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Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer
A significant consequence of equine arteritis virus (EAV) infection of horses is persistence of the virus in a variable percentage of infected stallions. We recently established an in vitro model of EAV persistence in cell culture for the purpose of furthering our understanding of EAV biology in gen...
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/PMC7114391/ https://www.ncbi.nlm.nih.gov/pubmed/20206215 http://dx.doi.org/10.1016/j.virusres.2010.02.013 |
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author | Zhang, Jianqiang Stein, David A. Timoney, Peter J. Balasuriya, Udeni B.R. |
author_facet | Zhang, Jianqiang Stein, David A. Timoney, Peter J. Balasuriya, Udeni B.R. |
author_sort | Zhang, Jianqiang |
collection | PubMed |
description | A significant consequence of equine arteritis virus (EAV) infection of horses is persistence of the virus in a variable percentage of infected stallions. We recently established an in vitro model of EAV persistence in cell culture for the purpose of furthering our understanding of EAV biology in general and viral persistence in the stallion in particular. In this study we investigated whether persistently infected HeLa cells could be cured of EAV infection by treatment with an antisense peptide-conjugated phosphorodiamidate morpholino oligomer (PPMO) designed to target the 5′-terminal region of the EAV genome. We found that persistently infected HeLa cells passaged three times in the presence of 5–10 μM EAV-specific PPMO produced no detectable virus. The PPMO-cured HeLa cells were free of infectious virus, viral antigen and EAV RNA as measured by plaque assay, indirect immunofluorescence assay and RT-PCR, respectively. Furthermore, when re-challenged with EAV at several passages after discontinuation of PPMO treatments, PPMO-cured HeLa cells were found to be refractory to re-infection and to the re-establishment of viral persistence. While these findings demonstrate that PPMO can be used to eliminate persistent EAV infection in cell culture, the efficacy of PPMO against EAV in vivo remains to be addressed. |
format | Online Article Text |
id | pubmed-7114391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71143912020-04-02 Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer Zhang, Jianqiang Stein, David A. Timoney, Peter J. Balasuriya, Udeni B.R. Virus Res Article A significant consequence of equine arteritis virus (EAV) infection of horses is persistence of the virus in a variable percentage of infected stallions. We recently established an in vitro model of EAV persistence in cell culture for the purpose of furthering our understanding of EAV biology in general and viral persistence in the stallion in particular. In this study we investigated whether persistently infected HeLa cells could be cured of EAV infection by treatment with an antisense peptide-conjugated phosphorodiamidate morpholino oligomer (PPMO) designed to target the 5′-terminal region of the EAV genome. We found that persistently infected HeLa cells passaged three times in the presence of 5–10 μM EAV-specific PPMO produced no detectable virus. The PPMO-cured HeLa cells were free of infectious virus, viral antigen and EAV RNA as measured by plaque assay, indirect immunofluorescence assay and RT-PCR, respectively. Furthermore, when re-challenged with EAV at several passages after discontinuation of PPMO treatments, PPMO-cured HeLa cells were found to be refractory to re-infection and to the re-establishment of viral persistence. While these findings demonstrate that PPMO can be used to eliminate persistent EAV infection in cell culture, the efficacy of PPMO against EAV in vivo remains to be addressed. Elsevier B.V. 2010-06 2010-03-03 /pmc/articles/PMC7114391/ /pubmed/20206215 http://dx.doi.org/10.1016/j.virusres.2010.02.013 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 Zhang, Jianqiang Stein, David A. Timoney, Peter J. Balasuriya, Udeni B.R. Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
title | Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
title_full | Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
title_fullStr | Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
title_full_unstemmed | Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
title_short | Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
title_sort | curing of hela cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114391/ https://www.ncbi.nlm.nih.gov/pubmed/20206215 http://dx.doi.org/10.1016/j.virusres.2010.02.013 |
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