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Exploring antiviral activity of Betanin and Glycine Betaine against dengue virus type-2 in transfected Hela cells.
- Source :
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Microbial pathogenesis [Microb Pathog] 2024 Oct; Vol. 195, pp. 106894. Date of Electronic Publication: 2024 Aug 29. - Publication Year :
- 2024
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Abstract
- Dengue virus (DENV) infection is a worldwide public health concern infecting approximately 400 million individuals and about 40,000 mortalities yearly. Despite this, no licensed or readily available antiviral medication is currently available specifically for DENV infection, and therapy is typically symptomatic. Therefore, the objective of the study was to investigate the antiviral activity of Beta vulgaris L. phytoconstituents against DENV-2 targeting NS3 protein. The antiviral activity of phytochemicals was examined through virtual ligand-based screening, antiviral inhibition and dosage response assays, western blotting analysis and MD simulations. We conducted toxicological, and pharmacokinetic analysis to assess plant-based natural compound's efficacy, safety, and non-toxic doses. Molecular docking and MD simulation results revealed that the nonstructural protein-3 (NS3) might prove as a funamental target for Betanin and Glycine Betaine against Dengue virus. Betanin and Glycine betaine were initially studied for their non-toxic doses in HeLa, CHO, and Vero cells via MTT assay. HeLa cells were transiently transfected with cloned vector pcDNA3.1/Zeo(+)/DENV-2 NS3 along with non-toxic doses (80 μM-10 μM) of selected phytochemicals. The dose-response assay illustrated downregulated expression of DENV-2 NS3 gene after administration of Betanin (IC50 = 4.35 μM) and Glycine Betaine (IC50 = 4.49 μM). Dose response analysis of Betanin (80 μM-10 μM) depicted the significant inhibition of NS3 protein expression as well. These results suggested downregulated expression of DENV-2 NS3 at mRNA and protein level portraying the DENV replication inhibition. Based on our study findings, NS3 protease is depicted as distinctive DENV-2 inhibitor target. We will channel our study further into in vitro characterization employing the mechanistic study to understand the role of host factors in anti-flavi therapeutic.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)
- Subjects :
- Humans
HeLa Cells
Animals
Chlorocebus aethiops
Vero Cells
Viral Nonstructural Proteins metabolism
Viral Nonstructural Proteins genetics
Betacyanins pharmacology
CHO Cells
Cricetulus
Phytochemicals pharmacology
Molecular Dynamics Simulation
Virus Replication drug effects
Serine Endopeptidases metabolism
Serine Endopeptidases genetics
Dengue drug therapy
Dengue virology
Viral Proteases
Dengue Virus drug effects
Dengue Virus genetics
Antiviral Agents pharmacology
Molecular Docking Simulation
Betaine pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1096-1208
- Volume :
- 195
- Database :
- MEDLINE
- Journal :
- Microbial pathogenesis
- Publication Type :
- Academic Journal
- Accession number :
- 39214424
- Full Text :
- https://doi.org/10.1016/j.micpath.2024.106894