Molecular docking analyses of Avicennia marina-derived phytochemicals against white spot syndrome virus (WSSV) envelope protein-VP28

被引:14
作者
Sahu, Sunil Kumar [1 ]
Kathiresan, Kandasamy [1 ]
Singh, Reena [1 ]
Senthilraja, Poomalai [2 ]
机构
[1] Annamalai Univ, Fac Marine Sci, Ctr Adv Study Marine Biol, Parangipettai 608502, Tamil Nadu, India
[2] Annamalai Univ, Dept Zool, Chidambaram 608002, Tamil Nadu, India
关键词
White spot syndrome virus (wssv); VP28 envelope protein; Mangroves; Avicennia marina; Molecular docking; Phytochemicals;
D O I
10.6026/97320630008897
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
White spot syndrome (WSS) is one of the most common and most disastrous diseases of shrimp worldwide. It causes up to 100% mortality within 3 to 4 days in commercial shrimp farms, resulting in large economic losses to the shrimp farming industry. VP28 envelope protein of WSSV is reported to play a key role in the systemic infection in shrimps. Considering the most sombre issue of viral disease in cultivated shrimp, the present study was undertaken to substantiate the inhibition potential of Avicennia marina-derived phytochemicals against the WSSV envelope protein VP28. Seven A. marina-derived phytochemicals namely stigmasterol, triterpenoid, betulin, lupeol, avicenol-A, betulinic acid and quercetin were docked against the WSSV protein VP28 by using Argus lab molecular docking software. The chemical structures of the phytochemicals were retrieved from Pubchem database and generated from SMILES notation. Similarly the protein structure of the envelope protein was obtained from protein data bank (PDB-ID: 2ED6). Binding sites were predicted by using ligand explorer software. Among the phytochemicals screened, stigmasterol, lupeol and betulin showed the best binding exhibiting the potential to block VP28 envelope protein of WSSV, which could possibly inhibit the attachment of WSSV to the host species. Further experimental studies will provide a clear understanding on the mode of action of these phytochemicals individually or synergistically against WSSV envelope protein and can be used as an inhibitory drug to reduce white spot related severe complications in crustaceans.
引用
收藏
页码:897 / 900
页数:4
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