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Updated: Jul 7, 2026

A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
[Expression and study of the functional proteins of hepatitis C virus in CHO cell line]
Jia Guo1, Ran Yan, Guo-Dong Xu
1State Key Laboratory of Virology, College of Life Scicences, Wuhan University, Wuhan 430072, China.
Abstract:
Recently, the interactions between hepatitis C virus (HCV) genes and the host cell factors were the focus of this field. Cell factors in the different biochemical pathway were approved to be interfered when HCV infection. To make sure which HCV gene(s) was the major factor during the interaction process, ten eukaryotic expression plasmids containing different functional genes of HCV: Core, E1, E2, p7, NS2, NS3, NS4A, NS4B, NS5A and NS5B were transfected into the CHO-K1 cells respectively. Then ten stable cell lines expressing different HCV functional proteins were constructed under the selective pressure of G418. DNA and mRNA of the HCV genes were both detected by PCR and RT-PCR respectively in the corresponding stable cell lines, freezation and anabiosis would not lose the HCV genes. Besides, the El, E2 and NS5B proteins were detected by Western-blot which demonstrated that the HCV genes have formed stable expression in the host cells. The activity of UDP-glucose ceramide glucosyltransferase (UGCG) in the stable cell lines increased in different degree by TLC assay. For example, the activity of UGCG in CHO-K1-E2 and CHO-K1-p7 was doubled according to the control cells,and in CHO-K1-NS2 and CHO-K1-NS5A was about 1.6 times compared with the control cells. The establishment of the stable cell lines containing different single HCV gene will provide foundation for investigating the interactions between the virus and the host factors, and for the filtration of antiviral medicine.
Insights
Researchers created stable cell lines expressing individual hepatitis C virus (HCV) genes to study host interactions. Certain HCV genes significantly increased UDP-glucose ceramide glucosyltransferase (UGCG) activity, aiding antiviral drug discovery.
Area of Science:
- Virology
- Molecular Biology
- Biochemistry
Background:
- Hepatitis C virus (HCV) infection disrupts host cell pathways.
- Identifying specific HCV genes responsible for these disruptions is crucial.
Purpose of the Study:
- To construct stable cell lines expressing individual HCV genes.
- To investigate the impact of single HCV genes on host cell factors, specifically UDP-glucose ceramide glucosyltransferase (UGCG) activity.
Main Methods:
- Transfection of CHO-K1 cells with eukaryotic expression plasmids for ten HCV genes (Core, E1, E2, p7, NS2, NS3, NS4A, NS4B, NS5A, NS5B).
- Selection of stable cell lines using G418.
- Confirmation of gene and protein expression using PCR, RT-PCR, and Western blot.
- Assay of UDP-glucose ceramide glucosyltransferase (UGCG) activity using TLC.
Main Results:
- Ten stable cell lines expressing individual HCV genes were successfully established.
- Stable expression of HCV genes (E1, E2, NS5B proteins) was confirmed.
- UGCG activity increased in cell lines expressing E2, p7, NS2, and NS5A, with E2 and p7 doubling activity.
Conclusions:
- The established stable cell lines provide a valuable platform for studying HCV-host interactions.
- Specific HCV genes modulate host UGCG activity, offering potential targets for antiviral drug development.
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