Anti-Dengue Activity of Lipophilic Fraction of Ocimum basilicum L. Stem

被引:6
作者
Joshi, Rajesh Kumar [1 ]
Agarwal, Shivankar [1 ]
Patil, Poonam [2 ]
Alagarasu, Kalichamy [2 ]
Panda, Kingshuk [2 ]
Cherian, Sarah [2 ]
Parashar, Deepti [2 ]
Roy, Subarna [1 ]
机构
[1] ICMR, Natl Inst Tradit Med, Belagavi 590010, Karnataka, India
[2] ICMR, Natl Inst Virol, 20-A,Dr Ambedkar Rd, Pune 411001, Maharashtra, India
关键词
dengue; chikungunya; antiviral; Ocimum basilicum L; Merr; phytosterols; CHEMICAL-COMPOSITION; ESSENTIAL OILS; SWEET BASIL; GC-MS; VIRUS; CONSTITUENTS; ANTIOXIDANT; EXTRACT; MEDICINE; LEAVES;
D O I
10.3390/molecules28031446
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ocimum basilicum L. is used to cure many types of fever in traditional medicine. This study aims to explore the antiviral activity of the lipophilic fraction of the stem of O. basilicum (LFOB) against dengue virus (DENV) and chikungunya virus (CHIKV). The LFOB was analyzed using GC-FID and GC-MS. The antiviral activity of LFOB was studied using the Vero CCL-81 cell line. The cytotoxicity assay was performed using 3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT). In vitro antiviral activity and FFU assay were used to determine and confirm antiviral activity against DENV and CHIKV. Twenty-six compounds were identified in LFOB using GC/MS. The most abundant compounds were beta-sitosterol (22.9%), stigmasterol (18.7%), and campesterol (12.9%). Significant reduction in DENV titre was observed under pre- and post-infection treatment conditions at a concentration of 3.125 mu g/mL, but no anti-CHIKV activity was observed. Our earlier and the present AutoDock-Vina-based in silico docking study revealed that beta-sitosterol and stigmasterol could form strong interactions with the DENV E glycoprotein and DENV RdRp domain, respectively. Our findings suggest that LFOB can inhibit DENV infection and might act as a potent prophylactic/therapeutic agent against DENV-2. In silico results suggested that beta-sitosterol and stigmasterol may block the viral entry by inhibiting the fusion process and viral replication respectively.
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页数:12
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