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首页> 外文期刊>Vaccine >Residual virulence and immunogenicity of CGV26 and CGV2631 B. melitensis Rev. 1 deletion mutant strains in sheep after subcutaneous or conjunctival vaccination
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Residual virulence and immunogenicity of CGV26 and CGV2631 B. melitensis Rev. 1 deletion mutant strains in sheep after subcutaneous or conjunctival vaccination

机译:皮下或结膜疫苗接种后,绵羊CGV26和CGV2631 melitensis Rev.1缺失突变株的残留毒力和免疫原性

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The CGV26 and CGV2631 strains are novel engineered Brucella melitensis Rev.1 mutant strains deleted for the bp26 gene or for both bp26 and omp31 genes, respectively, coding for proteins of diagnostic significance. The residual virulence and immunogenicity of both mutants were compared to the parental Rev.1 strain in sheep after subcutaneous or conjunctival vaccination. The deletion of the bp26 gene or both bp26 and omp31 genes had no significant effect on the intracellular survival of the Rev.1 strain in ovine macrophage cultures. The kinetics of infection induced by both mutants in sheep was similar to the Rev.1 strain, and inoculation by the subcutaneous route produced wider and more generalized infections than the conjunctival route. All strains were cleared from lymph nodes and organs within 3 months after inoculation. The CGV26 and CGV2631 mutants induced both specific systemic antibody response and lymphoproliferation in sheep. The kinetics of the responses induced by the mutants was quite similar to that of the parental Rev.1 strain, except for the intensity of the lymphoproliferative response, which was attenuated for the CGV2631 mutant. In conclusion, the residual virulence of both CGV26 and CGV2631 mutants in sheep was similar to that of the parental Rev.1 vaccine strain. These mutants induced also significant specific antibody and cell-mediated immunity in sheep and are suitable to be evaluated as potential vaccine candidates against B. melitensis and B. ovis infections in sheep.
机译:CGV26和CGV2631菌株是新型工程改造的布鲁氏布鲁氏菌Rev.1突变株,分别缺失bp26基因或bp26和omp31基因,编码具有诊断意义的蛋白质。皮下或结膜疫苗接种后,将这两个突变体的残留毒力和免疫原性与绵羊亲本Rev.1菌株进行了比较。 bp26基因或bp26和omp31基因的缺失对绵羊巨噬细胞培养物中Rev.1菌株的细胞内存活没有明显影响。两种突变体在绵羊中诱导的感染动力学与Rev.1菌株相似,皮下途径接种比结膜途径感染更广泛,更普遍。接种后3个月内清除所有淋巴结和器官的菌株。 CGV26和CGV2631突变体诱导了绵羊的特异性全身抗体反应和淋巴增殖。突变体诱导的反应动力学与亲本Rev.1菌株非常相似,除了淋巴增生反应的强度对CGV2631突变体减弱。总之,CGV26和CGV2631突变体在绵羊中的残留毒力与亲代Rev.1疫苗株相似。这些突变体还在绵羊中诱导了显着的特异性抗体和细胞介导的免疫,并且适于被评估为针对绵羊中的B.melitensis和B.ovis感染的潜在疫苗候选物。

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