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肠炎沙门菌lpfC基因缺失株的构建及基本生物学特性研究
  • ISSN号:1004-311X
  • 期刊名称:《生物技术》
  • 时间:0
  • 分类:Q933[生物学—微生物学]
  • 作者机构:[1]扬州大学江苏省人兽共患病学重点实验室/江苏高校动物重要疫病与人兽共患病防控协同创新中心,江苏扬州225009
  • 相关基金:国家自然科学基金项目(“肠炎沙门菌炎症反应机制及抗炎药物舒洛地特作用机制的研究” No.31320103907;“鸡白痢沙门菌致病岛-2 T3SS效应蛋白致病与免疫的分子机制” No.31230070); 公益性行业(农业)科研专项(“动物源性沙门菌病防控技术研究与示范” No.201403054); 国家“863”计划项目(“鸡白痢;鸡伤寒;禽大肠杆菌基因工程疫苗研发” No.2011AA10A212)资助 National Natural Science Foundation of China under Grant No. 31320103907 ( Molecular mechanism of inflammatory response caused by Sal- monella enteritidis and the evaluation of anti - inflammatory effect by sulodexide ), the National Natural Science Foundation of China under Grant No. 31230070 ( Molecular mechanisms on the pathogenicity and immunity of SPI -2 T3 SS effectors in Salmonella enterica serovar pullorum) , Special Fund for Agro -scientific Research in the Public Interest under Grant No. 201403054 (Studies and demonstration of prevention and control techniques on animal Salmo- nellosis) , the National 863 Program under Grant No. 2011AA10A212 (Development of genetically engineering vaccine for Salmonella pullorum, Salmonella gallinarum and avian E. coll. )
中文摘要:

[目的]为研究与Lpf菌毛合成相关的lpfC基因对肠炎沙门菌致病性的影响。[方法]利用自杀质粒介导的同源重组技术构建肠炎沙门菌C50041株的lpfC基因缺失株C50041ΔlpfC,并进行PCR和测序鉴定。同时,将lpfC基因克隆至质粒pBR322并电转入缺失株中,构建回复株C50041ΔlpfCR。比较野生株C50041、缺失株C50041ΔlpfC及回复株C50041ΔlpfCR的基本生物学特性。[结果]成功构建了缺失株C50041ΔlpfC及回复株C50041ΔlpfCR,且lpfC基因的缺失不影响C50041的生长特性和生化特性。该缺失株具有良好的遗传稳定性,但缺失株对BALB/c小鼠的LD50是野生株的2倍。[结论]lpfC基因的缺失使肠炎沙门菌对BALB/c小鼠的毒力降低,为进一步研究肠炎沙门菌Lpf菌毛的功能奠定了基础。

英文摘要:

[Objective]To study the role of lpfC gene which encodes a putative outer membrane usher for Lpf fimbrial assembly of Salmonella enteritidis in pathogenesis.[Methods]We constructed a lpfC mutant of Salmonella Enteritidis strain C50041 via suicide plasmid p GMB151,and its complementary strain C50041 ΔlpfCR in this study.Then the biological characteristics and virulence were determined.[Results]Among the three strains,there are no obviously differences in growth property and biochemical properties,while pass-generation test showed that hereditary property ofC50041 ΔlpfC was stable.However,the mouse lethal test showed that the LD50 of the C50041 ΔlpfC was 2 times than that of the parent strain C50041.[Conclusion]This study provided basic data for further study of the functions of the lpfC gene,and make a significant contribution to study the Lpf fimbriae function of Salmonella enteritidis.

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期刊信息
  • 《生物技术》
  • 北大核心期刊(2014版)
  • 主管单位:黑龙江省科学院
  • 主办单位:黑龙江省科学院微生物研究所 黑龙江省微生物学会 黑龙江省生物工程学会
  • 主编:张介驰
  • 地址:哈尔滨市道里区兆麟街68号
  • 邮编:150010
  • 邮箱:swjszz@163.com
  • 电话:0451-84615121
  • 国际标准刊号:ISSN:1004-311X
  • 国内统一刊号:ISSN:23-1319/Q
  • 邮发代号:14-225
  • 获奖情况:
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  • 被引量:13503