Minor nucleotide substitutions in the omp31 gene of Brucella ovis result in antigenic differences in the major outer membrane protein that it encodes compared to those of the other Brucella species

被引:43
作者
Vizcaíno, N
Kittelberger, R
Cloeckaert, A
Marín, CM
Fernández-Lago, L
机构
[1] Univ Salamanca, Edificio Departmental, Dept Genet & Microbiol, Salamanca 37007, Spain
[2] Diputac Gen Aragon, Serv Invest Agroalimentaria, Unidad Sanidad Anim, Zaragoza 50080, Spain
[3] Minist Agr & Forestry, Natl Ctr Dis Invest, Upper Hutt, New Zealand
[4] INRA, Ctr Tours, Pathol Aviaire & Parasitol Stn, F-37380 Nouzilly, France
关键词
D O I
10.1128/IAI.69.11.7020-7028.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gene coding for the major outer membrane protein Omp31 was sequenced in five Brucella species and their biovars. Although the omp31 genes appeared to be highly conserved in the genus Brucella, nine nucleotide substitutions were detected in the gene of Brucella ovis compared to that of Brucella melitensis. As shown by differential binding properties of monoclonal antibodies (MAbs) to the two Brucella species, these nucleotide substitutions result in different antigenic properties of Omp31. The antigenic differences were also evidenced when sera from B. ovis-infected rams were tested by Western blotting with the recombinant B. melitensis or B. ovis Omp31 proteins. Twelve available sera reacted with recombinant B. ovis Omp31, but only four of them reacted with recombinant B. melitensis Omp31. These results validate previous evidence for the potential of Omp31 as a diagnostic antigen for B. ovis infection in rams and demonstrate that B. ovis Omp31, instead of B. melitensis Omp31, should be used to evaluate this point. The antigenic differences between the A melitensis and B. ovis Omp31 proteins should also be taken into account when Omp31 is evaluated as a candidate for the development of subcellular vaccines against B. ovis infection. No reactivity against recombinant B. melitensis Omp31 was detected, by Western blotting, with sera from B. melitensis-infected sheep. Accordingly, Omp31 does not seem to be a good diagnostic antigen for B. melitensis infections in sheep. Two immunodominant regions were identified on the B. ovis Omp31 protein by using recombinant DNA techniques and specific MAbs. Sera from B. ovis-infected rams that reacted with the recombinant protein were tested by Western blotting against one of these immunodominant regions shown to be exposed at the bacterial surface. Only 4 of the 12 sera reacted, but with strong intensity.
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收藏
页码:7020 / 7028
页数:9
相关论文
共 37 条
[1]   CHARACTERIZATION OF BRUCELLA-OVIS LIPOPOLYSACCHARIDE AND ITS USE FOR DIAGNOSIS OF RAM EPIDIDYMITIS BY ENZYME-LINKED IMMUNOSORBENT-ASSAY [J].
AFZAL, M ;
TENGERDY, RP ;
SQUIRE, PG ;
ELLIS, RP .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 20 (06) :1159-1164
[2]  
ALTON G. G., 1988, TECHNIQUES BRUCELLOS
[3]  
BLASCO JM, 1990, ANIMAL BRUCELLOSIS, P157
[4]   SURFACE EXPOSURE OF OUTER-MEMBRANE PROTEIN AND LIPOPOLYSACCHARIDE EPITOPES IN BRUCELLA SPECIES STUDIED BY ENZYME-LINKED-IMMUNOSORBENT-ASSAY AND FLOW-CYTOMETRY [J].
BOWDEN, RA ;
CLOECKAERT, A ;
ZYGMUNT, MS ;
BERNARD, S ;
DUBRAY, G .
INFECTION AND IMMUNITY, 1995, 63 (10) :3945-3952
[5]   OUTER-MEMBRANE PROTEIN-SPECIFIC AND ROUGH LIPOPOLYSACCHARIDE-SPECIFIC MONOCLONAL-ANTIBODIES PROTECT MICE AGAINST BRUCELLA-OVIS [J].
BOWDEN, RA ;
CLOECKAERT, A ;
ZYGMUNT, MS ;
DUBRAY, G .
JOURNAL OF MEDICAL MICROBIOLOGY, 1995, 43 (05) :344-347
[6]   Identification of protective outer membrane antigens of Brucella ovis by passive immunization of mice with monoclonal antibodies [J].
Bowden, RA ;
Estein, SM ;
Zygmunt, MS ;
Dubray, G ;
Cloeckaert, A .
MICROBES AND INFECTION, 2000, 2 (05) :481-488
[7]   BACTERIAL ANTIGENIC VARIATION, HOST IMMUNE-RESPONSE, AND PATHOGEN-HOST COEVOLUTION [J].
BRUNHAM, RC ;
PLUMMER, FA ;
STEPHENS, RS .
INFECTION AND IMMUNITY, 1993, 61 (06) :2273-2276
[8]   IDENTIFICATION OF 7 SURFACE-EXPOSED BRUCELLA OUTER-MEMBRANE PROTEINS BY USE OF MONOCLONAL-ANTIBODIES - IMMUNOGOLD LABELING FOR ELECTRON-MICROSCOPY AND ENZYME-LINKED-IMMUNOSORBENT-ASSAY [J].
CLOECKAERT, A ;
DEWERGIFOSSE, P ;
DUBRAY, G ;
LIMET, JN .
INFECTION AND IMMUNITY, 1990, 58 (12) :3980-3987
[9]   Nucleotide sequence and expression of the gene encoding the major 25-kilodalton outer membrane protein of Brucella ovis: Evidence for antigenic shift, compared with other Brucella species, due to a deletion in the gene [J].
Cloeckaert, A ;
Verger, JM ;
Grayon, M ;
Zygmunt, MS ;
Grepinet, O .
INFECTION AND IMMUNITY, 1996, 64 (06) :2047-2055
[10]   RESTRICTION SITE POLYMORPHISM OF THE GENES ENCODING THE MAJOR 25 KDA AND 36 KDA OUTER-MEMBRANE PROTEINS OF BRUCELLA [J].
CLOECKAERT, A ;
VERGER, JM ;
GRAYON, M ;
GREPINET, O .
MICROBIOLOGY-UK, 1995, 141 :2111-2121