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乌拉圭乙型肝炎病毒的基因变异性:D/F、A/F基因型重组体

Genetic variability of hepatitis B virus in Uruguay: D/F, A/F genotype recombinants.

作者信息

Lopez L, Flichman D, Mojsiejczuk L, Gonzalez M V, Uriarte R, Campos R, Cristina J, Garcia-Aguirre Laura

机构信息

Laboratorio de Virología Molecular, Facultad de Ciencias, Centro de Investigaciones Nucleares, Udelar, Montevideo, Uruguay.

出版信息

Arch Virol. 2015 Sep;160(9):2209-17. doi: 10.1007/s00705-015-2477-0. Epub 2015 Jun 23.

Abstract

Hepatitis B virus (HBV) infection is a serious global health problem. Approximately 2 billion people worldwide have been infected, and approximately 350 million individuals currently suffer from HBV-induced chronic liver infection, which causes 600,000 deaths annually from chronic hepatitis, cirrhosis and hepatocellular carcinoma. HBV is classified in eight genotypes (A-H), and two more have been proposed (I-J). In this paper, complete genome sequences of nine Uruguayan HBV are reported. Five samples belong to genotype F1b and one to genotype A2. Three HBV recombinants were detected: A1/F1b, A2/F1b and D3/F1b. The following mutations were detected: a G1896A substitution, a 33-nucleotide deletion from position 2896 to 2928 in the Pre-S1 region involving Pre-S1 residues 3-13, a 33-nt deletion in the Pre-S1 region involving nt 2913-2945 and Pre-S1 residues 9-19. More F genotypes strains than expected were detected in this study, supporting the hypothesis that there are more people of indigenous origin than declared in our population. Also, one third of the samples analyzed were recombinants. This cannot be explained by the low HBV prevalence in Uruguay, but a high HBV infection rate in drug addicts and dialysis patients could act in favor of multiple-genotype HBV infections that could lead to recombination.

摘要

乙型肝炎病毒(HBV)感染是一个严重的全球健康问题。全球约有20亿人曾感染过HBV,目前约有3.5亿人患有HBV引起的慢性肝脏感染,每年有60万人死于慢性肝炎、肝硬化和肝细胞癌。HBV分为八种基因型(A - H),另外还有两种基因型被提出(I - J)。本文报道了9株乌拉圭HBV的全基因组序列。5个样本属于F1b基因型,1个属于A2基因型。检测到3株HBV重组体:A1/F1b、A2/F1b和D3/F1b。检测到以下突变:一个G1896A替换,前S1区从第2896位到2928位有33个核苷酸缺失,涉及前S1区第3 - 13位残基;前S1区有33个核苷酸缺失,涉及第2913 - 2945位核苷酸和前S1区第9 - 19位残基。本研究中检测到的F基因型菌株比预期的多,这支持了一种假说,即我们人群中具有本土血统的人比申报的要多。此外,分析的样本中有三分之一是重组体。这不能用乌拉圭较低的HBV流行率来解释,但吸毒者和透析患者中较高的HBV感染率可能有利于多基因型HBV感染,进而导致重组。

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