ANTIBODY REACTIVITY TO THE IMMUNODOMINANT EPITOPES OF THE CAPRINE ARTHRITIS-ENCEPHALITIS VIRUS GP38 TRANSMEMBRANE PROTEIN ASSOCIATES WITH THE DEVELOPMENT OF ARTHRITIS

被引:60
作者
BERTONI, G
ZAHNO, ML
ZANONI, R
VOGT, HR
PETERHANS, E
RUFF, G
CHEEVERS, WP
SONIGO, P
PANCINO, G
机构
[1] UNIV BERN,INST VET VIROL,CH-3012 BERN,SWITZERLAND
[2] UNIV BERN,INST ANIM BREEDING,DEPT IMMUNOGENET,CH-3012 BERN,SWITZERLAND
[3] WASHINGTON STATE UNIV,COLL VET MED,DEPT VET MICROBIOL & PATHOL,PULLMAN,WA 99164
[4] INST COCHIN GENET MOLEC,F-75014 PARIS,FRANCE
关键词
D O I
10.1128/JVI.68.11.7139-7147.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
High titers of antibodies to caprine arthritis-encephalitis virus (CAEV) envelope (Env) glycoproteins are found in infected goats developing a progressive arthritis. In order to identify linear B epitopes of the CAEV Env, which may be involved in the immunopathology of arthritis, we constructed a lambda gt11 Env expression library. By combining library screening with sera from naturally infected Swiss goats with an enzyme immunoassay with overlapping peptides (pepscan), four group-specific epitopes could be precisely defined in the transmembrane envelope proteins: TM1 to TM4, including a conserved structure (TM3) that corresponds to the immunodominant epitope of human immunodeficiency virus type 1 and other lentiviruses. A panel of 190 CAEV naturally infected goat serum samples, obtained from animals with defined clinical status, was tested for reactivity to synthetic peptides corresponding to the TM epitopes in an enzyme-linked immunosorbent assay. Antibody reactivity to two epitopes was highly associated (TM3, P = 0.002, and TM4, P < 0.001) with the presence of clinically detectable arthritis. Such an association is absent for anti-Gag antibody. Antibodies to the immunodominant structures of the TM glycoprotein could thus have an important role in the immunopathogenic process leading to disease.
引用
收藏
页码:7139 / 7147
页数:9
相关论文
共 46 条
[1]   SEROLOGICAL DIAGNOSIS OF FELINE IMMUNODEFICIENCY VIRUS-INFECTION BASED ON SYNTHETIC PEPTIDES FROM ENV GLYCOPROTEINS [J].
AVRAMEAS, A ;
STROSBERG, AD ;
MORAILLON, A ;
SONIGO, P ;
PANCINO, G .
RESEARCH IN VIROLOGY, 1993, 144 (03) :209-218
[2]   PRECURSOR POLYPEPTIDES OF CAPRINE ARTHRITIS ENCEPHALITIS LENTIVIRUS STRUCTURAL PROTEINS [J].
CHEEVERS, WP ;
STEM, TA ;
KNOWLES, DP ;
MCGUIRE, TC .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :675-681
[3]   ANALYSIS OF EQUINE HUMORAL IMMUNE-RESPONSES TO THE TRANSMEMBRANE ENVELOPE GLYCOPROTEIN (GP45) OF EQUINE INFECTIOUS-ANEMIA VIRUS [J].
CHONG, YH ;
BALL, JM ;
ISSEL, CJ ;
MONTELARO, RC ;
RUSHLOW, KE .
JOURNAL OF VIROLOGY, 1991, 65 (02) :1013-1018
[4]   CONSERVED CYSTEINE RESIDUES IN THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 TRANSMEMBRANE ENVELOPE PROTEIN ARE ESSENTIAL FOR PRECURSOR ENVELOPE CLEAVAGE [J].
DEDERA, D ;
GU, RL ;
RATNER, L .
JOURNAL OF VIROLOGY, 1992, 66 (02) :1207-1209
[5]  
DEVEREUX J, 1991, PROGRAM MANUAL GCG P
[6]  
DUMOND DC, 1962, BR J EXP PATHOL, V43, P363
[7]   AN ANTI-GP41 HUMAN MONOCLONAL-ANTIBODY THAT ENHANCES HIV-1 INFECTION IN THE ABSENCE OF COMPLEMENT [J].
EATON, AM ;
UGEN, KE ;
WEINER, DB ;
WILDES, T ;
LEVY, JA .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1994, 10 (01) :13-18
[8]   EVALUATION OF FELINE IMMUNODEFICIENCY VIRUS AND FELINE LEUKEMIA-VIRUS TRANSMEMBRANE PEPTIDES FOR SEROLOGICAL DIAGNOSIS [J].
FONTENOT, JD ;
HOOVER, EA ;
ELDER, JH ;
MONTELARO, RC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (07) :1885-1890
[9]   A GENERAL-MODEL FOR THE TRANSMEMBRANE PROTEINS OF HIV AND OTHER RETROVIRUSES [J].
GALLAHER, WR ;
BALL, JM ;
GARRY, RF ;
GRIFFIN, MC ;
MONTELARO, RC .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1989, 5 (04) :431-440
[10]   FINE MAPPING OF AN IMMUNODOMINANT DOMAIN IN THE TRANSMEMBRANE GLYCOPROTEIN OF HUMAN-IMMUNODEFICIENCY-VIRUS [J].
GNANN, JW ;
NELSON, JA ;
OLDSTONE, MBA .
JOURNAL OF VIROLOGY, 1987, 61 (08) :2639-2641