Detection of lamivudine- or adefovir-resistant hepatitis B virus mutations by a liquid array

被引:9
作者
Liu, Hongyan [1 ,2 ]
Mao, Richeng [1 ,2 ]
Fan, Lili [3 ]
Xia, Jiahui [3 ]
Li, Yiliang [3 ]
Yin, Yongxi [3 ]
Li, Xinyan [1 ,2 ]
Zhao, Xu [1 ,2 ]
Guo, Hongying [1 ,2 ]
Zhu, Haoxiang [1 ,2 ]
Zhang, Yongmei [1 ,2 ]
Kang, Yaoyue [1 ,2 ]
Zhang, Jiming [1 ,2 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Infect Dis, Shanghai 200040, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Key Lab Med Mol Virol, Shanghai 200040, Peoples R China
[3] Shanghai Fudan Zhang Jiang Biopharmaceu Corp, Shanghai 201210, Peoples R China
关键词
Beads or microspheres; Chronic hepatitis B; Hepatitis B virus; Liquid array; Luminex; Lamivudine- or adefovir-resistance; LONG-TERM THERAPY; LINE PROBE ASSAY; DIPIVOXIL; PCR; MUTANTS; QUANTITATION; STRAINS;
D O I
10.1016/j.jviromet.2011.04.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel polymerase chain reaction (PCR)-Luminex assay was developed for rapid, accurate, and high-throughput detection of the most important hepatitis B virus (HBV) variants, including those with reverse transcriptase (RI) domain L180M, M204I/V, A181T/V/S, I233V and N2361 mutations associated with resistance to lamivudine (LAM) or adefovir (ADV). Using mixtures of mutant and wild-type HBV, this method was sufficiently sensitive for detecting 103 HBV m1(-1) and could detect minor mutants when they comprised 5% of the total viral population. Comparison of the PCR-Luminex assay with INNO-LiPA for detecting clinical LAM- or ADV-resistant chronic hepatitis B virus infection in 64 patients confirmed the following: the 2 methods were 97.9% (48 of 49) and 93.3% (14 of 15) concordant for detecting LAM- or ADV-resistance mutations, respectively. The agreement with direct sequencing was 70.3% (45 of 64). The PCR-Luminex assay or multi-analyte suspension array can detect simultaneously and efficiently minor populations HBV mutants early during infection in many clinical samples. It is a simple, cost-effective method for resistance surveillance or selecting appropriate antiviral agents and initiating timely rescue treatment before the development drug-resistance related virus or biochemical breakthrough. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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