Bourinbaiar A S, Lee-Huang S
Department of Biochemistry, New York University School of Medicine, New York 10016, USA.
Biochem Biophys Res Commun. 1996 Feb 27;219(3):923-9. doi: 10.1006/bbrc.1996.0334.
We examined the effect on anti-HIV proteins MAP30 and GAP31, from Momordica charantia and Gelonium multiflorum, on the infection and replication of Herpes Simplex Viruses (HSV). Human lung WI-38 fibroblasts cultured in the presence of tenfold dilutions of MAP30 or GAP31 were exposed to HSV and viral yield was measured at 24-48 hours by ELISA. The effective concentrations for 50% inhibitions (EC50) were 0.1-0.2 microM for HSV-2, and 0.3-0.5 microM for HSV-1 for MAP30 and GAP31, respectively. In comparison, the EC(50) for acyclovir (ACV), a commonly used anti-HSV drug, was 0.2 and 1.7 microM for HSV-2 and HSV-1, respectively. The cytotoxicity of all three antivirals was negligible and comparable. However, the antiherpetic activity of the plant proteins against acyclovir-resistant strains was two to three logs more potent than ACV. These results suggest that MAP30 and GAP31, previously shown to be active against HIV, may be useful for the therapy of herpesvirus infections.
我们研究了来自苦瓜和多花巴豆的抗HIV蛋白MAP30和GAP31对单纯疱疹病毒(HSV)感染和复制的影响。在存在10倍稀释的MAP30或GAP31的情况下培养的人肺WI-38成纤维细胞暴露于HSV,并在24至48小时通过ELISA测量病毒产量。对于MAP30和GAP31,HSV-2的50%抑制有效浓度(EC50)为0.1 - 0.2微摩尔,HSV-1的为0.3 - 0.5微摩尔。相比之下,常用的抗HSV药物阿昔洛韦(ACV)对HSV-2和HSV-1的EC50分别为0.2和1.7微摩尔。所有三种抗病毒药物的细胞毒性可忽略不计且相当。然而,植物蛋白对阿昔洛韦耐药菌株的抗疱疹活性比ACV强两到三个对数。这些结果表明,先前显示对HIV有活性的MAP30和GAP31可能对疱疹病毒感染的治疗有用。