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Efficacy of geraniin on dengue virus type-2 infected BALB/c mice

BACKGROUND: Dengue continues to be a major international public health concern. Despite that, there is no clinically approved antiviral for treatment of dengue virus (DENV) infections. In this study, geraniin extracted from the rind of Nephelium lappaceum was shown to inhibit the replication of DENV...

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Autores principales: Abdul Ahmad, Siti Aisyah, Palanisamy, Uma D., Khoo, Joon Joon, Dhanoa, Amreeta, Syed Hassan, Sharifah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391806/
https://www.ncbi.nlm.nih.gov/pubmed/30813954
http://dx.doi.org/10.1186/s12985-019-1127-7
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author Abdul Ahmad, Siti Aisyah
Palanisamy, Uma D.
Khoo, Joon Joon
Dhanoa, Amreeta
Syed Hassan, Sharifah
author_facet Abdul Ahmad, Siti Aisyah
Palanisamy, Uma D.
Khoo, Joon Joon
Dhanoa, Amreeta
Syed Hassan, Sharifah
author_sort Abdul Ahmad, Siti Aisyah
collection PubMed
description BACKGROUND: Dengue continues to be a major international public health concern. Despite that, there is no clinically approved antiviral for treatment of dengue virus (DENV) infections. In this study, geraniin extracted from the rind of Nephelium lappaceum was shown to inhibit the replication of DENV-2 in both in vitro and in vivo experiments. METHODS: The effect of geraniin on DENV-2 RNA synthesis in infected Vero cells was tested using quantitative RT-PCR. The in vivo efficacy of geraniin in inhibiting DENV-2 infection was then tested using BALB/c mice with geraniin administered at three different times. The differences in spleen to body weight ratio, DENV-2 RNA load and liver damage between the three treatment groups as compared to DENV-2 infected mice without geraniin administration were determined on day eight post-infection. RESULTS: Quantitative RT-PCR confirmed the decrease in viral RNA synthesis of infected Vero cells when treated with geraniin. Geraniin seemed to provide a protective effect on infected BALB/c mice liver when given at 24 h pre- and 24 h post-infection as liver damage was observed to be very mild even though a significant reduction of DENV-2 RNA load in serum was not observed in these two treatment groups. However, when administered at 72 h post-infection, severe liver damage in the form of necrosis and haemorrhage had prevailed despite a substantial reduction of DENV-2 RNA load in serum. CONCLUSIONS: Geraniin was found to be effective in reducing DENV-2 RNA load when administered at 72 h post-infection while earlier administration could prevent severe liver damage caused by DENV-2 infection. These results provide evidence that geraniin is a potential candidate for the development of anti-dengue drug.
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spelling pubmed-63918062019-03-11 Efficacy of geraniin on dengue virus type-2 infected BALB/c mice Abdul Ahmad, Siti Aisyah Palanisamy, Uma D. Khoo, Joon Joon Dhanoa, Amreeta Syed Hassan, Sharifah Virol J Research BACKGROUND: Dengue continues to be a major international public health concern. Despite that, there is no clinically approved antiviral for treatment of dengue virus (DENV) infections. In this study, geraniin extracted from the rind of Nephelium lappaceum was shown to inhibit the replication of DENV-2 in both in vitro and in vivo experiments. METHODS: The effect of geraniin on DENV-2 RNA synthesis in infected Vero cells was tested using quantitative RT-PCR. The in vivo efficacy of geraniin in inhibiting DENV-2 infection was then tested using BALB/c mice with geraniin administered at three different times. The differences in spleen to body weight ratio, DENV-2 RNA load and liver damage between the three treatment groups as compared to DENV-2 infected mice without geraniin administration were determined on day eight post-infection. RESULTS: Quantitative RT-PCR confirmed the decrease in viral RNA synthesis of infected Vero cells when treated with geraniin. Geraniin seemed to provide a protective effect on infected BALB/c mice liver when given at 24 h pre- and 24 h post-infection as liver damage was observed to be very mild even though a significant reduction of DENV-2 RNA load in serum was not observed in these two treatment groups. However, when administered at 72 h post-infection, severe liver damage in the form of necrosis and haemorrhage had prevailed despite a substantial reduction of DENV-2 RNA load in serum. CONCLUSIONS: Geraniin was found to be effective in reducing DENV-2 RNA load when administered at 72 h post-infection while earlier administration could prevent severe liver damage caused by DENV-2 infection. These results provide evidence that geraniin is a potential candidate for the development of anti-dengue drug. BioMed Central 2019-02-27 /pmc/articles/PMC6391806/ /pubmed/30813954 http://dx.doi.org/10.1186/s12985-019-1127-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://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/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Abdul Ahmad, Siti Aisyah
Palanisamy, Uma D.
Khoo, Joon Joon
Dhanoa, Amreeta
Syed Hassan, Sharifah
Efficacy of geraniin on dengue virus type-2 infected BALB/c mice
title Efficacy of geraniin on dengue virus type-2 infected BALB/c mice
title_full Efficacy of geraniin on dengue virus type-2 infected BALB/c mice
title_fullStr Efficacy of geraniin on dengue virus type-2 infected BALB/c mice
title_full_unstemmed Efficacy of geraniin on dengue virus type-2 infected BALB/c mice
title_short Efficacy of geraniin on dengue virus type-2 infected BALB/c mice
title_sort efficacy of geraniin on dengue virus type-2 infected balb/c mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391806/
https://www.ncbi.nlm.nih.gov/pubmed/30813954
http://dx.doi.org/10.1186/s12985-019-1127-7
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