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首页> 外文期刊>Biomedical Research >Fucoidan inhibits parainfluenza virus type 2 infection to LLCMK2 cells
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Fucoidan inhibits parainfluenza virus type 2 infection to LLCMK2 cells

机译:Fucoidan抑制2型副流感病毒对LLCMK2细胞的感染

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摘要

The effects of fucoidan and L-fucose, a fundamental major component of fucoidan, on the growth of human parainfluenza virus type 2 (hPIV-2) in LLCMK2 cells were investigated. Fucoidan inhibited cell fusion and hemadsorption, but L-fucose only partly inhibited both. Virus RNA was not detected in the hPIV-2 infected cells cultured with fucoidan. However, L-fucose did not inhibit virus RNA synthesis. Indirect immunofluorescence study showed that virus protein synthesis was inhibited by fucoidan, but not by L-fucose. Furthermore, using a recombinant, green fluorescence protein-expressing hPIV-2, it was found that virus entry was inhibited by fucoidan, but not by L-fucose. These results suggested that fucoidan inhibited virus adsorption to the surface of the cells by binding to the cell surface and prevented infection, indicating that the sulfated polysaccharide form was important for the inhibition by fucoidan.
机译:研究了岩藻依聚糖和岩藻依聚糖的基本主要成分L-岩藻糖对LLCMK2细胞中人类2型副流感病毒(hPIV-2)生长的影响。岩藻依聚糖抑制细胞融合和溶血作用,但L-岩藻糖仅部分抑制两者。在用岩藻依聚糖培养的hPIV-2感染的细胞中未检测到病毒RNA。但是,L-岩藻糖不能抑制病毒RNA的合成。间接免疫荧光研究表明,岩藻依聚糖能抑制病毒蛋白的合成,而L-岩藻糖却不能。此外,使用表达绿色荧光蛋白的重组hPIV-2,发现岩藻依聚糖抑制了病毒的进入,而L-岩藻糖则没有。这些结果表明,岩藻依聚糖通过与细胞表面结合而抑制病毒吸附到细胞表面并防止感染,表明硫酸化多糖形式对于岩藻依聚糖的抑制是重要的。

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