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疾病进展和肝细胞癌背景下的丙型肝炎病毒全基因组遗传分析

HCV genome-wide genetic analyses in context of disease progression and hepatocellular carcinoma.

作者信息

Donlin Maureen J, Lomonosova Elena, Kiss Alexi, Cheng Xiaohong, Cao Feng, Curto Teresa M, Di Bisceglie Adrian, Tavis John E

机构信息

Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, Saint Louis, Missouri, United States of America; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, Missouri, United States of America.

Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, Saint Louis, Missouri, United States of America.

出版信息

PLoS One. 2014 Jul 31;9(7):e103748. doi: 10.1371/journal.pone.0103748. eCollection 2014.

Abstract

Hepatitis C virus (HCV) is a major cause of hepatitis and hepatocellular carcinoma (HCC) world-wide. Most HCV patients have relatively stable disease, but approximately 25% have progressive disease that often terminates in liver failure or HCC. HCV is highly variable genetically, with seven genotypes and multiple subtypes per genotype. This variation affects HCV's sensitivity to antiviral therapy and has been implicated to contribute to differences in disease. We sequenced the complete viral coding capacity for 107 HCV genotype 1 isolates to determine whether genetic variation between independent HCV isolates is associated with the rate of disease progression or development of HCC. Consensus sequences were determined by sequencing RT-PCR products from serum or plasma. Positions of amino acid conservation, amino acid diversity patterns, selection pressures, and genome-wide patterns of amino acid covariance were assessed in context of the clinical phenotypes. A few positions were found where the amino acid distributions or degree of positive selection differed between in the HCC and cirrhotic sequences. All other assessments of viral genetic variation and HCC failed to yield significant associations. Sequences from patients with slow disease progression were under a greater degree of positive selection than sequences from rapid progressors, but all other analyses comparing HCV from rapid and slow disease progressors were statistically insignificant. The failure to observe distinct sequence differences associated with disease progression or HCC employing methods that previously revealed strong associations with the outcome of interferon α-based therapy implies that variable ability of HCV to modulate interferon responses is not a dominant cause for differential pathology among HCV patients. This lack of significant associations also implies that host and/or environmental factors are the major causes of differential disease presentation in HCV patients.

摘要

丙型肝炎病毒(HCV)是全球范围内导致肝炎和肝细胞癌(HCC)的主要原因。大多数HCV患者病情相对稳定,但约25%的患者病情呈进展性,常最终发展为肝衰竭或HCC。HCV在基因上高度可变,有7种基因型,每种基因型又有多个亚型。这种变异影响HCV对抗病毒治疗的敏感性,并被认为与疾病差异有关。我们对107株HCV 1型分离株的完整病毒编码能力进行了测序,以确定独立HCV分离株之间的基因变异是否与疾病进展速度或HCC的发生有关。通过对血清或血浆中的逆转录聚合酶链反应(RT-PCR)产物进行测序来确定一致序列。在临床表型的背景下,评估了氨基酸保守位点、氨基酸多样性模式、选择压力以及全基因组氨基酸共变模式。发现在少数位点上,HCC和肝硬化序列中的氨基酸分布或正选择程度存在差异。所有其他关于病毒基因变异与HCC的评估均未得出显著关联。疾病进展缓慢患者的序列比快速进展者的序列受到更大程度的正选择,但所有其他比较快速和缓慢疾病进展者的HCV分析在统计学上均无显著意义。采用先前揭示与基于干扰素α治疗结果有强关联的方法却未能观察到与疾病进展或HCC相关的明显序列差异,这意味着HCV调节干扰素反应的可变能力不是HCV患者间病理差异的主要原因。这种缺乏显著关联也意味着宿主和/或环境因素是HCV患者疾病表现差异的主要原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e551/4117537/7168cdd3396d/pone.0103748.g001.jpg

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