Bunikis J, Noppa L, Ostberg Y, Barbour A G, Bergström S
Department of Microbiology, Umeå University, Sweden.
Infect Immun. 1996 Dec;64(12):5111-6. doi: 10.1128/iai.64.12.5111-5116.1996.
A chromosomally encoded 66-kDa protein (P66) of Borrelia spp. that cause Lyme disease has previously been shown to be associated with the spirochetal outer membrane. A topological model of P66 predicts a surface-exposed fragment which links the N- and C-terminal intramembranous domains of the protein (J. Bunikis, L. Noppa, and S. Bergström, FEMS Microbiol. Lett. 131:139-145, 1995). In the present study, an immunogenic determinant of P66 was identified by a comparison of the immunoreactivities of different fragments of P66 generated either by proteolytic treatment of intact spirochetes or as recombinant proteins expressed in Escherichia coli. The immune response to P66 during natural infection was found to be directed against the predicted surface domain which comprises amino acids at positions 454 through 491. A sequence comparison revealed considerable polymorphism of the surface domains of P66 proteins of different Lyme disease-causing Borrelia species. Five sequence patterns of this domain were observed in the B. garinii strains studied. In contrast, sequences of the relevant part of P66 of the B. afzelii and B. burgdorferi sensu stricto isolates studied were identical within the respective species. In immunoblotting, 5 of 17 (29.4%) sera from North American patients with early disseminated or persistent Lyme disease reacted against P66 of B. burgdorferi sensu stricto B31. These sera, however, failed to recognize P66 of B. afzelii and B. garinii, as well as an analog of P66 in the relapsing fever agent, B. hermsii. In conclusion, the topological model of P66 is supported by the demonstration of an apparent surface localization of an immunoreactive domain of this protein. Furthermore, analogous to the plasmid-encoded borrelial outer surface proteins, the predicted surface-exposed portion of chromosomally encoded P66 appears to be antigenically heterogenous.
引起莱姆病的疏螺旋体属的一种染色体编码的66 kDa蛋白(P66)先前已被证明与螺旋体外膜相关。P66的拓扑模型预测有一个表面暴露片段,该片段连接蛋白质的N端和C端膜内结构域(J. Bunikis、L. Noppa和S. Bergström,《FEMS微生物学快报》131:139 - 145,1995年)。在本研究中,通过比较完整螺旋体经蛋白水解处理产生的不同P66片段或大肠杆菌中表达的重组蛋白的免疫反应性,确定了P66的一个免疫原性决定簇。发现自然感染期间对P66的免疫反应针对的是预测的表面结构域,该结构域包含454至491位的氨基酸。序列比较显示,不同引起莱姆病的疏螺旋体物种的P66蛋白表面结构域存在相当大的多态性。在所研究的加氏疏螺旋体菌株中观察到该结构域的五种序列模式。相比之下,所研究的阿氏疏螺旋体和狭义伯氏疏螺旋体分离株的P66相关部分序列在各自物种内是相同的。在免疫印迹中,17份来自北美早期播散性或持续性莱姆病患者的血清中有5份(29.4%)与狭义伯氏疏螺旋体B31的P66发生反应。然而,这些血清未能识别阿氏疏螺旋体和加氏疏螺旋体的P66,以及回归热病原体赫氏疏螺旋体中P66的类似物。总之,P66的拓扑模型得到了该蛋白免疫反应性结构域明显表面定位的证明的支持。此外,类似于质粒编码的疏螺旋体外表面蛋白,染色体编码的P66预测的表面暴露部分在抗原性上似乎是异质的。