Dynamics of hepatitis C virus quasispecies turnover during interferon-alpha treatment

J Viral Hepat. 2003 Nov;10(6):413-22. doi: 10.1046/j.1365-2893.2003.00457.x.

Abstract

Interferon-alpha (IFN) has been shown to accelerate the evolution of hepatitis C virus (HCV) variants (quasispecies) in nonresponder patients. Different sensitivities of HCV variants to IFN are discussed as a possible mechanism. In the present study, quasispecies were investigated in detail by a newly established and validated direct solid-phase sequencing of the hypervariable region 1 (HVR1), during the initial 3 months of IFN therapy. According to single strand conformation polymorphism (SSCP) analysis, 14 of 26 (54%) virologic nonresponders with quasispecies evolution were identified. Six representative patients with SSCP changes were selected for frequent HVR1 sequencing. Pre-existing variants were identified by cloning and sequencing of the pretreatment serum HCV sample. In one patient the major type was substituted by a minor variant within 3 days of treatment while in the majority of patients the pretreatment major type did not decline before days 26-57 of treatment. Total serum HCV RNA levels remained constant in all patients. In conclusion, although quasispecies evolution during IFN therapy is common, it occurs after a wide range of time intervals after initiation of therapy. Thus, nonresponse to IFN cannot exclusively be explained by changes in the quasispecies.

MeSH terms

  • Adult
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • Base Sequence
  • DNA Mutational Analysis
  • Evolution, Molecular*
  • Female
  • Genetic Variation / drug effects
  • Genotype
  • Hepacivirus / classification
  • Hepacivirus / drug effects*
  • Hepacivirus / genetics*
  • Hepacivirus / isolation & purification
  • Hepatitis C / drug therapy*
  • Hepatitis C / virology*
  • Humans
  • Interferon-alpha / pharmacology
  • Interferon-alpha / therapeutic use*
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Polymorphism, Single-Stranded Conformational
  • RNA, Viral / blood
  • RNA, Viral / chemistry
  • RNA, Viral / isolation & purification
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Alignment
  • Sequence Analysis, DNA
  • Viral Load
  • Viral Proteins / chemistry
  • Viral Proteins / genetics

Substances

  • Antiviral Agents
  • HVR1 protein, Hepatitis C virus
  • Interferon-alpha
  • RNA, Viral
  • Viral Proteins