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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...

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Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Inc. 2008
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.
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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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