AFRICAN SWINE FEVER VIRUS STRUCTURAL PROTEIN P72 CONTAINS A CONFORMATIONAL NEUTRALIZING EPITOPE

被引:64
|
作者
BORCA, MV [1 ]
IRUSTA, P [1 ]
CARRILLO, C [1 ]
AFONSO, CL [1 ]
BURRAGE, T [1 ]
ROCK, DL [1 ]
机构
[1] USDA ARS, PLUM ISL ANIM DIS CTR, GREENPORT, NY 11948 USA
关键词
D O I
10.1006/viro.1994.1311
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have previously described a monoclonal antibody (mAb 135D4) to an unidentified 70- to 72-kDa African swine fever virus (ASFV) protein that exhibited high levels of neutralizing activity against various virulent AsFV isolates. Here, we identify the reactive ASFV protein as the major virus structural protein p72. in vitro-translated products of the p72 protein gene were specifically immunoprecipitated by mAb 135D4. Immunoprecipitation of a nested set of truncated p72 in vitro translation products defined the region between amino acid residues 400 and 404 as necessary for mAb 135D4 reactivity. Five partially overlapping peptides (15mers) covering residues 388-446 failed to react with mAb 135D4, suggesting the conformational dependence of the epitope. Supporting this interpretation, larger in vitro translation products representing residues 56-282, 159-361, 360-508, and 507-646 also failed to react with mAb 135D4. Consistent with its involvement in virus neutralization, immunoelectromicroscopy, using a rabbit antiserum against mAb 135D4-purified p72, located the protein on the surface of unenveloped virus particles. (C) 1994 Academic Press, Inc.
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页码:413 / 418
页数:6
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