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脾脏重塑的单细胞图谱揭示巨噬细胞亚群驱动的非洲猪瘟病毒发病机制。

Single-Cell Atlas of Spleen Remodeling Reveals Macrophage Subset-Driven ASFV Pathogenesis.

作者信息

Wang Liyuan, Sun Shouzhang, Liu Lei, Chen Yun, Zheng Haixue, Tang Zhonglin

机构信息

Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518124, China.

Key Laboratory of Livestock and Poultry Multi-Omics of MARA, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518124, China.

出版信息

Biology (Basel). 2025 Jul 18;14(7):882. doi: 10.3390/biology14070882.

Abstract

African swine fever virus (ASFV) causes global swine outbreaks, but its cellular pathogenesis is poorly understood. Using single-cell RNA data from ASFV-infected pig spleens across four timepoints, we identified macrophages as the primary viral reservoir, with infection driving lymphoid depletion and myeloid expansion. We characterized four functionally distinct macrophage subsets, including a metabolically reprogrammed SusceptibleMac population serving as the major viral niche and an AntiviralMac subset rapidly depleted during infection. Viral gene expression analysis revealed E165R as a central hub in viral replication networks, while host transcriptomics uncovered disruption of Netrin signaling pathways that may facilitate immune evasion. Pseudotime analysis revealed dynamic macrophage state transitions during infection. These findings provide a high-resolution cellular atlas of ASFV pathogenesis, revealing macrophage subset-specific responses that shape disease outcomes and identifying potential targets for therapeutic intervention.

摘要

非洲猪瘟病毒(ASFV)引发了全球猪群疫情,但对其细胞发病机制的了解却十分有限。我们利用在四个时间点采集的感染ASFV的猪脾脏单细胞RNA数据,确定巨噬细胞是主要的病毒储存库,感染导致淋巴细胞耗竭和髓细胞扩张。我们对四个功能不同的巨噬细胞亚群进行了表征,包括一个代谢重编程的易感巨噬细胞群体,它是主要的病毒生态位,以及一个在感染期间迅速耗竭的抗病毒巨噬细胞亚群。病毒基因表达分析显示E165R是病毒复制网络的核心枢纽,而宿主转录组学揭示了可能促进免疫逃逸的Netrin信号通路的破坏。伪时间分析揭示了感染期间巨噬细胞状态的动态转变。这些发现提供了一个高分辨率的ASFV发病机制细胞图谱,揭示了塑造疾病结果的巨噬细胞亚群特异性反应,并确定了治疗干预的潜在靶点。

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