畜牧兽医学报 ›› 2012, Vol. 43 ›› Issue (9): 1437-1443.doi:

• 预防兽医 • 上一篇    下一篇

布鲁菌糖基转移酶对细胞炎症反应的影响

张豫,张辉*,张艳,孟茹,王震,陈瑞花,张俊波,鲁芝子,陈创夫*   

  1. (石河子大学动物科技学院 新疆地方与民族高发病教育部重点实验室,石河子 832003)
  • 出版日期:2012-09-25 发布日期:2012-09-25
  • 通讯作者: 陈创夫,教授,E-mail:ccf-xb@163.com; 张辉,副教授,E-mail: allanzhh@yahoo.com
  • 作者简介:张豫(1985-),女,新疆石河子人,硕士生,主要从事布鲁菌致病机制的研究,E-mail:llb@shzu.edu.cn,Tel:09932060217
  • 基金资助:

    国家“973项目”(2010CB30203);国家自然科学基金(31001046/30960288);高层次人才科研启动资金(RCZX200914)

The Effect of Cellular Inflammatory Response by Glycosyltransferase of Brucella

ZHANG Yu, ZHANG Hui*, ZHANG Yan, MENG Ru, WANG Zheng, CHEN Run-hua,
 ZHANG Jun-bo, LU Zhi-zi, CHEN Chuang-fu*   

  1. (Key Laboratory of Xinjiang Endemic and Ethnic Disease, College of Animal
    Science &Technologe, Shihezi University, Shihezi 832003, China)
  • Online:2012-09-25 Published:2012-09-25

摘要: 本研究旨在研究布鲁菌糖基转移酶(WboA)在诱发胚胎滋养层细胞(HTP-8)炎症反应中的作用。以羊种布鲁菌M5-90为模板,扩增WboA基因,构建pET28a(+)-WboA重组表达质粒,转化重组质粒在BL21(DE3)中表达,通过SDS-PAGE和Western blot鉴定,并对重组WboA蛋白进行纯化。构建自杀载体pGEM-7zf-ΔWboA-SacB,通过同源重组的方法,筛选布鲁菌WboA基因缺失株ΔWboA,并进行PCR鉴定和遗传稳定性检测。然后将纯化的WboA蛋白与ΔWboA分别作用于胚胎滋养层细胞,ELISA检测IL-6、IL-10、TNF-α和乳酸脱氢酶(LDH)的相对变化量。结果成功纯化了WboA蛋白,构建了ΔWboA,ΔWboA侵染胚胎滋养层细胞诱导产生炎症细胞因子IL-6、IL-10和TNF-α均低于M5-90对照组,差异显著(P<0.05),WboA蛋白作用胚胎滋养层细胞时,炎症细胞因子IL-6、TNF-α和LDH均高于PBS对照组,差异极显著(P<0.01)。本研究表明WboA蛋白具有细胞毒作用,布鲁菌的致炎作用与脂多糖O链相关,为进一步阐明布鲁菌感染宿主细胞的发病机制奠定了基础。

Abstract: The study explored the role of glycosyltransferase in inflammation response of embryo trophoblast cells infection by Brucella. WboA gene was amplified from Brucella melitensis M5-90 strain by PCR and cloned into vector pET-28a(+). The constructed recombinant plasmid pET-WboA was transformed to competent E. coli BL21. The protein WboA was identified by SDS-PAGE, Western blot, and purified. The suicide plasmid pGEM-7zf-ΔWboA-SacB was constructed. The WboA gene was knocked out of the genomic DNA of Brucella melitensis vaccine M5-90 strain by homologous recombination. Then purified the WboA protein and ΔWboA affects in the embryo trophoblast cells separately, the inflammatory cytokines of IL-6, IL-10, TNF-α and the lactic dehydrogenase (LDH) were ELISA examination. The protein WboA was successfully purified and the mutant ΔWboA was constructed. Compared with the M5-90 infected group, the HPT-8 cells infected by ΔWboA released much less inflammatory cytokine IL-6, IL-10 and TNF-α (P<0.05). The inflammatory cytokine IL-6, TNF-α  and LDH released by HPT-8 effected with WboA protein were significantly higher than the PBS control group(P<0.01). These results indicate that the protein WboA has the function of cytotoxin and the inflammation response of Brucella is related to the Lipopolysaccharides O chain.

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