中国寄生虫学与寄生虫病杂志

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田鼠巴贝虫隐性感染鼠再感染、免疫抑制或盲传后的虫密度消长规律研究

蔡玉春1,2, 陈韶红2, 卢艳2, 艾琳2, 杨春利2, 陈家旭2*   

  1.  1 复旦大学生命科学学院, 上海 200433; 2 中国疾病预防控制中心寄生虫病预防控制所, 世界卫生组织热带病合作中心, 科技部国家级热带病国际联合中心, 卫生部寄生虫病原与媒介生物学重点实验室, 上海200025
  • 出版日期:2017-08-30 发布日期:2017-09-14

Dynamic changes of density of Babesia microti in mice with latent infection after re-infection, immunosuppression, or random transmission to healthy mice

CAI Yu-chun1,2, CHEN Shao-hong2, LU Yan2, AI Lin2, YANG Chun-li2, CHEN Jia-xu2*   

  1. 1 School of Life Sciences, Fudan University, Shanghai, 200433, China; 2 National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention; Key Laboratory of Parasite and Vector Biology, Ministry of Health; WHO Collaborating Centre for Tropical Diseases, National Center for International Research on Tropical Diseases, Ministry of Science and Technology, Shanghai 200025, China
  • Online:2017-08-30 Published:2017-09-14

摘要:

目的 观察田鼠巴贝虫(Babesia microti)隐性感染期小鼠经再感染、免疫抑制或盲传健康小鼠后的外周血红细胞内虫体密度的消长规律。 方法 取1只感染种鼠的外周血(虫密度为20%), 腹腔接种6周龄雌性BALB/c健康小鼠12只, 100 μl/只, 用随机数字表法分为对照组、再感染组、免疫抑制组和盲传组, 每组3只。4组感染小鼠连续28 d尾部采血, 吉氏染色法观察田鼠巴贝虫形态变化, 并计算红细胞染虫率, 构建隐性感染小鼠模型。再感染组隐性感染小鼠再次腹腔接种相同剂量的田鼠巴贝虫感染种鼠血; 免疫抑制组隐性感染小鼠腹腔注射地塞米松, 0.5 mg/只, 连续注射5 d; 盲传组3只隐性感染小鼠取眼眶血, 分别腹腔盲传接种健康雌性BALB/c小鼠各3只, 100 μl/只。3组小鼠继续尾部采血28 d, 镜下计数感染红细胞, 计算染虫率, 并观察田鼠巴贝虫形态变化。 结果 对照组、再感染组、免疫抑制组和盲传组小鼠外周血均于感染后第3天查见田鼠巴贝虫体, 第7天红细胞染虫率最高, 分别为73.2%、78.0%、76.2%及79.0%, 随后染虫率逐渐下降, 至第28天外周血镜检阴性, 进入隐性感染阶段。再感染组小鼠再次感染后28 d内, 每天染虫率均为0。免疫抑制组小鼠在免疫抑制后第2天查见虫体, 第12天染虫率再次达到高峰, 为65.2%, 随后逐渐下降, 至第22天再次进入隐性感染期。盲传组新感染的9只小鼠在感染后第4天查见虫体, 第9~10 天染虫率达到高峰, 为35.0%~39.0%, 随后逐渐下降, 至第28天小鼠进入隐性感染阶段。各组感染的田鼠巴贝虫形态变化基本一致, 染虫初期以小环状体居多; 染虫高峰期多见大环状体和长丝状体; 有多虫寄生现象。 结论 田鼠巴贝虫隐性感染期小鼠有带虫免疫现象, 并可作为传染源; 经免疫抑制后虫体被激化, 可出现与首次感染相同的虫体密度消长规律。

关键词: 巴贝虫病, 田鼠巴贝虫, 隐性感染, 输血感染, 免疫抑制

Abstract:

Objective To observe the infection dynamics of Babesia microti in mice with latent infection after re-infection, immunosuppression, or random transmission to healthy mice. Methods Twelve healthy BALB/c mice at the age of six weeks were intraperitoneally (i.p.) injected with 100 μl peripheral blood collected from infected mice (B. microti density, 20%) and then divided into 4 groups (control group, re-infection group, immunosuppression group and random transmission group, n = 3 in each). Tail blood collection was performed for 28 consecutive days to observe morphological changes of B. microti using Giemsa staining, calculate red blood cell (RBC) infection rate, and establish the mouse model of B. microti latent infection. Then the re-infection group once again received an i.p. injection of infected blood at the same dose as above and the immunosuppressive group received i.p. injection of dexamethasone (an immunosuppressant) for five consecutive days(0.5 mg/day). Orbital blood samples were collected in the random transmission group, which were then i.p. injected into 9 healthy BALB/c mice (1 ∶ 3). Tail blood was collected from the 3 groups of mice for consecutive 28 days to calculate RBC infection rate with microscopy and observe morphological changes of B. microti. Results B. microti parasites were first seen in RBC on day 3 in all the 4 groups. The RBC infection rate peaked on day 7(73.2%, 78.0%, 76.2% and 79.0% in control, re-infection, immunosuppression and random transmission groups, respectively), and gradually declined thereafter till the negative infection under a microscope, suggesting a latent infection phase. In the re-infection group, the rate of re-infection was 0 throughout the 28 days, while in the immune suppression group, re-infection was detected from day 2, reached a peak on day 12 (65.2%), and declined thereafter till 0 on day 22 (a latent infection phase). B. microti were firstly seen on day 4 in the transmitted nine mice, reached a peak on day 12 (35.0%-39.0%), and declined thereafter till the latent infection phase. The morphological changes of B. microti were basically similar among various groups. The early stage of infection was characterized by small ring bodies, while the peak stage was mainly composed of large ring bodies and filamentous bodies. Mmultiple parasitisms were also seen. Conclusion Premunition can be seen in mice with latent infection, which can be a source of infection. Immunosuppression of these mice may be followed by occurrences of similar density change dynamics as that observed after the first infection.

Key words: Babesiosis, Babesia microti, Latent infection, Transfusion infection, Immunosuppression