VARIANTS OF VENEZUELAN EQUINE ENCEPHALITIS-VIRUS THAT RESIST NEUTRALIZATION DEFINE A DOMAIN OF THE E2 GLYCOPROTEIN

被引:62
|
作者
JOHNSON, BJB
BRUBAKER, JR
ROEHRIG, JT
TRENT, DW
机构
关键词
D O I
10.1016/0042-6822(90)90533-W
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Stable neutralization (N) escape variants of Venezuelan equine encephalitis (VEE) virus were selected by anti-E2 glycoprotein monoclonal antibodies (MAbs) that neutralize viral infectivity, block viral hemagglutination, and passively protect mice. The nucleotide sequence of the Et, E2, and E3 genes of four variants revealed a clustering of single mutations in a domain spanning E2-182 to E2-207. The conformation of this short linear sequence affects antigenicity in the N domain because reduction and alkylation of virus disrupted binding of some E2 neutralizing MAbs. Serologic evidence for interaction of E2 epitopes also was obtained. Mutations in the N domain of VEE virus did not alter the kinetics of binding to Vero cells. They did, in some cases, produce attenuation of virulence in mice. © 1990.
引用
收藏
页码:676 / 683
页数:8
相关论文
共 50 条