A bifunctional anti-enterovirus compound that inhibits replication and the early stage of enterovirus 71 infection

被引:37
作者
Arita, Minetaro [1 ]
Takebe, Yutaka [2 ]
Wakita, Takaji [1 ]
Shimizu, Hiroyuki [1 ]
机构
[1] Natl Inst Infect Dis, Dept Virol 2, Musashimurayama, Tokyo 2080011, Japan
[2] Natl Inst Infect Dis, AIDS Res Ctr, Lab Mol Virol & Epidemiol, Shinjuku Ku, Tokyo 1628640, Japan
关键词
POLIOVIRUS RNA; BREFELDIN-A; ENVIROXIME TARGETS; CAPSID RESIDUES; PULMONARY-EDEMA; CODING REGION; PROTEIN; POLIOMYELITIS; PERSISTENT; MUTATIONS;
D O I
10.1099/vir.0.023374-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Enviroxime is an anti-enterovirus compound that targets viral protein 3A and/or 3AB and suppresses a replication step of enterovirus by an unknown mechanism. To date, a number of anti-enterovirus compounds that have little structural similarity to enviroxime but induce common resistance mutations in the 3A-encoding region have been identified. The present study identified a novel type of functionally enviroxime-like compound, AN-12-H5. This compound had no structural similarity to enviroxime or to known enviroxime-like compounds, including TTP-8307, GW5074 and Flt3 Inhibitor II. A resistance phenotype of poliovirus (PV) to these compounds was conferred by a major enviroxime-resistance mutation of PV (G531 8A, 3A-Ala70Thr), but not by resistance mutations to guanidine hydrochloride and brefeldin A. AN-12-H5 had a common structure with the anti-enterovirus 71 (EV71) compound AN-23-F6. AN-12-H5 and AN-23-F6 inhibited an early stage of EV71 infection after virus binding to the cells. Mutations in capsid proteins (G3112A, VP1-Ala224Thr, and G2396A, VP3-Arg227Lys mutations) were determined as resistant mutations to AN-12-H5 and AN-23-F6 in the early stage of EV71 infection. These results suggest that AN-12-H5 is a bifunctional anti-enterovirus compound that belongs to a novel class of enviroxime-like compounds and targets both a replication step and an early stage of EV71 infection.
引用
收藏
页码:2734 / 2744
页数:11
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