[Expression and Detection of Lentivirus-mediated Green Fluorescent Protein in Schistosoma japonicum].

Yue Xin, Nan Zhao, Qing Li, Wei Hu
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Abstract

Objective: To test if the green fluorescent protein gene can be expressed in Schistosoma japonicum and produce green fluorescence signals there.

Methods: The spontaneous fluorescence in Schistosoma japonicum at different developmental stages was observed by fluorescence microscopy. The cultured 14-day schistosomula were infected with the lentiviral vector containing cyto megalo virus (CMV)-driven zsGreen gene, or were incubated with RPMI 1640 medium containing 10% fetal bovine serum as a negative control. At 48 h after infection, genomic DNA and total RNA were extracted, and cDNA was synthesized. PCR was performed to detect the genomic integration of zsGreen gene and the expression of zsGreen mRNA. Green fluorescence was observed under a fluorescence microscope at 24 h and 48 h after infection, and at various time points after replacement with fresh culture medium.

Results: There was no obvious spontaneous fluorescence in schistosomula, but the adult worms showed clear spontaneous fluorescence. PCR results showed a specific band of 173 bp from the schistosomula genomic DNA, which corresponded to the zsGreen gene. Gene sequencing also confirmed this result. At 24 h after infection, green fluorescence was seen in the intestine of schistosomula, which was, however, suspected to be food residues. At 48 h after infection, evenly-distributed green fluorescence emerged across the intestine, and the fluorescence was brighter than the background fluorescence of the lentiviral culture medium. The fluorescence weakened on day 3 after replacement with fresh 1640 medium, and disappeared a week later. The green fluorescence re-emerged 2 weeks after replacement with the lentivirus-containing 1640 medium. No fluorescence was seen in the negative control group.

Conclusion: The exogenous green fluorescent protein gene can be expressed in Schistosoma japonicum. However, the green fluorescence seen under the fluorescence microscope needs further verification.

慢病毒介导的绿色荧光蛋白在日本血吸虫中的表达与检测
目的:研究绿色荧光蛋白基因能否在日本血吸虫中表达并产生绿色荧光信号。方法:用荧光显微镜观察日本血吸虫不同发育阶段的自发荧光。用含有巨细胞病毒(CMV)驱动的zsGreen基因的慢病毒载体感染培养的14天血吸虫,或用含有10%胎牛血清的RPMI 1640培养基孵育。感染后48 h提取基因组DNA和总RNA,合成cDNA。采用PCR检测zsGreen基因的基因组整合和zsGreen mRNA的表达。在感染后24 h和48 h,以及更换新鲜培养基后的不同时间点,荧光显微镜下观察到绿色荧光。结果:血吸虫无明显的自发荧光,成虫有明显的自发荧光。PCR结果显示,该血吸虫基因组DNA中有173 bp的特异条带,与zsGreen基因对应。基因测序也证实了这一结果。感染24 h后,血吸虫肠内可见绿色荧光,怀疑为食物残留。感染后48 h,肠内出现均匀分布的绿色荧光,荧光比慢病毒培养基的背景荧光更亮。用新鲜的1640培养基替换后第3天荧光减弱,1周后荧光消失。用含慢病毒的1640培养基替换2周后,绿色荧光再次出现。阴性对照组未见荧光。结论:外源绿色荧光蛋白基因可在日本血吸虫中表达。但是,在荧光显微镜下看到的绿色荧光需要进一步验证。
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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