MONOCLONAL-ANTIBODY CHARACTERIZATION OF JAMESTOWN CANYON (CALIFORNIA SEROGROUP) VIRUS TOPOTYPES ISOLATED IN CANADA

被引:5
作者
ARTSOB, H
SPENCE, L
BRODEUR, BR
THNG, C
机构
[1] UNIV TORONTO,DEPT MICROBIOL,TORONTO M5S 1A1,ONTARIO,CANADA
[2] NATL LAB IMMUNOL,LAB CTR DIS CONT,BUR MICROBIOL,OTTAWA,ONTARIO,CANADA
关键词
D O I
10.1089/vim.1992.5.233
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Jamestown Canyon (JC) virus of the California (CAL) serogroup has been isolated in 12 American states and 6 Canadian provinces. A study was undertaken to produce monoclonal antibodies (MAbs) to JC virus and to use these MAbs to assay for possible heterogeneity among naturally occurring JC topotypes in Canada. MAbs were produced to the prototype strain of JC virus using BALB/c mice. Twenty-seven secreting MAbs were obtained and three of these MAbs were propagated and studied. All three MAbs, M1 (IgG 1), M2 (IgG2b), and M3 (IgG2a), were reactive by immunofluorescent antibody assay against JC-infected vero cells and by ELISA against JC antigen. MAb M2 reacted with all members of the Melao complex, MAb M1 reacted only with Keystone virus, while MAb M3 exhibited no reactivity with other CAL serogroup viruses. Only MAb M3 possessed neutralization and hemagglutination inhibition activities against JC virus. The MAbs were also tested by ELISA and for neutralizing activity against 13 JC topotypes isolated in 5 provinces from Newfoundland to Saskatchewan. ELISA confirmed closer identity of the Canadian topotypes to JC as opposed to the closely related South River virus. The MAbs verified all Canadian topotypes to be JC virus but revealed different patterns of reactivity between these topotypes and prototype JC virus.
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页码:233 / 242
页数:10
相关论文
共 27 条
[1]  
ARTSOB H, 1984, J CLIN MICROBIOL, V20, P276, DOI 10.1128/JCM.20.2.276-280.1984
[2]  
ARTSOB H, 1985, CAN MED ASSOC J, V133, P1026
[3]  
BISHOP DHK, 1980, COMPREHENSIVE VIROLO, V14, P1
[4]   PARAMETERS AFFECTING ASCITES TUMOR-FORMATION IN MICE AND MONOCLONAL-ANTIBODY PRODUCTION [J].
BRODEUR, BR ;
TSANG, P ;
LAROSE, Y .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 71 (02) :265-272
[5]   HIGH-YIELD MONOCLONAL-ANTIBODY PRODUCTION IN ASCITES [J].
BRODEUR, BR ;
TSANG, PS .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 86 (02) :239-241
[6]   PROTECTION AGAINST INFECTION WITH NEISSERIA-MENINGITIDIS GROUP-B SEROTYPE-2B BY PASSIVE-IMMUNIZATION WITH SEROTYPE-SPECIFIC MONOCLONAL-ANTIBODY [J].
BRODEUR, BR ;
LAROSE, Y ;
TSANG, P ;
HAMEL, J ;
ASHTON, F ;
RYAN, A .
INFECTION AND IMMUNITY, 1985, 50 (02) :510-516
[7]   NEW MONOCLONAL-ANTIBODIES FOR THE DETECTION OF IMMEDIATE EARLY ANTIGENS OF CYTOMEGALOVIRUS [J].
BRODEUR, BR ;
LUSSIER, M ;
LAROSE, Y ;
ROSSIER, E ;
MILLER, H ;
NAKAGAWA, C ;
EVELEGH, M .
VIRAL IMMUNOLOGY, 1992, 5 (01) :61-69
[8]  
Calisher C H, 1983, Prog Clin Biol Res, V123, P1
[9]   TECHNIQUES FOR HEMAGGLUTINATION AND HEMAGGLUTINATION-INHIBITION WITH ARTHROPOD-BORNE VIRUSES [J].
CLARKE, DH ;
CASALS, J .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1958, 7 (05) :561-573
[10]  
DEIBEL R, 1983, CALIFORNIA SEROGROUP, P313