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Two Methods of Heterokaryon Formation to Discover HCV Restriction Factors
Published on: July 16, 2012
Variations in the core region of hepatitis C virus genomes in patients with chronic hepatitis
M Kurosaki1, N Enomoto, F Marumo
1Second Department of Internal Medicine, Faculty of Medicine, Tokyo Medical and Dental University, Japan.
Insights
Hepatitis C virus (HCV) core region sequences change during chronic infection, with greater diversity observed in patients with higher alanine aminotransferase levels. These findings suggest core region variations may influence HCV's cytopathic effects.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Hepatitis C virus (HCV) exists as quasispecies, with rapid sequence changes noted in the hypervariable region.
- The HCV core region's potential role in immune recognition and sequence variation remained unclear.
Purpose of the Study:
- To investigate sequence diversity and temporal changes within the HCV core region during chronic infection.
- To determine if core region variations correlate with disease severity markers like alanine aminotransferase (ALT) levels.
Main Methods:
- RNA extraction from plasma of four chronic HCV patients.
- cDNA synthesis, polymerase chain reaction (PCR) amplification of the core region.
- Single strand conformation polymorphism (SSCP) analysis to assess sequence diversity.
Main Results:
- SSCP analysis revealed distinct nucleotide sequences within the HCV core region in each patient.
- Quasispecies populations within the core region exhibited temporal changes throughout the chronic infection course.
- Sequence variation was more pronounced in patients with high serum ALT levels compared to those with low levels.
Conclusions:
- Sequential variations occur within the HCV core region in infected individuals.
- The population of HCV quasispecies, based on core region sequences, evolves during chronic infection.
- Core region sequence changes may be linked to the cytopathic effects of hepatitis C virus.
Abstract:
In each infected patient, the population of hepatitis C virus is composed of quasispecies that differ in their nucleotide sequences. Among regions in hepatitis C virus genomes, nucleotide sequences of the hypervariable region have been shown to change quickly during the course of infection. It is not known, however, whether these variations exist in the core region that has recently been suggested to contain human lymphocyte antigen class 1 restricted sites for cytotoxic T cell recognition. To clarify this, RNA was extracted from the plasma of four patients with chronic hepatitis C. After cDNA synthesis, DNA fragments that contain the core region were amplified by the polymerase chain reaction and the diversity of the core region was analyzed by the single strand conformation polymorphism analysis. Using this method, single or multiple DNA bands were observed in each patient, and representative bands showed different nucleotide sequences. Comparison of single strand conformation polymorphism patterns revealed that the population of quasispecies changed during the course of chronic infection. These changes were more remarkable in patients with high serum alanine aminotransferase levels than those with low serum alanine aminotransferase levels. Thus, sequential variations exist in the core region of hepatitis C virus in same individuals, and the population of quasispecies as determined by the sequence of the core region changes during the course of infection, which might be related to cytopathic effects of hepatitis C virus.
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