Genotyping hepatitis B virus dual infections using population-based sequence data

被引:17
作者
Beggel, Bastian [1 ]
Neumann-Fraune, Maria [2 ]
Doering, Matthias [1 ]
Lawyer, Glenn [1 ]
Kaiser, Rolf [2 ]
Verheyen, Jens [2 ]
Lengauer, Thomas [1 ]
机构
[1] Max Planck Inst Informat, Dept Computat Biol & Appl Algorithm, Saarbrucken, Germany
[2] Univ Cologne, Inst Virol, D-50931 Cologne, Germany
关键词
HEPATOCELLULAR-CARCINOMA; HBV GENOTYPE; ANTIGEN; COINFECTION; STRAINS; MANAGEMENT; RESISTANCE; LAMIVUDINE; MUTATIONS; THERAPY;
D O I
10.1099/vir.0.043042-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The hepatitis B virus (HBV) is classified into distinct genotypes A-H that are characterized by different progression of hepatitis B and sensitivity to interferon treatment. Previous computational genotyping methods are not robust enough regarding HBV dual infections with different genotypes. The correct classification of HBV sequences into the present genotypes is impaired due to multiple ambiguous sequence positions. We present a computational model that is able to identify and genotype inter- and intragenotype dual infections using population-based sequencing data. Model verification on synthetic data showed 100 % accuracy for intergenotype dual infections and 36.4% sensitivity in intragenotype dual infections. Screening patient sera (n=241) revealed eight putative cases of intergenotype dual infection (one A-D, six A-G and one D-G) and four putative cases of intragenotype dual infection (one A-A, two D-D and one E-E). Clonal experiments from the original patient material confirmed three out of three of our predictions. The method has been integrated into geno2pheno([hbv]), an established web-service in clinical use for analysing HBV sequence data. It offers exact and detailed identification of HBV genotypes in patients with dual infections that helps to optimize antiviral therapy regimens. geno2pheno([hbv]) is available under http://www.genafor.org/g2p_hbv/index.php.
引用
收藏
页码:1899 / 1907
页数:9
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