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Molecular identification of hepatitis B virus genotypes/subgenotypes: Revised classification hurdles and updated resolutions

机译:乙型肝炎病毒基因型/亚基因型的分子鉴定:修订的分类障碍和更新的解决方案

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摘要

The clinical course of infections with the hepatitis B virus (HBV) substantially varies between individuals, as a consequence of a complex interplay between viral, host, environmental and other factors. Due to the high genetic variability of HBV, the virus can be categorized into different HBV genotypes and subgenotypes, which considerably differ with respect to geographical distribution, transmission routes, disease progression, responses to antiviral therapy or vaccination, and clinical outcome measures such as cirrhosis or hepatocellular carcinoma. However, HBV (sub)genotyping has caused some controversies in the past due to misclassifications and incorrect interpretations of different genotyping methods. Thus, an accurate, holistic and dynamic classification system is essential. In this review article, we aimed at highlighting potential pitfalls in genetic and phylogenetic analyses of HBV and suggest novel terms for HBV classification. Analyzing full-length genome sequences when classifying genotypes and subgenotypes is the foremost prerequisite of this classification system. Careful attention must be paid to all aspects of phylogenetic analysis, such as bootstrapping values and meeting the necessary thresholds for (sub)genotyping. Quasi-subgenotype refers to subgenotypes that were incorrectly suggested to be novel. As many of these strains were misclassified due to genetic differences resulting from recombination, we propose the term “recombino-subgenotype”. Moreover, immigration is an important confounding facet of global HBV distribution and substantially changes the geographic pattern of HBV (sub)genotypes. We therefore suggest the term “immigro-subgenotype” to distinguish exotic (sub)genotypes from native ones. We are strongly convinced that applying these two proposed terms in HBV classification will help harmonize this rapidly progressing field and allow for improved prophylaxis, diagnosis and treatment.
机译:由于病毒,宿主,环境和其他因素之间复杂的相互作用,乙型肝炎病毒(HBV)感染的临床过程在个体之间存在很大差异。由于HBV的高遗传变异性,该病毒可分为不同的HBV基因型和亚基因型,在地理分布,传播途径,疾病进展,对抗病毒疗法或疫苗的反应以及临床结局指标(例如肝硬化)方面存在很大差异或肝细胞癌。但是,由于分类错误和对不同基因型方法的错误解释,HBV(亚)基因型在过去引起了一些争议。因此,准确,全面和动态的分类系统至关重要。在这篇评论文章中,我们旨在突出HBV遗传和系统发育分析中的潜在陷阱,并为HBV分类提出新的术语。在对基因型和亚基因型进行分类时,分析全长基因组序列是此分类系统的首要前提。必须认真注意系统发育分析的所有方面,例如自举值和达到(亚)基因分型的必要阈值。准亚基因型是指被错误地认为是新颖的亚基因型。由于由于重组引起的遗传差异,这些菌株中有许多是错误分类的,因此我们建议使用术语“重组亚基因型”。此外,移民是全球HBV分布的一个重要混杂因素,它极大地改变了HBV(亚)基因型的地理格局。因此,我们建议使用术语“异基因亚型”来区分外来(亚)基因型和本地基因型。我们坚信,将这两个提议的术语应用到HBV分类中将有助于协调这个快速发展的领域,并可以提高预防,诊断和治疗的水平。

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