Antibody to the E3 Glycoprotein Protects Mice against Lethal Venezuelan Equine Encephalitis Virus Infection

被引:29
作者
Parker, Michael D. [1 ]
Buckley, Marilyn J. [3 ]
Melanson, Vanessa R. [1 ]
Glass, Pamela J. [1 ]
Norwood, David [2 ]
Hart, Mary Kate [1 ,4 ]
机构
[1] USA, Med Res Inst Infect Dis, Div Virol, Frederick, MD 21702 USA
[2] Diagnost Syst Div, Frederick, MD USA
[3] Integrated Toxicol Div, Frederick, MD USA
[4] DynPort Vaccine Co, Frederick, MD USA
关键词
SEMLIKI-FOREST-VIRUS; SINDBIS-VIRUS; MONOCLONAL-ANTIBODIES; MEMBRANE-PROTEINS; ENCEPHALOMYELITIS VIRUS; ATTENUATED VACCINES; FURIN; EXPRESSION; FUSION; LIVE;
D O I
10.1128/JVI.01345-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Six monoclonal antibodies were isolated that exhibited specificity for a furin cleavage site deletion mutant (V3526) of Venezuelan equine encephalitis virus (VEEV). These antibodies comprise a single competition group and bound the E3 glycoprotein of VEEV subtype I viruses but failed to bind the E3 glycoprotein of other alphaviruses. These antibodies neutralized V3526 virus infectivity but did not neutralize the parental strain of Trinidad donkey (TrD) VEEV. However, the E3-specific antibodies did inhibit the production of virus from VEEV TrD-infected cells. In addition, passive immunization of mice demonstrated that antibody to the E3 glycoprotein provided protection against lethal VEEV TrD challenge. This is the first recognition of a protective epitope in the E3 glycoprotein. Furthermore, these results indicate that E3 plays a critical role late in the morphogenesis of progeny virus after E3 appears on the surfaces of infected cells.
引用
收藏
页码:12683 / 12690
页数:8
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