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In vitro characterization of the antiviral activity of fucoidan from Cladosiphon okamuranus against Newcastle Disease Virus

机译:克拉多芬中岩藻糖聚糖抗新城疫病毒的体外抗病毒活性

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Background Newcastle Disease Virus (NDV) causes a serious infectious disease in birds that results in severe losses in the worldwide poultry industry. Despite vaccination, NDV outbreaks have increased the necessity of alternative prevention and control measures. Several recent studies focused on antiviral compounds obtained from natural resources. Many extracts from marine organisms have been isolated and tested for pharmacological purposes, and their antiviral activity has been demonstrated in vitro and in vivo. Fucoidan is a sulfated polysaccharide present in the cell wall matrix of brown algae that has been demonstrated to inhibit certain enveloped viruses with low toxicity. This study evaluated the potential antiviral activity and the mechanism of action of fucoidan from Cladosiphon okamuranus against NDV in the Vero cell line. Methods The cytotoxicity of fucoidan was determined by the MTT assay. To study its antiviral activity, fusion and plaque-forming unit (PFU) inhibition assays were conducted. The mechanism of action was determined by time of addition, fusion inhibition, and penetration assays. The NDV vaccine strain (La Sota) was used in the fusion inhibition assays. PFU and Western blot experiments were performed using a wild-type lentogenic NDV strain. Results Fucoidan exhibited antiviral activity against NDV La Sota, with an obtained IS50 >2000. In time of addition studies, we observed viral inhibition in the early stages of infection (0–60 min post-infection). The inhibition of viral penetration experiments with a wild-type NDV strain supported this result, as these experiments demonstrated a 48% decrease in viral infection as well as reduced HN protein expression. Ribavirin, which was used as an antiviral control, exhibited lower antiviral activity than fucoidan and high toxicity at active doses. In the fusion assays, the number of syncytia was significantly reduced (70% inhibition) when fucoidan was added before cleavage of the fusion protein, perhaps indicating a specific interaction between fucoidan and the F0 protein. Conclusion The results of this study suggest that fucoidan from C. okamuranus represents a potential low-toxicity antiviral compound for the poultry industry, and our findings provide a better understanding of the mode of action of sulfated polysaccharides.
机译:背景技术新城疫病毒(NDV)在鸟类中引起严重的传染病,导致全球禽业遭受严重损失。尽管进行了疫苗接种,但NDV暴发增加了替代性预防和控制措施的必要性。最近的一些研究集中于从自然资源获得的抗病毒化合物。已从海洋生物中提取了许多提取物并进行了药理学测试,并且已在体外和体内证明了其抗病毒活性。褐藻糖胶是存在于褐藻细胞壁基质中的一种硫酸化多糖,已被证明能以低毒性抑制某些包膜病毒。这项研究评估了潜在的抗病毒活性和冈比亚克拉多夫中岩藻依聚糖对Vero细胞系中NDV的作用机理。方法采用MTT法测定岩藻依聚糖的细胞毒性。为了研究其抗病毒活性,进行了融合和噬菌斑形成单位(PFU)抑制试验。作用机理通过添加时间,融合抑制和渗透测定来确定。 NDV疫苗株(La Sota)用于融合抑制试验。使用野生型迟发型NDV株进行PFU和Western blot实验。结果岩藻糖聚糖对NDV La Sota具有抗病毒活性,其IS 50

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