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Autori principali: Kim, Eun-A, Kang, Nalae, Heo, Jun-Ho, Park, Areumi, Heo, Seong-Yeong, Kim, Hyun-Soo, Heo, Soo-Jin
Natura: Artículo científico
Lingua:en
Pubblicazione: International journal of molecular sciences 2024
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Accesso online:https://pubmed.ncbi.nlm.nih.gov/39769456/
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author Kim, Eun-A
Kang, Nalae
Heo, Jun-Ho
Park, Areumi
Heo, Seong-Yeong
Kim, Hyun-Soo
Heo, Soo-Jin
author_facet Kim, Eun-A
Kang, Nalae
Heo, Jun-Ho
Park, Areumi
Heo, Seong-Yeong
Kim, Hyun-Soo
Heo, Soo-Jin
Kim, Eun-A
Kang, Nalae
Heo, Jun-Ho
Park, Areumi
Heo, Seong-Yeong
Kim, Hyun-Soo
Heo, Soo-Jin
collection PubMed - marine biology
contents Antiviral Activity of Extracts and Dieckol Against Zika Virus. Kim, Eun-A Kang, Nalae Heo, Jun-Ho Park, Areumi Heo, Seong-Yeong Kim, Hyun-Soo Heo, Soo-Jin Zika Virus Antiviral Agents Animals Chlorocebus aethiops Vero Cells Benzofurans Phaeophyceae Molecular Docking Simulation Virus Replication Plant Extracts Zika Virus Infection Viral Nonstructural Proteins RNA-Dependent RNA Polymerase Humans Viral Proteases Serine Endopeptidases Nucleoside-Triphosphatase DEAD-box RNA Helicases and its major compound dieckol, both natural marine products, possess antioxidant, anti-inflammatory, and metabolic-regulating effects. Zika virus (ZIKV), an arbovirus from the family, is transmitted by mosquitoes and causes serious illnesses in humans. This study aimed to evaluate the anti-ZIKV potential of and dieckol. The antiviral activity of extract (ECE), prepared with 80% ethanol, was assessed in ZIKV-infected Vero E6 cells through MTT assay, plaque assay, and quantitative polymerase chain reaction (qPCR), demonstrating no cytotoxicity and a significant reduction in viral titers and ZIKV mRNA levels. In addition, ECE decreased the expression of tumor necrosis factor-α and interferon-induced protein with tetratricopeptide repeats in the ZIKV-infected cells. Dieckol, the primary active compound in ECE, exhibited potent anti-ZIKV activity, with a half maximal inhibitory concentration (IC), value of 4.8 µM. In silico molecular docking analysis revealed that dieckol forms stable complexes with key ZIKV proteins, including the envelope, NS2B/NS3, and RNA-dependent RNA polymerase (RdRp) protein, exhibiting high binding energies of -438.09 kcal/mol, -1040.51 kcal/mol, and -1043.40 kcal/mol, respectively. Overall, our findings suggest that ECE and dieckol are promising candidates for the development of anti-ZIKV agents.
format Artículo científico
id pubmed_39769456
institution PubMed
language en
publishDate 2024
publisher International journal of molecular sciences
record_format pubmed
spellingShingle Antiviral Activity of Extracts and Dieckol Against Zika Virus.
Kim, Eun-A
Kang, Nalae
Heo, Jun-Ho
Park, Areumi
Heo, Seong-Yeong
Kim, Hyun-Soo
Heo, Soo-Jin
Zika Virus
Antiviral Agents
Animals
Chlorocebus aethiops
Vero Cells
Benzofurans
Phaeophyceae
Molecular Docking Simulation
Virus Replication
Plant Extracts
Zika Virus Infection
Viral Nonstructural Proteins
RNA-Dependent RNA Polymerase
Humans
Viral Proteases
Serine Endopeptidases
Nucleoside-Triphosphatase
DEAD-box RNA Helicases
Antiviral Activity of Extracts and Dieckol Against Zika Virus. Kim, Eun-A Kang, Nalae Heo, Jun-Ho Park, Areumi Heo, Seong-Yeong Kim, Hyun-Soo Heo, Soo-Jin Zika Virus Antiviral Agents Animals Chlorocebus aethiops Vero Cells Benzofurans Phaeophyceae Molecular Docking Simulation Virus Replication Plant Extracts Zika Virus Infection Viral Nonstructural Proteins RNA-Dependent RNA Polymerase Humans Viral Proteases Serine Endopeptidases Nucleoside-Triphosphatase DEAD-box RNA Helicases and its major compound dieckol, both natural marine products, possess antioxidant, anti-inflammatory, and metabolic-regulating effects. Zika virus (ZIKV), an arbovirus from the family, is transmitted by mosquitoes and causes serious illnesses in humans. This study aimed to evaluate the anti-ZIKV potential of and dieckol. The antiviral activity of extract (ECE), prepared with 80% ethanol, was assessed in ZIKV-infected Vero E6 cells through MTT assay, plaque assay, and quantitative polymerase chain reaction (qPCR), demonstrating no cytotoxicity and a significant reduction in viral titers and ZIKV mRNA levels. In addition, ECE decreased the expression of tumor necrosis factor-α and interferon-induced protein with tetratricopeptide repeats in the ZIKV-infected cells. Dieckol, the primary active compound in ECE, exhibited potent anti-ZIKV activity, with a half maximal inhibitory concentration (IC), value of 4.8 µM. In silico molecular docking analysis revealed that dieckol forms stable complexes with key ZIKV proteins, including the envelope, NS2B/NS3, and RNA-dependent RNA polymerase (RdRp) protein, exhibiting high binding energies of -438.09 kcal/mol, -1040.51 kcal/mol, and -1043.40 kcal/mol, respectively. Overall, our findings suggest that ECE and dieckol are promising candidates for the development of anti-ZIKV agents.
title Antiviral Activity of Extracts and Dieckol Against Zika Virus.
topic Zika Virus
Antiviral Agents
Animals
Chlorocebus aethiops
Vero Cells
Benzofurans
Phaeophyceae
Molecular Docking Simulation
Virus Replication
Plant Extracts
Zika Virus Infection
Viral Nonstructural Proteins
RNA-Dependent RNA Polymerase
Humans
Viral Proteases
Serine Endopeptidases
Nucleoside-Triphosphatase
DEAD-box RNA Helicases
url https://pubmed.ncbi.nlm.nih.gov/39769456/