ANTIBODIES TO AUJESZKYS DISEASE VIRUS IN PIGS IMMUNIZED WITH PURIFIED VIRUS GLYCOPROTEINS

被引:10
作者
IGLESIAS, G
MOLITOR, T
REED, D
LITALIEN, J
机构
[1] UNIV MINNESOTA,COLL VET MED,DEPT LARGE ANIM CLIN SCI,ST PAUL,MN 55108
[2] MOLEC GENET INC,MINNETONKA,MN
关键词
D O I
10.1016/0378-1135(90)90045-W
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antibodies to Aujeszky's disease virus (ADV) glycoproteins gII, gIII, and gp50 were compared using four in vitro tests. Antibodies generated by vaccination with a modified-live vaccine (MLV) were also compared. The serological assays employed were: serum neutralization test (SNT), complement facilitated serum neutralization test (C'SNT), complement-mediated cytolysis and antibody dependent cellular cytotoxicity (ADCC). Pigs were immunized with single glycoproteins twice 14 days apart, or once with the modified-live vaccine. Fourteen days after the second immunization, sera were collected. Virus neutralizing activity (SNT) was demonstrated in the sera from all pigs immunized with gp50 and in one out of three immunized with gIII. Sera from the MLV group all had neutralization titers higher than animals immunized with single glycoproteins. Addition of guinea pig complement to the serum neutralization test (i.e., C'SNT) produced an enhancement of antibody titers in all groups except the pigs immunized with gIII. The complement-mediated cytolysis test rendered antibody titers similar in magnitude for all pigs immunized with single glycoproteins, but slightly lower than values for MLV vaccinated pigs. ADCC activity was clearly displayed in sera from pigs immunized with gIII or vaccinated with MLV, whereas sera from pigs immunized with gII or gp50 had a minimal response. The results indicate that the relative efficiency of antibodies against ADV glycoproteins in protection should be considered for selecting or producing gene-deleted strains for use in vaccine production. © 1990.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 27 条
[1]   PROTECTION OF CATTLE FROM BOVINE HERPESVIRUS TYPE-I (BHV-1) INFECTION BY IMMUNIZATION WITH INDIVIDUAL VIRAL GLYCOPROTEINS [J].
BABIUK, LA ;
LITALIEN, J ;
LITTELVANDENHURK, SV ;
ZAMB, T ;
LAWMAN, MJP ;
HUGHES, G ;
GIFFORD, GA .
VIROLOGY, 1987, 159 (01) :57-66
[2]   LOCALIZATION OF THE REGIONS OF HOMOLOGY BETWEEN THE GENOMES OF HERPES-SIMPLEX VIRUS, TYPE-1, AND PSEUDORABIES VIRUS [J].
BENPORAT, T ;
VEACH, RA ;
IHARA, S .
VIROLOGY, 1983, 127 (01) :194-204
[3]   OCULAR INFECTION WITH HERPES-SIMPLEX VIRUS TYPE-1 - PREVENTION OF ACUTE HERPETIC ENCEPHALITIS BY SYSTEMIC ADMINISTRATION OF VIRUS-SPECIFIC ANTIBODY [J].
DAVIS, WB ;
TAYLOR, JA ;
OAKES, JE .
JOURNAL OF INFECTIOUS DISEASES, 1979, 140 (04) :534-540
[4]   IDENTIFICATION OF THE PSEUDORABIES VIRUS GLYCOPROTEIN-GP50 AS A MAJOR TARGET OF NEUTRALIZING ANTIBODIES [J].
ELOIT, M ;
FARGEAUD, D ;
LHARIDON, R ;
TOMA, B .
ARCHIVES OF VIROLOGY, 1988, 99 (1-2) :45-56
[5]   IMMUNOGENICITY OF HERPES-SIMPLEX VIRUS GLYCOPROTEIN-GC AND GLYCOPROTEIN-GB AND THEIR ROLE IN PROTECTIVE IMMUNITY [J].
GLORIOSO, J ;
SCHRODER, CH ;
KUMEL, G ;
SZCZESIUL, M ;
LEVINE, M .
JOURNAL OF VIROLOGY, 1984, 50 (03) :805-812
[6]   INDUCED PROTEINS IN CELLS INFECTED WITH PSEUDORABIES VIRUS [J].
HAHN, EC ;
HAHN, PS .
ARCHIVES OF VIROLOGY, 1987, 94 (3-4) :247-257
[7]   CHARACTERIZATION OF THE ENVELOPE PROTEINS OF PSEUDORABIES VIRUS [J].
HAMPL, H ;
BENPORAT, T ;
EHRLICHER, L ;
HABERMEHL, KO ;
KAPLAN, AS .
JOURNAL OF VIROLOGY, 1984, 52 (02) :583-590
[8]  
JAKUBIK J, 1987, ZENTRALBL VET MED B, V15, P741
[9]   PATHOGENESIS OF HERPES-SIMPLEX VIRUS IN CONGENITALLY ATHYMIC MICE - THE RELATIVE ROLES OF CELL-MEDIATED AND HUMORAL IMMUNITY [J].
KAPOOR, AK ;
NASH, AA ;
WILDY, P ;
PHELAN, J ;
MCLEAN, CS ;
FIELD, HJ .
JOURNAL OF GENERAL VIROLOGY, 1982, 60 (JUN) :225-233
[10]  
KUMEL G, 1985, J VIROL, V56, P930