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Immunological and Molecular Analyses of the Borrelia hermsii Factor H and Factor H-Like Protein 1 Binding Protein FhbA: Demonstration of Its Utility as a Diagnostic Marker and Epidemiological Tool for Tick-Borne Relapsing Fever

机译:伯氏疏螺旋体H因子和H因子样蛋白1结合蛋白FhbA的免疫学和分子分析:证明其作为Tick-Borne复发热的诊断标记和流行病学工具的效用

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摘要

It has been demonstrated that Borrelia hermsii, a causative agent of relapsing fever, produces a factor H (FH) and FH-like protein 1 (FHL-1) binding protein. The binding protein has been designated FhbA. To determine if FH/FHL-1 binding is widespread among B. hermsii isolates, a diverse panel of strains was tested for the FH/FHL-1 binding phenotype and FhbA production. Most isolates (23/24) produced FhbA and bound FH/FHL-1. Potential variation in FhbA among isolates was analyzed by DNA sequence analyses. Two genetically distinct FhbA types, designated fhbA1 and fhbA2, were delineated, and type-specific PCR primers were generated to allow for rapid differentiation. Pulsed-field gel electrophoresis and hybridization analyses demonstrated that all isolates that possess the gene carry it on a 200-kb linear plasmid (lp200), whereas isolates that lack the gene lack lp200 and instead carry an lp170. To determine if FhbA is antigenic during infection and to assess the specificity of the response, recombinant FhbA1 (rFhbA1) and rFhbA2 were screened with serum from infected mice and humans. FhbA was found to be expressed and antigenic and to elicit a potentially type-specific FhbA response. To localize the epitopes of FhbA1 and FhbA2, truncations were generated and screened with infection serum. The epitopes were determined to be conformationally defined. Collectively, these analyses indicate that FH/FHL-1 binding is a widespread virulence mechanism for B. hermsii and provide insight into the genetic and antigenic structure of FhbA. The data also have potential implications for understanding the epidemiology of relapsing fever in North America and can be applied to the future development of species-specific diagnostic tools.
机译:业已证明,复发性发热的致病菌-伯氏疏螺旋体会产生H因子(FH)和FH样蛋白1(FHL-1)结合蛋白。结合蛋白被称为FhbA。为了确定FH / FHL-1结合是否在贺氏芽孢杆菌分离物中广泛分布,测试了多种菌株的FH / FHL-1结合表型和FhbA产生。大多数分离株(23/24)产生FhbA并结合FH / FHL-1。通过DNA序列分析分析了分离株之间FhbA的潜在变异。描绘了两种遗传上不同的FhbA类型,分别称为fhbA1和fhbA2,并生成了类型特异性PCR引物以实现快速分化。脉冲场凝胶电泳和杂交分析表明,所有拥有该基因的分离株都在200kb线性质粒(lp200)上携带该基因,而缺乏该基因的分离株则缺少lp200,而携带lp170。为了确定FhbA在感染期间是否具有抗原性并评估反应的特异性,用来自感染小鼠和人类的血清筛选了重组FhbA1(rFhbA1)和rFhbA2。发现FhbA表达并具有抗原性,并引发潜在的类型特异性FhbA反应。为了定位FhbA1和FhbA2的表位,产生了截短并用感染血清进行了筛选。确定表位是构象确定的。总体而言,这些分析表明FH / FHL-1结合是一种广泛存在的致病性芽孢杆菌毒力机制,并为FhbA的遗传和抗原结构提供了见识。这些数据对于理解北美复发性发热的流行病学也具有潜在的意义,并可用于将来开发特定物种的诊断工具。

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