《中国畜牧兽医》 ›› 2019, Vol. 46 ›› Issue (4): 986-993.doi: 10.16431/j.cnki.1671-7236.2019.04.004

• 生物技术 • 上一篇    下一篇

布鲁氏菌vceA基因缺失株的构建及生物学特性研究

王小凤, 李明奇, 郭嘉, 赵天艺, 刘航, 张樊, 孙晓露, 何家琪, 王震, 张辉   

  1. 石河子大学动物科技学院, 动物疾病防控兵团重点实验室, 石河子 832003
  • 收稿日期:2018-09-03 出版日期:2019-04-20 发布日期:2019-04-22
  • 通讯作者: 王震, 张辉 E-mail:530469380@qq.com;allanzhh@yahoo.com
  • 作者简介:王小凤(1991-),女,河南安阳人,硕士生,研究方向:人兽共患病致病机制与防控,E-mail:1205135930@qq.com
  • 基金资助:

    国家自然科学基金项目(31460650);兵团人才项目(CZ027202、2017CB002);国家SRP项目(201810759011)

Construction and Biological Characteristics of Brucella vceA Gene Deletion Strain

WANG Xiaofeng, LI Mingqi, GUO Jia, ZHAO Tianyi, LIU Hang, ZHANG Fan, SUN Xiaolu, HE Jiaqi, WANG Zhen, ZHANG Hui   

  1. Key Laboratory of Xinjiang Endemic and Ethnic Disease, College of Animal Science & Technology, Shihezi University, Shihezi 832003, China
  • Received:2018-09-03 Online:2019-04-20 Published:2019-04-22

摘要:

试验旨在构建布鲁氏菌Ⅳ型分泌系统vceA基因缺失株,分析其生长特征及其在人胚胎滋养层细胞(HPT-8)中的存活能力。以布鲁氏菌S2308为模板,PCR扩增vceA基因上、下游同源臂,以pUC19K质粒为模板扩增kan基因,然后利用融合PCR技术将3段基因进行融合,再将此片段与pMD19-T载体连接,电转至大肠杆菌DH5α感受态细胞中,构建ΔvceA基因缺失株(S2308ΔvceA),通过卡那抗性对缺失株进行连续筛选,并检测其遗传稳定性。在相同培养条件下,观察亲本株S2308和S2308ΔvceA的生长变化趋势,以侵染复数(MOI)100:1侵染HPT-8细胞,通过CFU计数检测亲本株S2308和缺失株S2308ΔvceA在细胞内的生存能力。结果显示,试验成功获得片段大小为372、510、1 093 bp的vceA基因上、下游同源臂和kan基因;且成功构建pMD19-T-vceA-kan自杀载体,将其电转入大肠杆菌DH5α感受态细胞,构建基因缺失株,连续传代10次未发现基因回复突变;在体外相同培养条件下,缺失株S2308ΔvceA与亲本株S2308生长趋势相似,均在12 h达到对数生长期,30 h进入平台期;侵染HPT-8细胞12 h时,缺失株S2308ΔvceA在细胞中的数量显著低于亲本株S2308(P<0.05)。综上所述,本试验成功构建并获得了具有良好遗传稳定性的布鲁氏菌vceA基因缺失株,该缺失株在体外培养条件下与亲本株生长趋势相似;但该缺失株在HPT-8细胞内的存活能力显著变弱。

关键词: 布鲁氏菌; vceA基因缺失株; 生长曲线; 生物学特性

Abstract:

This study was aimed to construct Brucella 2308 (S2308) vceA gene mutants then analyse its growth character and survival ability in human embryonic trophoblast cells (HPT-8).The upstream,downstream homologous arms of vceA gene and kan gene were amplified by PCR method with wild S2308 strain as template.The fusion PCR technology was used to fuse the three genes fragments and connected to pMD19-T vector and then electric transported to E. coli DH5α competent cells to construct S2308ΔvceA strain.The genetic stability of the mutant strain was tested by screening continuously with kanar resistance,and the growth rates between the S2308ΔvceA and S2308 strains were compared.The HPT-8 cells were infected with S2308ΔvceA and S2308 strains at a multiplicity of infection of 100:1 and the intracellular survival ability was determined by CFU counting.The results showed that the target gene fragments of upstream homologous arms (372 bp),downstream homologous arms (510 bp) of vceA gene and kan gene (1 093 bp) were amplified respectively.The mutants was successfully constructed and the virulence not recover after culture at least 10 generations.The growth curves of S2308ΔvceA and S2308 strains were similar under the same condition.These two strains reached the logarithm growth phase at 12 h,entered in platform period after 30 h.However,the survival rates of the S2308ΔvceA strain was significantly lower than its parent strain S2308 after the infection of HPT-8 cells at 12 h (P<0.05).In conclusion,This experiment successfully constructed and obtained a vceA gene deletion strain of Brucella with good genetic stability,and the growth trend of this deleted strain was similar to parent strain under the condition of in vitro culture.However,the viability of the deleted strain in HPT-8 cells was significantly weakened.

Key words: Brucella; vceA gene mutant strain; growth curve; biological characteristics

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