Pujol C A, Coto C E, Damonte E B
Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina.
Rev Argent Microbiol. 1995 Apr-Jun;27(2):91-8.
The effects of different experimental conditions on the antiviral activity of the sulphated xylomannan F6, isolated from the red seaweed Nothogenia fastigiata, against the replication of herpes simplex virus type 1 and 2 (HSV-1 and HSV-2) were studied. The compound was equally effective against several strains of HSV-1 (F, KOS, B-2006 and Field) and HSV-2 (G) in different cell lines (Vero, HEp-2 and BHK-21). Furthermore, the antiviral activity of F6 was independent of the method employed to determine the 50% inhibitory concentration (IC50) (virus yield or plaque reduction tests). The value of the IC50 against HSV-1 was not significantly affected by the initial virus concentration since a variation in the multiplicity of infection from 0.0001 to 0.1 UFP/cell only increased twofold the IC50 from 0.61 to 1.35 micrograms/ml, respectively. The potent inhibitory effect of F6 against high doses of HSV-1 represents a significant advantage for this sulphated polysaccharide with respect to other compounds only active against low viral inocula.
研究了不同实验条件对从红藻Nothogenia fastigiata中分离得到的硫酸化木聚糖F6抗1型和2型单纯疱疹病毒(HSV-1和HSV-2)复制的抗病毒活性的影响。该化合物在不同细胞系(Vero、HEp-2和BHK-21)中对几种HSV-1毒株(F、KOS、B-2006和Field)和HSV-2毒株(G)同样有效。此外,F6的抗病毒活性与用于确定50%抑制浓度(IC50)的方法(病毒产量或蚀斑减少试验)无关。针对HSV-1的IC50值不受初始病毒浓度的显著影响,因为感染复数从0.0001增加到0.1个感染单位/细胞时,IC50仅分别从0.61微克/毫升增加到1.35微克/毫升两倍。F6对高剂量HSV-1的强效抑制作用相对于其他仅对低病毒接种量有活性的化合物而言,是这种硫酸化多糖的一个显著优势。