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Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers
The genus Alphavirus contains members that threaten human health, both as natural pathogens and as potential biological weapons. Peptide-conjugated phosphorodiamidate morpholino oligomers (PPMO) enter cells readily and can inhibit viral replication through sequence-specific steric blockade of viral...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447162/ https://www.ncbi.nlm.nih.gov/pubmed/18468653 http://dx.doi.org/10.1016/j.virol.2008.03.032 |
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author | Paessler, Slobodan Rijnbrand, Rene Stein, David A. Ni, Haolin Yun, Nadezhda E. Dziuba, Natallia Borisevich, Viktoriya Seregin, Alexey Ma, Yinghong Blouch, Robert Iversen, Patrick L. Zacks, Michele A. |
author_facet | Paessler, Slobodan Rijnbrand, Rene Stein, David A. Ni, Haolin Yun, Nadezhda E. Dziuba, Natallia Borisevich, Viktoriya Seregin, Alexey Ma, Yinghong Blouch, Robert Iversen, Patrick L. Zacks, Michele A. |
author_sort | Paessler, Slobodan |
collection | PubMed |
description | The genus Alphavirus contains members that threaten human health, both as natural pathogens and as potential biological weapons. Peptide-conjugated phosphorodiamidate morpholino oligomers (PPMO) enter cells readily and can inhibit viral replication through sequence-specific steric blockade of viral RNA. Sindbis virus (SINV) has low pathogenicity in humans and is regularly utilized as a model alphavirus. PPMO targeting the 5′-terminal and AUG translation start site regions of the SINV genome blocked the production of infectious SINV in tissue culture. PPMO designed against corresponding regions in Venezuelan equine encephalitis virus (VEEV) were likewise found to be effective in vitro against several strains of VEEV. Mice treated with PPMO before and after VEEV infection were completely protected from lethal outcome while mice receiving only post-infection PPMO treatment were partially protected. Levels of virus in tissue samples correlated with animal survival. Uninfected mice suffered no apparent ill-effects from PPMO treatment. Thus, PPMO appear promising as candidates for therapeutic development against alphaviruses. |
format | Text |
id | pubmed-2447162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-24471622009-07-05 Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers Paessler, Slobodan Rijnbrand, Rene Stein, David A. Ni, Haolin Yun, Nadezhda E. Dziuba, Natallia Borisevich, Viktoriya Seregin, Alexey Ma, Yinghong Blouch, Robert Iversen, Patrick L. Zacks, Michele A. Virology Article The genus Alphavirus contains members that threaten human health, both as natural pathogens and as potential biological weapons. Peptide-conjugated phosphorodiamidate morpholino oligomers (PPMO) enter cells readily and can inhibit viral replication through sequence-specific steric blockade of viral RNA. Sindbis virus (SINV) has low pathogenicity in humans and is regularly utilized as a model alphavirus. PPMO targeting the 5′-terminal and AUG translation start site regions of the SINV genome blocked the production of infectious SINV in tissue culture. PPMO designed against corresponding regions in Venezuelan equine encephalitis virus (VEEV) were likewise found to be effective in vitro against several strains of VEEV. Mice treated with PPMO before and after VEEV infection were completely protected from lethal outcome while mice receiving only post-infection PPMO treatment were partially protected. Levels of virus in tissue samples correlated with animal survival. Uninfected mice suffered no apparent ill-effects from PPMO treatment. Thus, PPMO appear promising as candidates for therapeutic development against alphaviruses. Elsevier Inc. 2008-07-05 2008-05-12 /pmc/articles/PMC2447162/ /pubmed/18468653 http://dx.doi.org/10.1016/j.virol.2008.03.032 Text en Copyright © 2008 Elsevier Inc. 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 Paessler, Slobodan Rijnbrand, Rene Stein, David A. Ni, Haolin Yun, Nadezhda E. Dziuba, Natallia Borisevich, Viktoriya Seregin, Alexey Ma, Yinghong Blouch, Robert Iversen, Patrick L. Zacks, Michele A. Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
title | Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
title_full | Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
title_fullStr | Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
title_full_unstemmed | Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
title_short | Inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
title_sort | inhibition of alphavirus infection in cell culture and in mice with antisense morpholino oligomers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447162/ https://www.ncbi.nlm.nih.gov/pubmed/18468653 http://dx.doi.org/10.1016/j.virol.2008.03.032 |
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