Antiviral actions of flavanoid-derived compounds on dengue virus type-2

<p>Dengue viruses, mosquito-borne members of the Flaviviridae family, are the causative agents of dengue fever and its associated complications, dengue haemorrhagic fever and dengue shock syndrome. To date, more than 2.5 billion people in over 100 countries are at risk of infection, and approx...

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Main Author: Mudiana Muhamad, Lee Yean Kee, Noorsaadah Abd. Rahman, Rohana Yusof
Format: Article
Language:English
Published: Ivyspring International Publisher 2010-01-01
Series:International Journal of Biological Sciences
Online Access:http://www.biolsci.org/v06p0294.htm
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spelling doaj-befaf73f7b9648ed9e5a6100ab45805b2020-11-24T22:31:41ZengIvyspring International PublisherInternational Journal of Biological Sciences1449-22882010-01-0163294302Antiviral actions of flavanoid-derived compounds on dengue virus type-2Mudiana Muhamad, Lee Yean Kee, Noorsaadah Abd. Rahman, Rohana Yusof<p>Dengue viruses, mosquito-borne members of the Flaviviridae family, are the causative agents of dengue fever and its associated complications, dengue haemorrhagic fever and dengue shock syndrome. To date, more than 2.5 billion people in over 100 countries are at risk of infection, and approximately 20 million infections were reported annually. There is currently no treatment or vaccine available for dengue infection. This study employed a whole-cell organism model or <i>in vitro</i> methods to study the inhibitory property of the flavanoid-derived compounds against DENV2 activity. Results showed that at concentration not exceeding the maximum non-toxic dose (MNTD), these compounds completely prevented DENV2 infection in HepG2 cells as indicated by the absence of cytophatic effects. The <i>in vitro</i> antiviral activity assessed in HepG2 cells employing virus inhibition assay showed high inhibitory activity in a dose dependent manner. At concentration below MNTD, compounds exhibited inhibitory activity against DENV2 with a range of potency strengths of 72% to 100%. The plaque forming unit per ml (pfu/ml) was reduced prominently with a maximum reduction of 98% when the infected HepG2 cells were treated with the highest non-toxic dose of compounds. The highly potent activity of the compounds against DENV2 infection strongly suggests their potential as a lead antiviral agent for dengue.</p>http://www.biolsci.org/v06p0294.htm
collection DOAJ
language English
format Article
sources DOAJ
author Mudiana Muhamad, Lee Yean Kee, Noorsaadah Abd. Rahman, Rohana Yusof
spellingShingle Mudiana Muhamad, Lee Yean Kee, Noorsaadah Abd. Rahman, Rohana Yusof
Antiviral actions of flavanoid-derived compounds on dengue virus type-2
International Journal of Biological Sciences
author_facet Mudiana Muhamad, Lee Yean Kee, Noorsaadah Abd. Rahman, Rohana Yusof
author_sort Mudiana Muhamad, Lee Yean Kee, Noorsaadah Abd. Rahman, Rohana Yusof
title Antiviral actions of flavanoid-derived compounds on dengue virus type-2
title_short Antiviral actions of flavanoid-derived compounds on dengue virus type-2
title_full Antiviral actions of flavanoid-derived compounds on dengue virus type-2
title_fullStr Antiviral actions of flavanoid-derived compounds on dengue virus type-2
title_full_unstemmed Antiviral actions of flavanoid-derived compounds on dengue virus type-2
title_sort antiviral actions of flavanoid-derived compounds on dengue virus type-2
publisher Ivyspring International Publisher
series International Journal of Biological Sciences
issn 1449-2288
publishDate 2010-01-01
description <p>Dengue viruses, mosquito-borne members of the Flaviviridae family, are the causative agents of dengue fever and its associated complications, dengue haemorrhagic fever and dengue shock syndrome. To date, more than 2.5 billion people in over 100 countries are at risk of infection, and approximately 20 million infections were reported annually. There is currently no treatment or vaccine available for dengue infection. This study employed a whole-cell organism model or <i>in vitro</i> methods to study the inhibitory property of the flavanoid-derived compounds against DENV2 activity. Results showed that at concentration not exceeding the maximum non-toxic dose (MNTD), these compounds completely prevented DENV2 infection in HepG2 cells as indicated by the absence of cytophatic effects. The <i>in vitro</i> antiviral activity assessed in HepG2 cells employing virus inhibition assay showed high inhibitory activity in a dose dependent manner. At concentration below MNTD, compounds exhibited inhibitory activity against DENV2 with a range of potency strengths of 72% to 100%. The plaque forming unit per ml (pfu/ml) was reduced prominently with a maximum reduction of 98% when the infected HepG2 cells were treated with the highest non-toxic dose of compounds. The highly potent activity of the compounds against DENV2 infection strongly suggests their potential as a lead antiviral agent for dengue.</p>
url http://www.biolsci.org/v06p0294.htm
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