Evolution of hepatitis C viral quasispecies after liver transplantation
- PMID: 12404223
- DOI: 10.1053/gast.2002.36546
Evolution of hepatitis C viral quasispecies after liver transplantation
Abstract
Background & aims: To determine whether HCV quasispecies diversity correlated positively with liver disease progression after orthotopic liver transplantation (OLT).
Methods: We studied 11 patients undergoing OLT for HCV-related cirrhosis with recurrent hepatitis C in 2 groups according to the stage of hepatic fibrosis on follow-up. The mild group had stage 1 or 2 fibrosis; the severe group, stage 3 or 4 fibrosis. HCV quasispecies diversity was assessed by cloning and sequencing in pretransplantation and posttransplantation serum samples.
Results: In the mild fibrosis group, intrasample hypervariable region 1 (HVR1) genetic distance and nonsynonymous substitutions increased after OLT, whereas in the severe fibrosis group, these parameters decreased in follow-up. In contrast, intrasample diversity progressed similarly in both groups in the adjacent sequences flanking HVR1. There was an inverse correlation between the stage of hepatic fibrosis and amino acid complexity after OLT. Among all patients, the estimated rate of amino acid change was greater initially and became more constant after 36 months.
Conclusions: After OLT, a more complex HCV HVR1 quasispecies population was associated with mild disease recurrence. Among those patients with severe recurrent hepatitis C, HCV appeared to be under greater immune pressure. The greatest change in viral amino acid sequences occurred in the first 36 months after OLT.
Comment in
-
Hepatitis C virus in solid organ transplantation: not always a bad thing?Gastroenterology. 2002 Nov;123(5):1729-33. doi: 10.1053/gast.2002.36852. Gastroenterology. 2002. PMID: 12404247 Review. No abstract available.
Similar articles
-
Hepatitis C virus quasi-species dynamics predict progression of fibrosis after liver transplantation.J Infect Dis. 2004 Jun 1;189(11):2037-46. doi: 10.1086/386338. Epub 2004 May 10. J Infect Dis. 2004. PMID: 15143471
-
Influence of the dynamics of the hypervariable region 1 of hepatitis C virus (HCV) on the histological severity of HCV recurrence after liver transplantation.J Med Virol. 2001 Oct;65(2):266-75. doi: 10.1002/jmv.2029. J Med Virol. 2001. PMID: 11536232
-
Genetic complexity and serum reactivity of HVR1 quasispecies of hepatitis C virus in patients with cirrhosis.Am J Gastroenterol. 2002 Jun;97(6):1489-95. doi: 10.1111/j.1572-0241.2002.05794.x. Am J Gastroenterol. 2002. PMID: 12094871
-
E2 quasispecies specificity of hepatitis C virus association with allografts immediately after liver transplantation.Liver Transpl. 2004 Feb;10(2):208-16. doi: 10.1002/lt.20060. Liver Transpl. 2004. PMID: 14762858
-
Pretransplantation hepatitis C virus quasispecies may be predictive of outcome after liver transplantation.Hepatology. 2000 Aug;32(2):375-81. doi: 10.1053/jhep.2000.9089. Hepatology. 2000. PMID: 10915745
Cited by
-
Hepatitis C virus envelope glycoprotein co-evolutionary dynamics during chronic hepatitis C.Virology. 2008 Jun 5;375(2):580-91. doi: 10.1016/j.virol.2008.02.012. Epub 2008 Mar 17. Virology. 2008. PMID: 18343477 Free PMC article.
-
HCV in liver transplantation.Semin Immunopathol. 2013 Jan;35(1):101-10. doi: 10.1007/s00281-012-0329-5. Epub 2012 Jul 25. Semin Immunopathol. 2013. PMID: 22829333
-
Theoretical aspects of immunity.Annu Rev Chem Biomol Eng. 2010;1:247-76. doi: 10.1146/annurev-chembioeng-073009-100952. Annu Rev Chem Biomol Eng. 2010. PMID: 22432581 Free PMC article. Review.
-
Evidence of an Exponential Decay Pattern of the Hepatitis Delta Virus Evolution Rate and Fluctuations in Quasispecies Complexity in Long-Term Studies of Chronic Delta Infection.PLoS One. 2016 Jun 30;11(6):e0158557. doi: 10.1371/journal.pone.0158557. eCollection 2016. PLoS One. 2016. PMID: 27362848 Free PMC article.
-
Analysis of a non-structural gene reveals evidence of possible hepatitis C virus (HCV) compartmentalization.J Med Virol. 2012 Feb;84(2):242-52. doi: 10.1002/jmv.22269. J Med Virol. 2012. PMID: 22170544 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases