Department of Biological Sciences, Mississippi State University, Starkville, Mississippi, United States of America.
PLoS Negl Trop Dis. 2013 Sep 19;7(9):e2454. doi: 10.1371/journal.pntd.0002454. eCollection 2013.
Relapsing fever spirochetes are global yet neglected pathogens causing recurrent febrile episodes, chills, nausea, vomiting, and pregnancy complications. Given these nonspecific clinical manifestations, improving diagnostic assays for relapsing fever spirochetes will allow for identification of endemic foci and expedite proper treatment. Previously, an antigen designated the Borrelia immunogenic protein A (BipA) was identified in the North American species Borrelia hermsii. Thus far, BipA appears unique to relapsing fever spirochetes. The antigen remains unidentified outside of these pathogens, while interspecies amino acid identity for BipA in relapsing fever spirochetes is only 24-36%. The current study investigated the immunogenicity of BipA in Borrelia turicatae, a species distributed in the southern United States and Latin America.
METHODOLOGY/PRINCIPAL FINDINGS: bipA was amplified from six isolates of Borrelia turicatae, and sequence analysis demonstrated that the gene is conserved among isolates. A tick transmission system was developed for B. turicatae in mice and a canine, two likely vertebrate hosts, which enabled the evaluation of serological responses against recombinant BipA (rBipA). These studies indicated that BipA is antigenic in both animal systems after infection by tick bite, yet serum antibodies failed to bind to B. hermsii rBipA at a detectable level. Moreover, mice continued to generate an antibody response against BipA one year after the initial infection, further demonstrating the protein's potential toward identifying endemic foci for B. turicatae.
CONCLUSIONS/SIGNIFICANCE: These initial studies support the hypothesis that BipA is a spirochete antigen unique to a relapsing fever Borrelia species, and could be used to improve efforts for identifying B. turicatae endemic regions.
回归热螺旋体是全球性的被忽视的病原体,可引起反复发作的发热、寒战、恶心、呕吐和妊娠并发症。鉴于这些非特异性临床表现,改进用于回归热螺旋体的诊断检测将有助于确定地方性流行区域并加快适当的治疗。以前,在北美的 Borrelia hermsii 物种中发现了一种被称为 Borrelia 免疫原性蛋白 A(BipA)的抗原。到目前为止,BipA 似乎是回归热螺旋体所特有的。该抗原在这些病原体之外仍然无法识别,而回归热螺旋体中 BipA 的种间氨基酸同一性仅为 24-36%。本研究调查了 Borrelia turicatae 中的 BipA 免疫原性,Borrelia turicatae 分布于美国南部和拉丁美洲。
方法/主要发现:从 Borrelia turicatae 的六个分离株中扩增了 bipA,序列分析表明该基因在分离株中是保守的。在小鼠和犬中开发了一种用于 Borrelia turicatae 的蜱传播系统,这两种可能的脊椎动物宿主使针对重组 BipA(rBipA)的血清反应评估成为可能。这些研究表明,在通过蜱叮咬感染后,BipA 在两种动物系统中均具有抗原性,但血清抗体未能在可检测水平上与 Borrelia hermsii rBipA 结合。此外,在初次感染一年后,小鼠仍继续针对 BipA 产生抗体反应,进一步证明了该蛋白在确定 Borrelia turicatae 地方性流行区域方面的潜力。
结论/意义:这些初步研究支持了 BipA 是一种回归热 Borrelia 物种特有的螺旋体抗原的假设,并且可用于改进识别 Borrelia turicatae 地方性流行区域的努力。