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Biological characteristics of the rtA181T/sW172* mutant strain of Hepatitis B virus in animal model

机译:乙型肝炎病毒rtA181T / sW172 *突变株在动物模型中的生物学特性

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Background The effects of Hepatitis B virus (HBV) rtA181T/sW172* mutation on viral replication and pathogenicity was concerned recently. This study aimed to investigate the biological characteristics of rtA181T/sW172* mutant strain of HBV in animal model. Methods The rtA181T/sW172* mutant plasmid was constructed using the pHBV4.1 (wild type HBV) as a template. The wild and mutant HBV replication mouse models were established utilizing a hydrodynamic technique. The titers of hepatitis B surface antigen (HBsAg), hepatitis B e antigen, and HBV DNA in serum, and the levels of HBsAg, hepatitis B core antigen(HBcAg), HBV DNA replication intermediates (HBV DNA RI) and HBV RNA in liver were measured after 1, 3, 5, 7, 10, 12 and 15 days of plasmid injection. Results In wild-type HBV replication mouse model, serum HBsAg was high on day 1, 3, and 5, but became lower since day 7; while in mutant HBV mouse model, serum HBsAg was always at very low level. In liver tissues, HBV DNA RI of wild type HBV was detected on day 1 after transfection. The level subsequently peaked on day 3, gradually declined after day 5, and was almost undetectable on day 10. However, the HBV DNA RI levels of the mutant strain were always higher and lasted longer until day 15. Consistently, the expression levels of HBsAg and HBcAg in liver of the mutant group were significantly increased. Conclusions In the case of the HBV rtA181T/sW172* mutation, the secretion of serum HBsAg was impaired, whereas HBV DNA replication and HBsAg/HBcAg expression were increased in liver. These results suggest that the mutation can impair HBsAg secretion, and may cause the accumulation of viral core particles in liver.
机译:背景技术最近,人们开始关注乙型肝炎病毒(HBV)rtA181T / sW172 *突变对病毒复制和致病性的影响。本研究旨在探讨动物模型中HBV rtA181T / sW172 *突变株的生物学特性。方法以pHBV4.1(野生型HBV)为模板构建rtA181T / sW172 *突变质粒。利用流体力学技术建立了野生型和突变型HBV复制小鼠模型。血清中乙型肝炎表面抗原(HBsAg),乙型肝炎e抗原和HBV DNA的滴度以及肝脏中HBsAg,乙型肝炎核心抗原(HBcAg),HBV DNA复制中间体(HBV DNA RI)和HBV RNA的水平在质粒注射后1、3、5、7、10、12和15天后测量细胞因子。结果在野生型HBV复制小鼠模型中,血清HBsAg在第1、3和5天较高,但从第7天开始降低;而在突变型HBV小鼠模型中,血清HBsAg始终处于非常低的水平。在肝组织中,转染后第1天检测到野生型HBV的HBV DNA RI。该水平随后在第3天达到峰值,在第5天后逐渐下降,在第10天几乎未检测到。但是,突变株的HBV DNA RI水平始终较高,并持续到第15天。一致地,HBsAg的表达水平突变组肝脏中HBcAg和HBcAg明显升高。结论HBV rtA181T / sW172 *突变会损害血清HBsAg的分泌,而肝脏中HBV DNA复制和HBsAg / HBcAg表达增加。这些结果表明,该突变可损害HBsAg分泌,并可能导致肝脏中病毒核心颗粒的积累。

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