Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China.
Lett Appl Microbiol. 2010 Nov;51(5):564-9. doi: 10.1111/j.1472-765X.2010.02935.x. Epub 2010 Sep 16.
Genes uniquely expressed in vivo may contribute to the overall pathogenicity of an organism and are likely to serve as potential targets for the development of new vaccine. This study aims to screen the genes expressed in vivo after Vibrio anguillarum infection by in vivo-induced antigen technology (IVIAT).
The convalescent-phase sera were obtained from turbot (Scophthalmus maximus) survived after infection by the virulent V. anguillarum M3. The pooled sera were thoroughly adsorbed with M3 cells and Escherichia coli BL21 (DE3) cells. A genomic expression library of M3 was constructed and screened for the identification of immunogenic proteins by colony immunoblot analysis with the adsorbed sera. After three rounds of screening, 19 putative in vivo-induced (ivi) genes were obtained. These ivi genes were catalogued into four functional groups: regulator/signalling, metabolism, biological process and hypothetical proteins. Three ivi genes were insertion-mutated, and the growth and 50% lethal dose (LD(50) ) of these mutants were evaluated.
The identification of ivi genes in V. anguillarum M3 sheds light on understanding the bacterial pathogenesis and provides novel targets for the development of new vaccines and diagnostic reagents.
To the best of our knowledge, this is the first report describing in vivo-expressed genes of V. anguillarum using IVIAT. The screened ivi genes in this study could be new virulent factors and targets for the development of vaccine, which may have implications for the development of diagnostic regents.
在体内特异性表达的基因可能有助于生物体的整体致病性,并可能成为开发新型疫苗的潜在靶点。本研究旨在通过活体诱导抗原技术(IVIAT)筛选鳗弧菌感染后体内表达的基因。
从感染鳗弧菌 M3 后存活的大菱鲆(Scophthalmus maximus)的恢复期血清中获得。将混合血清用 M3 细胞和大肠杆菌 BL21(DE3)细胞充分吸附。构建了 M3 的基因组表达文库,并通过与吸附血清的菌落免疫印迹分析筛选鉴定免疫原性蛋白。经过三轮筛选,获得了 19 个假定的体内诱导(ivi)基因。这些 ivi 基因被分为四个功能组:调节剂/信号、代谢、生物过程和假设蛋白。三个 ivi 基因被插入突变,评估了这些突变体的生长和 50%致死剂量(LD50)。
在鳗弧菌 M3 中鉴定出的 ivi 基因有助于了解细菌发病机制,并为开发新型疫苗和诊断试剂提供了新的靶标。
据我们所知,这是首次使用 IVIAT 描述鳗弧菌体内表达基因的研究。本研究筛选出的 ivi 基因可能是新的毒力因子和疫苗开发的靶点,这可能对诊断试剂的开发具有重要意义。