Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells

Dengue virus (DENV) infection causes mild to severe illness in humans that can lead to fatality in severe cases. Currently, no specific drug is available for the treatment of DENV infection. Thus, the development of an anti-DENV drug is urgently required. Cordycepin (3′-deoxyadenosine), which is a m...

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Main Authors: Aussara Panya, Pucharee Songprakhon, Suthida Panwong, Kanyaluck Jantakee, Thida Kaewkod, Yingmanee Tragoolpua, Nunghathai Sawasdee, Vannajan Sanghiran Lee, Piyarat Nimmanpipug, Pa-thai Yenchitsomanus
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/11/3118
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spelling doaj-e56ff7af62ec4caca4f7f6461359324a2021-06-01T00:52:40ZengMDPI AGMolecules1420-30492021-05-01263118311810.3390/molecules26113118Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero CellsAussara Panya0Pucharee Songprakhon1Suthida Panwong2Kanyaluck Jantakee3Thida Kaewkod4Yingmanee Tragoolpua5Nunghathai Sawasdee6Vannajan Sanghiran Lee7Piyarat Nimmanpipug8Pa-thai Yenchitsomanus9Center of Excellence for Innovation in Analytical Science and Technology, Chiang Mai University, Chiang Mai 50200, ThailandDivision of Molecular Medicine, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, ThailandDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, ThailandDivision of Molecular Medicine, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, ThailandDepartment of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603, MalaysiaCenter of Excellence for Innovation in Analytical Science and Technology, Chiang Mai University, Chiang Mai 50200, ThailandDivision of Molecular Medicine, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, ThailandDengue virus (DENV) infection causes mild to severe illness in humans that can lead to fatality in severe cases. Currently, no specific drug is available for the treatment of DENV infection. Thus, the development of an anti-DENV drug is urgently required. Cordycepin (3′-deoxyadenosine), which is a major bioactive compound in Cordyceps (ascomycete) fungus that has been used for centuries in Chinese traditional medicine, was reported to exhibit antiviral activity. However, the anti-DENV activity of cordycepin is unknown. We hypothesized that cordycepin exerts anti-DENV activity and that, as an adenosine derivative, it inhibits DENV replication. To test this hypothesis, we investigated the anti-DENV activity of cordycepin in DENV-infected Vero cells. Cordycepin treatment significantly decreased DENV protein at a half-maximal effective concentration (EC50) of 26.94 μM. Moreover, DENV RNA was dramatically decreased in cordycepin-treated Vero cells, indicating its effectiveness in inhibiting viral RNA replication. Via in silico molecular docking, the binding of cordycepin to DENV non-structural protein 5 (NS5), which is an important enzyme for RNA synthesis, at both the methyltransferase (MTase) and RNA-dependent RNA polymerase (RdRp) domains, was predicted. The results of this study demonstrate that cordycepin is able to inhibit DENV replication, which portends its potential as an anti-dengue therapy.https://www.mdpi.com/1420-3049/26/11/3118bioactive compoundcordycepincordyceps extractdengue virusantiviral activity
collection DOAJ
language English
format Article
sources DOAJ
author Aussara Panya
Pucharee Songprakhon
Suthida Panwong
Kanyaluck Jantakee
Thida Kaewkod
Yingmanee Tragoolpua
Nunghathai Sawasdee
Vannajan Sanghiran Lee
Piyarat Nimmanpipug
Pa-thai Yenchitsomanus
spellingShingle Aussara Panya
Pucharee Songprakhon
Suthida Panwong
Kanyaluck Jantakee
Thida Kaewkod
Yingmanee Tragoolpua
Nunghathai Sawasdee
Vannajan Sanghiran Lee
Piyarat Nimmanpipug
Pa-thai Yenchitsomanus
Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells
Molecules
bioactive compound
cordycepin
cordyceps extract
dengue virus
antiviral activity
author_facet Aussara Panya
Pucharee Songprakhon
Suthida Panwong
Kanyaluck Jantakee
Thida Kaewkod
Yingmanee Tragoolpua
Nunghathai Sawasdee
Vannajan Sanghiran Lee
Piyarat Nimmanpipug
Pa-thai Yenchitsomanus
author_sort Aussara Panya
title Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells
title_short Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells
title_full Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells
title_fullStr Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells
title_full_unstemmed Cordycepin Inhibits Virus Replication in Dengue Virus-Infected Vero Cells
title_sort cordycepin inhibits virus replication in dengue virus-infected vero cells
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-05-01
description Dengue virus (DENV) infection causes mild to severe illness in humans that can lead to fatality in severe cases. Currently, no specific drug is available for the treatment of DENV infection. Thus, the development of an anti-DENV drug is urgently required. Cordycepin (3′-deoxyadenosine), which is a major bioactive compound in Cordyceps (ascomycete) fungus that has been used for centuries in Chinese traditional medicine, was reported to exhibit antiviral activity. However, the anti-DENV activity of cordycepin is unknown. We hypothesized that cordycepin exerts anti-DENV activity and that, as an adenosine derivative, it inhibits DENV replication. To test this hypothesis, we investigated the anti-DENV activity of cordycepin in DENV-infected Vero cells. Cordycepin treatment significantly decreased DENV protein at a half-maximal effective concentration (EC50) of 26.94 μM. Moreover, DENV RNA was dramatically decreased in cordycepin-treated Vero cells, indicating its effectiveness in inhibiting viral RNA replication. Via in silico molecular docking, the binding of cordycepin to DENV non-structural protein 5 (NS5), which is an important enzyme for RNA synthesis, at both the methyltransferase (MTase) and RNA-dependent RNA polymerase (RdRp) domains, was predicted. The results of this study demonstrate that cordycepin is able to inhibit DENV replication, which portends its potential as an anti-dengue therapy.
topic bioactive compound
cordycepin
cordyceps extract
dengue virus
antiviral activity
url https://www.mdpi.com/1420-3049/26/11/3118
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