Department of Biotechnology, Chemistry and Pharmacy, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.
Department of Experimental and Clinical Medicine, University of Florence, Viale Morgagni 48, 50134 Florence, Italy.
Int J Mol Sci. 2024 Feb 19;25(4):2437. doi: 10.3390/ijms25042437.
Zika virus (ZIKV) is a positive-sense single-stranded virus member of the family. Among other arboviruses, ZIKV can cause neurological disorders such as Guillain Barré syndrome, and it can have congenital neurological manifestations and affect fertility. ZIKV nonstructural protein 5 (NS5) is essential for viral replication and limiting host immune detection. Herein, we performed virtual screening to identify novel small-molecule inhibitors of the ZIKV NS5 methyltransferase (MTase) domain. Compounds were tested against the MTases of both ZIKV and DENV, demonstrating good inhibitory activities against ZIKV MTase. Extensive molecular dynamic studies conducted on the series led us to identify other derivatives with improved activity against the MTase and limiting ZIKV infection with an increased selectivity index. Preliminary pharmacokinetic parameters have been determined, revealing excellent stability over time. Preliminary in vivo toxicity studies demonstrated that the hit compound is well tolerated after acute administration. Our results provide the basis for further optimization studies on novel non-nucleoside MTase inhibitors.
Zika 病毒(ZIKV)是黄病毒科的正链单股病毒成员。与其他虫媒病毒一样,ZIKV 可引起神经疾病,如格林-巴利综合征,还可导致先天性神经发育异常和影响生育能力。ZIKV 非结构蛋白 5(NS5)是病毒复制所必需的,可限制宿主免疫检测。在此,我们进行了虚拟筛选,以鉴定 ZIKV NS5 甲基转移酶(MTase)结构域的新型小分子抑制剂。对 ZIKV 和 DENV 的 MTases 进行了化合物测试,结果表明这些化合物对 ZIKV MTase 具有良好的抑制活性。对该系列化合物进行了广泛的分子动力学研究,使我们发现了其他具有改善 MTase 活性和增加对 ZIKV 感染选择性指数的衍生物。已经确定了初步的药代动力学参数,显示出随时间推移的优异稳定性。初步的体内毒性研究表明,在急性给药后,该化合物的命中化合物 耐受性良好。我们的研究结果为进一步优化新型非核苷 MTase 抑制剂的研究提供了基础。