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Oroxylin A shows limited antiviral activity towards dengue virus

OBJECTIVE: The mosquito transmitted dengue virus (DENV) the causative agent of dengue fever (DF) remains a significant public health burden in many countries. Thailand, along with many countries in Asia and elsewhere, has a long history of using traditional medicines to combat febrile diseases such...

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Autores principales: Ratanakomol, Thippayawan, Roytrakul, Sittiruk, Wikan, Nitwara, Smith, Duncan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066930/
https://www.ncbi.nlm.nih.gov/pubmed/35509105
http://dx.doi.org/10.1186/s13104-022-06040-0
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author Ratanakomol, Thippayawan
Roytrakul, Sittiruk
Wikan, Nitwara
Smith, Duncan R.
author_facet Ratanakomol, Thippayawan
Roytrakul, Sittiruk
Wikan, Nitwara
Smith, Duncan R.
author_sort Ratanakomol, Thippayawan
collection PubMed
description OBJECTIVE: The mosquito transmitted dengue virus (DENV) the causative agent of dengue fever (DF) remains a significant public health burden in many countries. Thailand, along with many countries in Asia and elsewhere, has a long history of using traditional medicines to combat febrile diseases such as DF. Screening bioactive compounds from traditional medicines reported to have antipyretic or anti-inflammatory activity may lead to the development of potent antivirals. In this study oroxylin A (OA), a flavonoid derivative found in Oroxylum indicum (commonly called the Indian trumpet flower or tree of Damocles), was screened for antiviral activity towards DENV. RESULTS: Cytotoxicity analysis in BHK-21 cells showed a 50% cytotoxic concentration (CC(50)) of 534.17 µM. The compound showed no direct virucidal activity towards DENV, and pre-treatment of cells had no effect on virus production. A deficit was seen in virus production when cells were post-infection treated with oroxylin A. Under conditions of post-infection treatment, the EC(50) value was 201.1 µM, giving a selectivity index (SI) value of 2.66. Accumulation of DENV E protein inside the cell was seen under conditions of post-infection treatment, suggesting that oroxylin A may exert some effects at the virus assembly/egress stages of the replication cycle. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-022-06040-0.
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spelling pubmed-90669302022-05-04 Oroxylin A shows limited antiviral activity towards dengue virus Ratanakomol, Thippayawan Roytrakul, Sittiruk Wikan, Nitwara Smith, Duncan R. BMC Res Notes Research Note OBJECTIVE: The mosquito transmitted dengue virus (DENV) the causative agent of dengue fever (DF) remains a significant public health burden in many countries. Thailand, along with many countries in Asia and elsewhere, has a long history of using traditional medicines to combat febrile diseases such as DF. Screening bioactive compounds from traditional medicines reported to have antipyretic or anti-inflammatory activity may lead to the development of potent antivirals. In this study oroxylin A (OA), a flavonoid derivative found in Oroxylum indicum (commonly called the Indian trumpet flower or tree of Damocles), was screened for antiviral activity towards DENV. RESULTS: Cytotoxicity analysis in BHK-21 cells showed a 50% cytotoxic concentration (CC(50)) of 534.17 µM. The compound showed no direct virucidal activity towards DENV, and pre-treatment of cells had no effect on virus production. A deficit was seen in virus production when cells were post-infection treated with oroxylin A. Under conditions of post-infection treatment, the EC(50) value was 201.1 µM, giving a selectivity index (SI) value of 2.66. Accumulation of DENV E protein inside the cell was seen under conditions of post-infection treatment, suggesting that oroxylin A may exert some effects at the virus assembly/egress stages of the replication cycle. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-022-06040-0. BioMed Central 2022-05-04 /pmc/articles/PMC9066930/ /pubmed/35509105 http://dx.doi.org/10.1186/s13104-022-06040-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . 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 in a credit line to the data.
spellingShingle Research Note
Ratanakomol, Thippayawan
Roytrakul, Sittiruk
Wikan, Nitwara
Smith, Duncan R.
Oroxylin A shows limited antiviral activity towards dengue virus
title Oroxylin A shows limited antiviral activity towards dengue virus
title_full Oroxylin A shows limited antiviral activity towards dengue virus
title_fullStr Oroxylin A shows limited antiviral activity towards dengue virus
title_full_unstemmed Oroxylin A shows limited antiviral activity towards dengue virus
title_short Oroxylin A shows limited antiviral activity towards dengue virus
title_sort oroxylin a shows limited antiviral activity towards dengue virus
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066930/
https://www.ncbi.nlm.nih.gov/pubmed/35509105
http://dx.doi.org/10.1186/s13104-022-06040-0
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