畜牧兽医学报 ›› 2023, Vol. 54 ›› Issue (8): 3406-3414.doi: 10.11843/j.issn.0366-6964.2023.08.025

• 预防兽医 • 上一篇    下一篇

影响非洲猪瘟病毒对培养细胞感染性的因素分析

冯永智1,2, 龚婷2,3, 吴东东1,2, 高琦1,3,4, 郑晓宇1,3, 张桂红1,2,3,4, 孙彦阔1,2,4*   

  1. 1. 华南农业大学兽医学院国家非洲猪瘟区域实验室(广州), 广州 510642;
    2. 广东省动物源性人兽共患病预防与控制重点实验室, 广州 510642;
    3. 岭南现代农业科学与技术广东省实验室茂名分中心, 茂名 525000;
    4. 农业农村部人畜共患病重点实验室, 广州 510642
  • 收稿日期:2022-10-31 出版日期:2023-08-23 发布日期:2023-08-22
  • 通讯作者: 孙彦阔,主要从事猪病毒病的流行病学、病原致病性和疫苗等方面研究,E-mail:yankuosun@scau.edu.cn
  • 作者简介:冯永智(1997-),男,山东潍坊人,硕士,主要从事非洲猪瘟病毒致病机制研究,E-mail:fyz@stu.scau.edu.cn
  • 基金资助:
    “十四五”国家重点研发计划项目(2021YFD1800100);广州市基础与应用基础研究项目(202201010490);财政部和农业农村部:国家现代农业产业技术体系、茂名实验室科研启动项目(2021TDQD002)

Analysis of Factors Affecting the Infectivity of African Swine Fever Virus on Cultured Cells

FENG Yongzhi1,2, GONG Ting2,3, WU Dongdong1,2, GAO Qi1,3,4, ZHENG Xiaoyu1,3, ZHANG Guihong1,2,3,4, SUN Yankuo1,2,4*   

  1. 1. National Regional Laboratory of African Swine Fever (Guangzhou), College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China;
    2. Key Laboratory of Prevention and Control of Animal-borne Zoonoses in Guangdong Province, Guangzhou 510642, China;
    3. Lingnan Modern Agricultural Science and Technology Guangdong Provincial Laboratory Maoming Branch, Maoming 525000, China;
    4. Key Laboratory of Zoonotic Diseases, Ministry of Agriculture and Rural Affairs, Guangzhou 510642, China 510642
  • Received:2022-10-31 Online:2023-08-23 Published:2023-08-22

摘要: 猪原代肺泡巨噬细胞(PAMs)是非洲猪瘟病毒(ASFV)的主要靶细胞,除宿主单核/巨噬细胞外,ASFV难以在其他体外细胞系中持续生长繁殖。本研究旨在研究影响ASFV在体外感染能力的因素。通过比较ASFV接种易感细胞PAMs和非易感细胞系3D4/21、PK15细胞的全基因组转录谱差异;使用小分子药物改变细胞代谢或周期、物理方法改变细胞黏附;通过荧光定量PCR、Western blot、红细胞吸附检测病毒在3D4/21和PK15细胞系中的增殖情况。结果表明:ASFV接种3D4/21和PK15两种细胞与PAMs细胞的共同差异基因显著富集在细胞黏附、细胞周期和细胞代谢等方面;使用多种调控细胞周期、细胞代谢的小分子药物处理细胞后对ASFV感染PK15和3D4/21细胞的能力无显著影响;通过悬浮培养来调节细胞的黏附后,显著提高ASFV感染PK15和3D4/21细胞的能力,但随着传代次数的增加,病毒的复制能力逐渐下降。综上所述,细胞黏附可能是影响ASFV体外感染能力的重要因素之一,但是改变细胞黏附后并不能维持ASFV的复制能力。本研究为ASFV体外细胞系的建立提供了初步参考。

关键词: 非洲猪瘟病毒, 全基因组转录谱, 悬浮培养, 体外感染细胞系

Abstract: Porcine primary alveolar macrophages (PAMs) were the main target cells of African swine fever virus (ASFV), and it was difficult for ASFV to grow and multiply continuously in other in vitro cell lines except host monocytes/macrophages. The aim of this study was to investigate the factors affecting ASFV in in vitro passaging cultures. By comparing the genome-wide transcriptional profile differences between ASFV inoculated susceptible cells PAMs and non-susceptible cell lines 3D4/21 and PK15 cells; Using small molecule drugs to alter cell metabolism or cycle, physical methods to alter cell adhesion; detecting virus proliferation in 3D4/21 and PK15 cell lines by fluorescence quantitative PCR, Western blot, red cell adsorption. The results showed that:ASFV inoculation of both 3D4/21 and PK15 cells and PAMs cells were significantly enriched in genes common to both cell adhesion, cell cycle and cell metabolism; The ability of ASFV to infect PK15 and 3D4/21 cells was not significantly affected by treatment of cells with various small molecule drugs that regulate cell cycle and cell metabolism; The ability of ASFV to infect PK15 and 3D4/21 cells was significantly affected by suspension culture to regulate The ability of ASFV to infect PK15 and 3D4/21 cells was significantly improved after cell adhesion was regulated by suspension culture, but the replication ability of the virus gradually decreased with the increase in the number of passages. In conclusion, cell adhesion may be one of the important factors affecting the in vitro infection ability of ASFV, but altering cell adhesion did not maintain the replication ability of ASFV. This study provides a preliminary reference for the establishment of ASFV in vitro cell lines.

Key words: African swine fever virus, genome-wide transcriptional profiling, suspension culture, in vitro infected cell line

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