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Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus

BACKGROUND: Hepatitis C virus (HCV) infection is a major worldwide health problem that can cause liver fibrosis and hepatocellular carcinoma (HCC). The clinical treatment of HCV infection mainly relies on the use of direct-acting antivirals (DAAs) that are usually expensive and have side effects. Th...

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Autores principales: Sarhan, Moustafa, El-Bitar, Alaa M. H., Mohammadein, Amaal, Elshehaby, Mohammed, Hotta, Hak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609606/
https://www.ncbi.nlm.nih.gov/pubmed/34868283
http://dx.doi.org/10.1590/1678-9199-JVATITD-2021-0039
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author Sarhan, Moustafa
El-Bitar, Alaa M. H.
Mohammadein, Amaal
Elshehaby, Mohammed
Hotta, Hak
author_facet Sarhan, Moustafa
El-Bitar, Alaa M. H.
Mohammadein, Amaal
Elshehaby, Mohammed
Hotta, Hak
author_sort Sarhan, Moustafa
collection PubMed
description BACKGROUND: Hepatitis C virus (HCV) infection is a major worldwide health problem that can cause liver fibrosis and hepatocellular carcinoma (HCC). The clinical treatment of HCV infection mainly relies on the use of direct-acting antivirals (DAAs) that are usually expensive and have side effects. Therefore, achieving the discovery of more successful agents is always urgent. In this context, antiviral compounds that inhibit viral infections and disease progression with important therapeutic activities have been identified in animal venoms including arthropod toxins. This indicates that arthropod venoms represent a good natural source of promising candidates for new antivirals. METHODS: The antiviral activity of the wasp venom (WV), isolated from the Oriental hornet (Vespa orientalis), was assessed using cell culture technique with human hepatocellular carcinoma-derived cell line (Huh7it-1) and the recombinant strain of HCV genotype 2a (JFH1). RESULTS: The results revealed that WV inhibited HCV infectivity with 50% inhibitory concentration (IC(50)) of 10 ng/mL, while the 50% cytotoxic concentration (CC(50)) was 11,000 ng/mL. Time of addition experiment showed that the WV blocked HCV attachment/entry to the cells probably through virucidal effect. On the other hand, the venom showed no inhibitory effect on HCV replication. CONCLUSION: WV can inhibit the entry stage of HCV infection at non-cytotoxic concentrations. Therefore, it could be considered a potential candidate for characterization of natural anti-HCV agents targeting the entry step.
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spelling pubmed-86096062021-12-03 Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus Sarhan, Moustafa El-Bitar, Alaa M. H. Mohammadein, Amaal Elshehaby, Mohammed Hotta, Hak J Venom Anim Toxins Incl Trop Dis Research BACKGROUND: Hepatitis C virus (HCV) infection is a major worldwide health problem that can cause liver fibrosis and hepatocellular carcinoma (HCC). The clinical treatment of HCV infection mainly relies on the use of direct-acting antivirals (DAAs) that are usually expensive and have side effects. Therefore, achieving the discovery of more successful agents is always urgent. In this context, antiviral compounds that inhibit viral infections and disease progression with important therapeutic activities have been identified in animal venoms including arthropod toxins. This indicates that arthropod venoms represent a good natural source of promising candidates for new antivirals. METHODS: The antiviral activity of the wasp venom (WV), isolated from the Oriental hornet (Vespa orientalis), was assessed using cell culture technique with human hepatocellular carcinoma-derived cell line (Huh7it-1) and the recombinant strain of HCV genotype 2a (JFH1). RESULTS: The results revealed that WV inhibited HCV infectivity with 50% inhibitory concentration (IC(50)) of 10 ng/mL, while the 50% cytotoxic concentration (CC(50)) was 11,000 ng/mL. Time of addition experiment showed that the WV blocked HCV attachment/entry to the cells probably through virucidal effect. On the other hand, the venom showed no inhibitory effect on HCV replication. CONCLUSION: WV can inhibit the entry stage of HCV infection at non-cytotoxic concentrations. Therefore, it could be considered a potential candidate for characterization of natural anti-HCV agents targeting the entry step. Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) 2021-11-19 /pmc/articles/PMC8609606/ /pubmed/34868283 http://dx.doi.org/10.1590/1678-9199-JVATITD-2021-0039 Text en https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sarhan, Moustafa
El-Bitar, Alaa M. H.
Mohammadein, Amaal
Elshehaby, Mohammed
Hotta, Hak
Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus
title Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus
title_full Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus
title_fullStr Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus
title_full_unstemmed Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus
title_short Virucidal activity of oriental hornet Vespa orientalis venom against hepatitis C virus
title_sort virucidal activity of oriental hornet vespa orientalis venom against hepatitis c virus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609606/
https://www.ncbi.nlm.nih.gov/pubmed/34868283
http://dx.doi.org/10.1590/1678-9199-JVATITD-2021-0039
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