Univ. Bordeaux, CNRS, MFP, UMR 5234, 146 rue Léo Saignat, Bordeaux cedex, 33076, France.
Fédération de Recherche "TransbioMed", Bordeaux, France.
Sci Rep. 2017 Jun 2;7(1):2697. doi: 10.1038/s41598-017-03038-8.
Mosquito- and tick-borne pathogens including Chikungunya, Dengue, Japanese encephalitis, West Nile, Yellow fever and Zika virus, represent a new economic and public health challenge. In the absence of effective vaccines and specific therapies, only supportive regimens are administrated for most of these infections. Thus, the development of a targeted therapy is mandatory to stop the rapid progression of these pathogens and preoccupant associated burdens such as Guillain-Barre syndrome, microcephaly. For this, it is essential to develop biochemical tools to help study and target key viral enzymes involved in replication such as helicase complexes, methyl-transferases and RNA-dependent RNA polymerases. Here, we show that a highly purified ZIKV polymerase domain is active in vitro. Importantly, we show that this isolated domain is capable of de novo synthesis of the viral genome and efficient elongation without terminal nucleotide transferase activity. Altogether, this isolated polymerase domain will be a precious tool to screen and optimize specific nucleoside and non-nucleoside inhibitors to fight against Zika infections.
蚊媒和蜱媒病原体包括基孔肯雅热、登革热、日本脑炎、西尼罗河热、黄热病和寨卡病毒,它们给经济和公共卫生带来了新的挑战。由于缺乏有效的疫苗和特效疗法,对于大多数此类感染,仅能提供支持性治疗方案。因此,必须开发靶向疗法来阻止这些病原体的快速传播,并解决与吉兰-巴雷综合征、小头畸形等相关的负担。为此,开发生化工具来帮助研究和针对参与复制的关键病毒酶(如解旋酶复合物、甲基转移酶和 RNA 依赖性 RNA 聚合酶)至关重要。在这里,我们证明了高度纯化的寨卡病毒聚合酶结构域在体外具有活性。重要的是,我们表明这个分离的结构域能够从头合成病毒基因组并进行有效的延伸,而没有末端核苷酸转移酶活性。总之,这个分离的聚合酶结构域将成为筛选和优化针对寨卡病毒感染的特定核苷和非核苷抑制剂的宝贵工具。