Kawahara M, Suto C, Rikihisa Y, Yamamoto S, Tsuboi Y
Nagoya City Public Health Research Institute, Japan.
J Clin Microbiol. 1993 Jan;31(1):89-96. doi: 10.1128/jcm.31.1.89-96.1993.
An infectious agent was isolated from the enlarged spleen of a wild mouse, Eothenomys kageus, by intraperitoneal inoculation of the spleen homogenate into laboratory mice. The laboratory mice developed splenomegaly, and the agent was maintained by serial passage of spleen homogenates in laboratory mice. The agent in the spleen homogenate was inactivated after incubation at 37 or 50 degrees C. Tetracyclines were effective in preventing infection of mice with this agent, but penicillin and sulfonamides were ineffective. Cytoplasmic inclusion bodies were observed in the peritoneal macrophages of infected mice. Electron microscopy revealed numerous small pleomorphic cocci within membrane-lined vacuoles in the cytoplasm of splenic macrophages. Morphologically similar to the ehrlichial organisms, each organism was surrounded by a distinct plasma membrane and rippled outer cell membrane without a distinct peptidoglycan layer. The agent did not grow in chicken embryos, and the Weil-Felix test result was negative. In the indirect fluorescent-antibody test, the agent reciprocally cross-reacted with Ehrlichia canis and cross-reacted somewhat with Ehrlichia sennetsu but did not cross-react with Ehrlichia risticii, Neorickettsia helminthoeca, Rickettsia tsutsugamushi, or Chlamydia spp. The mouse antiserum against this agent reacted with 64-, 47-, 46-, 44-, and 40-kDa proteins of E. canis by Western blotting (immunoblotting). Since E. canis and closely related Ehrlichia chaffeensis and Ehrlichia ewingii are not known to proliferate or cause splenomegaly in mice, these results suggest that the agent is a new species within the tribe Ehrlichieae of the family Rickettsiaceae. The finding suggests that wild rodents may serve as reservoirs for pathogenic ehrlichiae.
通过将一只野生日本田鼠(Eothenomys kageus)肿大脾脏的匀浆腹腔接种到实验小鼠体内,从该野生小鼠的脾脏中分离出一种感染因子。实验小鼠出现脾肿大,通过在实验小鼠中连续传代脾脏匀浆来维持该因子。脾脏匀浆中的因子在37或50摄氏度孵育后失活。四环素可有效预防小鼠感染该因子,但青霉素和磺胺类药物无效。在感染小鼠的腹腔巨噬细胞中观察到细胞质包涵体。电子显微镜显示,在脾脏巨噬细胞细胞质中被膜包裹的空泡内有许多小的多形性球菌。形态上与埃立克体属生物相似,每个生物体都被一层独特的质膜和有波纹的外细胞膜所包围,没有明显的肽聚糖层。该因子在鸡胚中不生长,外斐试验结果为阴性。在间接荧光抗体试验中,该因子与犬埃立克体相互交叉反应,与嗜人类埃立克体也有一定交叉反应,但与里氏埃立克体、蠕虫新立克次体、恙虫病立克次体或衣原体属不交叉反应。通过蛋白质印迹法(免疫印迹法),针对该因子的小鼠抗血清与犬埃立克体的64、47、46、44和40 kDa蛋白质发生反应。由于犬埃立克体以及密切相关的恰菲埃立克体和尤因埃立克体在小鼠中不会增殖或引起脾肿大,这些结果表明该因子是立克次体科埃立克体族内的一个新物种。这一发现表明野生啮齿动物可能是致病性埃立克体的储存宿主。