›› 2008, Vol. 28 ›› Issue (4): 246-250.

• 论文 • 上一篇    下一篇

脑炎微孢子虫病豚鼠模型的实验研究

  

  1. 1.南方医科大学比较医学研究所,广州 510515;2.南方医科大学珠江医院病理科,广州 510282
  • 收稿日期:2008-06-04 出版日期:2008-04-30 发布日期:2008-04-30

Experimental Study on Establishment of Encephalitozoonosis Model with FMMU Albino Guinea-pig

  1. 1. Institute of Comparative Medicine, Southern Medical University, Guangzhou 510515, China;2. Department of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510282, China
  • Received:2008-06-04 Online:2008-04-30 Published:2008-04-30

摘要: 目的 建立FMMU白化豚鼠脑炎微孢子虫病动物模型。方法 动物分为免疫抑制组和非免疫抑制对照组两组。从患病兔分离纯化兔脑炎微孢子虫,豚鼠灌胃接种,免疫抑制剂组肌肉注射氢化可的松。粪便检查虫体,观察临床症状,光镜检查内脏组织病理学变化,电镜观察微孢子虫超微结构,评价FMMU白化豚鼠作为脑炎微孢子虫感染动物模型的可行性。结果 免疫抑制豚鼠于感染后第3天检出原虫,比非免疫抑制豚鼠检出时间早1 d。免疫抑制豚鼠于第6天全部检出原虫,比对照组豚鼠早2 d。对照组豚鼠除少数有食欲下降和消瘦外,其余无症状。免疫抑制豚鼠感染后出现消瘦、腹水等症状,5只于感染后35 d出现神经症状和少尿、排尿痛苦等泌尿系统症状。造模后40 d免疫抑制豚鼠死亡率达25%。光镜观察发现主要在脑、肾、肝等内脏器官中存在局灶性淋巴上皮样肉芽肿病变。电镜观察表明脑炎微孢子虫具三层结构的孢子壁,孢子内部极管呈6圈螺旋排列。结论 成功建立免疫抑制FMMU白化豚鼠脑炎微孢子虫感染模型,可作为动物及人类的急性脑炎微孢子虫病动物模型用于相关研究。

关键词: 脑炎微孢子虫, FMMU白化豚鼠, 免疫抑制剂, 脑炎微孢子虫病

Abstract: Objective To establish encephalitozoonosis model of FMMU albino guinea-pig. Method FMMU albino guinea-pigs were divided into 2 groups: immunosuppressed group, non-immunosuppressed control group. Encephalitozoon cuniculi were isolated and purified from diseased rabbit, guinea-pigs were infected by intragas trie administration of E. cuniculi, and hydrocortisone was administered by intramuscular injection. E. cuniculi in faeces,clinical manifestations, and histopathologic changes in major organs were observed, the ultrastructure of E. cuniculi was observed by electron microscope(EM). Result E. cuniculi were detected from hydrocortisone-immunosuppressed guinea-pigs at day 3 post infection, one day earlier than that of non-immunosuppressed ones, and all immunosuppressed guinea-pigs were detected with E. cuniculi at day 6, ahead of control group 2 days. Minority of guinea-pigs in control group showed loss of appetite and emaciation, others were asymptomatic. Emaciation and ascites could be seen in immunosuppressed guinea-pigs, and 5 of which had neurological and urinary symptoms such as wryneck, convulsion, oliguria and painful urination at day 35 post infection. Mortality rate was 25% at day 40 post infection in immunosuppressed group. Under light microscope there were focal lymphoepithelioid granuloma in internal organ, such as brain, kidney and liver. EM observation showed that E. cuniculi spore has a trilaminar wall, the interior polar tube was arranged into 6 coils. Conclusion E. cunicul infection model of immunosuppressed FMMU albino guinea-pig was established successfully and could be used as acute Encephalitozoonosis animal model for human and other animals.

Key words: Encephalitozoon cuniculi, FMMU albino guinea-pig, Immunosuppression, Encephalitozoonosis