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Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro
Background: The emergence of drug-resistant strains of herpes simplex virus type 1 (HSV-1) has been increasingly reported. Therefore, attempts to discover new antiviral agents in particular from natural compounds are required. In this study, we evaluated the possible inhibitory effects of hydroalcoh...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Iran University of Medical Sciences
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111625/ https://www.ncbi.nlm.nih.gov/pubmed/33996660 http://dx.doi.org/10.47176/mjiri.35.9 |
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author | Ghaffari, Hadi Ataei-Pirkooh, Angila Mirghazanfari, Sayid Mahdi Barati, Mohammad |
author_facet | Ghaffari, Hadi Ataei-Pirkooh, Angila Mirghazanfari, Sayid Mahdi Barati, Mohammad |
author_sort | Ghaffari, Hadi |
collection | PubMed |
description | Background: The emergence of drug-resistant strains of herpes simplex virus type 1 (HSV-1) has been increasingly reported. Therefore, attempts to discover new antiviral agents in particular from natural compounds are required. In this study, we evaluated the possible inhibitory effects of hydroalcoholic extract of Sambucus ebulus (S. ebulus ) against HSV-1. Methods: S. ebulus extract was produced by maceration method. MTT assay was used to evaluate the cytotoxicity effects of the S. ebulus extract; also, antiviral effects were measured both by test TCID50 and quantitative real-time PCR methods. To study the inhibitory impact of S. ebulus extract on the expression of HSV-1 antigens, indirect immunofluorescence assay (IFA) was also performed. All analyses were performed using the GraphPad Prism software v. 7.0. Results: In the postexposure assay of HSV-1 with S. ebulus extract at the highest nontoxic concentration (75 μg/mL), S. ebulus extract led to 2.6 log10 TCID50 reduction in infectious virus titer. At the highest nontoxic concentration, the S. ebulus extract led to inhibition rates of 91.2%, based on the quantitative real-time PCR assay results (p<0.001). Also, in the immunofluorescence assay, a significant reduction was observed in fluorescence emission intensity in HSV-1-infected cell treated with S. ebulus extract compared to the control group. Conclusion: S. ebulus extract is a novel and effective natural compound in reducing HSV-1 titer and future studies should be conducted to discover the complete mechanism of antiviral effect of this natural compound. |
format | Online Article Text |
id | pubmed-8111625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Iran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-81116252021-05-13 Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro Ghaffari, Hadi Ataei-Pirkooh, Angila Mirghazanfari, Sayid Mahdi Barati, Mohammad Med J Islam Repub Iran Original Article Background: The emergence of drug-resistant strains of herpes simplex virus type 1 (HSV-1) has been increasingly reported. Therefore, attempts to discover new antiviral agents in particular from natural compounds are required. In this study, we evaluated the possible inhibitory effects of hydroalcoholic extract of Sambucus ebulus (S. ebulus ) against HSV-1. Methods: S. ebulus extract was produced by maceration method. MTT assay was used to evaluate the cytotoxicity effects of the S. ebulus extract; also, antiviral effects were measured both by test TCID50 and quantitative real-time PCR methods. To study the inhibitory impact of S. ebulus extract on the expression of HSV-1 antigens, indirect immunofluorescence assay (IFA) was also performed. All analyses were performed using the GraphPad Prism software v. 7.0. Results: In the postexposure assay of HSV-1 with S. ebulus extract at the highest nontoxic concentration (75 μg/mL), S. ebulus extract led to 2.6 log10 TCID50 reduction in infectious virus titer. At the highest nontoxic concentration, the S. ebulus extract led to inhibition rates of 91.2%, based on the quantitative real-time PCR assay results (p<0.001). Also, in the immunofluorescence assay, a significant reduction was observed in fluorescence emission intensity in HSV-1-infected cell treated with S. ebulus extract compared to the control group. Conclusion: S. ebulus extract is a novel and effective natural compound in reducing HSV-1 titer and future studies should be conducted to discover the complete mechanism of antiviral effect of this natural compound. Iran University of Medical Sciences 2021-01-18 /pmc/articles/PMC8111625/ /pubmed/33996660 http://dx.doi.org/10.47176/mjiri.35.9 Text en © 2021 Iran University of Medical Sciences https://creativecommons.org/licenses/by-nc-sa/1.0/This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial-ShareAlike 1.0 License (CC BY-NC-SA 1.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Ghaffari, Hadi Ataei-Pirkooh, Angila Mirghazanfari, Sayid Mahdi Barati, Mohammad Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro |
title |
Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro
|
title_full |
Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro
|
title_fullStr |
Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro
|
title_full_unstemmed |
Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro
|
title_short |
Inhibition of herpes simplex virus type 1 infection by Sambucus ebulus extract in vitro
|
title_sort | inhibition of herpes simplex virus type 1 infection by sambucus ebulus extract in vitro |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111625/ https://www.ncbi.nlm.nih.gov/pubmed/33996660 http://dx.doi.org/10.47176/mjiri.35.9 |
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