湖北农业科学 ›› 2022, Vol. 61 ›› Issue (6): 112-116.doi: 10.14088/j.cnki.issn0439-8114.2022.06.021

• 畜牧·兽医 • 上一篇    下一篇

小鼠IL-1β原核表达及其与在布鲁氏杆菌侵染巨噬细胞中差异表达的初步研究

杨馨, 邹德颖, 张凯, 常江, 常恒祯, 战俊澎, 郭珣, 刘益辛, 程梦妍, 韩成, 胡盼, 卢士英, 李岩松, 柳增善, 任洪林   

  1. 吉林大学人兽共患病研究教育部重点实验室/人兽共患病研究所/动物医学学院,长春 130062
  • 收稿日期:2021-12-09 出版日期:2022-03-25 发布日期:2022-04-18
  • 通讯作者: 任洪林(1974-),男,教授,博士,博士生导师,主要从事人兽共患细菌病、食品安全快检技术及分子生物学与毒理学研究,(电子信箱)renhl@jlu.edu.cn。
  • 作者简介:杨馨(1995-),女,陕西西安人,在读硕士研究生,研究方向为兽医公共卫生学,(电话)18392364878(电子信箱)1971908850@qq.com。
  • 基金资助:
    吉林省科技发展计划资助项目(20200402059NC); 中央高校基本科研业务费专项资金资助项目(45121031B007)

Prokaryotic expression of mouse IL-1β and preliminary study on its differential expression in Brucella infection

YANG Xin, ZOU De-ying, ZHANG Kai, CHANG Jiang, CHANG Heng-zhen, ZHAN Jun-peng, GUO Xun, LIU Yi-xin, CHENG Meng-yan, HAN Cheng, HU Pan, LU Shi-ying, LI Yan-song, LIU Zeng-shan, REN Hong-lin   

  1. Key Laboratory of Zoonosis Research, Ministry of Education/Institute of Zoonosis/College of Veterinary Medicine, Jilin University, Changchun 130062, China
  • Received:2021-12-09 Online:2022-03-25 Published:2022-04-18

摘要: 为研究IL-1β在布鲁氏杆菌(Brucella)侵染小鼠巨噬细胞过程中的表达情况,首先构建重组小鼠IL-1β原核稳定表达系统,免疫新西兰兔获得多克隆抗体,通过ELISA检测血清效价,并通过Western blot分析其活性,再以感染复数(multiplicity of infection,MOI)为1∶100(细菌∶细胞)建立猪种布鲁氏杆菌S2株侵染小鼠巨噬细胞RAW264.7的模型,利用RT-PCR检测细菌侵染过程中IL-1βMyD88 mRNA的变化水平;Western blot分析IL-1β在蛋白水平的变化。结果表明,重组蛋白IL-1β分子质量31 ku,多克隆抗体效价为1∶256 000,并且具有良好的特异性;与对照组相比,感染后IL-1β mRNA和IL-1β蛋白表达上调,胞内细菌数减少。猪种布鲁氏杆菌S2株侵染巨噬细胞IL-1β的表达量随时间变化并影响胞内活菌数。

关键词: 布鲁氏杆菌(Brucella), 原核表达, 多克隆抗体, IL-1β, MyD88

Abstract: To explore the expression of IL-1β during the infection of host cells by Brucella, the prokaryotic expression of IL-1β in mouse was constructed, polyclonal antibodies was obtained by immunization, and its activity was detected by ELISA and Western blot. The 1∶100 (bacterial∶cell) multiplicity of infection was then used to model the infection of RAW264.7 macrophages by Brucella suis S2. Expression of IL-1β mRNA and MyD88 mRNA was detected by RT-PCR; IL-1β protein was analyzed by Western blot. The molecular weight of the recombinant protein was about 31 ku. And the titer of the polyclonal antibody prepared by ELISA was 1∶25 600, with good immunoreactivity and specificity. The expression of IL-1β mRNA and IL-1β protein increased after infection. And the number of intracellular bacteria decreased. The expression of IL-1β in macrophages infected with Brucella suis S2 varied over time and affected the intracellular bacteria。

Key words: Brucella, prokaryotic expression, polyclonal antibody, IL-1β, MyD88

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