Talarico L B, Pujol C A, Zibetti R G M, Faría P C S, Noseda M D, Duarte M E R, Damonte E B
Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
Antiviral Res. 2005 Jun;66(2-3):103-10. doi: 10.1016/j.antiviral.2005.02.001. Epub 2005 Feb 26.
Two homogeneous sulfated polysaccharides obtained from the red seaweeds Gymnogongrus griffithsiae and Cryptonemia crenulata, the kappa/iota/nu 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% (IC50) values around 1 microg/ml and selectivity indices > 1000. The compounds had a lower antiviral effect against DENV-3 (IC50 values in the range 13.9-14.2 microg/ml), an even lower effect against DENV-4 (IC50 values in the range 29.3 to > 50 microg/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.
从红藻Gymnogongrus griffithsiae和Cryptonemia crenulata中提取的两种均一硫酸化多糖,即κ/ι/ν卡拉胶G3d和dl-半乳聚糖混合物C2S-3,在不同宿主细胞类型中针对四种血清型登革热病毒(DENV)的抗病毒特性进行了测定。两种海藻衍生物都是Vero细胞中DENV-2增殖的选择性抑制剂,其半数抑制浓度(IC50)值约为1微克/毫升,选择性指数>1000。这些化合物对DENV-3的抗病毒作用较低(IC50值在13.9-14.2微克/毫升范围内),对DENV-4的作用更低(IC50值在29.3至>50微克/毫升范围内),对DENV-1完全无活性。就宿主细胞而言,多硫酸盐在人肝癌HepG2和包皮PH细胞中是DENV-2和DENV-3的抑制剂,抗病毒效果与在Vero细胞中相似,但在蚊C6/36 HT细胞中完全无活性。机制研究表明,G3d和C2S-3仅在与病毒一起添加或感染后早期才是活性DENV-2抑制剂,病毒吸附和内化的初始过程都是这些化合物的主要靶点。因此,多糖抗病毒活性因病毒血清型和宿主细胞而异,可能归因于导致病毒进入的病毒-细胞相互作用的差异。