van Dellen A F, Stewart C G, Botha W S
Division of Pathobiology, Wilford Hall (USAF) Medical Center, San Antonio, Texas 78236-5300.
Onderstepoort J Vet Res. 1989 Mar;56(1):1-22.
Encephlitozoonosis was induced in 35 of 38 vervet monkeys (Cercopithecus pygerythrus). They were either directly (orally) inoculated with Encephlitozoon cuniculi or indirectly exposed to this protozoan parasite. Cell-culture-grown spores of E. cuniculi, isolated from the kidneys of dogs with natural, fatal disease, were administered orally to 29 of these monkeys. Another 5 were exposed in utero by orally infecting pregnant females, and 3 were exposed to horizontal infection by nursing infected infants. Only one was given an intravenous inoculation of spores. The disease was induced in non-gravid and late-pregnant adults, immunocompetent infants, and in infants that were immunologically compromised by parenteral steroid administration, as well as in one infant that was immunologically immature because of its premature birth. The effects of age, dosage, post-inoculation (PI) interval, passage level of the parasite in cell culture and immunological status of the host were correlated with macroscopical and microscopical lesions. The experimentally induced infection was confirmed either by reisolation of the parasite in cell culture or by observation of spores in tissue sections. Both confirmatory methods were supported by serological examination. Reisolation of the organism in primary cell culture prepared from kidneys usually resulted in more frequent isolates and larger yields of spores from infants than from adult vervets. Infection with E. cuniculi invariably induced subclinical disease. Based on histology, lesions were minimal to moderately severe, depending on age, PI interval, and immunological status of the host. Alimentary tract infections were seen histologically as early as three days PI. Subsequently, infections resulted in detectable lesions most consistently in the liver, kidneys and brain. Lesions in these organs were generally granulomatous and were similar to those found in canine encephalitozoonosis. In addition, multifocal interstitial pneumonitis and myocarditis as well as vasculitis and perivasculitis were seen in other tissues and organs. Infants had more severe and more widespread lesions than adults. Although lesions and spores were still present in the brain of one immunocompetent infant 36 weeks after initial infection, the disease in immunocompetent infants and adults is thought to be self-limiting. However, infection may persist. Immunological depression favoured increased growth and multiplication of the organism, and resulted in detection of more spores within inflammatory lesions as well as more intracellular colonies of the organism that were free of inflammatory reaction.(ABSTRACT TRUNCATED AT 400 WORDS)
38只绿猴(赤猴)中有35只感染了脑胞内原虫病。它们要么直接(经口)接种兔脑胞内原虫,要么间接接触这种原生动物寄生虫。从患有自然致命疾病的狗的肾脏中分离出的兔脑胞内原虫细胞培养生长的孢子经口给予其中29只猴子。另外5只在子宫内通过感染怀孕雌性而暴露,3只通过哺乳受感染的幼崽而暴露于水平感染。只有一只接受了孢子的静脉注射。该疾病在未怀孕和怀孕后期的成年动物、免疫功能正常的幼崽、因肠胃外给予类固醇而免疫受损的幼崽以及一只因早产而免疫不成熟的幼崽中诱发。年龄、剂量、接种后(PI)间隔、寄生虫在细胞培养中的传代水平以及宿主的免疫状态的影响与宏观和微观病变相关。通过在细胞培养中重新分离寄生虫或通过观察组织切片中的孢子来确认实验性诱导的感染。两种确认方法均得到血清学检查的支持。从肾脏制备的原代细胞培养中重新分离该生物体通常导致幼崽比成年绿猴更频繁地分离出该生物体且孢子产量更高。感染兔脑胞内原虫总是诱发亚临床疾病。根据组织学,病变从轻微到中度严重,这取决于宿主的年龄、PI间隔和免疫状态。早在接种后三天,在组织学上就可见消化道感染。随后,感染最一致地导致在肝脏、肾脏和大脑中出现可检测到的病变。这些器官中的病变通常是肉芽肿性的,并且与犬脑胞内原虫病中发现的病变相似。此外,在其他组织和器官中可见多灶性间质性肺炎和心肌炎以及血管炎和血管周围炎。幼崽的病变比成年动物更严重且更广泛。尽管在初次感染36周后,一只免疫功能正常的幼崽的大脑中仍存在病变和孢子,但免疫功能正常的幼崽和成年动物中的疾病被认为是自限性的。然而,感染可能持续存在。免疫抑制有利于该生物体的生长和繁殖增加,并导致在炎症病变中检测到更多的孢子以及更多无炎症反应的该生物体的细胞内菌落。(摘要截断于400字)