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新型颠茄制剂通过抑制 p65 核易位和 TNF-α 介导的 NF-κB 信号通路对日本脑炎病毒的抗病毒和抗炎活性。

Antiviral and anti-inflammatory activity of novel belladonna formulation against Japanese encephalitis virus via inhibition of p65 nuclear translocation and TNF-α mediated NF-kB signaling.

机构信息

Centre for Advanced Research, Faculty of Medicine, King George's Medical University, Lucknow, India.

CCRH, Ministry of Ayush, Janakpuri, India.

出版信息

Biotechnol Genet Eng Rev. 2023 Oct;39(2):937-959. doi: 10.1080/02648725.2023.2166258. Epub 2023 Jan 31.

Abstract

Japanese encephalitis (JE) is a mosquito-borne flavivirus infection, a major cause of viral encephalitis in South-East Asia with a CFR of ~30% and no specific treatment. Therefore, a novel belladonna formulation (BCT) was prepared and its antiviral and anti-inflammatory activity was elucidated during Japanese encephalitis virus (JEV) infection. Anti-JEV role of BCT was investigated aiming to prevent the infection in the peripheral immune cells. Antiviral activity of BCT was evaluated by plaque reduction assay, cell survival and apoptosis assay. BCT-mediated reduction in JEV-envelope expression was measured by indirect immunofluorescence, RT-PCR and Western blot assays. NF-κB expression and p65 nuclear translocation assays were determined to explore the mechanism of the action of BCT. TNF-α level was measured to evaluate the anti-inflammatory role of BCT during JEV infection. Consequently, molecular docking was performed with the TRAF2-TRADD complex. Our data suggested that BCT treatment reduces the JEV-plaque formation, JEV-induced cytopathic effects and increases cell survival. The antiviral effect of BCT was confirmed by reduction in the JEV-envelope protein expression. Moreover, BCT treatment and prevents the NF-κB activation via preventing the nuclear translocation of p65 and reduces the TNF-α levels. Our molecular docking analysis suggested that belladonna alkaloids interfere with the TRAF2-TRADD complex that results in inhibition of TNF-induced NF-κB signaling. For the first time, our data suggested that BCT reduces JEV expression and interferes with TNF-induced NF-κB signaling, thereby increasing cell survival via preventing the p65 nuclear translocation and may be used for the treatment and prevention of JE.: CFR: Case fatality rate; CAM: Complementary and alternative medicines; COX-2: Cyclooxygenase-2; IκB: Inhibitor kappa B; JE: Japanese encephalitis; JEV: Japanese encephalitis virus; NF-κB: Nuclear factor kappa-light-chain-enhancer of activated B cells; ORF: Open reading frame; TNFR: Tumor necrosis factor receptor; TNF-α: Tumor necrosis factor-α; TRADD: TNFR1-associated death domain protein; TRAF2: TNF Receptor Associated Factor 2.

摘要

日本脑炎 (JE) 是一种由蚊子传播的黄病毒感染,是东南亚主要的病毒性脑炎病因之一,病死率约为 30%,且无特效治疗方法。因此,我们制备了一种新型颠茄制剂 (BCT),并在日本脑炎病毒 (JEV) 感染期间研究了其抗病毒和抗炎活性。本研究旨在通过预防外周免疫细胞感染来探索 BCT 的抗 JEV 作用。通过空斑减少试验、细胞存活和凋亡试验评估 BCT 的抗病毒活性。通过间接免疫荧光、RT-PCR 和 Western blot 试验测定 BCT 介导的 JEV-包膜表达减少。通过 NF-κB 表达和 p65 核易位试验来探索 BCT 作用的机制。通过测量 TNF-α 水平来评估 BCT 在 JEV 感染期间的抗炎作用。随后,用 TRAF2-TRADD 复合物进行分子对接。我们的数据表明,BCT 处理可减少 JEV 噬斑形成、JEV 诱导的细胞病变效应并增加细胞存活。BCT 减少 JEV 包膜蛋白表达证实了其抗病毒作用。此外,BCT 处理可通过防止 p65 核易位来抑制 NF-κB 激活并降低 TNF-α 水平。我们的分子对接分析表明,颠茄生物碱干扰 TRAF2-TRADD 复合物,从而抑制 TNF 诱导的 NF-κB 信号传导。这是首次表明 BCT 可降低 JEV 表达并干扰 TNF 诱导的 NF-κB 信号传导,从而通过防止 p65 核易位增加细胞存活,并可能用于 JE 的治疗和预防。CFR:病死率;CAM:补充和替代医学;COX-2:环氧化酶-2;IκB:κB 抑制蛋白;JE:日本脑炎;JEV:日本脑炎病毒;NF-κB:核因子 kappaB;ORF:开放阅读框;TNFR:肿瘤坏死因子受体;TNF-α:肿瘤坏死因子-α;TRADD:TNFR1 相关死亡结构域蛋白;TRAF2:肿瘤坏死因子受体相关因子 2。

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