Sitnik Roberta, Pinho João Renato Rebello, Bertolini Dennis Armando, Bernardini Antonio Plinio, Da Silva Luiz Caetano, Carrilho Flair José
Serviço de Virologia, Instituto Adolfo Lutz, Av. Brigadeiro Luiz Antonio, 4701, 01401-002 São Paulo, SP, Brazil.
J Clin Microbiol. 2004 Jun;42(6):2455-60. doi: 10.1128/JCM.42.6.2455-2460.2004.
A method for genotyping hepatitis B virus by partial HBsAg gene sequencing with primers common to all known genotypes was developed. Mutations related to anti-HBs resistance are also detected with this method. Samples from 103 Brazilian patients were analyzed. Precore and core region of these viruses were also sequenced in 101 patients. Genotypes A, B, C, D, and F were found with frequencies of 49.5, 2.9, 13.6, 24.3, and 9.7%, respectively. Genotypes B and C were found only in Asian patients, whereas genotypes A, D, and F were more common in patients without an Asian background. Precore mutants were found in 32 (31.7%) of 101 patients, with a higher frequency in those infected with genotype D (22 of 25 [88.0%]). Analysis of nucleotide 1858 showed presence of thymine in all patients with genotypes B, C, and D and in a few patients with genotypes A (10.0%) and F (30.0%), who showed more frequently the presence of cytosine. This nucleotide was closely related to the presence of precore mutants. Mutations in the basal core promoter were found in 64 of 101 (63.4%) samples. These mutations were more frequent in patients infected with genotype F (90.0%) and less frequent in patients infected with genotype B (33.3%). Deletions in this region were found in two genotype C-infected patients.
开发了一种通过使用所有已知基因型通用的引物对乙型肝炎病毒进行部分乙肝表面抗原(HBsAg)基因测序来进行基因分型的方法。该方法还可检测与抗HBs耐药性相关的突变。分析了103名巴西患者的样本。还对其中101名患者的这些病毒的前核心区和核心区进行了测序。发现A、B、C、D和F基因型,其频率分别为49.5%、2.9%、13.6%、24.3%和9.7%。B和C基因型仅在亚洲患者中发现,而A、D和F基因型在无亚洲背景的患者中更常见。在101名患者中的32名(31.7%)发现了前核心突变体,在感染D基因型的患者中频率更高(25名中的22名[88.0%])。对核苷酸1858的分析显示,所有B、C和D基因型患者以及少数A基因型(10.0%)和F基因型(30.0%)患者中存在胸腺嘧啶,而这些患者中更频繁地存在胞嘧啶。该核苷酸与前核心突变体的存在密切相关。在101个样本中的64个(63.4%)发现了核心启动子基础区的突变。这些突变在感染F基因型的患者中更常见(90.0%),而在感染B基因型的患者中较不常见(33.3%)。在两名感染C基因型的患者中发现了该区域的缺失。