Antiviral Activity of <i>Ecklonia cava</i> Extracts and Dieckol Against Zika Virusopen access
- Authors
- Kim, Eun-A; Kang, Nalae; Heo, Jun-Ho; Park, Areumi; Heo, Seong-Yeong; Kim, Hyun-Soo; Heo, Soo-Jin
- Issue Date
- Dec-2024
- Publisher
- Multidisciplinary Digital Publishing Institute (MDPI)
- Keywords
- <italic>Ecklonia cava</italic>; dieckol; Zika virus; Vero E6 cells; in silico assays
- Citation
- International Journal of Molecular Sciences, v.25, no.24
- Indexed
- SCIE
SCOPUS
- Journal Title
- International Journal of Molecular Sciences
- Volume
- 25
- Number
- 24
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/75643
- DOI
- 10.3390/ijms252413694
- ISSN
- 1661-6596
1422-0067
- Abstract
- Ecklonia cava and its major compound dieckol, both natural marine products, possess antioxidant, anti-inflammatory, and metabolic-regulating effects. Zika virus (ZIKV), an arbovirus from the Flaviviridae family, is transmitted by mosquitoes and causes serious illnesses in humans. This study aimed to evaluate the anti-ZIKV potential of Ecklonia cava and dieckol. The antiviral activity of Ecklonia cava 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-alpha 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 (IC50), value of 4.8 mu M. 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.
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