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白足鼠大脑转录组对波瓦桑病毒感染的反应。

Peromyscus leucopus mouse brain transcriptome response to Powassan virus infection.

机构信息

Biology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, NIAID/NIH, Hamilton, MT, 59840, USA.

Rocky Mountain Veterinary Branch, Rocky Mountain Laboratories, NIAID/NIH, Hamilton, MT, 59840, USA.

出版信息

J Neurovirol. 2018 Feb;24(1):75-87. doi: 10.1007/s13365-017-0596-y. Epub 2017 Nov 16.

DOI:10.1007/s13365-017-0596-y
PMID:29147886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5790856/
Abstract

Powassan virus (POWV) is a tick-borne Flavivirus responsible for life-threatening encephalitis in North America and some regions of Russia. The ticks that have been reported to transmit the virus belong to the Ixodes species, and they feed on small-to-medium-sized mammals, such as Peromyscus leucopus mice, skunks, and woodchucks. We previously developed a P. leucopus mouse model of POWV infection, and the model is characterized by a lack of clinical signs of disease following intraperitoneal or intracranial inoculation. However, intracranial inoculation results in mild subclinical encephalitis from 5 days post infection (dpi), but the encephalitis resolves by 28 dpi. We used RNA sequencing to profile the P. leucopus mouse brain transcriptome at different time points after intracranial challenge with POWV. At 24 h post infection, 42 genes were significantly differentially expressed and the number peaked to 232 at 7 dpi before declining to 31 at 28 dpi. Using Ingenuity Pathway Analysis, we determined that the genes that were significantly expressed from 1 to 15 dpi were mainly associated with interferon signaling. As a result, many interferon-stimulated genes (ISGs) were upregulated. Some of the ISGs include an array of TRIMs (genes encoding tripartite motif proteins). These results will be useful for the identification of POWV restriction factors.

摘要

波瓦桑病毒(POWV)是一种蜱传黄病毒,可导致北美的致命性脑炎和俄罗斯的一些地区发生脑炎。已知传播该病毒的蜱虫属于硬蜱属,它们以中小体型的哺乳动物为食,如白足鼠、臭鼬和土拨鼠。我们之前开发了一种 POWV 感染的白足鼠模型,该模型的特点是在腹腔内或颅内接种后缺乏疾病的临床症状。然而,颅内接种会导致轻度亚临床脑炎,从感染后 5 天开始,但脑炎会在 28 天内消退。我们使用 RNA 测序技术,在 POWV 颅内感染后不同时间点对白足鼠大脑转录组进行了分析。在感染后 24 小时,有 42 个基因显著差异表达,在感染后 7 天达到峰值(232 个),然后在感染后 28 天下降至 31 个。使用 IPA 分析,我们确定在感染后 1 至 15 天表达显著的基因主要与干扰素信号通路有关。因此,许多干扰素刺激基因(ISGs)被上调。一些 ISGs 包括一系列 TRIMs(编码三肽基序蛋白的基因)。这些结果将有助于鉴定 POWV 的限制因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/09afbc874aed/13365_2017_596_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/7092fc75226c/13365_2017_596_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/acf871da9ff4/13365_2017_596_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/2490c6f8cb37/13365_2017_596_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/09afbc874aed/13365_2017_596_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/7092fc75226c/13365_2017_596_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/acf871da9ff4/13365_2017_596_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/2490c6f8cb37/13365_2017_596_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89f6/5790856/09afbc874aed/13365_2017_596_Fig4_HTML.jpg

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