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来自动物病毒的受体结合蛋白与人类细胞进入因子具有广泛的兼容性。

Receptor-binding proteins from animal viruses are broadly compatible with human cell entry factors.

作者信息

Dufloo Jérémy, Andreu-Moreno Iván, Moreno-García Jorge, Valero-Rello Ana, Sanjuán Rafael

机构信息

Institute for Integrative Systems Biology, Universitat de València - Consejo Superior de Investigaciones Científicas, Paterna, Spain.

出版信息

Nat Microbiol. 2025 Feb;10(2):405-419. doi: 10.1038/s41564-024-01879-4. Epub 2025 Jan 2.

Abstract

Cross-species transmission of animal viruses poses a threat to human health. However, systematic experimental assessments of these risks remain scarce. A critical step in viral infection is cellular internalization mediated by viral receptor-binding proteins (RBPs). Here we constructed viral pseudotypes bearing the RBPs of 102 enveloped RNA viruses and assayed their infectivity across 5,202 RBP-cell combinations. This showed that most of the tested viruses have the potential to enter human cells. Pseudotype infectivity varied widely among the 14 viral families examined and was influenced by RBP characteristics, host of origin and target cell type. Cellular gene expression data revealed that the availability of specific cell-surface receptors is not necessarily the main factor limiting viral entry and that additional host factors must be considered. Altogether, these results suggest weak interspecies barriers in the early stages of infection and advance our understanding of the molecular interactions driving viral zoonosis.

摘要

动物病毒的跨物种传播对人类健康构成威胁。然而,对这些风险的系统性实验评估仍然匮乏。病毒感染的关键步骤是由病毒受体结合蛋白(RBP)介导的细胞内化。在此,我们构建了携带102种包膜RNA病毒RBP的病毒假型,并在5202种RBP-细胞组合中检测了它们的感染性。这表明大多数测试病毒都有进入人类细胞的潜力。在所检测的14个病毒家族中,假型感染性差异很大,并且受RBP特性、病毒起源宿主和靶细胞类型的影响。细胞基因表达数据显示,特定细胞表面受体的可用性不一定是限制病毒进入的主要因素,还必须考虑其他宿主因素。总之,这些结果表明在感染早期种间屏障较弱,并增进了我们对驱动病毒人畜共患病的分子相互作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fc4/11790484/1f2fac3ad940/41564_2024_1879_Fig1_HTML.jpg

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