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Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins

Novel therapeutic options are urgently needed to improve global treatment of virus infections. Herbal products with confirmed clinical safety features are attractive starting material for the identification of new antiviral activities. Here we demonstrate that Cistus incanus (Ci) herbal products inh...

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Autores principales: Rebensburg, Stephanie, Helfer, Markus, Schneider, Martha, Koppensteiner, Herwig, Eberle, Josef, Schindler, Michael, Gürtler, Lutz, Brack-Werner, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735868/
https://www.ncbi.nlm.nih.gov/pubmed/26833261
http://dx.doi.org/10.1038/srep20394
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author Rebensburg, Stephanie
Helfer, Markus
Schneider, Martha
Koppensteiner, Herwig
Eberle, Josef
Schindler, Michael
Gürtler, Lutz
Brack-Werner, Ruth
author_facet Rebensburg, Stephanie
Helfer, Markus
Schneider, Martha
Koppensteiner, Herwig
Eberle, Josef
Schindler, Michael
Gürtler, Lutz
Brack-Werner, Ruth
author_sort Rebensburg, Stephanie
collection PubMed
description Novel therapeutic options are urgently needed to improve global treatment of virus infections. Herbal products with confirmed clinical safety features are attractive starting material for the identification of new antiviral activities. Here we demonstrate that Cistus incanus (Ci) herbal products inhibit human immunodeficiency virus (HIV) infections in vitro. Ci extract inhibited clinical HIV-1 and HIV-2 isolates, and, importantly, a virus isolate with multiple drug resistances, confirming broad anti-HIV activity. Antiviral activity was highly selective for virus particles, preventing primary attachment of the virus to the cell surface and viral envelope proteins from binding to heparin. Bioassay-guided fractionation indicated that Ci extract contains numerous antiviral compounds and therefore has favorably low propensity to induce virus resistance. Indeed, no resistant viruses emerged during 24 weeks of continuous propagation of the virus in the presence of Ci extracts. Finally, Ci extracts also inhibited infection by virus particles pseudotyped with Ebola and Marburg virus envelope proteins, indicating that antiviral activity of Ci extract extends to emerging viral pathogens. These results demonstrate that Ci extracts show potent and broad in vitro antiviral activity against viruses that cause life-threatening diseases in humans and are promising sources of agents that target virus particles.
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spelling pubmed-47358682016-02-05 Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins Rebensburg, Stephanie Helfer, Markus Schneider, Martha Koppensteiner, Herwig Eberle, Josef Schindler, Michael Gürtler, Lutz Brack-Werner, Ruth Sci Rep Article Novel therapeutic options are urgently needed to improve global treatment of virus infections. Herbal products with confirmed clinical safety features are attractive starting material for the identification of new antiviral activities. Here we demonstrate that Cistus incanus (Ci) herbal products inhibit human immunodeficiency virus (HIV) infections in vitro. Ci extract inhibited clinical HIV-1 and HIV-2 isolates, and, importantly, a virus isolate with multiple drug resistances, confirming broad anti-HIV activity. Antiviral activity was highly selective for virus particles, preventing primary attachment of the virus to the cell surface and viral envelope proteins from binding to heparin. Bioassay-guided fractionation indicated that Ci extract contains numerous antiviral compounds and therefore has favorably low propensity to induce virus resistance. Indeed, no resistant viruses emerged during 24 weeks of continuous propagation of the virus in the presence of Ci extracts. Finally, Ci extracts also inhibited infection by virus particles pseudotyped with Ebola and Marburg virus envelope proteins, indicating that antiviral activity of Ci extract extends to emerging viral pathogens. These results demonstrate that Ci extracts show potent and broad in vitro antiviral activity against viruses that cause life-threatening diseases in humans and are promising sources of agents that target virus particles. Nature Publishing Group 2016-02-02 /pmc/articles/PMC4735868/ /pubmed/26833261 http://dx.doi.org/10.1038/srep20394 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Rebensburg, Stephanie
Helfer, Markus
Schneider, Martha
Koppensteiner, Herwig
Eberle, Josef
Schindler, Michael
Gürtler, Lutz
Brack-Werner, Ruth
Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins
title Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins
title_full Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins
title_fullStr Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins
title_full_unstemmed Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins
title_short Potent in vitro antiviral activity of Cistus incanus extract against HIV and Filoviruses targets viral envelope proteins
title_sort potent in vitro antiviral activity of cistus incanus extract against hiv and filoviruses targets viral envelope proteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735868/
https://www.ncbi.nlm.nih.gov/pubmed/26833261
http://dx.doi.org/10.1038/srep20394
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