Barbet A F, Meeus P F M, Bélanger M, Bowie M V, Yi J, Lundgren A M, Alleman A R, Wong S J, Chu F K, Munderloh U G, Jauron S D
Department of Pathobiology, College of Veterinary Medicine, University of Florida, PO Box 110880, Gainesville, FL 32611, USA.
Infect Immun. 2003 Apr;71(4):1706-18. doi: 10.1128/IAI.71.4.1706-1718.2003.
Anaplasma phagocytophilum is the causative agent of an emerging tick-borne zoonosis in the United States and Europe. The organism causes a febrile illness accompanied by other nonspecific symptoms and can be fatal, especially if treatment is delayed. Persistence of A. phagocytophilum within mammalian reservoir hosts is important for ensuring continued disease transmission. In the related organism Anaplasma marginale, persistence is associated with antigenic variation of the immunoprotective outer membrane protein MSP2. Extensive diversity of MSP2 is achieved by combinatorial gene conversion of a genomic expression site by truncated pseudogenes. The major outer membrane protein of A. phagocytophilum, MSP2(P44), is homologous to MSP2 of A. marginale, has a similar organization of conserved and variable regions, and is also encoded by a multigene family containing some truncated gene copies. This suggests that the two organisms could use similar mechanisms to generate diversity in outer membrane proteins from their small genomes. We define here a genomic expression site for MSP2(P44) in A. phagocytophilum. As in A. marginale, the msp2(p44) gene in this expression site is polymorphic in all populations of organisms we have examined, whether organisms are obtained from in vitro culture in human HL-60 cells, from culture in the tick cell line ISE6, or from infected human blood. Changes in culture conditions were found to favor the growth and predominance of certain msp2(p44) variants. Insertions, deletions, and substitutions in the region of the genomic expression site encoding the central hypervariable region matched sequence polymorphisms in msp2(p44) mRNA. These data suggest that, similarly to A. marginale, A. phagocytophilum uses combinatorial mechanisms to generate a large array of outer membrane protein variants. Such gene polymorphism has profound implications for the design of vaccines, diagnostic tests, and therapy.
嗜吞噬细胞无形体是美国和欧洲一种新出现的蜱传人畜共患病的病原体。该生物体引发一种伴有其他非特异性症状的发热性疾病,可能致命,尤其是治疗延迟时。嗜吞噬细胞无形体在哺乳动物储存宿主内持续存在对于确保疾病的持续传播很重要。在相关生物体边缘无形体中,持续存在与免疫保护性外膜蛋白MSP2的抗原变异有关。MSP2的广泛多样性是通过基因组表达位点被截短的假基因进行组合基因转换实现的。嗜吞噬细胞无形体的主要外膜蛋白MSP2(P44)与边缘无形体的MSP2同源,具有相似的保守区和可变区组织,并且也由一个包含一些截短基因拷贝的多基因家族编码。这表明这两种生物体可能利用相似机制从其小基因组中产生外膜蛋白的多样性。我们在此定义了嗜吞噬细胞无形体中MSP2(P44)的一个基因组表达位点。与边缘无形体一样,该表达位点中的msp2(p44)基因在我们检测的所有生物体群体中都是多态性的,无论生物体是从人HL - 60细胞的体外培养物、蜱细胞系ISE6的培养物中获得,还是从受感染的人血液中获得。发现培养条件的变化有利于某些msp2(p44)变体的生长和优势。基因组表达位点编码中央高变区的区域中的插入、缺失和替换与msp2(p44)mRNA中的序列多态性相匹配。这些数据表明,与边缘无形体类似,嗜吞噬细胞无形体利用组合机制产生大量外膜蛋白变体。这种基因多态性对疫苗、诊断测试和治疗的设计具有深远影响。