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Sp140L是一种新型疱疹病毒限制因子。

Sp140L Is a Novel Herpesvirus Restriction Factor.

作者信息

Cable Jana M, Wongwiwat Wiyada, Grabowski Jenna C, White Robert E, Luftig Micah A

机构信息

Duke University School of Medicine, Department of Molecular Genetics and Microbiology, Duke Center for Virology, Durham, NC, USA.

Section of Virology, Department of Infectious Disease, Imperial College London, London, United Kingdom.

出版信息

bioRxiv. 2024 Dec 14:2024.12.13.628399. doi: 10.1101/2024.12.13.628399.

Abstract

Herpesviruses, including the oncogenic Epstein-Barr Virus (EBV), must bypass host DNA sensing mechanisms to establish infection. The first viral latency protein expressed, EBNA-LP, is essential for transformation of naïve B cells, yet its role in evading host defenses remains unclear. Using single-cell RNA sequencing of EBNA-LP-Knockout (LPKO)-infected B cells, we reveal an antiviral response landscape implicating the 'speckled proteins' as key restriction factors countered by EBNA-LP. Specifically, loss of or the primate-specific reverses the restriction of LPKO, suppresses a subset of canonically interferon-stimulated genes, and restores viral gene transcription and cellular proliferation. Notably, we also identify Sp140L as a restriction target of the herpesvirus saimiri ORF3 protein, implying a role in immunity to other DNA viruses. This study reveals Sp140L as a restriction factor that we propose links sensing and transcriptional suppression of viral DNA to an IFN-independent innate immune response, likely relevant to all nuclear DNA viruses.

摘要

疱疹病毒,包括致癌的爱泼斯坦-巴尔病毒(EBV),必须绕过宿主DNA传感机制才能建立感染。首个表达的病毒潜伏蛋白EBNA-LP对于原始B细胞的转化至关重要,但其在逃避宿主防御中的作用仍不清楚。通过对EBNA-LP基因敲除(LPKO)感染的B细胞进行单细胞RNA测序,我们揭示了一种抗病毒反应格局,表明“斑点蛋白”是EBNA-LP对抗的关键限制因子。具体而言,缺失 或灵长类特异性的 可逆转LPKO的限制,抑制一部分典型的干扰素刺激基因,并恢复病毒基因转录和细胞增殖。值得注意的是,我们还确定Sp140L是赛米利疱疹病毒ORF3蛋白的限制靶点,这意味着其在对其他DNA病毒的免疫中发挥作用。这项研究揭示Sp140L是一种限制因子,我们认为它将病毒DNA的传感和转录抑制与不依赖干扰素的先天免疫反应联系起来,这可能与所有核DNA病毒都相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5cd/11661405/0a153a95c930/nihpp-2024.12.13.628399v1-f0001.jpg

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