4.6 Article

Naturally occurring mutations in the reverse transcriptase region of hepatitis B virus polymerase from treatment- naive Korean patients infected with genotype C2

Journal

WORLD JOURNAL OF GASTROENTEROLOGY
Volume 23, Issue 23, Pages 4222-4232

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.3748/wjg.v23.i23.4222

Keywords

Hepatitis B virus; Polymerase; Reverse transcriptase; Potential nucleos (t) ide analog resistance; Chronic hepatitis; Hepatocellular carcinoma

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF)-Ministry of Education, Science and Technology [NRF-2015R1C1A1A02037267]
  2. Korea Health Technology R&D Project through the Korea Health Industry Development Institute-Ministry of Health and Welfare, South Korea [HI14C0955]

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AIM To report naturally occurring mutations in the reverse transcriptase region (RT) of hepatitis B virus (HBV) polymerase from treatment naive Korean chronic patients infected with genotype C2. METHODS Here, full-length HBV reverse transcriptase RT sequences were amplified and sequenced from 131 treatment naive Korean patients chronically infected with hepatitis B genotype C2. The patients had two distinct clinical statuses: 59 patients with chronic hepatitis (CH) and 72 patients with hepatocellular carcinoma (HCC). The deduced amino acids (AAs) at 42 previously reported potential nucleos(t) ide analog resistance (NAr) mutation positions in the RT region were analyzed. RESULTS Potential NAr mutations involving 24 positions were found in 79 of the 131 patients (60.3%). Notably, AA substitutions at 2 positions (rt184 and rt204) involved in primary drug resistance and at 2 positions (rt80 and rt180) that functioned as secondary/compensatory mutations were detected in 10 patients (1 CH patient and 9 HCC patients) and 7 patients (1 CH and 6 HCC patients), respectively. The overall mutation frequencies in the HCC patients (3.17%, 96/3024 mutations) were significantly higher than the frequencies in the CH patients (2.09%, 52/2478 mutations) (P = 0.003). In addition, a total of 3 NAr positions, rt80, rt139 and rt204 were found to be significantly related to HCC from treatment naive Korean patients. CONCLUSION Our data showed that naturally occurring NAr mutations in South Korea might contribute to liver disease progression (particularly HCC generation) in chronic patients with genotype C2 infections.

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