期刊文献+

布鲁氏菌ery操纵子突变株生物学特性分析 被引量:3

Biological Characterization of an ery Operon Promoter Mutant in Brucella
原文传递
导出
摘要 布鲁氏菌ery操纵子参与赤藓醇代谢.赤藓醇能够促进布鲁氏菌的生长.为进一步研究布鲁氏菌引发宿主流产的分子机制,采用基因重组技术构建布鲁氏菌ery操纵子启动子缺失株(△ery),通过体内外实验探讨布鲁氏菌ery操纵子的生物学功能.研究结果显示,获得了布鲁氏菌ery操纵子缺失株;布鲁氏菌ery操纵子缺失株侵染胚胎滋养层细胞脱落较亲本株明显下降;巨噬细胞CFU计数缺失株作用组和亲本株作用组差异显著(P<0.05).试管凝集和虎红平板实验结果显示均出现凝集现象;检测血清中细胞因子IL-10和TNF-α的表达水平,△ery诱导机体产生的IL-10和TNF-α明显低于亲本株(P<0.05).小鼠脾脏细菌CFU计数结果显示,△ery较亲本株毒力明显下降.本研究表明,布鲁氏菌ery操纵子启动子缺失株毒力较亲本株明显下降,为进一步揭示布鲁氏菌引起流产的致病机制提供了一定的理论依据. The ery operon is important for the metabolism of erythritol in Brucella, and erythritol was known to promote the growth of Brucella. To study the molecular mechanisms of Brucella-induced host abortion, an ery operon promoter deletion mutant strain (△ery) was constructed by DNA recombination to explore the biological function of Brucella ery operon in vivo and in vitro. The results showed that the exfoliative human trophoblast cells (HTP-8) infected with the △ery strain was significantly decreased as compared those infected with the wild type in clone forming units (CFU) (P〈0.05). In tube agglutination and rose bengal plate agglutination tests, the results showed that the degree of agglutination, as well as the levels of IL-10 and TNF-α were significantly lower in △ery groups (P〈0.05) than in the controls. The mouse spleen CFU results showed that the virulence of △ery was significantly decreased. This study provided useful evidence indicating the ery operon could be important for the pathogenesis of Brucella in abortion.
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2013年第1期76-83,共8页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家重点基础研究发展规划(973项目 No.2010CB30203) 国家自然科学基金(No.31001046/30960288) 高层次人才科研启动资金(No.RCZX200914)~~
关键词 布鲁氏菌 ery操纵子 缺失株 毒力 Brucella ery operon deletion mutant virulence
  • 相关文献

参考文献19

  • 1Dawson CE, Stubberfield EJ, Perrett LL, et al. Phenotypic andmolecular characterization of Brucella isolates from marinemammals [J]. BMC Microbiol, 2008,8: 224.
  • 2Pappas G, Papadimitriou P, Akritidis N, et al. The new globalmap of human brucellosis [ J]. Lancet Infect Dis,2006,6(2):91-99.
  • 3Greenfield RA,Drevets DA,Machado LJ,et al. Bacterialpathogens as biological weapons and agents of bioterrorism [ J].Am J Med Sci, 2002,323(6) : 299-315.
  • 4Kuplulu 0,Sariraehmetoglu B. Isolation and identification ofBrucella spp. in ice cream [ J]. Food Control, 2004,15: 511-514.
  • 5Cortea A,Scarcelli E,Soares RM,et al. Detection of BrucilaDNA from aborted bovine foetuses by polymerase chain reaction[J]. Aust Vet J, 2001, 79(7) : 500-501.
  • 6Hawk ET, Greenwood A, Gritz E R, ei al. The translationalresearch working group developmental pathway for lifestylealterations [J].Clin Cancer Res, 2008, 14(18) : 5707-5713.
  • 7Ko J, Splitter G A. Molecular host-pathogen interaction inbrucellosis : current understanding and future approaches tovaccine development for mice and humans [ J ]. Clin MicrobiolRev, 2003,16(1) : 65-78.
  • 8尚德秋.中国布鲁氏菌病防治科研50年[J].中华流行病学杂志,2000,21(1):55-57. 被引量:97
  • 9Sangari FJ, Agiiero J, Garcia-Lobo JM. The genes for erythritolcatabolism are organized as an inducible operon in Brucellaabortus [ J ] - Microbiology, 2000,146( Pt2) : 487-495.
  • 10Sperry JF, Robertson DC. Erythritol catabolism by Brucellaabortus[J]. J Bacteriol, 1975,121(2) : 619-630.

二级参考文献29

共引文献114

同被引文献16

引证文献3

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部