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Published on: July 16, 2012
HCV selection and HVR1 evolution in a chimpanzee chronically infected with HCV-1 over 12 years
Ling Lu1, Nakano Tatsunori, Chunhua Li
1Division of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Utah, Utah, USA.
Insights
Hepatitis C virus (HCV) selection occurred in a chimpanzee over 12 years, with distinct viral strains and hypervariable region-1 (HVR1) patterns emerging during acute and chronic infections.
Area of Science:
- Virology
- Immunology
- Genetics
Background:
- Hepatitis C virus (HCV) infection is a global health concern.
- Understanding viral evolution is crucial for developing effective treatments.
- Chimpanzees are valuable models for studying HCV infection.
Purpose of the Study:
- To investigate the selection and evolution of HCV and its hypervariable region-1 (HVR1) in a chimpanzee over a 12-year period.
- To analyze viral changes following inoculation with contaminated factor VIII concentrate.
Main Methods:
- HCV fragments, including HVR1, were amplified from inoculum and chimpanzee plasma samples (12 years).
- Cloning and sequencing were performed on amplified HCV fragments.
- Viral sequences were analyzed to track subtype evolution and HVR1 changes.
Main Results:
- The inoculum contained multiple HCV subtypes (1a, 1b, 2a, 2b, 3a).
- The chimpanzee initially harbored two 1a strains, which evolved into a single HCV-1 strain.
- Over time, HVR1 patterns showed irregular changes, with a decrease in diversity and increased similarity to the 1a consensus sequence in later years, correlating with higher viral load.
Conclusions:
- HCV selection was evident at multiple stages: transmission, acute hepatitis, and chronic infection.
- Selection occurred among subtypes, isolates, and quasispecies.
- Viral evolution, particularly in HVR1, reflects adaptation and immune pressure during chronic HCV infection.
Aim:
To study hepatitis C virus (HCV) selection and hypervariable region-1 (HVR1) evolution in a chimpanzee chronically infected with HCV-1 over 12 years after inoculation with a human factor VIII concentrate contaminated with HCV.
Methods:
From the inoculum, the earliest chimpanzee plasma and 12 annual plasma samples, HCV fragments including HVR1 were amplified followed by cloning and sequencing.
Results:
Five HCV subtypes - 1a, 1b, 2a, 2b, 3a - and multiple 1a strains were identified in the inoculum. Two 1a strains were found in the earliest chimpanzee sample, while a single HCV-1 strain was detected in the 12 annual samples. None of the chimpanzee sequences were identical to those found in the inoculum. Over 12 years, HVR1 patterns changed irregularly, but a few patterns showed identical nucleotide or amino acid sequences. In the last three years, the variety of HVR1 patterns decreased, while the proportion of major patterns increased. These corresponded to a higher virus load and a lower number of amino acid substitutions. Simultaneously, the HVR1 sequences became more similar to the consensus sequence of the 1a subtype.
Conclusion:
HCV selection was observed from the inoculum to the inoculated chimpanzee and from the early acute hepatitis to the persistent chronic infection. The selection occurred at three levels: among subtypes after transmission, among isolates during acute hepatitis and among quasispecies in chronic infection.
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