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猫免疫缺陷病毒感染诱导的基因表达变化在上皮细胞和淋巴细胞中有所不同。

Gene-expression changes induced by Feline immunodeficiency virus infection differ in epithelial cells and lymphocytes.

作者信息

Dowling R J O, Bienzle D

机构信息

Department of Pathobiology, University of Guelph, Guelph, Ontario, Canada N1G 2W1.

出版信息

J Gen Virol. 2005 Aug;86(Pt 8):2239-2248. doi: 10.1099/vir.0.80735-0.

Abstract

Infection of cats with Feline immunodeficiency virus (FIV) is an important model for understanding comparative lentivirus biology. In vivo, FIV infects lymphocytes and monocyte/macrophages, but in vitro infection is commonly investigated in epithelial Crandell-Reese Feline Kidney (CRFK) cells. In this study, the transcriptional responses of CRFK cells and primary lymphocytes to infection with FIV 34TF, a cloned subtype A virus, and FIV USgaB01, a biological subtype B isolate, were determined. Reverse-transcribed mRNA from both cell types was hybridized to microarrays containing 1700 human expressed sequence tags in duplicate and data were analysed with Significance Analysis of Microarrays (sam) software. Results from six experiments assessing homeostatic cross-species hybridization excluded 3.48 % inconsistently detected transcripts. Analysis of data from five time points over 48 h after infection identified 132 and 24 differentially expressed genes in epithelial cells and lymphocytes, respectively. Genes involved in protein synthesis, the cell cycle, structure and metabolism were affected. The magnitude of gene-expression changes ranged from 0.62 to 1.62 and early gene induction was followed by downregulation after 4 h. Transcriptional changes in CRFK cells were distinct from those in lymphocytes, except for heat-shock cognate protein 71, which was induced at multiple time points in both cell types. These findings indicate that FIV infection induces transcriptional changes of a modest magnitude in a wide range of genes, which is probably reflective of the relatively non-cytopathic nature of virus infection.

摘要

猫感染猫免疫缺陷病毒(FIV)是理解慢病毒比较生物学的重要模型。在体内,FIV感染淋巴细胞和单核细胞/巨噬细胞,但体外感染通常在上皮性克兰德尔 - 里斯猫肾(CRFK)细胞中进行研究。在本研究中,测定了CRFK细胞和原代淋巴细胞对克隆的A亚型病毒FIV 34TF和生物学B亚型分离株FIV USgaB01感染的转录反应。将两种细胞类型的逆转录mRNA与包含1700个人类表达序列标签的微阵列进行重复杂交,并用微阵列显著性分析(sam)软件分析数据。来自六个评估稳态跨物种杂交实验的结果排除了3.48%检测不一致的转录本。对感染后48小时内五个时间点的数据进行分析,分别在上皮细胞和淋巴细胞中鉴定出132个和24个差异表达基因。参与蛋白质合成、细胞周期、结构和代谢的基因受到影响。基因表达变化的幅度范围为0.62至1.62,早期基因诱导后4小时出现下调。CRFK细胞中的转录变化与淋巴细胞中的不同,除了热休克同源蛋白71,它在两种细胞类型的多个时间点均被诱导。这些发现表明,FIV感染在广泛的基因中诱导适度幅度的转录变化,这可能反映了病毒感染相对非细胞病变的性质。

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