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Identification of Virulence-Associated Genes of Pseudomonas viridiflava Activated During Infection by Use of a Novel IVET Promoter Probing Plasmid

机译:通过使用新型IVET启动子探测质粒鉴定感染过程中激活的假单胞菌毒力相关基因。

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Analysis of virulence mechanisms of plant pathogens is often limited by the lack of genetic tools that can be used to identify genes that are preferentially expressed during their interactions with plants. In the present study, we used the newly constructed IVET (in vivo expression technique) plasmid pIviGK and the corresponding antibiotic resistance-based selection method to identify genes that encode pathogenicity factors of the soft rot-causing bacterium Pseudomonas viridiflava. These included pel, the gene encoding pectate lyase, which is responsible for the development of soft rot symptoms. We have also isolated and characterized the gene mviN(pv) encoding a putative novel membrane associated virulence factor of P. viridiflava. A mutation in mviN(pv) was shown to influence motility as well as virulence of P. viridiflava. The mviN(pv) gene is expressed to a moderate level in LB media and its expression increases under inducing conditions as was shown by measuring in planta expression dynamics of the fused gfp reporter gene.
机译:植物病原体毒力机制的分析通常受到缺乏遗传工具的限制,这些遗传工具可用于鉴定在与植物相互作用期间优先表达的基因。在本研究中,我们使用了新构建的IVET(体内表达技术)质粒pIviGK和相应的基于抗生素抗性的选择方法来鉴定编码软腐病细菌绿假单胞菌致病性因子的基因。其中包括pel,果胶酸裂合酶的编码基因,负责产生软腐病症状。我们还分离和表征了基因mviN(pv)编码假定的新型膜相关毒力因子P. viridiflava。已显示mviN(pv)中的突变会影响运动性以及vi.ifridiflava的毒性。 mviN(pv)基因在LB培养基中表达到中等水平,并且在诱导条件下其表达增加,如通过测量融合的gfp报告基因的植物表达动态所显示的。

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