Halbur, Patrick G. Meng, Xiang-Jin Iversen, Patrick L. Zhang, Yan-Jin Antiviral Res Article Porcine reproductive and respiratory syndrome (PRRS) has been devastating the global swine industry for more than a decade, and current strategies to control PRRS are inadequate. In this study we characterized the inhibition of PRRS virus (PRRSV) replication by antisense phosphorodiamidate morpholino oligomers (PMO). Of 12 peptide-conjugated PMO (PPMO), four were found to be highly effective at inhibiting PRRSV replication in cell culture in a dose-dependant and sequence-specific manner. PPMO 5UP2 and 5HP are complementary to sequence in the 5′ end of the PRRSV genome, and 6P1 and 7P1 to sequence in the translation initiation regions of ORF6 and ORF7, respectively. Treatment of cells with 5UP2 or 5HP caused a 4.5 log(10) reduction in PRRSV yield, compared to a control PPMO. Combination of 6P1 and 7P1 led to higher level reduction than 6P1 or 7P1 alone. 5UP2, 5HP, and a combination of 6P1 and 7P1 inhibited PRRSV replication in porcine alveolar macrophages and protected the cells from PRRSV-induced cytopathic effect. Northern blot and real-time RT-PCR results demonstrated that the effective PPMO led to a reduction of PRRSV RNA level. 5UP2 and 5HP inhibited virus replication of 10 other strains of PRRSV. Results from this study suggest potential applications of PPMO for PRRS control. Elsevier B.V. 2008-02 2007-10-04 /pmc/articles/PMC7114306/ /pubmed/17959259 http://dx.doi.org/10.1016/j.antiviral.2007.09.002 Text en Copyright © 2007 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 Patel, Deendayal Opriessnig, Tanja Stein, David A. Halbur, Patrick G. Meng, Xiang-Jin Iversen, Patrick L. Zhang, Yan-Jin Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
title | Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
title_full | Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
title_fullStr | Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
title_full_unstemmed | Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
title_short | Peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
title_sort | peptide-conjugated morpholino oligomers inhibit porcine reproductive and respiratory syndrome virus replication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114306/ https://www.ncbi.nlm.nih.gov/pubmed/17959259 http://dx.doi.org/10.1016/j.antiviral.2007.09.002 |
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