恒河猴肝细胞中丙型肝炎病毒正、负链RNA和蛋白的超微结构定位

S. Majerowicz, C. Grief, M. A. Pinto, M. L. Baptista, Â. T. Pinhão, Renata C. Airano, C. Vitral, R. Marchevsky, C. Yoshida, O. Barth, En Qg Inglaterra. Nibsc. Potters Bar. Herts
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引用次数: 1

摘要

用电子显微镜分析了实验感染丙型肝炎病毒(HCV)的恒河猴肝脏的形态学变化。利用原位杂交和免疫电镜技术证实了肝细胞内病毒RNA和蛋白质的定位。这些动物通过不同的途径接种。仅通过脾内入路对HCV感染的自体肝细胞移植感染是成功的。用于感染肝细胞的接种物为基因3型,RNA拷贝数为107个/mL。用特异性引物制成的互补负链和正链探针进行原位杂交。尽管HCV感染水平被认为很低,但我们能够在感染肝细胞的粗内质网改变膜中检测和定位病毒阳性和阴性RNA链和病毒蛋白,显示病毒在体内复制的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrastructural localization of Hepatitis C virus positive and negative strand RNA and proteins in Hepatocytes of a Rhesus Monkey (Macaca Mulatta)
Morphological alterations of the liver from rhesus macaque (Macaca mulatta) experimentally infected with hepatitis C virus (HCV) were analyzed using electron microscopy. The localization of viral RNA and proteins inside hepatocytes was demonstrated using in situ hybridization and immunoelectron microscopy techniques. The animals were inoculated by different routes. The infection was successful only by use of the intrasplenic approach to HCV infected autogenic hepatocyte transplant. The inoculum used to infect the hepatocytes was characterized as genotype 3 with 107 RNA copies/mL. In situ hybridization was performed using a complementary negative and positive strand probe made with the specific primer. Despite that the level of HCV infection was considered to be low, we were able to detect and localize viral positive and negative RNA strands and viral proteins in altered membranes of the rough endoplasmic reticulum in infected liver cells, showing evidence of viral replication in vivo.
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