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体外培养的嵌合体丙型肝炎病毒感染Huh7.5细胞的透射电镜观察
引用本文:马力,魏欣,张野,王平忠,连建奇,贾战生.体外培养的嵌合体丙型肝炎病毒感染Huh7.5细胞的透射电镜观察[J].中华微生物学和免疫学杂志,2009,29(6).
作者姓名:马力  魏欣  张野  王平忠  连建奇  贾战生
作者单位:第四军医大学唐都医院全军感染病诊疗中心,西安,710038
基金项目:国家高技术研究发展计划(863计划) 
摘    要:目的 通过透射电子显微镜技术观察体外培养的嵌合体丙型肝炎病毒(HCV)感染Huh7.5细胞后胞内病毒颗粒的形态学特征及细胞内部超微结构的变化.方法 将含有全长HCV嵌合基因组的质粒pFL-J6/JFH体外转录为HCV RNA,电穿孔转染至Huh7.5细胞,实时定量聚合酶链反应(qRT-PCR)测定培养上清中病毒数量;间接免疫荧光检测病毒蛋白的表达;收取转染后细胞培养上清感染原始Huh7.5细胞,制作超薄细胞切片,透射电子显微镜技术观察被感染细胞中病毒颗粒的形态学特征及细胞超微结构的变化.结果 qRT-PCR显示不同时间点收取的转染后细胞培养上清中含有高水平的病毒量;间接免疫荧光显示病毒NSSA非结构蛋白高表达;透射电子显微镜观察到被感染的Huh7.5细胞内含有大量有包膜或无包膜的病毒样颗粒,细胞质内部分膜性细胞器增生,出现黄病毒科病毒感染后特征性结构及某种未知结构等.结论 体外培养的嵌合体HCV具有HCV颗粒的形态学特征,并能够有效感染人源性肝细胞Huh7.5.

关 键 词:丙型肝炎病毒  体外转录  透射电子显微镜

Observation of chimeric hepatitis C virus In infected Huh7.5 cell through transmission electron microscopy
MA Li,WEI Xin,ZHANG Ye,WANG Ping-zhong,LIAN Jian-qi,JIA Zhan-sheng.Observation of chimeric hepatitis C virus In infected Huh7.5 cell through transmission electron microscopy[J].Chinese Journal of Microbiology and Immunology,2009,29(6).
Authors:MA Li  WEI Xin  ZHANG Ye  WANG Ping-zhong  LIAN Jian-qi  JIA Zhan-sheng
Abstract:Objective To observe the morphological characteristics of HCV particles and intracel-lular ultrastructure changes in Huh7. 5 cells which was infected with chimeric HCV via transmission electron microscopy. Methods Plasmid J6/JFH encoding the full length HCV chimeric genome was transcribed to HCV RNA in vitro and the RNA was transfected into Huh7.5 cells by electroporation. Quantitative real-time PCR(qRT-PCR) was used to assay HCV copies of the supernatant of transfected cells. Indirect immunofluo-rescence was used to detect the expression of HCV proteins. The cell culture superoatant were used to infect narve Huh7.5 cells, transmission electron microscopy was used to observe morphological characteristics of vi-rus particles and intracellular ultrastructure changes in infected Huh7. 5 cells. Results qRT-PCR showed high level virus copies in supernatant of transfected cells collected in different times, indirect immuno-fluo-rescencc proved high expression of HCV NS5A proteins in the transfected cells. Large numbers of enveloped or unenveloped virus-like particles (VLPs) were observed in infected Huh7. 5 cells via transmission electronmicroscopy. We also found hyperplasia of some membrane-enclosed organelles in the cytoplasm. Several fea-tures characterizing flavivirus infected cells and a cytoplasmic inclusion of unknown origin were observed. Conclusion The chimeric HCV from in vitro cell culture system is proved to be intact virus particles which can efficiently infect Huh7.5 cells.
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