中国丙型肝炎病毒3b亚型高感染性假颗粒的制备及糖蛋白的鉴定

Gesi Tao, Fei Ye, Yao Deng, Ling Zhang, Sha Lu, Xiaozhen Bo, Congli Li, Xiaoling Shen, Wenjie Tan
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摘要

我们希望对中国丙型肝炎病毒(HCV)的包膜蛋白编码基因进行表征,并制备3b亚型的HCV假颗粒(HCVpp)。从中国HCV患者中克隆了两个HCV基因型3b包膜蛋白编码基因(C27、C30),并进行了测序分析。构建两个包膜蛋白表达质粒,并用western blotting对其进行表征。制备了HCVpp,并在体外靶向感染细胞。结果表明,HCV亚型3b包膜蛋白编码基因C27、C30的核苷酸和氨基酸序列具有高度同源性(98。5%和98。与国际参考菌株3b TrKj有密切的系统发育关系。在C27和C30的包膜蛋白编码区有10个氨基酸位点被取代。C27包膜蛋白的表达明显高于HCV亚型1 (Conl)和C30。相应的HCVpp在体外的感染性也有显著差异,因此可以利用C27制备具有高感染性的HCVpp亚型3b。总之,我们对HCV亚型3b的两个包膜蛋白编码基因进行了测序,并对其体外表达进行了研究。这是首次报道制备具有高传染性的HCVpp亚型3b。本研究可为丙型肝炎病毒的研究和疫苗的开发提供有效的工具。
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Characterization of Glycoproteins and Preparation of HCV Pseudoparticles with High Infectivity of Subtype 3b from Chinese Patients.

We wished to characterize the envelope protein coding gene of the hepatitis-C virus (HCV) from Chinese patients and prepare HCV pseudoparticles (HCVpp) of subtype 3b. Two of the HCV genotype 3b envelope protein coding genes (C27, C30) were cloned from Chinese HCV patients followed by sequencing analyses. Then, two envelope protein expression plasmids were constructed and characterized by western blotting. HCVpp were prepared and target cells infected in vitro. Results showed that the sequences of nucleotides and amino acids from two HCV subtype 3b envelope protein encoding genes (C27, C30) had high homology (98. 5% and 98. 2%, respectively) and had a close phylogenetic relationship with the international reference strain 3b TrKj. Ten amino-acid sites were substituted in the envelope protein coding region of C27 and C30. Expression of the C27 envelope protein was significantly higher than that of HCV subtype 1 (Conl) and C30. The corresponding HCVpp infectivity in vitro was also significantly different, whereby C27 could be used to prepare HCVpp subtype 3b with high infectivity. In conclusion, two envelope protein encoding genes of HCV subtype 3b were sequenced and their expression in vitro investigated. This is the first report on preparation of HCVpp subtype 3b with high infectivity. This study might provide an effective tool for HCV research and development of a vaccine for HCV.

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