Wang Chuan, Zhang Fuqin, Yang Jianglong, Khanniche Asma, Shen Hao
Department of Medical Technology, West China School of Public Health, Sichuan University, Chengdu, PR China.
J Mol Microbiol Biotechnol. 2014;24(3):191-5. doi: 10.1159/000363450. Epub 2014 Jun 27.
Listeria ivanovii (LI) possesses a facultative intracellular life cycle in macrophages and non-professional phagocytes thus making it a potential novel vaccine vector. We have developed a genome site-specific integration system as a universal tool for constructing the live LI-based vaccines. Using this system, the porcine reproductive and respiratory syndrome virus (PRRSV) orf5 and orf6 genes, coding for PRRSV membrane-associated protein GP5 and M, respectively, were integrated into the LI genome. Genome PCR and sequencing results showed that the orf5 or orf6 gene had been integrated into the LI genome downstream of orfXYZ or mpl gene. Western blot analysis of the non-secreted and secreted bacterial protein samples showed the expression and secretion of GP5 or M protein from the recombinant LI strains. The secretion of the heterologous proteins is a key step for bacterial vaccine vectors to deliver the antigens to the immune system to stimulate antigen-specific immune responses. Therefore, this integration system may be a potential tool for constructing novel vaccines using live LI as vector.
伊氏李斯特菌(LI)在巨噬细胞和非专职吞噬细胞中具有兼性胞内生命周期,因此使其成为一种潜在的新型疫苗载体。我们已经开发了一种基因组位点特异性整合系统,作为构建基于活LI的疫苗的通用工具。利用该系统,分别编码猪繁殖与呼吸综合征病毒(PRRSV)膜相关蛋白GP5和M的PRRSV orf5和orf6基因被整合到LI基因组中。基因组PCR和测序结果表明,orf5或orf6基因已整合到LI基因组中orfXYZ或mpl基因的下游。对非分泌型和分泌型细菌蛋白样品的蛋白质印迹分析显示,重组LI菌株表达并分泌了GP5或M蛋白。异源蛋白的分泌是细菌疫苗载体将抗原递送至免疫系统以刺激抗原特异性免疫反应的关键步骤。因此,该整合系统可能是使用活LI作为载体构建新型疫苗的潜在工具。