乙型肝炎病毒(HBV)临床分离株的分子特征和流行及其重要性

Vatsal Parashar, Dimple Raina, S. Sahni
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引用次数: 0

摘要

乙型肝炎病毒(HBV) DNA定量为治疗和治愈HBV和肝细胞癌(HCC)提供了见解。本研究涉及HBV DNA病毒载量的分子分析和HBV DNA基因型的分子研究(Revill et al., 2019)。本研究对不同基因型在种群中的分布进行了研究。从印度北阿坎德邦德拉敦Shri Mahant Indresh医院不同科室(包括门诊和ipd)的疑似HBV反应患者共采集102份EDTA血清样本。DNA提取后进行实时定量。巢式PCR技术进行HBV基因型鉴定。在收集的102个血清学检测样本中,60个样本HBsAg呈阳性,并进行了进一步的生化分析。测定样本中HBV病毒载量,滴度在34 IU/mL ~ 1.10×108 IU/mL之间,其中16.7%(10例)未检测到靶病毒,83.3%(50例)为高病毒载量。采用巢式PCR对50份病毒载量较高的样品进行基因分型。HBV基因型以d型最常见,占65.62%,共32例。由于主要致病因素的差异,HBV基因型的存在在不同的地理条件下存在差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular profiling and prevalence of hepatitis B virus (HBV) in clinical isolates and its importance
Hepatitis B virus (HBV) DNA quantification provides insight for treating and curing HBV and hepatic cell carcinoma (HCC). This study deals with the molecular profiling of HBV DNA viral load and the molecular investigation of the HBV DNA genotypes (Revill et al., 2019). The distribution of various genotypes among the population has been studied in this research. Total 102 EDTA serum samples were taken from suspected HBV reactive patients from the different Departments, including OPDs and IPDs of Shri Mahant Indresh Hospital, Dehradun, Uttarakhand, India. After DNA extraction real-time quantification was performed. Nested PCR technology did the HBV genotypic characterization. Out of 102 samples collected for the serological test, 60 samples were found positive for HBsAg and further biochemical profiling was performed. The HBV viral load was quantified in the samples and their titer values were observed between 34 IU/mL to 1.10×108 IU/mL in which, 16.7% (10 cases) were in which the target was not detected and 83.3%, i.e., 50 cases were with high viral load. Then genotyping of these 50 samples with high viral load was performed by Nested PCR. Genotype d of HBV was found to be most prevalent in 65.62% of cases i.e. 32 cases in total. The presence of HBV genotype varies within the different geographical conditions because of the differences in the major causative factors.
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