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  4. Micro-evolution of the hepatitis B virus genome in hepatitis B e-antigen-positive carriers: Comparison of genotypes B and C at various immune stages
 
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Micro-evolution of the hepatitis B virus genome in hepatitis B e-antigen-positive carriers: Comparison of genotypes B and C at various immune stages

Journal
Journal of Gastroenterology and Hepatology (Australia)
Journal Volume
30
Journal Issue
1
Pages
172-177
Date Issued
2015
Author(s)
CHUN-JEN LIU  
Chen T.-C.
PEI-JER CHEN  
HURNG-YI WANG  
TAI-CHUNG TSENG  
Cheng H.-R.
CHEN-HUA LIU  
DING-SHINN CHEN  
JIA-HORNG KAO  
DOI
10.1111/jgh.12654
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84919655097&doi=10.1111%2fjgh.12654&partnerID=40&md5=236fc47bb8dc718b4670e0b282876131
https://scholars.lib.ntu.edu.tw/handle/123456789/505147
Abstract
Background and Aim: Patients with hepatitis B virus (HBV) genotype B infection experience hepatitis B e-antigen (HBeAg) seroconversion at an earlier stage than do patients with genotype C infection. Therefore, this study investigated whether the differential phenotypes are related to HBV genomic evolution. Methods: Thirty-three HBeAg-positive patients with a mean follow-up of 3.1 years were enrolled: 16 at the immune tolerance stage (group I) and 17 at the immune clearance stage (group II). The evolution rates of paired viral genomes at enrollment and at the final follow-up in the full-length genome (μf), nonoverlapping regions (synonymous [μs] and nonsynonymous [μa]), and overlapping regions (μ) were calculated. The evolution rates were then compared according to serum alanine aminotransferase (ALT) levels and HBV genotype. Results: The overall μf evolution rate was lower in group I than in group II (1.4×10-5±3.3×10-5 vs 1.2×10-3±1.2×10-3 nucleotide substitution/site/year, P<0.001). We observed similar results for the μs, μa, and μ evolution rates. All evolution parameters were comparable between genotypes B and C. We determined a positive correlation between μa/y and the area under the average ALT time curve in genotype B (R2=0.6935, P<0.0001), but not in genotype C (R2=0.1606, P=0.124). Conclusion: The evolution rate of the HBV genome is higher at the immune clearance stage than at the immune tolerance stage. Host immune selection might play a role in triggering evolution of genotype B. ? 2014 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd.
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; hepatitis B(e) antigen; nucleotide; alanine aminotransferase; hepatitis B(e) antigen; adult; alanine aminotransferase blood level; Article; clinical article; controlled study; evolution; female; hepatitis B; Hepatitis B virus genotype B; Hepatitis B virus genotype C; hepatitis C; human; immune clearance; immune status; immunity; immunological tolerance; male; nonhuman; phenotype; priority journal; virus genome; blood; follow up; genetics; genotype; hepatitis B; Hepatitis B virus; heterozygote; immunology; molecular evolution; time; virology; virus genome; young adult; Adult; Alanine Transaminase; Carrier State; Evolution, Molecular; Female; Follow-Up Studies; Genome, Viral; Genotype; Hepatitis B; Hepatitis B e Antigens; Hepatitis B virus; Humans; Male; Time Factors; Young Adult
Publisher
Blackwell Publishing
Type
journal article

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