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Expression of interferon-induced antiviral genes is delayed in a STAT1 knockout mouse model of Crimean-Congo hemorrhagic fever

机译:克里米亚-刚果出血热的STAT1基因敲除小鼠模型中干扰素诱导的抗病毒基因的表达被延迟

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Background Crimean Congo hemorrhagic fever (CCHF) is a tick-borne hemorrhagic zoonosis associated with high mortality. Pathogenesis studies and the development of vaccines and antivirals against CCHF have been severely hampered by the lack of suitable animal model. We recently developed and characterized a mature mouse model for CCHF using mice carrying STAT1 knockout (KO). Findings Given the importance of interferons in controlling viral infections, we investigated the expression of interferon pathway-associated genes in KO and wild-type (WT) mice challenged with CCHF virus. We expected that the absence of the STAT1 protein would result in minimal expression of IFN-related genes. Surprisingly, the KO mice showed high levels of IFN-stimulated gene expression, beginning on day 2 post-infection, while in WT mice challenged with virus the same genes were expressed at similar levels on day 1. Conclusions We conclude that CCHF virus induces similar type I IFN responses in STAT1 KO and WT mice, but the delayed response in the KO mice permits rapid viral dissemination and fatal illness.
机译:背景克里米亚刚果出血热(CCHF)是由tick传播的出血性人畜共患病,与高死亡率相关。缺乏合适的动物模型严重阻碍了发病机制研究以及针对CCHF的疫苗和抗病毒药物的开发。我们最近使用携带STAT1基因敲除(KO)的小鼠开发并鉴定了CCHF的成熟小鼠模型。发现鉴于干扰素在控制病毒感染中的重要性,我们调查了受CCHF病毒攻击的KO和野生型(WT)小鼠中干扰素途径相关基因的表达。我们预期STAT1蛋白的缺失将导致IFN相关基因的最低表达。令人惊讶的是,KO小鼠从感染后第2天开始表现出高水平的IFN刺激基因表达,而在受病毒攻击的WT小鼠中,第1天以相同水平表达了相同基因。结论我们得出结论,CCHF病毒诱导了相似的表达。 STAT1 KO和WT小鼠的I型IFN应答,但KO小鼠的延迟应答允许快速的病毒传播和致命的疾病。

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