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Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2

Dengue has long been a serious health burden to the global community, especially for those living in the tropics. Despite the availability of vaccines, effective treatment for the infection is still needed and currently remains absent. In the present study, the antiviral properties of the Streptomyc...

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Autores principales: Zulkifli, Nurfatihah, Khairat, Jasmine-Elanie, Azman, Adzzie-Shazleen, Baharudin, Nur-Faralyza Mohd, Malek, Nurul-Adila, Zainal Abidin, Syafiq-Asnawi, AbuBakar, Sazaly, Hassandarvish, Pouya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459629/
https://www.ncbi.nlm.nih.gov/pubmed/37632115
http://dx.doi.org/10.3390/v15081773
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author Zulkifli, Nurfatihah
Khairat, Jasmine-Elanie
Azman, Adzzie-Shazleen
Baharudin, Nur-Faralyza Mohd
Malek, Nurul-Adila
Zainal Abidin, Syafiq-Asnawi
AbuBakar, Sazaly
Hassandarvish, Pouya
author_facet Zulkifli, Nurfatihah
Khairat, Jasmine-Elanie
Azman, Adzzie-Shazleen
Baharudin, Nur-Faralyza Mohd
Malek, Nurul-Adila
Zainal Abidin, Syafiq-Asnawi
AbuBakar, Sazaly
Hassandarvish, Pouya
author_sort Zulkifli, Nurfatihah
collection PubMed
description Dengue has long been a serious health burden to the global community, especially for those living in the tropics. Despite the availability of vaccines, effective treatment for the infection is still needed and currently remains absent. In the present study, the antiviral properties of the Streptomyces sp. KSF 103 methanolic extract (Streptomyces KSF 103 ME), which consists of a number of potential antiviral compounds, were investigated against dengue virus serotype 2 (DENV-2). The effects of this extract against DENV-2 replication were determined using the quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Findings from the study suggested that the Streptomyces KSF 103 ME showed maximum inhibitory properties toward the virus during the virus entry stage at concentrations of more than 12.5 µg/mL. Minimal antiviral activities were observed at other virus replication stages; adsorption (42% reduction at 50 µg/mL), post-adsorption (67.6% reduction at 50 µg/mL), prophylactic treatment (68.4% and 87.7% reductions at 50 µg/mL and 25 µg/mL, respectively), and direct virucidal assay (48% and 56.8% reductions at 50 µg/mL and 25 µg/mL, respectively). The Streptomyces KSF 103 ME inhibited dengue virus replication with a 50% inhibitory concentration (IC(50)) value of 20.3 µg/mL and an International System of Units (SI) value of 38.9. The Streptomyces KSF 103 ME showed potent antiviral properties against dengue virus (DENV) during the entry stage. Further studies will be needed to deduce the antiviral mechanisms of the Streptomyces KSF 103 ME against DENV.
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spelling pubmed-104596292023-08-27 Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2 Zulkifli, Nurfatihah Khairat, Jasmine-Elanie Azman, Adzzie-Shazleen Baharudin, Nur-Faralyza Mohd Malek, Nurul-Adila Zainal Abidin, Syafiq-Asnawi AbuBakar, Sazaly Hassandarvish, Pouya Viruses Article Dengue has long been a serious health burden to the global community, especially for those living in the tropics. Despite the availability of vaccines, effective treatment for the infection is still needed and currently remains absent. In the present study, the antiviral properties of the Streptomyces sp. KSF 103 methanolic extract (Streptomyces KSF 103 ME), which consists of a number of potential antiviral compounds, were investigated against dengue virus serotype 2 (DENV-2). The effects of this extract against DENV-2 replication were determined using the quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Findings from the study suggested that the Streptomyces KSF 103 ME showed maximum inhibitory properties toward the virus during the virus entry stage at concentrations of more than 12.5 µg/mL. Minimal antiviral activities were observed at other virus replication stages; adsorption (42% reduction at 50 µg/mL), post-adsorption (67.6% reduction at 50 µg/mL), prophylactic treatment (68.4% and 87.7% reductions at 50 µg/mL and 25 µg/mL, respectively), and direct virucidal assay (48% and 56.8% reductions at 50 µg/mL and 25 µg/mL, respectively). The Streptomyces KSF 103 ME inhibited dengue virus replication with a 50% inhibitory concentration (IC(50)) value of 20.3 µg/mL and an International System of Units (SI) value of 38.9. The Streptomyces KSF 103 ME showed potent antiviral properties against dengue virus (DENV) during the entry stage. Further studies will be needed to deduce the antiviral mechanisms of the Streptomyces KSF 103 ME against DENV. MDPI 2023-08-20 /pmc/articles/PMC10459629/ /pubmed/37632115 http://dx.doi.org/10.3390/v15081773 Text en © 2023 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
Zulkifli, Nurfatihah
Khairat, Jasmine-Elanie
Azman, Adzzie-Shazleen
Baharudin, Nur-Faralyza Mohd
Malek, Nurul-Adila
Zainal Abidin, Syafiq-Asnawi
AbuBakar, Sazaly
Hassandarvish, Pouya
Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2
title Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2
title_full Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2
title_fullStr Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2
title_full_unstemmed Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2
title_short Antiviral Activities of Streptomyces KSF 103 Methanolic Extracts against Dengue Virus Type-2
title_sort antiviral activities of streptomyces ksf 103 methanolic extracts against dengue virus type-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459629/
https://www.ncbi.nlm.nih.gov/pubmed/37632115
http://dx.doi.org/10.3390/v15081773
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