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The antiviral activity of sulfated polysaccharides against dengue virus is dependent on virus serotype and host cell.

机译:硫酸多糖对登革热病毒的抗病毒活性取决于病毒的血清型和宿主细胞。

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Two homogeneous sulfated polysaccharides obtained from the red seaweeds Gymnogongrus griffithsiae and Cryptonemia crenulata, the kappa/iotau carrageenan G3d and the dl-galactan hybrid C2S-3, were assayed for their antiviral properties against the four serotypes of dengue virus (DENV) in different host cell types. Both seaweed derivatives were selective inhibitors of DENV-2 multiplication in Vero cells with inhibitory concentration 50% (IC(50)) values around 1mug/ml and selectivity indices >1000. The compounds had a lower antiviral effect against DENV-3 (IC(50) values in the range 13.9-14.2mug/ml), an even lower effect against DENV-4 (IC(50) values in the range 29.3 to >50mug/ml) and were totally inactive against DENV-1. With respect to the host cell, the polysulfates were inhibitors of DENV-2 and DENV-3 in the human hepatoma HepG2 and foreskin PH cells, with similar antiviral effectiveness as in Vero cells, but were totally inactive in mosquito C6/36 HT cells. Mechanistic studies demonstrated that G3d and C2S-3 were active DENV-2 inhibitors only when added together with the virus or early after infection, and both initial processes of virus adsorption and internalization are the main targets of these compounds. Therefore, the variations in antiviral activity of the polysaccharides depending on the viral serotype and the host cell may be ascribed to differences in the virus-cell interaction leading to virus entry.
机译:测定了两种从红海藻Gymnogongrus griffithsiae和Cryptonemia crenulata,κ/ iota / nu角叉菜胶G3d和dl-半乳聚糖杂种C2S-3获得的均质硫酸化多糖对四种登革热病毒血清型(DENV)的抗病毒特性。不同的宿主细胞类型。两种海藻衍生物都是Vero细胞中DENV-2增殖的选择性抑制剂,抑制浓度50%(IC(50))值约为1mug / ml,选择性指数> 1000。这些化合物对DENV-3的抗病毒作用较低(IC(50)值在13.9-14.2mug / ml范围内),对DENV-4的抗病毒作用较小(IC(50)值在29.3至> 50mug / ml范围内) ml),并且对DENV-1完全没有活性。对于宿主细胞,多硫酸盐是人肝癌HepG2和包皮PH细胞中的DENV-2和DENV-3抑制剂,具有与Vero细胞类似的抗病毒效果,但在蚊子C6 / 36 HT细胞中完全没有活性。机理研究表明,G3d和C2S-3仅在与病毒一起添加时或在感染后早期才是活性DENV-2抑制剂,并且病毒吸附和内在化的初始过程都是这些化合物的主要目标。因此,取决于病毒血清型和宿主细胞的多糖的抗病毒活性的变化可以归因于导致病毒进入的病毒-细胞相互作用的差异。

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