Rikihisa Y, Rota T, Lee T H, MacDonald A B, Ito S
Infect Immun. 1979 Nov;26(2):638-50. doi: 10.1128/iai.26.2.638-650.1979.
The immunolabeling characteristics of Rickettsia tsutsugamushi (Gilliam strain) were examined by using a purified immunoglobulin G fraction of antibody to R. tsutsugamushi raised in rabbits. Formalin-fixed rickettsiae were reacted with this antibody and then with ferritin-conjugated goat anti-rabbit Fc antibody. R. tsutsugamushi cultivated in yolk sacs was used to raise antibody for this study. When rickettsiae in BHK-21 cells infected from yolk sac seed material were immunoferritin labeled, the binding of ferritin was found to be dense and uniform on the outer surface of the rickettsiae in disrupted host cells. Immunolabeling of purified suspensions of extracellular rickettsiae resulted in the uniform ferritin labeling of the microorganism. Aggregation of these rickettsiae by antibody appeared to depend upon the purity of the pellets. Immunoferritin labeling examined at high magnification revealed ferritin very close to the outer dense leaflet of the outer membrane. On some rickettsiae or on focal sites of others, the labelin; was several ferritin particles thick, suggesting the presence of a thick coating. The immunoferritin labeling of R. tsutsugamushi during successive serial passages in BHK-21 cells revealed decreased labeling with each passage, and by the 10th passage there was no detectable labeling. However, these rickettsiae inoculated back into yolk sacs regained their immunoferritin labeling. R. tsutsugamushi passed back into yolk sacs after four serial propagations in BHK-21 cells regained their labeling on the first passage in yolk sacs. However, rickettsiae from the 20th serial passage in BHK-21 cells required five passages in yolk sacs to reestablish their previous labeling affinity. Rickettsiae which did not label after 20 passages in BHK cells regained some of their labeling characteristics when sonicated. Antibody against rickettsiae cultivated in BHK-21 cells continued labeling rickettsiae even after 9 serial passages in BHK-21 cells.
利用兔源抗恙虫病立克次体抗体的纯化免疫球蛋白G组分,检测了恙虫病立克次体(吉利亚姆株)的免疫标记特征。将福尔马林固定的立克次体与该抗体反应,然后与铁蛋白偶联的山羊抗兔Fc抗体反应。本研究使用在卵黄囊中培养的恙虫病立克次体来制备抗体。当用免疫铁蛋白标记从卵黄囊种子材料感染的BHK - 21细胞中的立克次体时,发现铁蛋白在破裂宿主细胞中立克次体的外表面结合紧密且均匀。细胞外立克次体纯化悬液的免疫标记导致微生物被铁蛋白均匀标记。这些立克次体被抗体聚集似乎取决于沉淀的纯度。在高倍镜下检查免疫铁蛋白标记发现,铁蛋白非常靠近外膜的外致密层。在一些立克次体上或其他立克次体的局部位点,标记有几层铁蛋白颗粒厚,表明存在厚涂层。恙虫病立克次体在BHK - 21细胞中连续传代期间的免疫铁蛋白标记显示,每传一代标记减少,到第10代时没有可检测到的标记。然而,将这些立克次体重新接种到卵黄囊中后又恢复了免疫铁蛋白标记。在BHK - 21细胞中连续传代4次后再接种到卵黄囊中的恙虫病立克次体在卵黄囊中的第一代就恢复了标记。然而,来自BHK - 21细胞第20代连续传代的立克次体需要在卵黄囊中传5代才能重新建立其先前的标记亲和力。在BHK细胞中传20代后未标记的立克次体经超声处理后恢复了一些标记特征。即使在BHK - 21细胞中连续传代9次后,针对在BHK - 21细胞中培养的立克次体的抗体仍能继续标记立克次体。