白藜芦醇对基孔肯雅病毒和日本脑炎病毒复制的体外抗病毒作用。

N H Nor Isamuddin, N F Hanuar, S AbuBakar, K K Tan, K L Chin, N Zainal
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引用次数: 0

摘要

基孔肯雅病毒(CHIKV)和日本脑炎病毒(JEV)是蚊媒虫媒病毒,构成重大公共卫生风险,特别是在马来西亚等热带地区。CHIKV与关节和肌肉疼痛有关,而乙脑病毒如不治疗可引起严重的神经系统疾病和脑炎。由于没有特定的治疗方法,研究潜在的抗病毒药物至关重要。本研究探讨了白藜芦醇(RES)对猪流感病毒和乙脑病毒的体外抑制作用。使用MTS法评估RES对人腺癌肺泡基底上皮细胞(A549)的细胞毒性,然后进行剂量依赖性分析以确定最佳抑制浓度。通过感染前、感染后、杀病毒和抗吸附实验探索抗病毒作用,并分别通过斑块和焦斑形成实验测量病毒滴度。结果显示,RES的感染前和感染后处理显著降低了两种病毒的滴度,并呈剂量依赖性。值得注意的是,无论是感染前还是感染后,用100µM RES处理后,CHIKV滴度降低了65%以上(p < 0.01)。对于乙脑病毒,仅感染后治疗降低了93%以上(p < 0.05),而单独感染前治疗没有显著降低。此外,猪乙脑病毒和猪乙脑病毒的孵育前和抗吸附实验均无显著结果。这些发现表明,RES可能通过调节宿主细胞机制而不是直接靶向病毒来抑制病毒复制。综上所述,本研究表明RES对CHIKV和JEV复制具有抗病毒特性,强调其作为一种有效的抗病毒药物的潜力。然而,需要进一步的体内研究来充分评估其治疗潜力和疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiviral effects of resveratrol against the replication of chikungunya and Japanese encephalitis viruses in vitro.

Chikungunya virus (CHIKV) and Japanese encephalitis virus (JEV) are mosquito-borne arboviruses that pose significant public health risks, especially in tropical regions like Malaysia. CHIKV is linked to joint and muscle pain, while JEV can cause severe neurological illnesses and encephalitis if untreated. With no specific treatments available, research into potential antivirals is crucial. This study investigates the inhibitory potential of resveratrol (RES) against CHIKV and JEV in vitro. Cytotoxicity of RES was assessed on human adenocarcinoma alveolar basal epithelial cells (A549) using the MTS assay, followed by dose-dependent analyses to determine optimal inhibitory concentrations. Antiviral effects were explored through pre-infection, post-infection, virucidal, and anti-adsorption assays, with virus titres measured via plaque and foci-forming assays for CHIKV and JEV, respectively. Results revealed that RES's pre- and post-infection treatments significantly reduced titres of both viruses in a dose-dependent manner. Notably, CHIKV titres were reduced by over 65% (p < 0.01) when treated with 100 µM RES, whether administered pre-infection or post-infection. For JEV, a reduction of over 93% (p < 0.05) was observed only with post-infection treatment, while pre-infection treatment alone did not yield a significant reduction. In addition, both pre-incubation and anti-adsorption assays for CHIKV and JEV showed no significant results. These findings suggest that RES likely inhibits viral replication by modulating host cellular mechanisms rather than directly targeting the viruses. In summary, this study demonstrates that RES exhibits antiviral properties against CHIKV and JEV replication, underscoring its potential as an effective antiviral agent. However, further in vivo studies are needed to fully evaluate its therapeutic potential and efficacy.

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