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Temperature-sensitive mutants of enterovirus 71 show attenuation in cynomolgus monkeys
被引:137
作者:
Arita, M
Shimizu, H
Nagata, N
Ami, Y
Suzaki, Y
Sata, T
Iwasaki, T
Miyamura, T
机构:
[1] Natl Inst Infect Dis, Dept Virol 2, Musashimurayama, Tokyo 2080011, Japan
[2] Natl Inst Infect Dis, Dept Pathol, Musashimurayama, Tokyo 2080011, Japan
[3] Natl Inst Infect Dis, Div Expt Anim Res, Musashimurayama, Tokyo 2080011, Japan
[4] Nagasaki Univ, Inst Trop Med, Div Clin Invest, Nagasaki 8528523, Japan
关键词:
D O I:
10.1099/vir.0.80784-0
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:
Enterovirus 71 (EV71) is one of the major causative agents of hand, foot and mouth disease and is sometimes associated with serious neurological disorders. In this study, an attempt was made to identify molecular determinants of EV71 attenuation of neurovirulence in a monkey infection model. An infectious cDNA clone of the virulent strain of EV71 prototype BrCr was constructed; temperature-sensitive (ts) mutations of an attenuated strain of EV71 or of poliovirus (PV) Sabin vaccine strains were then introduced into the infectious clone. In vitro and in vivo phenotypes of the parental and mutant viruses were analysed in cultured cells and in cynomolgus monkeys, respectively. Mutations in 3D polymerase (3D(pol)) and in the 3' non-translated region (NTR), corresponding to ts determinants of Sabin 1, conferred distinct temperature sensitivity to EV71. An EV71 mutant [EV71 (S1-3')] carrying mutations in the 5' NTR, 3D(pol) and in the 3' NTR showed attenuated neurovirulence, resulting in limited spread of virus in the central nervous system of monkeys. These results indicate that EV71 and PV1 share common genetic determinants of neurovirulence in monkeys, despite the distinct properties in their original pathogenesis.
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页码:1391 / 1401
页数:11
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