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Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1

Ficus rubiginosa plant extract showed antimicrobial activity, but no evidence concerning its antiviral properties was reported. The antiviral activity of the methanolic extract (MeOH) and its n-hexane (H) and ethyl acetate (EA) fractions against Herpes simplex virus-1 (HSV-1), Human coronavirus (HCo...

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Autores principales: Dell’Annunziata, Federica, Sellitto, Carmine, Franci, Gianluigi, Marcotullio, Maria Carla, Piovan, Anna, Della Marca, Roberta, Folliero, Veronica, Galdiero, Massimiliano, Filippelli, Amelia, Conti, Valeria, Delfino, Domenico Vittorio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607631/
https://www.ncbi.nlm.nih.gov/pubmed/36298811
http://dx.doi.org/10.3390/v14102257
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author Dell’Annunziata, Federica
Sellitto, Carmine
Franci, Gianluigi
Marcotullio, Maria Carla
Piovan, Anna
Della Marca, Roberta
Folliero, Veronica
Galdiero, Massimiliano
Filippelli, Amelia
Conti, Valeria
Delfino, Domenico Vittorio
author_facet Dell’Annunziata, Federica
Sellitto, Carmine
Franci, Gianluigi
Marcotullio, Maria Carla
Piovan, Anna
Della Marca, Roberta
Folliero, Veronica
Galdiero, Massimiliano
Filippelli, Amelia
Conti, Valeria
Delfino, Domenico Vittorio
author_sort Dell’Annunziata, Federica
collection PubMed
description Ficus rubiginosa plant extract showed antimicrobial activity, but no evidence concerning its antiviral properties was reported. The antiviral activity of the methanolic extract (MeOH) and its n-hexane (H) and ethyl acetate (EA) fractions against Herpes simplex virus-1 (HSV-1), Human coronavirus (HCoV) -229E, and Poliovirus-1 (PV-1) was investigated in the different phases of viral infection in the VERO CCL-81 cell line. To confirm the antiviral efficacy, a qPCR was conducted. The recorded cytotoxic concentration 50% was 513.1, 298.6, and 56.45 µg/mL for MeOH, H, and EA, respectively, assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay after 72 h of treatment. The Ficus rubiginosa leaf extract inhibited the replication of HSV-1 in the early stages of infection, showing a complete inhibition up to 0.62, 0.31, and 1.25 µg/mL. Against HCoV-229E, a total inhibition up to 1.25 µg/mL for MeOH and H as well as 5 µg/mL for EA was observed. Otherwise, no activity was recorded against PV-1. The leaf extract could act directly on the viral envelope, destructuring the lipid membrane and/or directly blocking the enriched proteins on the viral surface. The verified gene inhibition suggested that the treatments with M, H, and EA impaired HSV-1 and HCoV-229E replication, with a greater antiviral efficiency against HSV-1 compared to HCoV-229E, possibly due to a greater affinity of Ficus rubiginosa towards membrane glycoproteins and/or the different lipid envelopes.
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spelling pubmed-96076312022-10-28 Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1 Dell’Annunziata, Federica Sellitto, Carmine Franci, Gianluigi Marcotullio, Maria Carla Piovan, Anna Della Marca, Roberta Folliero, Veronica Galdiero, Massimiliano Filippelli, Amelia Conti, Valeria Delfino, Domenico Vittorio Viruses Article Ficus rubiginosa plant extract showed antimicrobial activity, but no evidence concerning its antiviral properties was reported. The antiviral activity of the methanolic extract (MeOH) and its n-hexane (H) and ethyl acetate (EA) fractions against Herpes simplex virus-1 (HSV-1), Human coronavirus (HCoV) -229E, and Poliovirus-1 (PV-1) was investigated in the different phases of viral infection in the VERO CCL-81 cell line. To confirm the antiviral efficacy, a qPCR was conducted. The recorded cytotoxic concentration 50% was 513.1, 298.6, and 56.45 µg/mL for MeOH, H, and EA, respectively, assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay after 72 h of treatment. The Ficus rubiginosa leaf extract inhibited the replication of HSV-1 in the early stages of infection, showing a complete inhibition up to 0.62, 0.31, and 1.25 µg/mL. Against HCoV-229E, a total inhibition up to 1.25 µg/mL for MeOH and H as well as 5 µg/mL for EA was observed. Otherwise, no activity was recorded against PV-1. The leaf extract could act directly on the viral envelope, destructuring the lipid membrane and/or directly blocking the enriched proteins on the viral surface. The verified gene inhibition suggested that the treatments with M, H, and EA impaired HSV-1 and HCoV-229E replication, with a greater antiviral efficiency against HSV-1 compared to HCoV-229E, possibly due to a greater affinity of Ficus rubiginosa towards membrane glycoproteins and/or the different lipid envelopes. MDPI 2022-10-14 /pmc/articles/PMC9607631/ /pubmed/36298811 http://dx.doi.org/10.3390/v14102257 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dell’Annunziata, Federica
Sellitto, Carmine
Franci, Gianluigi
Marcotullio, Maria Carla
Piovan, Anna
Della Marca, Roberta
Folliero, Veronica
Galdiero, Massimiliano
Filippelli, Amelia
Conti, Valeria
Delfino, Domenico Vittorio
Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1
title Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1
title_full Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1
title_fullStr Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1
title_full_unstemmed Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1
title_short Antiviral Activity of Ficus rubiginosa Leaf Extracts against HSV-1, HCoV-229E and PV-1
title_sort antiviral activity of ficus rubiginosa leaf extracts against hsv-1, hcov-229e and pv-1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607631/
https://www.ncbi.nlm.nih.gov/pubmed/36298811
http://dx.doi.org/10.3390/v14102257
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