Nucleoside Inhibitors of Zika Virus

被引:131
作者
Eyer, Ludek [1 ]
Nencka, Radim [2 ]
Huvarova, Ivana [1 ]
Palus, Martin [1 ,3 ,4 ]
Alves, Maria Joao [5 ]
Gould, Ernest A. [6 ]
De Clercq, Erik [7 ]
Ruzek, Daniel [1 ,3 ,4 ]
机构
[1] Vet Res Inst, Dept Virol, Brno, Czech Republic
[2] Acad Sci Czech Republic, Inst Organ Chem & Biochem, Prague, Czech Republic
[3] Acad Sci Czech Republic, Ctr Biol, Inst Parasitol, Prague, Czech Republic
[4] Univ South Bohemia, Fac Sci, Ceske Budejovice, Czech Republic
[5] Natl Inst Hlth Dr Ricardo Jorge CEVDI INSA, Aguas De Moura, Portugal
[6] Aix Marseille Univ, IRD French Inst Res Dev, EHESP French Sch Publ Hlth, EPV UMR D Emergence Pathol Virales 190, Marseille, France
[7] Katholieke Univ Leuven, Rega Inst Med Res, Leuven, Belgium
关键词
Zika virus; flavivirus; nucleoside analogue; antiviral; therapy; FLAVIVIRUS DRUG DISCOVERY;
D O I
10.1093/infdis/jiw226
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There is growing evidence that Zika virus (ZIKV) can cause devastating infant brain defects and other neurological disorders in humans. However, no specific antiviral therapy is available at present. We tested a series of 2'-C- or 2'-O-methyl-substituted nucleosides, 2'-C-fluoro-2'-C-methyl-substituted nucleosides, 3'-O-methyl-substituted nucleosides, 3'-deoxynucleosides, derivatives with 4'-C-azido substitution, heterobase-modified nucleosides, and neplanocins for their ability to inhibit ZIKV replication in cell culture. Antiviral activity was identified when 2'-C-methylated nucleosides were tested, suggesting that these compounds might represent promising lead candidates for further development of specific antivirals against ZIKV.
引用
收藏
页码:707 / 711
页数:5
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