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Silvestrol Inhibits Chikungunya Virus Replication

Silvestrol, a natural compound that is isolated from plants of the genus Aglaia, is a specific inhibitor of the RNA helicase eIF4A, which unwinds RNA secondary structures in 5′-untranslated regions (UTRs) of mRNAs and allows translation. Silvestrol has a broad antiviral activity against multiple RNA...

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Autores principales: Henss, Lisa, Scholz, Tatjana, Grünweller, Arnold, Schnierle, Barbara S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266838/
https://www.ncbi.nlm.nih.gov/pubmed/30380742
http://dx.doi.org/10.3390/v10110592
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author Henss, Lisa
Scholz, Tatjana
Grünweller, Arnold
Schnierle, Barbara S.
author_facet Henss, Lisa
Scholz, Tatjana
Grünweller, Arnold
Schnierle, Barbara S.
author_sort Henss, Lisa
collection PubMed
description Silvestrol, a natural compound that is isolated from plants of the genus Aglaia, is a specific inhibitor of the RNA helicase eIF4A, which unwinds RNA secondary structures in 5′-untranslated regions (UTRs) of mRNAs and allows translation. Silvestrol has a broad antiviral activity against multiple RNA virus families. Here, we show that silvestrol inhibits the replication of chikungunya virus (CHIKV), a positive single-stranded RNA virus. Silvestrol delayed the protein synthesis of non-structural (nsPs) and structural proteins, resulting in a delayed innate response to CHIKV infection. Interferon-α induced STAT1 phosphorylation was not inhibited nor did eIF2α become phosphorylated 16 h post infection in the presence of silvestrol. In addition, the host protein shut-off induced by CHIKV infection was decreased in silvestrol-treated cells. Silvestrol acts by limiting the amount of nsPs, and thereby reducing CHIKV RNA replication. From our results, we propose that inhibition of the host helicase eIF4A might have potential as a therapeutic strategy to treat CHIKV infections.
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spelling pubmed-62668382018-12-07 Silvestrol Inhibits Chikungunya Virus Replication Henss, Lisa Scholz, Tatjana Grünweller, Arnold Schnierle, Barbara S. Viruses Article Silvestrol, a natural compound that is isolated from plants of the genus Aglaia, is a specific inhibitor of the RNA helicase eIF4A, which unwinds RNA secondary structures in 5′-untranslated regions (UTRs) of mRNAs and allows translation. Silvestrol has a broad antiviral activity against multiple RNA virus families. Here, we show that silvestrol inhibits the replication of chikungunya virus (CHIKV), a positive single-stranded RNA virus. Silvestrol delayed the protein synthesis of non-structural (nsPs) and structural proteins, resulting in a delayed innate response to CHIKV infection. Interferon-α induced STAT1 phosphorylation was not inhibited nor did eIF2α become phosphorylated 16 h post infection in the presence of silvestrol. In addition, the host protein shut-off induced by CHIKV infection was decreased in silvestrol-treated cells. Silvestrol acts by limiting the amount of nsPs, and thereby reducing CHIKV RNA replication. From our results, we propose that inhibition of the host helicase eIF4A might have potential as a therapeutic strategy to treat CHIKV infections. MDPI 2018-10-30 /pmc/articles/PMC6266838/ /pubmed/30380742 http://dx.doi.org/10.3390/v10110592 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Henss, Lisa
Scholz, Tatjana
Grünweller, Arnold
Schnierle, Barbara S.
Silvestrol Inhibits Chikungunya Virus Replication
title Silvestrol Inhibits Chikungunya Virus Replication
title_full Silvestrol Inhibits Chikungunya Virus Replication
title_fullStr Silvestrol Inhibits Chikungunya Virus Replication
title_full_unstemmed Silvestrol Inhibits Chikungunya Virus Replication
title_short Silvestrol Inhibits Chikungunya Virus Replication
title_sort silvestrol inhibits chikungunya virus replication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266838/
https://www.ncbi.nlm.nih.gov/pubmed/30380742
http://dx.doi.org/10.3390/v10110592
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