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非常适合用于非洲猪瘟病毒复制及I型干扰素诱导免疫研究的LFBK细胞。

Highly suitable LFBK cells for African swine fever virus replication and type I interferon-induced immune studies.

作者信息

Lee Eun-Gyeong, Kang Sang-Min, Tark Dongseob

机构信息

Laboratory for Infectious Disease Prevention, Korea Zoonosis Research Institute, Jeonbuk National University, Iksan, 54531, Republic of Korea.

ViEL-T Corporate Research Institute, ViEL-T lnc., Jeonju Innovation Startup Hub SJ Bldg, Jeonju, 54852, Republic of Korea.

出版信息

Vet Res. 2025 Jun 11;56(1):116. doi: 10.1186/s13567-025-01543-7.

DOI:10.1186/s13567-025-01543-7
PMID:40500801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12153162/
Abstract

African swine fever virus (ASFV), the causative agent of African swine fever, is a fatal haemorrhagic virus affecting domestic pigs and wild boars. The primary target cells for ASFV infection are porcine alveolar macrophages (PAMs); however, PAM isolation and maintenance are technically challenging, and genetic manipulation of these cells is difficult. The lack of suitable cell lines that support ASFV infection and replication has significantly hindered vaccine development. This study aimed to overcome these limitations and advance ASFV research. The results demonstrate that the foetal porcine kidney cells (LFBK) are suitable for ASFV studies. We observed that ASFV replicated significantly more efficiently in LFBK cells than in PAMs. Furthermore, LFBK cells exhibited antiviral immune responses similar to PAMs following ASFV infection or DNA analog. These findings suggest that the LFBK cell line could provide a much-needed platform for studying ASFV replication and pathogenesis while serving as a valuable tool for understanding ASFV-induced immune mechanisms.

摘要

非洲猪瘟病毒(ASFV)是非洲猪瘟的病原体,是一种影响家猪和野猪的致命出血性病毒。ASFV感染的主要靶细胞是猪肺泡巨噬细胞(PAM);然而,PAM的分离和维持在技术上具有挑战性,并且对这些细胞进行基因操作也很困难。缺乏支持ASFV感染和复制的合适细胞系严重阻碍了疫苗的开发。本研究旨在克服这些限制并推进ASFV研究。结果表明,胎猪肾细胞(LFBK)适用于ASFV研究。我们观察到,ASFV在LFBK细胞中的复制效率明显高于在PAM中的复制效率。此外,在感染ASFV或DNA类似物后,LFBK细胞表现出与PAM相似的抗病毒免疫反应。这些发现表明,LFBK细胞系可以为研究ASFV复制和发病机制提供急需的平台,同时作为理解ASFV诱导的免疫机制的宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/0da322554912/13567_2025_1543_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/a4bb932514b0/13567_2025_1543_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/0cbd460511a1/13567_2025_1543_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/0da322554912/13567_2025_1543_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/a4bb932514b0/13567_2025_1543_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/0cbd460511a1/13567_2025_1543_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cc/12153162/0da322554912/13567_2025_1543_Fig3_HTML.jpg

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本文引用的文献

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Pathogens. 2023 Jun 6;12(6):805. doi: 10.3390/pathogens12060805.
2
CD1d facilitates African swine fever virus entry into the host cells via clathrin-mediated endocytosis.CD1d 通过网格蛋白介导的内吞作用促进非洲猪瘟病毒进入宿主细胞。
Emerg Microbes Infect. 2023 Dec;12(2):2220575. doi: 10.1080/22221751.2023.2220575.
3
Porcine Circovirus Modulates Swine Influenza Virus Replication in Pig Tracheal Epithelial Cells and Porcine Alveolar Macrophages.
猪圆环病毒调节猪气管上皮细胞和猪肺泡巨噬细胞中的猪流感病毒复制。
Viruses. 2023 May 20;15(5):1207. doi: 10.3390/v15051207.
4
CP204L Is a Multifunctional Protein of African Swine Fever Virus That Interacts with the VPS39 Subunit of the Homotypic Fusion and Vacuole Protein Sorting Complex and Promotes Lysosome Clustering.CP204L 是非洲猪瘟病毒的多功能蛋白,可与同源融合和液泡蛋白分选复合物的 VPS39 亚基相互作用,并促进溶酶体聚集。
J Virol. 2023 Feb 28;97(2):e0194322. doi: 10.1128/jvi.01943-22. Epub 2023 Feb 1.
5
Adaptation of African swine fever virus to porcine kidney cells stably expressing CD163 and Siglec1.非洲猪瘟病毒适应稳定表达 CD163 和 Siglec1 的猪肾细胞。
Front Immunol. 2022 Oct 27;13:1015224. doi: 10.3389/fimmu.2022.1015224. eCollection 2022.
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