Trek Therapeutics, PBC, 125 Cambridge Park Drive, Suite 301, Cambridge, MA 02140, USA.
Department of Pathology, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA.
Antiviral Res. 2018 Jan;149:34-40. doi: 10.1016/j.antiviral.2017.11.004. Epub 2017 Nov 8.
Zika virus (ZIKV), a member of the Flaviviridae family, has recently been linked to abnormal pregnancies, fetal death, microcephaly, and Guillain-Barré syndrome in humans. Merimepodib (MMPD, VX-497), a potent inhibitor of inosine-5'-monophosphate dehydrogenase (IMPDH), has shown antiviral activity against HCV and a variety of DNA and RNA viruses in vitro. In this report, we expand the antiviral spectrum of MMPD, and demonstrate that MMPD inhibits ZIKV RNA replication with an EC of 0.6 μM. Furthermore, MMPD reduces the virus production of ZIKV as well as several other important emerging viral pathogens such as Ebola, Lassa, Chikungunya, and Junin viruses. The inhibition can be reversed by addition of exogenous guanosine to culture media, consistent with the mechanism of action of MMPD as an IMPDH inhibitor. We also provide evidence that MMPD can be used in combination with other antivirals such as ribavirin and T-705 (favipiravir) to enhance suppression of virus production.
寨卡病毒(ZIKV)属于黄病毒科,最近被发现与人类异常妊娠、胎儿死亡、小头畸形和格林-巴利综合征有关。Merimepodib(MMPD,VX-497)是一种有效的肌苷-5'-单磷酸脱氢酶(IMPDH)抑制剂,已在体外显示出对 HCV 以及多种 DNA 和 RNA 病毒的抗病毒活性。在本报告中,我们扩展了 MMPD 的抗病毒谱,并证明 MMPD 以 EC50 为 0.6 μM 的浓度抑制 ZIKV RNA 复制。此外,MMPD 还能降低 ZIKV 以及其他几种重要的新兴病毒病原体(如埃博拉、拉萨、基孔肯雅和胡宁病毒)的病毒产量。在培养基中添加外源性鸟苷可逆转抑制作用,与 MMPD 作为 IMPDH 抑制剂的作用机制一致。我们还提供了证据表明,MMPD 可与其他抗病毒药物(如利巴韦林和 T-705(法匹拉韦))联合使用,以增强对病毒产生的抑制作用。