Genotype-specific mutations in the polymerase gene of hepatitis B virus potentially associated with resistance to oral antiviral therapy

被引:39
|
作者
Mirandola, Silvia [1 ]
Sebastiani, Giada [2 ]
Rossi, Cristina [3 ]
Velo, Emanuela
Erne, Elke Maria [4 ]
Vario, Alessandro
Tempesta, Diego [2 ]
Romualdi, Chiara [5 ]
Campagnolo, Davide [1 ,6 ]
Alberti, Alfredo [1 ,6 ]
机构
[1] VIMM, I-35129 Padua, Italy
[2] Angelo Hosp, Hepatol & Clin Nutr Dept, Venice, Italy
[3] S Maria di Ca Foncello Hosp, Infect Dis Unit, Treviso, Italy
[4] Azienda Osped Padova, Infect & Trop Dis Unit, Padua, Italy
[5] Univ Padua, Dept Biol, I-35100 Padua, Italy
[6] Univ Padua, Dept Mol Med, I-35100 Padua, Italy
关键词
HBV-genotype; Chronic hepatitis B; Nucleot(s)ide analogues therapy; YMDD mutations; LONG-TERM LAMIVUDINE; REVERSE-TRANSCRIPTASE SEQUENCES; TREATMENT-NAIVE PATIENTS; ADEFOVIR DIPIVOXIL; CHINESE PATIENTS; LIVER-DISEASE; ENTECAVIR; HBV; MONOTHERAPY; TENOFOVIR;
D O I
10.1016/j.antiviral.2012.09.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The evolution of hepatitis B virus (HBV) and the role of different variants during antiviral therapy may be influenced by HBV genotype. We have therefore analysed substitutions potentially related to nudeos(t)ide analogues (NAs) resistance at 42 positions within RI-region in a cohort of patients with chronic hepatitis B in relation to HBV-genotype. RT mutations analysis was performed by direct sequencing in 200 NAs-naive patients and in 64 LAM or LAM + ADV experienced patients with NAs resistance, infected mainly by HBV-genotypes D and A. 27 polymorphic-sites were identified among the 42 positions analysed and 64 novel mutations were detected in 23 positions. Genotype-D displayed the highest mutation frequency (6.4%) among all HBV-genotypes analysed. Single or multiple mutations were detected in 80% of naive patients. Overall, the most frequent single mutations were at residues rt54, rt53 and rt91 which may associate with significantly lower HBV-DNA levels (p = 0.001). Comparison with sequencing data of patients failing LMV or LAM + ADV therapy revealed an higher frequency of novel genotype-specific mutations if compared with naive patients: 3 mutations under LAM monotherapy in HBV-D (rtS85F; rtL911; rtC256G) and 3 mutations under ADV therapy in HBV-A (rtI53V; rtW153R; rtF221Y). In HBV-D treated patients the dominant resistance mutation was rtL80V (31.4%) and rtM204I (60%) in LAM + ADV group while LAM-treated patients showed a preference of rtM204V (51.9%). Interestingly, none of HBV-A patients had mutation rtM204I under ADV add-on treatment but all of them had the "V" AA substitution. These results suggested that in patients with CHB, HBV-genotype might be relevant in the evolution and development of drug resistance showing also different mutation patterns in the YMDD motif between HBV genotype D and A. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:422 / 429
页数:8
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