[The effect of leptin transgenic Plasmodium yoelii on mouse body weight].

Kai Li, Hong Zheng, Feng Zhu, Yong Fu, Wen-yue Xu
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引用次数: 0

Abstract

Objective: To investigate the effect of leptin transgenic Plasmodium yoelii on mouse body weight.

Methods: To construct the leptin gene-containing CRISPR/Cas9 recombinant plasmid which had the 5′UTR and 3′UTR of MIF(macrophage migration inhibitory factor) of Plasmodium yoelli 17XNL strain at two ends, the exogenous mouse leptin gene was inserted downstream of MIF coding region through homologous recombination, resulting in the PYC-MIF-Leptin recombinant plasmid. The recombinant plasmid was then electroporated into P. y 17XNL mature schizonts, and the transgenic schizonts were used to infect a Kunming mouse via tail vein injection. The trangenic P. y clone was screened by pyrimethamine selection and identified by PCR. The trangenic or wild-type P. y was used to infect a C57BL/6 mouse respectively. Blood sample was collected through eye ball and tail vein, and immunofluorescence and RT-PCR were performed to determine the expression of leptin protein in the parasites. Finally, PBS (200 μl) containing trangenic or wild-type P. y (1 × 104) was injected through the tail vein into C57BL/6 mice(n = 5 respectively). The negative control received a same volume of PBS. The changes of parasitemia and body weight were recorded every two days.

Results: The leptin-expressing recombinant plasmid PYC-MIF-Leptin was constructed successfully. Results of DNA sequencing of transgenic parasites confirmed the integration of leptin gene at the downstream of MIF gene and successful transcription. Immunofluorescence results indicated successful expression of mouse leptin protein. The weight loss was significant in mice infected with transgenic parasites on day 17(17.26 ± 1.40)g, decreased by 10.7%, but not in the other two groups. Both transgenic and wild-type parasites began to decline when parasitemia reached about 10%, but the transgenic parasites proliferated more rapidly. Both disappeared at 23 days.

Conclusion: Infection with leptin transgenic parasites decreases the body weight of the infected mice.

[瘦素转基因约氏疟原虫对小鼠体重的影响]
目的:研究瘦素转基因约氏疟原虫对小鼠体重的影响。方法:构建两端分别含有约利疟原虫17XNL株巨噬细胞迁移抑制因子(MIF) 5′utr和3′utr的含瘦素基因的CRISPR/Cas9重组质粒,通过同源重组将外源小鼠瘦素基因插入MIF编码区下游,得到PYC-MIF-Leptin重组质粒。将重组质粒电穿孔至P. y . 17XNL成熟分裂体中,经尾静脉注射感染昆明小鼠。采用乙胺嘧啶筛选法对该转基因青豆克隆进行筛选和PCR鉴定。用转基因或野生型弓形虫分别感染C57BL/6小鼠。通过眼球和尾静脉采血,采用免疫荧光和RT-PCR检测瘦素蛋白在寄生虫体内的表达。最后将含有转基因或野生型P. y (1 × 104)的PBS (200 μl)经尾静脉注射到C57BL/6小鼠(n = 5)体内。阴性对照接受相同体积的PBS。每2 d记录一次寄生虫率和体重的变化。结果:成功构建了表达瘦素的重组质粒PYC-MIF-Leptin。转基因寄生虫的DNA测序结果证实了瘦素基因在MIF基因下游的整合和转录成功。免疫荧光结果显示小鼠瘦素蛋白成功表达。感染转基因寄生虫的小鼠在第17天体重减轻(17.26±1.40)g,降幅为10.7%,其他两组均无显著差异。当寄生率达到10%左右时,转基因和野生型寄生虫均开始下降,但转基因寄生虫的增殖速度更快。两人都在23天时失踪。结论:瘦素转基因寄生虫感染可降低感染小鼠的体重。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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