VACCINATION AGAINST TAENIA-TAENIAEFORMIS INFECTION IN RATS USING A RECOMBINANT PROTEIN AND PRELIMINARY-ANALYSIS OF THE INDUCED ANTIBODY-RESPONSE

被引:26
作者
ITO, A
BOGH, HO
LIGHTOWLERS, MW
MITCHELL, GF
TAKAMI, T
KAMIYA, M
ONITAKE, K
RICKARD, MD
机构
[1] CSIRO,DIV ANIM HLTH,MELBOURNE,VIC 3001,AUSTRALIA
[2] WALTER & ELIZA HALL INST MED RES,MELBOURNE,AUSTRALIA
[3] HOKKAIDO UNIV,FAC VET MED,DEPT PARASITOL,SAPPORO,HOKKAIDO 060,JAPAN
[4] GIFU UNIV,SCH MED,DEPT PATHOL,GIFU 500,JAPAN
[5] UNIV MELBOURNE,CTR VET CLIN,WERRIBEE,VIC 3030,AUSTRALIA
[6] YAMAGATA UNIV,FAC SCI,DEPT BIOL,YAMAGATA 990,JAPAN
基金
英国医学研究理事会;
关键词
D O I
10.1016/0166-6851(91)90219-V
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Primary screening of a cDNA expression library of Taenia taeniaeformis oncospheres in λgt11 bacteriophage was carried out using rabbit anti-T. taeniaeformis oncosphere serum affinity-purified from disrupted oncosphere pellets. From approximately 1.6 × 105 plaques, 21 single clones that were positive with the affinity-purified antibodies were isolated. Sibling analysis revealed that 17 clones out of the 21 could be assigned to five different antigen families. Only family 1 was strongly recognized by a serum prepared in a rabbit against a partially purified host-protective oncosphere antigen fraction. The fragments of λDNA were inserted into a pGEX plasmid vector that encodes glutathione S-transferase (GST) of Schistosoma japonicum. Clones designated TtO-18, -49, 53 (family 1), 46 (family 2), 15 (family 3), 40 (family 4) and 66 (family 5) were established as subclones in pGEX-1 plasmid vectors which produced GST fusion proteins. All GST fusion proteins were soluble and recognized by anti-GST and anti-TtO sera. Three vaccination experiments with these fusion proteins using specific-pathogen-free Wistar rats revealed that all three fusion proteins of family 1 were exclusively effective against T. taeniaeformis oncosphere challenge with approximately 95% and 91% reductions in cystic metacestode and total metacestode recoveries, respectively. Rats vaccinated with fusion proteins of family 1 produced antibodies which reacted with a 21-kDa oncosphere antigen component which appeared to be a major oncosphere stage-specific antigen. © 1991.
引用
收藏
页码:43 / 49
页数:7
相关论文
共 24 条
[1]   IDENTIFICATION OF A PARTICULAR ANTIGEN FROM A PARASITE CDNA LIBRARY USING ANTIBODIES AFFINITY PURIFIED FROM SELECTED PORTIONS OF WESTERN BLOTS [J].
BEALL, JA ;
MITCHELL, GF .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 86 (02) :217-223
[2]   STUDIES ON STAGE-SPECIFIC IMMUNITY AGAINST TAENIA-TAENIAEFORMIS METACESTODES IN MICE [J].
BOGH, HO ;
RICKARD, MD ;
LIGHTOWLERS, MW .
PARASITE IMMUNOLOGY, 1988, 10 (03) :255-264
[3]   STAGE-SPECIFIC IMMUNITY TO TAENIA-TAENIAEFORMIS INFECTION IN MICE - A HISTOLOGICAL STUDY OF THE COURSE OF INFECTION IN MICE VACCINATED WITH EITHER ONCOSPHERE OR METACESTODE ANTIGENS [J].
BOGH, HO ;
LIGHTOWLERS, MW ;
SULLIVAN, ND ;
MITCHELL, GF ;
RICKARD, MD .
PARASITE IMMUNOLOGY, 1990, 12 (02) :153-162
[4]   IMMUNOCHEMICAL ANALYSIS OF TAENIA-TAENIAEFORMIS ANTIGENS EXPRESSED IN ESCHERICHIA-COLI [J].
BOWTELL, DDL ;
SAINT, RB ;
RICKARD, MD ;
MITCHELL, GF .
PARASITOLOGY, 1986, 93 :599-610
[5]   EXPRESSION OF TAENIA TAENIAEFORMIS ANTIGENS IN ESCHERICHIA-COLI [J].
BOWTELL, DDL ;
SAINT, RB ;
RICKARD, MD ;
MITCHELL, GF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1984, 13 (02) :173-185
[6]  
BOWTELL DDL, 1983, EXP PARASITOL, V56, P417
[7]  
Ito A., 1987, Immune responses in parasitic infections: immunology, immunopathology, and immunoprophylaxis. Volume II: Trematodes and cestodes, P115
[8]  
ITO A, 1988, INT J PARASITOL, V18, P1019, DOI 10.1016/0020-7519(88)90071-9
[9]   STAGE-SPECIFIC ANTIGENS OF HYMENOLEPIS-MICROSTOMA RECOGNIZED IN BALB/C MICE [J].
ITO, A ;
ITOH, M ;
ANDREASSEN, J ;
ONITAKE, K .
PARASITE IMMUNOLOGY, 1989, 11 (05) :453-462
[10]  
IWAKI T, 1988, JAPAN J VET RES, V36, P156