Relationship between hepatitis B virus reverse transcriptase 181 mutation and S gene mutation in hepatitis B virus chronically infected patients

被引:0
|
作者
Wang, L-P. [1 ,2 ]
Han, F-Z. [2 ]
Yan, X-B. [2 ]
Fan, Y-C. [1 ]
Wang, K. [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Hepatol, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China
[2] Xuzhou Med Coll, Affiliated Hosp, Dept Infect Dis, Xuzhou, Peoples R China
关键词
Hepatitis B virus; genotype; rt181; resistant mutation; reverse transcriptase; HEPATOCELLULAR-CARCINOMA; LAMIVUDINE THERAPY; DRUG-RESISTANT; HBV MUTANTS; SELECTION; VACCINE; MONOTHERAPY; DELETION; RISK;
D O I
10.14715/cmb/2016.62.12.4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study aims to explore clinical significance of HBV rt181 mutation. Serum samples were collected from 226 CHB patients with no anti-viral treatment, and 72 patients with adefovir dipivoxil treatment over 1 year. HBV genes of reverse transcriptase regions were amplified by nested PCR. HBV DNA in pre-S/S regions sequences were determined by sequencing. Mutations in HBV were characterized by mutational analysis. Results indicated that resistant mutation was found in 16 samples (7.08%) with no anti-viral treatment. It showed higher prevalence in patients with adefovir dipivoxil treated samples 30/72(41.67%). Mutation sites of pre-existing and adefovir dipivoxil induced resistance were different (adefovir dipivoxil induced resistance mode is rtA181T/V, and pre-existing mode is the other). Resistance mutation was found just in genotype C patients. Among 25 containing rtA181T/V mutation patients, 7 rtA181T mutation cases with sW172L, 6 rtA181T mutation cases with sW172*, 12 rtA181V mutation cases with sL173F. In conclusion, mutation sites of pre-existing and adefovir dipivoxil induced resistance were different. HBV genotype C is prone to occur resistance mutation than genotype B. rtA181T mutation was accompanied with not only sW172 * mutation, but also sW172L mutation, rtA181V mutation was accompanied with sL173F mutation or Pre-S2 initiation codon to termination mutation.
引用
收藏
页码:18 / 23
页数:6
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