乙型肝炎病毒分离株不可分型的基因型限制模式和表面基因变异。

International journal of molecular epidemiology and genetics Pub Date : 2017-06-20 eCollection Date: 2017-01-01
Michael O Baclig, Karen G Reyes, Veni R Liles, Juliet Gopez-Cervantes
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摘要

慢性乙型肝炎是一个全球性的健康问题,是肝硬化和肝细胞癌的主要原因之一。乙型肝炎病毒(HBV)基因分型有助于制定HBV感染的临床管理决策,对流行病学研究也很重要。本研究的目的是调查菲律宾流行的HBV基因型的分布;分子表征不可分的基因型限制模式;并分析表面基因变异的存在。采用限制性内切片段长度多态性(RFLP)和DNA测序检测HBV基因型。三种基因型,HBV A (76%;73/96), HBV b (10%;10/96)和HBV C (14%;RFLP检测到13/96)。96株菌株中,9%的菌株RFLP分析无法分型。DNA测序和系统发育分析显示,这些分离株属于HBV基因型A (67%;6/9), b (11%;1/9)和C (22%;2/9)。在9株分离菌株中,55%的菌株表现出单个或多个变异,导致氨基酸发生变化。总的来说,无法分型的基因型鉴定可以通过S基因的序列和系统发育分析来解决,这种方法也可以用于检测单个或多个变异。我们的发现强调了通过DNA测序准确的基因分型和检测表面基因变异对优化临床管理的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Untypable genotype restriction patterns and surface gene variants of hepatitis B virus isolates.

Chronic hepatitis B is a global health problem, and is one of the leading causes of cirrhosis and hepatocellular carcinoma. Hepatitis B virus (HBV) genotyping helps in decision making for clinical management of HBV infection, and is important for epidemiological studies. The objectives of this study were to investigate the distribution of HBV genotypes circulating in the Philippines; molecularly characterize untypable genotype restriction patterns; and analyze the presence of surface gene variants. HBV genotypes were determined by restriction fragment length polymorphism (RFLP) and DNA sequencing. Three genotypes, HBV A (76%; 73/96), HBV B (10%; 10/96) and HBV C (14%; 13/96) were detected by RFLP. Out of the 96 isolates, 9% were untypable by RFLP analysis. DNA sequencing followed by phylogenetic analysis revealed that these isolates belonged to HBV genotypes A (67%; 6/9), B (11%; 1/9) and C (22%; 2/9). Out of the 9 isolates, 55% showed single or multiple variations which resulted to amino acid changes. Overall, the identification of untypable genotype can be resolved by sequence and phylogenetic analysis of the S gene and this approach can also be used to detect single or multiple variants. Our findings underscore the importance of accurate genotyping and detection of surface gene variants by DNA sequencing for optimal clinical management.

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