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病毒诱导的大脑转录变化包括与干扰素、细胞凋亡、白细胞介素 17 受体 A 和谷氨酸信号相关的基因的差异表达,以及 flavivirus 特异性上调 tRNA 合成酶。

Virus-induced transcriptional changes in the brain include the differential expression of genes associated with interferon, apoptosis, interleukin 17 receptor A, and glutamate signaling as well as flavivirus-specific upregulation of tRNA synthetases.

出版信息

mBio. 2014 Mar 11;5(2):e00902-14. doi: 10.1128/mBio.00902-14.

Abstract

Flaviviruses, particularly Japanese encephalitis virus (JEV) and West Nile virus (WNV), are important causes of virus-induced central nervous system (CNS) disease in humans. We used microarray analysis to identify cellular genes that are differentially regulated following infection of the brain with JEV (P3) or WNV (New York 99). Gene expression data for these flaviviruses were compared to those obtained following infection of the brain with reovirus (type 3 Dearing), an unrelated neurotropic virus. We found that a large number of genes were up-regulated by all three viruses (using the criteria of a change of >2-fold and a P value of <0.001), including genes associated with interferon signaling, the immune system, inflammation, and cell death/survival signaling. In addition, genes associated with glutamate signaling were down-regulated in infections with all three viruses (criteria, a >2-fold change and a P value of <0.001). These genes may serve as broad-spectrum therapeutic targets for virus-induced CNS disease. A distinct set of genes were up-regulated following flavivirus infection but not following infection with reovirus. These genes were associated with tRNA charging and may serve as therapeutic targets for flavivirus-induced CNS disease. IMPORTANCE Viral infections of the central nervous system (CNS) are an important cause of morbidity and mortality. Treatment options for virus-induced CNS disease are limited, and for many clinically important neurotropic viruses, no specific therapy of proven benefit is currently available. We performed microarray analysis to identify genes that are differentially regulated in the brain following virus infection in order to identify pathways that might provide novel therapeutic targets for virus-induced CNS disease. Although several studies have described gene expression changes following virus infection of the brain, this report is the first to directly compare large-scale gene expression data from different viruses. We identified genes that are differentially regulated in infection of the brain with viruses from different families and those which appear to be specific to flavivirus infections.

摘要

黄病毒,特别是日本脑炎病毒(JEV)和西尼罗河病毒(WNV),是人类中枢神经系统(CNS)病毒感染的重要原因。我们使用微阵列分析来鉴定感染大脑后的细胞基因,这些基因受 JEV(P3)或 WNV(纽约 99 号)感染的调节。这些黄病毒的基因表达数据与感染脑的呼肠孤病毒(3Dearing 型),一种无关的神经病毒的基因表达数据进行了比较。我们发现大量的基因被这三种病毒上调(使用变化> 2 倍和 P 值<0.001 的标准),包括与干扰素信号、免疫系统、炎症和细胞死亡/存活信号相关的基因。此外,感染这三种病毒后与谷氨酸信号相关的基因下调(标准为> 2 倍的变化和 P 值<0.001)。这些基因可能是病毒引起的中枢神经系统疾病的广谱治疗靶点。一组独特的基因在黄病毒感染后上调,但在呼肠孤病毒感染后未上调。这些基因与 tRNA 充电有关,可能是黄病毒引起的中枢神经系统疾病的治疗靶点。重要性中枢神经系统(CNS)的病毒感染是发病率和死亡率的一个重要原因。病毒引起的中枢神经系统疾病的治疗选择有限,而且对于许多临床上重要的神经病毒,目前没有经过验证的有效特定治疗方法。我们进行了微阵列分析,以鉴定在病毒感染后大脑中差异调节的基因,以便鉴定可能为病毒引起的中枢神经系统疾病提供新的治疗靶点的途径。尽管有几项研究描述了病毒感染大脑后的基因表达变化,但这是第一篇直接比较不同病毒的大规模基因表达数据的报告。我们鉴定了在感染不同病毒家族的大脑时差异调节的基因,以及那些似乎是黄病毒感染特有的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65cb/3952157/00a22454fb4f/mbo0011417670001.jpg

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