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感染非洲猪瘟病毒的猪的细胞因子、白细胞和全血转录组图谱的时间动态变化

Temporal dynamics of cytokine, leukocyte, and whole blood transcriptome profiles of pigs infected with African swine fever virus.

作者信息

Madden Daniel W, Artiaga Bianca Libanori, Trujillo Jessie D, Assato Patricia, McDowell Chester D, Fitz Isaac, Kwon Taeyong, Cool Konner, Li Yonghai, Gaudreault Natasha N, Morozov Igor, Richt Juergen A

机构信息

Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.

出版信息

bioRxiv. 2025 Aug 29:2025.08.29.673161. doi: 10.1101/2025.08.29.673161.

DOI:10.1101/2025.08.29.673161
PMID:40909556
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12407888/
Abstract

African swine fever virus (ASFV) is an important transboundary animal pathogen with significant impacts on the global swine industry. Overwhelming proinflammatory responses are a major virulence mechanism for ASFV, but the dynamics of these changes during clinical disease are not completely understood. We constructed a detailed portrait of the innate immune responses during acute African swine fever (ASF) at the cellular, transcriptomic, and cytokine levels. Samples serially obtained from infected piglets show progression of acute ASF is characterized by rapid increases in plasma type I interferons, TNF-α, IL-12p40, and IL-10, which coincide with the manifestation of clinical disease and viral DNAemia. Lymphocytes and natural killer (NK) cells progressively declined, with fluctuations in B cell, CD8+ T cell, and CD4+/CD8+ T cell populations. Blood monocytes and macrophages were highly variable throughout infection, with an abrupt spike in CD203+ mature macrophages immediately prior to death. Transcriptomic analysis of blood showed downregulation of cellular translation as early as 1 day post challenge (DPC), and significant upregulation of antiviral immune processes at 5 DPC and 7 DPC which overlapped with the onset of clinical disease. Together, these results present a highly detailed delineation of fatal ASF as involving an initial infection and damage of susceptible myeloid cells prior to symptomatic disease characterized by pro-inflammatory immune responses, lymphoid depletion, and clinical deterioration.

摘要

非洲猪瘟病毒(ASFV)是一种重要的跨界动物病原体,对全球养猪业有重大影响。压倒性的促炎反应是ASFV的主要致病机制,但这些变化在临床疾病期间的动态过程尚未完全了解。我们在细胞、转录组和细胞因子水平上构建了急性非洲猪瘟(ASF)期间先天免疫反应的详细图谱。从感染仔猪连续采集的样本显示,急性ASF的进展特征为血浆I型干扰素、TNF-α、IL-12p40和IL-10迅速增加,这与临床疾病和病毒血症的表现同时出现。淋巴细胞和自然杀伤(NK)细胞逐渐减少,B细胞、CD8 + T细胞以及CD4 + /CD8 + T细胞群体出现波动。在整个感染过程中,血液单核细胞和巨噬细胞变化很大,在死亡前CD203 +成熟巨噬细胞会突然激增。血液转录组分析显示,早在攻毒后1天(DPC)细胞翻译就下调,在5 DPC和7 DPC时抗病毒免疫过程显著上调,这与临床疾病的发作时间重叠。总之,这些结果对致命性ASF进行了高度详细的描述,即其在出现以促炎免疫反应、淋巴细胞耗竭和临床恶化为特征的症状性疾病之前,首先感染并损害易感髓样细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/8f876dfc83c4/nihpp-2025.08.29.673161v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/40cbe6606dd4/nihpp-2025.08.29.673161v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/8a730a1405da/nihpp-2025.08.29.673161v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/6b4cb5cf26a8/nihpp-2025.08.29.673161v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/ec563e49d0ed/nihpp-2025.08.29.673161v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/8f876dfc83c4/nihpp-2025.08.29.673161v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/40cbe6606dd4/nihpp-2025.08.29.673161v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/8a730a1405da/nihpp-2025.08.29.673161v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/6b4cb5cf26a8/nihpp-2025.08.29.673161v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/ec563e49d0ed/nihpp-2025.08.29.673161v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc4/12407888/8f876dfc83c4/nihpp-2025.08.29.673161v1-f0005.jpg

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本文引用的文献

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Vaccines (Basel). 2024 Sep 30;12(10):1125. doi: 10.3390/vaccines12101125.
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Genotype II Live-Attenuated ASFV Vaccine Strains Unable to Completely Protect Pigs against the Emerging Recombinant ASFV Genotype I/II Strain in Vietnam.II型基因工程减毒非洲猪瘟病毒疫苗株无法完全保护猪抵御越南出现的重组I/II型非洲猪瘟病毒株。
Vaccines (Basel). 2024 Sep 28;12(10):1114. doi: 10.3390/vaccines12101114.
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pK205R targets the proximal element of IFN-I signaling pathway to assist African swine fever virus to escape host innate immunity at the early stage of infection.
pK205R 通过靶向 IFN-I 信号通路的近端元件来协助非洲猪瘟病毒在感染早期逃避宿主固有免疫。
PLoS Pathog. 2024 Oct 15;20(10):e1012613. doi: 10.1371/journal.ppat.1012613. eCollection 2024 Oct.
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Transcriptome profiles of organ tissues from pigs experimentally infected with African swine fever virus in early phase of infection.感染非洲猪瘟病毒早期阶段实验感染猪的器官组织转录组谱。
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