The recombinant Omp31 from Brucella melitensis alone or associated with rough lipopolysaccharide induces protection against Brucella ovis infection in BALB/c mice

被引:70
作者
Estein, SM
Cassataro, J
Vizcaíno, N
Zygmunt, MS
Cloeckaert, A
Bowden, RA [1 ]
机构
[1] UNICEN, Fac Ciencias Vet, Dept Sanidad Anim & Med Prevent, Lab Immunoquim & Biotecnol, RA-7000 Tandil, Argentina
[2] Hosp Clin Jose San Martin, Fac Med, Immunogenet Lab, UBA, Buenos Aires, Argentina
[3] Univ Salamanca, Dept Genet & Microbiol, Salamanca 37007, Spain
[4] INRA, Ctr Rech Tours, Pathol Infect & Immunol Lab, F-37380 Nouzilly, France
[5] INRA, Ctr Rech Tours, Unite Pathol Aviaire & Parasitol, F-37380 Nouzilly, France
关键词
Brucella; vaccine; outer membrane protein;
D O I
10.1016/S1286-4579(02)00075-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunogenicity and protective activity against Brucella ovis of detergent-extracted recombinant Omp31 (rOmp31 extract) from Brucella melitensis produced in Escherichia coli, purified rough lipopolysaccharide, from B. ovis (R-LPS) and a mixture of rOmp31 extract and R-LPS (rOmp31 extract + R-LPS) were assessed in BALB/c mice. The experimental vaccines were compared with a hot saline extract (HS extract) from B. ovis mainly composed of outer membrane proteins (OMPs) and R-LPS, and known to be protective in mice against a B. ovis infection. Serum antibodies to Omp31 and R-LPS were detected in the corresponding mice using Western blotting with B. ovis whole-cell lysates and ELISA with purified antigens. Protection was evaluated by comparing the levels of infection in the spleens of vaccinated mice challenged with B. ovis. A significantly lower number of B. ovis colony-forming units in spleens relative to unimmunized (saline injected) controls were considered as protection. Mice immunized with rOmp31 extract or rOmp31 extract mixed with R-LPS developed antibodies that bound to the B. ovis surface with similar titers. Vaccination with rOmp31. extract plus R-LPS provided the best protection level, which was comparable with that given by HS extract. Similar protection was also obtained with rOmp31 extract alone and, to a lesser degree, with R-LPS. Comparisons between groups showed that an extract from E. coli-pUC19 (devoid of Omp31) provided no protection relative to either HS extract, rOmp31 extract or rOmp31 extract mixed with R-LPS. In conclusion, the recombinant Omp31 associated or not with B. ovis R-LPS, could be an interesting candidate for a subcellular vaccine against B. ovis infection. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:85 / 93
页数:9
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