An in-house real-time polymerase chain reaction: standardisation and comparison with the Cobas Amplicor HBV monitor and Cobas AmpliPrep/Cobas TaqMan HBV tests for the quantification of hepatitis B virus DNA

被引:3
|
作者
de Torres Santos, Ana Paula [1 ]
Levi, Jose Eduardo [2 ]
Lemos, Marcilio Figueiredo [3 ]
Calux, Samira Julien [3 ]
Oba, Isabel Takano [3 ]
Moreira, Regina Celia [3 ]
机构
[1] Univ Sao Paulo, Fac Med, Hosp Clin, Div Lab Cent,Lab Imunol, Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Inst Trop Med, Virol Lab, Sao Paulo, SP, Brazil
[3] Adolfo Lutz Inst, Ctr Virol, Nucleo Doencas Sanguineas & Sexuais, Sao Paulo, SP, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2016年 / 111卷 / 02期
基金
巴西圣保罗研究基金会;
关键词
HBV viral load; Cobas Amplicor HBV monitor; Cobas TaqMan HBV; HBVDNA; in-house rtPCR; RESISTANCE MUTATIONS; INFECTED PATIENTS; GENOTYPE-G; PCR ASSAY; QUANTITATION; SEQUENCE; PROBE; GENE;
D O I
10.1590/0074-02760150415
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
This study aimed to standardise an in-house real-time polymerase chain reaction (rtPCR) to allow quantification of hepatitis B virus (HBV) DNA in serum or plasma samples, and to compare this method with two commercial assays, the Cobas Amplicor HBV monitor and the Cobas AmpliPrep/Cobas TaqMan HBV test. Samples from 397 patients from the state of Sao Paulo were analysed by all three methods. Fifty-two samples were from patients who were human immunodeficiency virus and hepatitis C virus positive, but HBV negative. Genotypes were characterised, and the viral load was measure in each sample. The in-house rtPCR showed an excellent success rate compared with commercial tests; inter-assay and intra-assay coefficients correlated with commercial tests (r = 0.96 and r = 0.913, p < 0.001) and the in-house test showed no genotype-dependent differences in detection and quantification rates. The in-house assay tested in this study could be used for screening and quantifying HBV DNA in order to monitor patients during therapy.
引用
收藏
页码:134 / 140
页数:7
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