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Changes in the protein profile and antigenicity of different Borrelia burgdorferi strains after reintroduction to Ixodes ricinus ticks

机译:重新引入蓖麻短毛虱后不同博氏疏螺旋体菌株的蛋白质谱和抗原性变化

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摘要

Eight Swiss strains of , with various protein profiles and the North-American strain B31 were artificially introduced into ticks and reisolated 10 days later. All isolates were subsequently examined by SDS-PAGE analysis. Comparing initial isolates with the reisolates, we observed that 7 out of 9 strains changed their protein pattern with respect to the major proteins OspA, OspB and the 22 kDa protein after passage in the tick. The strains NE2, NE4 and NE83 with the initial phenotype of OspA and 22 kDa proteins changed to the phenotype of OspA and OspB, the strains B2 and NE202 with the initial phenotype of OspA acquired an additional protein of 22 kDa and the strain NE58 with the initial phenotype of OspA also acquired a protein of 22 kDa. Examination of these isolates by Western blot analysis demonstrated that the reaction with the monoclonal antibody H5332 and a monospecific polyclonal antibody PoAb/anti-22 kDa differed between the initial isolates and the reisolates.
机译:将八种具有不同蛋白质谱的瑞士菌株和北美菌株B31人工导入tick中,并在10天后重新分离。随后通过SDS-PAGE分析检查所有分离物。比较初始分离株和再分离株,我们观察到9个菌株中有7个在壁虱传代后相对于主要蛋白OspA,OspB和22 kDa蛋白改变了其蛋白模式。初始表型为OspA和22 kDa的NE2,NE4和NE83菌株变为OspA和OspB的表型,初始为OspA的B2和NE202菌株获得了22 kDa的另一种蛋白,而NE58的初始表型为OspA。 OspA的初始表型也获得了22 kDa的蛋白质。通过蛋白质印迹分析检查这些分离株表明,在最初的分离株和再分离株之间,与单克隆抗体H5332和单特异性多克隆抗体PoAb / anti-22 kDa的反应不同。

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