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Heterologous expression of pathogen-specific genes ligA and ligB in the saprophyte Leptospira biflexa confers enhanced adhesion to cultured cells and fibronectin

机译:病原体特异性基因ligA和ligB在腐生双螺旋钩端螺旋体中的异源表达增强了对培养细胞和纤连蛋白的附着力

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Background In comparison to other bacterial pathogens, our knowledge of the molecular basis of the pathogenesis of leptospirosis is extremely limited. An improved understanding of leptospiral pathogenetic mechanisms requires reliable tools for functional genetic analysis. Leptospiral immunoglobulin-like (Lig) proteins are surface proteins found in pathogenic Leptospira, but not in saprophytes. Here, we describe a system for heterologous expression of the Leptospira interrogans genes ligA and ligB in the saprophyte Leptospira biflexa serovar Patoc. Results The genes encoding LigA and LigB under the control of a constitutive spirochaetal promoter were inserted into the L. biflexa replicative plasmid. We were able to demonstrate expression and surface localization of LigA and LigB in L. biflexa. We found that the expression of the lig genes significantly enhanced the ability of transformed L. biflexa to adhere in vitro to extracellular matrix components and cultured cells, suggesting the involvement of Lig proteins in cell adhesion. Conclusions This work reports a complete description of the system we have developed for heterologous expression of pathogen-specific proteins in the saprophytic L. biflexa. We show that expression of LigA and LigB proteins from the pathogen confers a virulence-associated phenotype on L. biflexa, namely adhesion to eukaryotic cells and fibronectin in vitro. This study indicates that L. biflexa can serve as a surrogate host to characterize the role of key virulence factors of the causative agent of leptospirosis.
机译:背景与其他细菌性病原体相比,我们对钩端螺旋体病发病机理的分子基础的了解极为有限。对钩端螺旋体致病机制的进一步了解需要可靠的工具来进行功能遗传分析。钩端螺旋体样免疫球蛋白(Lig)蛋白是在致病性钩端螺旋体中发现的表面蛋白,但在腐生植物中却没有。在这里,我们描述了一种系统,用于在腐生双歧钩端螺旋体血清型Patoc中询问钩端螺旋体基因ligA和ligB的异源表达。结果在组成型螺旋形启动子的控制下,将编码LigA和LigB的基因插入到双弯曲乳杆菌复制质粒中。我们能够证明在L. biflexa中LigA和LigB的表达和表面定位。我们发现lig基因的表达显着增强了转化的双歧劳氏杆菌在体外粘附至细胞外基质成分和培养细胞的能力,表明Lig蛋白参与细胞粘附。结论这项工作报告了我们开发的系统,用于在腐生双挠线虫中异源表达病原体特异性蛋白。我们显示从病原体的LigA和LigB蛋白的表达赋予双挠L.,即对真核细胞和纤连蛋白的粘附力与毒力相关的表型。这项研究表明,双弯曲乳杆菌可以作为替代宿主来表征钩端螺旋体病病原体关键毒力因子的作用。

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