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猪呼吸道上皮细胞对猪流感病毒的先天抗病毒细胞因子反应。

Innate Antiviral Cytokine Response to Swine Influenza Virus by Swine Respiratory Epithelial Cells.

机构信息

Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis Tennessee.

出版信息

J Virol. 2021 Jul 12;95(15):e0069221. doi: 10.1128/JVI.00692-21.

Abstract

Swine influenza virus (SIV) can cause respiratory illness in swine. Swine contribute to influenza virus reassortment, as avian, human, and/or swine influenza viruses can infect swine and reassort, and new viruses can emerge. Thus, it is important to determine the host antiviral responses that affect SIV replication. In this study, we examined the innate antiviral cytokine response to SIV by swine respiratory epithelial cells, focusing on the expression of interferon (IFN) and interferon-stimulated genes (ISGs). Both primary and transformed swine nasal and tracheal respiratory epithelial cells were examined following infection with field isolates. The results show that IFN and ISG expression is maximal at 12 h postinfection (hpi) and is dependent on cell type and virus genotype. Swine are considered intermediate hosts that have facilitated influenza virus reassortment events that have given rise pandemics or genetically related viruses have become established in swine. In this study, we examine the innate antiviral response to swine influenza virus in primary and immortalized swine nasal and tracheal epithelial cells, and show virus strain- and host cell type-dependent differential expression of key interferons and interferon-stimulated genes.

摘要

猪流感病毒(SIV)可引起猪的呼吸道疾病。猪可促进流感病毒重配,因为禽、人、和/或猪流感病毒可感染猪并发生重配,从而出现新病毒。因此,确定影响 SIV 复制的宿主抗病毒反应非常重要。在这项研究中,我们通过猪呼吸道上皮细胞检测了针对 SIV 的先天抗病毒细胞因子反应,重点关注干扰素(IFN)和干扰素刺激基因(ISG)的表达。感染田间分离株后,对原代和转化的猪鼻和气管呼吸道上皮细胞进行了检测。结果表明,IFN 和 ISG 的表达在感染后 12 小时(hpi)达到最大值,并且依赖于细胞类型和病毒基因型。猪被认为是中间宿主,它们促进了流感病毒重配事件的发生,从而引发了大流行或使与流感病毒相关的病毒在猪中建立了种群。在这项研究中,我们检测了猪鼻和气管上皮细胞中针对猪流感病毒的先天抗病毒反应,并显示出病毒株和宿主细胞类型依赖性的关键干扰素和干扰素刺激基因的差异表达。

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