Takhampunya Ratree, Ubol Sukathida, Houng Huo-Shu, Cameron Craig E, Padmanabhan Radhakrishnan
Department of Microbiology, Faculty of Science, Mahidol University, 272 Rama VI Road, Bangkok 10400, Thailand.
Department of Microbiology and Immunology, Georgetown University School of Medicine, 3900 Reservoir Road, Washington, DC 20057, USA.
J Gen Virol. 2006 Jul;87(Pt 7):1947-1952. doi: 10.1099/vir.0.81655-0.
Dengue viruses (DEN), mosquito-borne members of the family Flaviviridae, are human pathogens of global significance. The effects of mycophenolic acid (MPA) and ribavirin (RBV) on DEN replication in monkey kidney (LLC-MK2) cells were examined. MPA (IC(50)=0.4+/-0.3 microM) and RBV (IC(50)=50.9+/-18 microM) inhibited DEN2 replication. Quantitative real-time RT-PCR of viral RNA and plaque assays of virions from DEN2-infected and MPA (10 microM)- and RBV (> or =200 microM)-treated cells showed a fivefold increase in defective viral RNA production by cells treated with each drug. Moreover, a dramatic reduction of intracellular viral replicase activity was seen by in vitro replicase assays. Guanosine reversed the inhibition of these compounds, suggesting that one mode of antiviral action of MPA and RBV is by inhibition of inosine monophosphate dehydrogenase and thereby depletion of the intracellular GTP pool. In addition, RBV may act by competing with guanine-nucleotide precursors in viral RNA translation, replication and 5' capping.
登革病毒(DEN)是黄病毒科的蚊媒病毒,是具有全球意义的人类病原体。研究了霉酚酸(MPA)和利巴韦林(RBV)对猴肾(LLC-MK2)细胞中登革病毒复制的影响。MPA(IC50 = 0.4±0.3微摩尔)和RBV(IC50 = 50.9±18微摩尔)抑制登革2型病毒的复制。对登革2型病毒感染以及用MPA(10微摩尔)和RBV(≥200微摩尔)处理的细胞进行病毒RNA的定量实时逆转录聚合酶链反应和病毒粒子的蚀斑测定,结果显示每种药物处理的细胞产生的缺陷病毒RNA增加了五倍。此外,通过体外复制酶测定发现细胞内病毒复制酶活性显著降低。鸟苷可逆转这些化合物的抑制作用,这表明MPA和RBV的一种抗病毒作用模式是通过抑制肌苷单磷酸脱氢酶,从而耗尽细胞内的鸟苷三磷酸池。此外,RBV可能通过在病毒RNA翻译、复制和5'加帽过程中与鸟嘌呤核苷酸前体竞争而起作用。