IDENTIFICATION OF 4 DISTINCT NEUTRALIZING EPITOPES ON BLUETONGUE VIRUS SEROTYPE-10 USING NEUTRALIZING MONOCLONAL-ANTIBODIES AND NEUTRALIZATION-ESCAPE VARIANTS

被引:23
作者
HEIDNER, HW [1 ]
ROSSITTO, PV [1 ]
MACLACHLAN, NJ [1 ]
机构
[1] UNIV CALIF DAVIS,SCH VET MED,DEPT VET PATHOL,DAVIS,CA 95616
关键词
D O I
10.1016/0042-6822(90)90041-O
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Neutralizing sites on bluetongue virus serotype 10 (BTV-10) were investigated with a panel of seven neutralizing monoclonal antibodies (MAbs Each MAb was coupled to agarose beads and tested against the other MAbs and a nonneutralizing control MAb in a competitive immunoprecipitation assay. In addition, neutralization-escape viral variants of BTV-10 were identified and cloned by selecting individual plaques that formed in the presence of neutralizing MAbs. Four antigenic variants were isolated, each under the selective pressure of a different MAb. Parental BTV-10 and the four antigenic variants were compared by microneutralization assay using the MAb panel. The panel of neutralizing MAbs was subdivided into four groups on the basis of these assays, indicating that at least four distinct neutralizing epitopes exist on the BTV-10 virion. These epitopes are individually defined by representative MAbs 034, 039, 041, and 045, and the results indicate that the four epitopes are interacting sites within a single antigenic domain on BTV-10 outer capsid protein VP2. This conclusion is further supported by the fact that a double-site neutralization-escape variant designated DE34/39 (sequentially produced against MAbs 034 and 039) was not neutralized by any MAb of the panel. © 1990.
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页码:658 / 661
页数:4
相关论文
共 17 条
[1]   MONOCLONAL-ANTIBODY ANALYSIS OF SEROTYPE-RESTRICTED AND UNRESTRICTED BLUETONGUE VIRAL ANTIGENIC DETERMINANTS [J].
APPLETON, JA ;
LETCHWORTH, GJ .
VIROLOGY, 1983, 124 (02) :286-299
[2]   CROSS-NEUTRALIZATION OF GENETIC REASSORTANTS OF BLUETONGUE VIRUS SEROTYPES 20 AND 21 [J].
COWLEY, JA ;
GORMAN, BM .
VETERINARY MICROBIOLOGY, 1989, 19 (01) :37-51
[3]   BLUETONGUE VIRUS GENOME REMAINS STABLE THROUGHOUT PROLONGED INFECTION OF CATTLE [J].
HEIDNER, HW ;
MACLACHLAN, NJ ;
FULLER, FJ ;
RICHARDS, RG ;
WHETTER, LE .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :2629-2636
[4]   A COMPARISON OF DIFFERENT CLONED BLUETONGUE VIRUS GENOME SEGMENTS AS PROBES FOR THE DETECTION OF VIRUS-SPECIFIED RNA [J].
HUISMANS, H ;
CLOETE, M .
VIROLOGY, 1987, 158 (02) :373-380
[5]  
HUISMANS H, 1981, ONDERSTEPOORT J VET, V48, P51
[6]  
Huismans H., 1983, Double-stranded RNA viruses. Proceedings of the First International Symposium, October 5-10, 1982, U.S. Virgin Islands, P165
[7]   MOLECULAR-BASIS OF BLUETONGUE VIRUS NEUTRALIZATION [J].
KAHLON, J ;
SUGIYAMA, K ;
ROY, P .
JOURNAL OF VIROLOGY, 1983, 48 (03) :627-632
[8]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[9]   HETEROGENEITY OF NEUTRALIZATION-RELATED EPITOPES WITHIN A BLUETONGUE VIRUS SEROTYPE [J].
LETCHWORTH, GJ ;
APPLETON, JA .
VIROLOGY, 1983, 124 (02) :300-307
[10]  
MACLACHLAN NJ, 1985, AM J VET RES, V46, P1238