raav2 - mfe77.43转移小鼠对日本血吸虫感染的耐药性研究

Hong-mei Wang, De-hui Xiong, Sai-qun Luo, Jie Yang, Yin-jun Qian, Zhi-qiang Qin
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引用次数: 0

摘要

目的:了解东方田鼠E77.43基因(MfE77.43)对日本血吸虫感染的抗性。方法:将MfE77.43构建到重组腺相关病毒AAV2中。采用磷酸钙DNA共沉淀法将AAV2-MfE77.43转染HEK293细胞。纯化重组rAAV2-MfE77.43,提取转染细胞的总RNA。RT-PCR检测E77.43的表达,SDS-PAGE分析rAAV2-MfE77.43的纯度。将18只KM小鼠分为3组,每组6只。实验组小鼠于第0、3、7天肌肉注射400 μl重组AAV2-MfE77.43病毒,该病毒在生理盐水中稀释5倍。阴性对照组和空白对照组小鼠给予等量pAAV或生理盐水。每次注射前经尾部采集静脉血,采用dot-ELISA法检测血浆中E77.43的表达。末次注射后,每只小鼠感染日本血吸虫尾蚴40只,感染后第41天处死。计算每克成虫和肝卵(LEPG)。分别计算除虫率和除卵率。HE染色观察鸡蛋肉芽肿。结果:RT-PCR检测出330bp的特异条带。病毒壳蛋白SDS-PAGE显示M(r)分别为87 000、72 000和62 000的3条蛋白带。Dot-ELISA结果显示,注射rAAV2-MfE77.43后第3天E77.43蛋白开始表达,并保持稳定至第41天。实验组成虫数和LEPG分别为20.16±3.93和19 800±2 715,虫卵减少率分别为27.3%和26.2%。阴性对照组虫数和LEPG分别为29.16±2.44和28 000±2 192(p)结论:E77.43基因对日本血吸虫感染具有保护作用,提示E77.43基因可能参与了东方田鼠对日本血吸虫感染的自然抗性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Resistance of rAAV2-MfE77.43-Transferred Mice to Schistosoma japonicum Infection].

Objective: To investigate the resistance of E77.43 gene of Microtus fortis(MfE77.43) to Schistosoma japonicum infection.

Methods: MfE77.43 was constructed into the recombinant Adeno-associated virus AAV2. The AAV2-MfE77.43 was transfected into HEK293 cells by the calcium phosphate DNA coprecipitation method. The recombinant rAAV2-MfE77.43 was purified and total RNA was extracted from the transfected cells. The expression of E77.43 was examined by RT-PCR and the purity of rAAV2-MfE77.43 was analyzed by SDS-PAGE. Eighteen KM mice were divided into three groups (n=6 in each group). Mice in the experiment group were intramuscularly injected on days 0, 3 and 7 with 400 μl recombinant AAV2-MfE77.43 virus which was 5-fold diluted in normal saline. Mice in negative control and blank control groups received same volume of pAAV or normal saline. Venous blood was collected through the tail before each injection, and E77.43 expression in plasma was detected by dot-ELISA method. After the last injection, each mouse was infected with 40 S. japonicum cercariae and sacrificed on day 41 after infection. Adult worms and liver eggs per gram(LEPG) were counted. Worm and egg reduction rate was calculated respectively. Egg granulomas were observed by HE staining.

Results: RT-PCR resulted in a 330 bp specific band. SDS-PAGE of virus shell protein revealed three protein bands with M(r) of 87 000, 72 000 and 62 000, respectively. Dot-ELISA showed that E77.43 protein began to be expressed on day 3 after rAAV2-MfE77.43 injection, remaining stable till day 41. The adult worm number and LEPG were 20.16±3.93 and 19 800±2 715, respectively, with a worm and egg reduction rate of 27.3% and 26.2% in the experiment group. While the worm number and LEPG in the negative control group were 29.16±2.44 and 28 000±2 192(P<0.01), respectively. HE staining and observation revealed fewer eosinophils and inflammatory cells around the liver eggs in the therapy group.

Conclusion: The E77.43 gene shows protective effects against S. japonicum infection, indicating that E77.43 may participate in the natural resistance of Microtus fortis to S. japonicum infection.

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