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Published on: July 16, 2012
Evolution of hepatitis C virus hypervariable region 1 in immunocompetent children born to HCV-infected mothers
M I Gismondi1, P D Becker, J M Díaz Carrasco
1Laboratorio de Biología Molecular, División Patología, Hospital de Niños Ricardo Gutiérrez, Buenos Aires, Argentina.
Insights
Hepatitis C virus (HCV) hypervariable region 1 (HVR1) showed remarkable amino acid stability in children over five years. This suggests evolutionary constraints and potential immune tolerance in pediatric HCV infections.
Area of Science:
- Virology
- Immunology
- Genetics
Background:
- Hepatitis C virus (HCV) hypervariable region 1 (HVR1) is known for its genomic variability.
- This variability is thought to reflect the complex interplay between the virus and host during chronic infection.
- Pediatric HCV infection can lead to liver disease.
Purpose of the Study:
- To investigate the evolutionary dynamics of HCV HVR1 and adjacent regions in children over a 5-year period.
- To understand the factors influencing viral evolution in pediatric HCV cases.
Main Methods:
- Longitudinal analysis of plasma samples from two HCV-positive children over 5 years.
- Sequencing and analysis of HVR1 and adjacent regions.
- Calculation of d(N)/d(S) rates and codon-level selection pressure analysis.
Main Results:
- HVR1 amino acid sequences remained nearly constant over time, despite nucleotide variations.
- Overall d(N)/d(S) ratios were below 1, indicating purifying selection.
- Analysis revealed few sites under selection and predominantly invariable positions within HVR1.
- HVR1 sequences exhibited expected antigenic properties.
Conclusions:
- Peculiar evolutionary dynamics were observed in pediatric HCV, characterized by nucleotide invariability and purifying selection on HVR1.
- The lack of HVR1 variability may indicate viral adaptation or immune tolerance in young patients.
Abstract:
Hepatitis C virus (HCV) hypervariable region 1 (HVR1) is the most variable region of the viral genome and its heterogeneity reflects the virus-host interplay during chronicity. Paediatric HCV-infected patients develop liver disease with typical clinical features. Here, the evolution of HVR1 and its adjacent regions were ascertained in plasma samples of two HCV-positive children during a 5-year follow-up period. We report an almost complete conservation of the HVR1 amino acid sequence over time, with underlying nucleotide variability both within and outside HVR1, suggesting some kind of constraint on virus evolution, particularly within HVR1. Although overall d(N)/d(S) rates [rates of nonsynonymous nucleotide substitutions per nonsynonymous site (d(N)) and synonymous nucleotide substitutions per synonymous site (d(S))] were <1 in both patients, a high resolution analysis of selection pressures exerted at the codon level revealed few sites subject to selection and an absolute predominance of invariable positions within HVR1. The HVR1 amino acid sequences showed the antigenic properties expected for this region. Taken together, these data suggest peculiar evolutionary dynamics in our patients, which could be attributed to a mechanism of nucleotide invariability along with purifying selection operating on the HVR1. The lack of HVR1 variability may reflect the adaptation of the virus to a particular environment within each patient or a phenomenon of immune tolerance generated in these immunocompetent patients earlier in life.
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