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Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
Published on: February 1, 2017
Hepatitis C Virus entry: the early steps in the viral replication cycle
1Department of Microbiology and Immunology, Tulane University Health Sciences Center, New Orleans, Louisiana, USA. asabahi@gmail.com
Insights
Hepatitis C virus (HCV) entry into cells was difficult to study. New HCV pseudo particle (HCVpp) and cell culture (HCVcc) systems now allow researchers to identify key cellular co-receptors involved in HCV infection.
Area of Science:
- Virology
- Cell Biology
- Immunology
Background:
- Hepatitis C virus (HCV) infects approximately 170 million people globally.
- Most acute HCV infections are asymptomatic, leading to chronic infection in many individuals.
- Studying HCV replication in vitro was challenging before the development of new systems.
Purpose of the Study:
- To review the literature on Hepatitis C virus (HCV) entry.
- To identify cellular co-receptors involved in HCV binding and entry.
- To contextualize findings based on experimental systems used.
Main Methods:
- Review of existing scientific literature.
- Analysis of studies using purified viral envelope proteins.
- Evaluation of data from HCV pseudo particle (HCVpp) and HCV cell culture (HCVcc) systems.
- Consideration of findings from patient sera.
Main Results:
- HCVpp and HCVcc systems have significantly advanced the understanding of HCV's early replication steps.
- These systems have facilitated the identification of cellular co-receptors essential for HCV binding and entry.
- The review synthesizes data from various experimental models.
Conclusions:
- The development of in vitro systems like HCVpp and HCVcc has been crucial for studying HCV entry.
- Understanding cellular co-receptors is key to deciphering the mechanisms of HCV infection.
- Further research into HCV entry pathways can inform therapeutic strategies.
Abstract:
Approximately 170 million are infected with the hepatitis C virus (HCV) world wide and an estimated 2.7 million are HCV RNA positive in the United States alone. The acute phase of the HCV infection, in majority of individuals, is asymptomatic. A large percentage of those infected with HCV are unable to clear the virus and become chronically infected. The study of the HCV replication cycle was hampered due to difficulties in growing and propagating the virus in an in vitro setting. The advent of the HCV pseudo particle (HCVpp) and HCV cell culture (HCVcc) systems have made possible the study of the HCV replication cycle, in vitro. Studies utilizing the HCVpp and HCVcc systems have increased our insight into the early steps of the viral replication cycle of HCV, such as the identification of cellular co-receptors for binding and entry. The aim of this article is to provide a review of the outstanding literature on HCV entry, specifically looking at cellular co-receptors involved and putting the data in the context of the systems used (purified viral envelope proteins, HCVpp system, HCVcc system and/or patient sera) and to also give a brief description of the cellular co-receptors themselves.
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