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Pathogenesis of Hepatitis E Virus and Hepatitis C Virus in Chimpanzees: Similarities and Differences

机译:黑猩猩戊型肝炎病毒和丙型肝炎病毒的发病机制:异同

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摘要

The chimpanzee is the only animal model for investigating the pathogenesis of viral hepatitis types A through E in humans. Studies of the host response, including microarray analyses, have relied on the close relationship between these two primate species: chimpanzee samples are commonly tested with human-based reagents. In this study, the host responses to two dissimilar viruses, hepatitis E virus (HEV) and hepatitis C virus (HCV), were compared in multiple experimentally infected chimpanzees. Affymetrix U133 + 2.0 human microarray chips were used to assess the entire transcriptome in serial liver biopsies obtained over the course of the infections. Respecting the limitations of microarray probes designed for human target transcripts to effectively assay chimpanzee transcripts, we conducted probe-level analysis of the microarray data in conjunction with a custom mapping of the probe sequences to the most recent human and chimpanzee genome sequences. Time points for statistical comparison were chosen based on independently measured viremia levels. Regardless of the viral infection, the alignment of differentially expressed genes to the human genome sequence resulted in a larger number of genes being identified when compared with alignment to the chimpanzee genome sequence. This probably reflects the lesser refinement of gene annotation for chimpanzees. In general, the two viruses demonstrated very distinct temporal changes in host response genes, although both RNA viruses induced genes that were involved in many of the same biological systems, including interferon-induced genes. The host response to HCV infection was more robust in the magnitude and number of differentially expressed genes compared to HEV infection.
机译:黑猩猩是唯一可用于调查人类A型至E型病毒性肝炎发病机制的动物模型。对宿主反应的研究(包括微阵列分析)依赖于这两种灵长类动物之间的密切关系:黑猩猩样品通常使用基于人的试剂进行测试。在这项研究中,在多种实验感染的黑猩猩中比较了宿主对两种不同病毒戊型肝炎病毒(HEV)和丙型肝炎病毒(HCV)的反应。 Affymetrix U133 + 2.0人类微阵列芯片用于评估在感染过程中获得的系列肝活检中的整个转录组。考虑到设计用于人类目标转录本以有效分析黑猩猩转录本的微阵列探针的局限性,我们结合定制序列将探针序列映射到最新的人类和黑猩猩基因组序列,对微阵列数据进行了探针级分析。根据独立测量的病毒血症水平选择统计比较的时间点。不管病毒感染如何,与黑猩猩基因组序列的比对相比,差异表达基因与人基因组序列的比对导致可识别出更多的基因。这可能反映了黑猩猩基因注释的细微改进。通常,两种病毒在宿主反应基因中均表现出非常明显的时间变化,尽管两种RNA病毒均诱导涉及许多相同生物系统的基因,包括干扰素诱导的基因。与HEV感染相比,宿主对HCV感染的反应在差异表达基因的数量和数量上更为强劲。

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