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[小鼠慢性弓形虫病发生发展及动态变化的初步观察]

[Preliminary observation on the development and dynamic changes of chronic toxoplasmosis in mice].

作者信息

Zhou G, Bai S, Li Y, Zhu G, Huang S

机构信息

College of Veterinary Medicine (Institute of Comparative Medicine), Yangzhou University, Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu 225009, China.

National Health Commission Key Laboratory of Parasitic Disease Control and Prevention, Jiangsu Provincial Key Laboratory on Parasite and Vector Control Technology, Jiangsu Provincial Medical Key Laboratory, Jiangsu Institute of Parasitic Diseases, China.

出版信息

Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2024 Jun 7;36(3):304-309. doi: 10.16250/j.32.1374.2024044.

Abstract

OBJECTIVE

To investigate the development and dynamic changes of cysts in the brain of mice following infection with different forms of , so as to provide insights into for toxoplasmosis prevention and control.

METHODS

ICR mice at ages of 6 to 8 weeks, each weighing 20 to 25 g, were intraperitoneally injected with tachyzoites of the PRU strain at a dose of 1 × 10 tachyzoites per mouse, orally administered with cysts at a dose of 20 oocysts per mouse or oocysts at a dose of 200 oocysts per mouse for modeling chronic infection in mice, and the clinical symptoms and survival of mice were observed post-infection. Mice were orally infected with cysts at doses of 10 (low-dose group), 20 (medium-dose group), 40 cysts per mouse (high-dose group), and the effect of different doses of infections on the number of cysts was examined in the mouse brain. Mice were orally administered with cysts at a dose of 20 cysts per mouse, and grouped according to gender (female and male) and time points of infections (20, 30, 60, 90, 120, 150, 180 days post-infection), and the effects of gender and time points of infections on the number of cysts was examined in the mouse brain. In addition, mice were divided into the tachyzoite group (Group T), the first-generation cyst group (Group C1), the second-generation cyst group (Group C2), the third-generation cyst (Group C3) and the fourth-generation cyst group (Group C4). Mice in the Group T were intraperitoneally injected with tachyzoites at a dose of 1 × 10 tachyzoites per mouse, and the cysts were collected from the mouse brain tissues 30 days post-infection, while mice in the Group C1 were orally infected with the collected cysts at a dose of 30 cysts per mouse. Continuous passage was performed by oral administration with cysts produced by the previous generation in mice, and the effect of continuous passage on the number of cysts was examined in the mouse brain.

RESULTS

Following infection with tachyzoites, cysts and oocysts in mice, obvious clinical symptoms were observed on days 6 to 13 and mice frequently died on days 7 to 12. The survival rates of mice were 67.0%, 87.0% and 53.0%, and the mean numbers of cysts were (516.0 ± 257.2), (1 203.0 ± 502.0) and (581.0 ± 183.1) in the mouse brain ( = 11.94, < 0.01) on day 30 post-infection with tachyzoites, cysts and oocysts, respectively, and the numbers of cysts in the brain tissues were significantly lower in mice infected with tachyzoites and oocysts than in those infected with cysts (all values < 0.01). The survival rates of mice were 87.0%, 87.0% and 60.0%, and the mean numbers of cysts were (953.0 ± 355.5), (1 084.0 ± 474.3) and (1 113.0 ± 546.0) in the mouse brain in the low-, medium- and high-dose groups on day 30 post-infection, respectively ( = 0.42, > 0.05). The survival rates of male and female mice were 73.0% and 80.0%, and the mean numbers of cysts were (946.4 ± 411.4) and (932.1 ± 322.4) in the brain tissues of male and female mice, respectively ( = 1.63, > 0.05). Following continuous passage, the mean numbers of cysts were (516.0 ± 257.2), (1 203.0 ± 502.0), (896.8 ± 332.3), (782.5 ± 423.9) and (829.2 ± 306.0) in the brain tissues of mice in the T, C1, C2, C3 and C4 groups, respectively ( = 4.82, < 0.01), and the number of cysts was higher in the mouse brain in Group 1 than in Group T ( < 0.01). Following oral administration of 20 cysts in mice, cysts were found in the moues brain for the first time on day 20 post-infection, and the number of cysts gradually increased over time, peaked on days 30 and 90 post-infection and then gradually decreased; however, the cysts were still found in the mouse brain on day 180 post-infection.

CONCLUSIONS

There is a higher possibility of developing chronic infection in mice following infection with cysts than with oocysts or tachyzoites and the most severe chronic infection is seen following infection with cysts. The number of cysts does not correlate with the severity of chronic infection, and the number of cysts peaks in the mouse brain on days 30 and 90 post-infection.

摘要

目的

研究小鼠感染不同形式的 后脑部囊肿的发育及动态变化,为弓形虫病的防控提供依据。

方法

选取6至8周龄、体重20至25 g的ICR小鼠,每只小鼠腹腔注射1×10 速殖子的PRU株,或每只小鼠口服20个卵囊或200个卵囊以建立小鼠慢性 感染模型,感染后观察小鼠的临床症状和存活情况。将小鼠分别口服感染10个(低剂量组)、20个(中剂量组)、40个囊肿/只小鼠(高剂量组),检测不同剂量 感染对小鼠脑部囊肿数量的影响。将小鼠每只口服20个囊肿,根据性别(雌性和雄性)和感染时间点(感染后20、30、60、90、120、150、180天)分组,检测性别和感染时间点对小鼠脑部囊肿数量的影响。此外,将小鼠分为速殖子组(T组)、第一代囊肿组(C1组)、第二代囊肿组(C2组)、第三代囊肿组(C3组)和第四代囊肿组(C4组)。T组小鼠每只腹腔注射1×10 速殖子,感染后30天从鼠脑组织中收集囊肿,C1组小鼠每只口服30个收集的囊肿。通过给小鼠口服上一代产生的囊肿进行连续传代,检测连续传代对小鼠脑部囊肿数量的影响。

结果

小鼠感染速殖子、囊肿和卵囊后,在第6至13天出现明显临床症状,第7至12天小鼠频繁死亡。感染速殖子、囊肿和卵囊后第30天,小鼠存活率分别为67.0%、87.0%和53.0%,小鼠脑内囊肿平均数分别为(516.0±257.2)、(1 203.0±502.0)和(581.0±183.1)( = 11.94, < 0.01),感染速殖子和卵囊的小鼠脑组织中的囊肿数量明显低于感染囊肿的小鼠(所有 值< 0.01)。低、中、高剂量组感染后第30天,小鼠存活率分别为87.0%、87.0%和60.0%,小鼠脑内囊肿平均数分别为(953.0±355.5)、(1 084.0±474.3)和(1 113.0±546.0)( = 0.42, > 0.05)。雄性和雌性小鼠存活率分别为73.0%和80.0%,雄性和雌性小鼠脑组织中的囊肿平均数分别为(946.4±411.4)和(932.1±322.4)( = 1.63, > 0.05)。连续传代后,T、C1、C2、C3和C4组小鼠脑组织中的囊肿平均数分别为(516.0±257.2)、(1 203.0±502.0)、(896.8±332.3)、(782.5±423.9)和(829.2±306.0)( = 4.82, < 0.01),C1组小鼠脑内囊肿数量高于T组( < 0.01)。小鼠口服20个囊肿后,感染后第20天首次在小鼠脑内发现囊肿,囊肿数量随时间逐渐增加,在感染后第30天和第90天达到峰值,然后逐渐下降;然而,感染后第180天小鼠脑内仍有囊肿。

结论

小鼠感染囊肿后发生慢性 感染的可能性高于感染卵囊或速殖子,且感染囊肿后慢性感染最为严重。囊肿数量与慢性 感染的严重程度无关,小鼠脑内囊肿数量在感染后第30天和第90天达到峰值。

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