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Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus
Hibiscus schizopetalus (Dyer) Hook.f. (Malvaceae) is an ornamental plant. The aim was to investigate its antimicrobial and antioxidant activities. In vitro antiviral, antibacterial, and antioxidant activities of the 70% ethanolic extract (Et-E) of the aerial parts of the plant were determined. The D...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692239/ https://www.ncbi.nlm.nih.gov/pubmed/33142982 http://dx.doi.org/10.3390/antibiotics9110756 |
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author | El-Shiekh, Riham A. Abdelmohsen, Usama Ramadan Ashour, Hossam M. Ashour, Rehab M. |
author_facet | El-Shiekh, Riham A. Abdelmohsen, Usama Ramadan Ashour, Hossam M. Ashour, Rehab M. |
author_sort | El-Shiekh, Riham A. |
collection | PubMed |
description | Hibiscus schizopetalus (Dyer) Hook.f. (Malvaceae) is an ornamental plant. The aim was to investigate its antimicrobial and antioxidant activities. In vitro antiviral, antibacterial, and antioxidant activities of the 70% ethanolic extract (Et-E) of the aerial parts of the plant were determined. The Dichloromethane Fraction (DCM-F) and the n-Butanol Fraction (Bu-F) were assessed using Liquid chromatography–mass spectrometry (LC-MS). The DCM-F showed higher antiviral activities against Coxsackie B4 (CoxB4) viruses (IC(50) = 64.13 µg/mL) and adenoviruses (IC(50) = 54.88 µg/mL) than acyclovir (IC(50) = 72.79 µg/mL for CoxB4 viruses; IC(50) = 91.92 µg/mL for adenoviruses). The DCM-F showed higher anti-helicobacter pylori activity (MIC = 3.9 µg/mL) than clarithromycin (MIC = 1.95 µg/mL). The DCM-F inhibited Herpes Simplex Virus (HSV) Type I (IC(50) = 29.85 µg/mL) and HSV Type II (IC(50) = 74.17 µg/mL). The Bu-F showed higher anti-mycobacterial activity (MIC = 7.81 µg/mL) than isoniazid (MIC = 0.24 µg/mL) and higher antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA)(MIC = 7.81 µg/mL) than vancomycin (MIC = 3.9 µg/mL). Antioxidant assays included total antioxidant capacity (TAC), 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS), 2,2-diphenyl-1-picryl-hydrazyl (DPPH), and iron reducing power. The Bu-F showed the highest antioxidant activity. Chemical profiles were analyzed using HPLC-HR–ESI–MS to identify the metabolites responsible for these biological activities. We identified more than 60 metabolites that belong to anthocyanins, flavonoids, phenolics, terpenes, sterols, and fatty acids. In conclusion, Hibiscus schizopetalus is endowed with metabolites that could be used against viruses and antibiotic-resistant bacteria. They can also be potent antioxidants. |
format | Online Article Text |
id | pubmed-7692239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76922392020-11-28 Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus El-Shiekh, Riham A. Abdelmohsen, Usama Ramadan Ashour, Hossam M. Ashour, Rehab M. Antibiotics (Basel) Article Hibiscus schizopetalus (Dyer) Hook.f. (Malvaceae) is an ornamental plant. The aim was to investigate its antimicrobial and antioxidant activities. In vitro antiviral, antibacterial, and antioxidant activities of the 70% ethanolic extract (Et-E) of the aerial parts of the plant were determined. The Dichloromethane Fraction (DCM-F) and the n-Butanol Fraction (Bu-F) were assessed using Liquid chromatography–mass spectrometry (LC-MS). The DCM-F showed higher antiviral activities against Coxsackie B4 (CoxB4) viruses (IC(50) = 64.13 µg/mL) and adenoviruses (IC(50) = 54.88 µg/mL) than acyclovir (IC(50) = 72.79 µg/mL for CoxB4 viruses; IC(50) = 91.92 µg/mL for adenoviruses). The DCM-F showed higher anti-helicobacter pylori activity (MIC = 3.9 µg/mL) than clarithromycin (MIC = 1.95 µg/mL). The DCM-F inhibited Herpes Simplex Virus (HSV) Type I (IC(50) = 29.85 µg/mL) and HSV Type II (IC(50) = 74.17 µg/mL). The Bu-F showed higher anti-mycobacterial activity (MIC = 7.81 µg/mL) than isoniazid (MIC = 0.24 µg/mL) and higher antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA)(MIC = 7.81 µg/mL) than vancomycin (MIC = 3.9 µg/mL). Antioxidant assays included total antioxidant capacity (TAC), 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS), 2,2-diphenyl-1-picryl-hydrazyl (DPPH), and iron reducing power. The Bu-F showed the highest antioxidant activity. Chemical profiles were analyzed using HPLC-HR–ESI–MS to identify the metabolites responsible for these biological activities. We identified more than 60 metabolites that belong to anthocyanins, flavonoids, phenolics, terpenes, sterols, and fatty acids. In conclusion, Hibiscus schizopetalus is endowed with metabolites that could be used against viruses and antibiotic-resistant bacteria. They can also be potent antioxidants. MDPI 2020-10-30 /pmc/articles/PMC7692239/ /pubmed/33142982 http://dx.doi.org/10.3390/antibiotics9110756 Text en © 2020 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 El-Shiekh, Riham A. Abdelmohsen, Usama Ramadan Ashour, Hossam M. Ashour, Rehab M. Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus |
title | Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus |
title_full | Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus |
title_fullStr | Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus |
title_full_unstemmed | Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus |
title_short | Novel Antiviral and Antibacterial Activities of Hibiscus schizopetalus |
title_sort | novel antiviral and antibacterial activities of hibiscus schizopetalus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692239/ https://www.ncbi.nlm.nih.gov/pubmed/33142982 http://dx.doi.org/10.3390/antibiotics9110756 |
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