Viral sequence evolution in acute hepatitis C virus infection
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Viral sequence evolution in acute hepatitis C virus infection. / Kuntzen, Thomas; Timm, Joerg; Berical, Andrew; Lewis-Ximenez, Lia L; Jones, Andrea; Nolan, Brian; Schulze zur Wiesch, Julian; Li, Bin; Schneidewind, Arne; Kim, Arthur Y; Chung, Raymond T; Lauer, Georg M; Allen, Todd M.
in: J VIROL, Jahrgang 81, Nr. 21, 11.2007, S. 11658-68.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Viral sequence evolution in acute hepatitis C virus infection
AU - Kuntzen, Thomas
AU - Timm, Joerg
AU - Berical, Andrew
AU - Lewis-Ximenez, Lia L
AU - Jones, Andrea
AU - Nolan, Brian
AU - Schulze zur Wiesch, Julian
AU - Li, Bin
AU - Schneidewind, Arne
AU - Kim, Arthur Y
AU - Chung, Raymond T
AU - Lauer, Georg M
AU - Allen, Todd M
PY - 2007/11
Y1 - 2007/11
N2 - CD8(+)-T-cell responses play an important role in the containment and clearance of hepatitis C virus (HCV) infection, and an association between viral persistence and development of viral escape mutations has been postulated. While escape from CD8+ -T-cell responses has been identified as a major driving force for the evolution of human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV), a broader characterization of this relationship is needed in HCV infection. To determine the extent, kinetics, and driving forces of HCV sequence evolution, we sequenced the entire HCV genome longitudinally in four subjects monitored for up to 30 months after acute infection. For two subjects the transmission sources were also available. Of 53 total non-envelope amino acid substitutions detected, a majority represented forward mutations away from the consensus sequence. In contrast to studies in HIV and SIV, however, only 11% of these were associated with detectable CD8+ T-cell responses. Interestingly, 19% of non-envelope mutations represented changes toward the consensus sequence, suggesting reversion in the absence of immune pressure upon transmission. Notably, the rate of evolution of forward and reverse mutations correlated with the conservation of each residue, which is indicative of structural constraints influencing the kinetics of viral evolution. Finally, the rate of sequence evolution was observed to decline over the course of infection, possibly reflective of diminishing selection pressure by dysfunctional CD8+ T cells. Taken together, these data provide insight into the extent to which HCV is capable of evading early CD8+ T-cell responses and support the hypothesis that dysfunction of CD8+ T cells may be associated with failure to resolve HCV infections.
AB - CD8(+)-T-cell responses play an important role in the containment and clearance of hepatitis C virus (HCV) infection, and an association between viral persistence and development of viral escape mutations has been postulated. While escape from CD8+ -T-cell responses has been identified as a major driving force for the evolution of human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV), a broader characterization of this relationship is needed in HCV infection. To determine the extent, kinetics, and driving forces of HCV sequence evolution, we sequenced the entire HCV genome longitudinally in four subjects monitored for up to 30 months after acute infection. For two subjects the transmission sources were also available. Of 53 total non-envelope amino acid substitutions detected, a majority represented forward mutations away from the consensus sequence. In contrast to studies in HIV and SIV, however, only 11% of these were associated with detectable CD8+ T-cell responses. Interestingly, 19% of non-envelope mutations represented changes toward the consensus sequence, suggesting reversion in the absence of immune pressure upon transmission. Notably, the rate of evolution of forward and reverse mutations correlated with the conservation of each residue, which is indicative of structural constraints influencing the kinetics of viral evolution. Finally, the rate of sequence evolution was observed to decline over the course of infection, possibly reflective of diminishing selection pressure by dysfunctional CD8+ T cells. Taken together, these data provide insight into the extent to which HCV is capable of evading early CD8+ T-cell responses and support the hypothesis that dysfunction of CD8+ T cells may be associated with failure to resolve HCV infections.
KW - Amino Acids/chemistry
KW - CD8-Positive T-Lymphocytes/metabolism
KW - Epitopes, T-Lymphocyte/chemistry
KW - Evolution, Molecular
KW - Genome, Viral
KW - HLA Antigens/chemistry
KW - Hepacivirus/genetics
KW - Hepatitis C/genetics
KW - Humans
KW - Interferon-gamma/metabolism
KW - Leukocytes, Mononuclear/metabolism
KW - Molecular Sequence Data
KW - Mutation
KW - Phylogeny
KW - T-Lymphocytes/metabolism
U2 - 10.1128/JVI.00995-07
DO - 10.1128/JVI.00995-07
M3 - SCORING: Journal article
C2 - 17699568
VL - 81
SP - 11658
EP - 11668
JO - J VIROL
JF - J VIROL
SN - 0022-538X
IS - 21
ER -