Borrelia miyamotoi BipA-like protein, BipM, is a candidate serodiagnostic antigen distinguishing between Lyme disease and relapsing fever Borrelia infections

IF 3.1 2区 医学 Q2 INFECTIOUS DISEASES Ticks and Tick-borne Diseases Pub Date : 2024-02-16 DOI:10.1016/j.ttbdis.2024.102324
Kevin S. Brandt, Brittany A. Armstrong, Irina Goodrich, Robert D. Gilmore
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Abstract

A Borrelia miyamotoi gene with partial homology to bipA of relapsing fever spirochetes Borrelia hermsii and Borrelia turicatae was identified by a GenBank basic alignment search analysis. We hypothesized that this gene product may be an immunogenic antigen as described for other relapsing fever Borrelia (RFB) and could serve as a serological marker for B. miyamotoi infections. The B. miyamotoi gene was a truncated version about half the size of the B. hermsii and B. turicatae bipA with a coding sequence of 894 base pairs. The gene product had a calculated molecular size of 32.7 kDa (including the signal peptide). Amino acid alignments with B. hermsii and B. turicatae BipA proteins and with other B. miyamotoi isolates showed conservation at the carboxyl end. We cloned the B. miyamotoi bipA-like gene (herein named bipM) and generated recombinant protein for serological characterization and for antiserum production. Protease protection analysis demonstrated that BipM was surface exposed. Serologic analyses using anti-B. miyamotoi serum samples from tick bite-infected and needle inoculated mice showed 94 % positivity against BipM. The 4 BipM negative serum samples were blotted against another B. miyamotoi antigen, BmaA, and two of them were seropositive resulting in 97 % positivity with both antigens. Serum samples from B. burgdorferi sensu stricto (s.s.)-infected mice were non-reactive against rBipM by immunoblot. Serum samples from Lyme disease patients were also serologically negative against BipM except for 1 sample which may have indicated a possible co-infection. A recently published study demonstrated that B. miyamotoi BipM was non-reactive against serum samples from B. hermsii, Borrelia parkeri, and B. turicatae infected animals. These results show that BipM has potential for a B. miyamotoi-infection specific and sensitive serodiagnostic to differentiate between Lyme disease and various RFB infections.

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宫本鲍瑞氏菌 BipA 样蛋白 BipM 是区分莱姆病和复发性热鲍瑞氏菌感染的候选血清诊断抗原
通过 GenBank 基本比对搜索分析,我们发现了宫本鲍雷氏菌的一个基因,该基因与赫氏鲍雷氏菌(Borrelia hermsii)和土里卡塔鲍雷氏菌(Borrelia turicatae)的复发性热螺旋体 bipA 有部分同源性。我们推测该基因产物可能是一种免疫原性抗原,如其他复发性热鲍曼(RFB)所描述的那样,并可作为宫本氏杆菌感染的血清学标志物。B. miyamotoi 基因是一个截短的版本,大小约为 B. hermsii 和 B. turicatae bipA 的一半,编码序列为 894 个碱基对。该基因产物的计算分子大小为 32.7 kDa(包括信号肽)。与 B. hermsii 和 B. turicatae BipA 蛋白以及其他 B. miyamotoi 分离物的氨基酸比对显示,其羧基末端是一致的。我们克隆了 B. miyamotoi bipA-like 基因(在此命名为 bipM),并生成了重组蛋白用于血清学鉴定和抗血清生产。蛋白酶保护分析表明,BipM 表面暴露。使用蜱虫叮咬感染小鼠和针刺接种小鼠的抗 B. miyamotoi 血清样本进行的血清学分析表明,BipM 的阳性率为 94%。将 4 份 BipM 阴性血清样本与另一种 B. miyamotoi 抗原 BmaA 进行印迹分析,其中两份血清呈阳性,两种抗原的阳性率均为 97%。严格意义上的布氏菌(B. burgdorferi sensu stricto,s.s.)感染小鼠的血清样本通过免疫印迹对 rBipM 无反应。莱姆病患者的血清样本也对 BipM 呈血清学阴性反应,只有一个样本除外,这可能表明可能存在合并感染。最近发表的一项研究表明,B. miyamotoi BipM 对 B. hermsii、Borrelia parkeri 和 B. turicatae 感染动物的血清样本无反应。这些结果表明,BipM 有可能成为宫本氏杆菌感染的特异性和敏感性血清诊断方法,以区分莱姆病和各种 RFB 感染。
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来源期刊
Ticks and Tick-borne Diseases
Ticks and Tick-borne Diseases INFECTIOUS DISEASES-MICROBIOLOGY
CiteScore
6.90
自引率
12.50%
发文量
185
审稿时长
6-12 weeks
期刊介绍: Ticks and Tick-borne Diseases is an international, peer-reviewed scientific journal. It publishes original research papers, short communications, state-of-the-art mini-reviews, letters to the editor, clinical-case studies, announcements of pertinent international meetings, and editorials. The journal covers a broad spectrum and brings together various disciplines, for example, zoology, microbiology, molecular biology, genetics, mathematical modelling, veterinary and human medicine. Multidisciplinary approaches and the use of conventional and novel methods/methodologies (in the field and in the laboratory) are crucial for deeper understanding of the natural processes and human behaviour/activities that result in human or animal diseases and in economic effects of ticks and tick-borne pathogens. Such understanding is essential for management of tick populations and tick-borne diseases in an effective and environmentally acceptable manner.
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