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In vitro inhibition of feline coronavirus replication by small interfering RNAs
Infection with virulent biotypes of feline coronavirus (FCoV) can result in the development of feline infectious peritonitis (FIP), a typically fatal immune mediated disease for which there is currently no effective antiviral treatment. In this study we demonstrate the ability of small interfering R...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117188/ https://www.ncbi.nlm.nih.gov/pubmed/21367541 http://dx.doi.org/10.1016/j.vetmic.2011.01.023 |
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author | McDonagh, Phillip Sheehy, Paul A. Norris, Jacqueline M. |
author_facet | McDonagh, Phillip Sheehy, Paul A. Norris, Jacqueline M. |
author_sort | McDonagh, Phillip |
collection | PubMed |
description | Infection with virulent biotypes of feline coronavirus (FCoV) can result in the development of feline infectious peritonitis (FIP), a typically fatal immune mediated disease for which there is currently no effective antiviral treatment. In this study we demonstrate the ability of small interfering RNA (siRNA) mediated RNA interference (RNAi) to inhibit the replication of virulent FCoV strain FIPV WSU 79-1146 in an immortalised feline cell line. A panel of eight synthetic siRNAs targeting four different regions of the FCoV genome were tested for antiviral effects. Efficacy was determined by qRT-PCR of intracellular viral genomic and messenger RNA, TCID50 infectivity assay of extracellular virus, and direct IFA for viral protein expression. All siRNAs demonstrated an inhibitory effect on viral replication in vitro. The two most effective siRNAs, targeting the untranslated 5′ leader sequence (L2) and the nucleocapsid gene (N1), resulted in a >95% reduction in extracellular viral titre. Further characterisation of these two siRNAs demonstrated their efficacy when used at low concentrations and in cells challenged with high viral loads. Taken together these findings provide important information for the potential therapeutic application of RNAi in treating FIP. |
format | Online Article Text |
id | pubmed-7117188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71171882020-04-02 In vitro inhibition of feline coronavirus replication by small interfering RNAs McDonagh, Phillip Sheehy, Paul A. Norris, Jacqueline M. Vet Microbiol Article Infection with virulent biotypes of feline coronavirus (FCoV) can result in the development of feline infectious peritonitis (FIP), a typically fatal immune mediated disease for which there is currently no effective antiviral treatment. In this study we demonstrate the ability of small interfering RNA (siRNA) mediated RNA interference (RNAi) to inhibit the replication of virulent FCoV strain FIPV WSU 79-1146 in an immortalised feline cell line. A panel of eight synthetic siRNAs targeting four different regions of the FCoV genome were tested for antiviral effects. Efficacy was determined by qRT-PCR of intracellular viral genomic and messenger RNA, TCID50 infectivity assay of extracellular virus, and direct IFA for viral protein expression. All siRNAs demonstrated an inhibitory effect on viral replication in vitro. The two most effective siRNAs, targeting the untranslated 5′ leader sequence (L2) and the nucleocapsid gene (N1), resulted in a >95% reduction in extracellular viral titre. Further characterisation of these two siRNAs demonstrated their efficacy when used at low concentrations and in cells challenged with high viral loads. Taken together these findings provide important information for the potential therapeutic application of RNAi in treating FIP. Elsevier B.V. 2011-06-02 2011-02-01 /pmc/articles/PMC7117188/ /pubmed/21367541 http://dx.doi.org/10.1016/j.vetmic.2011.01.023 Text en Copyright © 2011 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 McDonagh, Phillip Sheehy, Paul A. Norris, Jacqueline M. In vitro inhibition of feline coronavirus replication by small interfering RNAs |
title | In vitro inhibition of feline coronavirus replication by small interfering RNAs |
title_full | In vitro inhibition of feline coronavirus replication by small interfering RNAs |
title_fullStr | In vitro inhibition of feline coronavirus replication by small interfering RNAs |
title_full_unstemmed | In vitro inhibition of feline coronavirus replication by small interfering RNAs |
title_short | In vitro inhibition of feline coronavirus replication by small interfering RNAs |
title_sort | in vitro inhibition of feline coronavirus replication by small interfering rnas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117188/ https://www.ncbi.nlm.nih.gov/pubmed/21367541 http://dx.doi.org/10.1016/j.vetmic.2011.01.023 |
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