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Inhibition of Junín virus replication by small interfering RNAs

Junín virus (JUNV), the etiological agent of the Argentine hemorrhagic fever, has a single-stranded RNA genome with ambisense expression which encodes for five proteins. In previous works we have demonstrated that the Z arenavirus matrix protein represents an attractive target for antiviral therapy....

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Autores principales: Artuso, María C., Ellenberg, Paula C., Scolaro, Luis A., Damonte, Elsa B., García, Cybele C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114203/
https://www.ncbi.nlm.nih.gov/pubmed/19591878
http://dx.doi.org/10.1016/j.antiviral.2009.07.001
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author Artuso, María C.
Ellenberg, Paula C.
Scolaro, Luis A.
Damonte, Elsa B.
García, Cybele C.
author_facet Artuso, María C.
Ellenberg, Paula C.
Scolaro, Luis A.
Damonte, Elsa B.
García, Cybele C.
author_sort Artuso, María C.
collection PubMed
description Junín virus (JUNV), the etiological agent of the Argentine hemorrhagic fever, has a single-stranded RNA genome with ambisense expression which encodes for five proteins. In previous works we have demonstrated that the Z arenavirus matrix protein represents an attractive target for antiviral therapy. With the aim of studying a new alternative therapeutic mechanism, four Z-specific siRNAs (Z1- to Z4-siRNAs) were tested showing variable efficacy. The most effective inhibitor was Z2-siRNA targeted at the region encompassed by nt 179–197 of Z gene. The efficacy of this Z2-siRNA against JUNV was also demonstrated in virus-infected cells, by testing infectious virus plaque formation (92.8% JUNV yield reduction), viral RNA level or antigen expression, as well as in cells transfected with Z-specific reporter plasmids (91% reduction in expression of Z-EGFP fusion protein). Furthermore, the lack of effect of this Z-siRNA on the expression of other JUNV proteins, such as N and GPC, confirmed the specificity of action exerted by Z2-siRNA on Z transcript. Thus, the present study represents the first report of virus inhibition mediated by RNA interference for a New World arenavirus.
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spelling pubmed-71142032020-04-02 Inhibition of Junín virus replication by small interfering RNAs Artuso, María C. Ellenberg, Paula C. Scolaro, Luis A. Damonte, Elsa B. García, Cybele C. Antiviral Res Article Junín virus (JUNV), the etiological agent of the Argentine hemorrhagic fever, has a single-stranded RNA genome with ambisense expression which encodes for five proteins. In previous works we have demonstrated that the Z arenavirus matrix protein represents an attractive target for antiviral therapy. With the aim of studying a new alternative therapeutic mechanism, four Z-specific siRNAs (Z1- to Z4-siRNAs) were tested showing variable efficacy. The most effective inhibitor was Z2-siRNA targeted at the region encompassed by nt 179–197 of Z gene. The efficacy of this Z2-siRNA against JUNV was also demonstrated in virus-infected cells, by testing infectious virus plaque formation (92.8% JUNV yield reduction), viral RNA level or antigen expression, as well as in cells transfected with Z-specific reporter plasmids (91% reduction in expression of Z-EGFP fusion protein). Furthermore, the lack of effect of this Z-siRNA on the expression of other JUNV proteins, such as N and GPC, confirmed the specificity of action exerted by Z2-siRNA on Z transcript. Thus, the present study represents the first report of virus inhibition mediated by RNA interference for a New World arenavirus. Elsevier B.V. 2009-10 2009-07-08 /pmc/articles/PMC7114203/ /pubmed/19591878 http://dx.doi.org/10.1016/j.antiviral.2009.07.001 Text en Copyright © 2009 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
Artuso, María C.
Ellenberg, Paula C.
Scolaro, Luis A.
Damonte, Elsa B.
García, Cybele C.
Inhibition of Junín virus replication by small interfering RNAs
title Inhibition of Junín virus replication by small interfering RNAs
title_full Inhibition of Junín virus replication by small interfering RNAs
title_fullStr Inhibition of Junín virus replication by small interfering RNAs
title_full_unstemmed Inhibition of Junín virus replication by small interfering RNAs
title_short Inhibition of Junín virus replication by small interfering RNAs
title_sort inhibition of junín virus replication by small interfering rnas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114203/
https://www.ncbi.nlm.nih.gov/pubmed/19591878
http://dx.doi.org/10.1016/j.antiviral.2009.07.001
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