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福氏2a志贺氏菌2457T HtpG蛋白诱导小鼠炎性反应
引用本文:卜歆,朱力,刘先凯,赵格,冯尔玲,张静飞,袁静,王恒樑.福氏2a志贺氏菌2457T HtpG蛋白诱导小鼠炎性反应[J].微生物学报,2008,48(7):905-910.
作者姓名:卜歆  朱力  刘先凯  赵格  冯尔玲  张静飞  袁静  王恒樑
作者单位:1. 西北农林科技大学食品科学与工程学院,杨凌712100;军事医学科学院生物工程研究所,病原微生物生物安全国家重点实验室,北京,100071
2. 军事医学科学院生物工程研究所,病原微生物生物安全国家重点实验室,北京,100071
基金项目:国家自然科学基金 , 国家重点基础研究发展计划(973计划)
摘    要:目的]构建福氏2a志贺氏菌2457T株的htpG缺失突变株和回复株,对HtpG蛋白的功能进行初步研究.方法]采用X-Red重组系统对htpG基因进行缺失突变,构建了福氏2a志贺氏菌2457T株的htpG缺失突变株,并利用低拷贝质粒构建了htpG突变株的回复株.在此基础上,对野生株、突变株和回复株的生长曲线、生化反应、豚鼠角膜试验进行了比较分析,并考察了野生株、突变株和回复株腹腔注射引起小鼠炎症反应的强弱.结果]HtpG蛋白功能与福氏志贺氏菌的基本生化代谢无关,也不影响细菌穿透上皮细胞的能力,但腹腔注射后能够引起小鼠强烈的炎症反应.结论]HtpG蛋白功能可能与细菌的免疫致病性相关.

关 键 词:福氏2a志贺氏菌2457T株  热休克蛋白HtpG  缺失突变株  炎症因子  福氏志贺氏菌  蛋白诱导  小鼠  炎性反应  mice  inflammatory  response  strain  相关  致病性  免疫  能力  上皮细胞  穿透  细菌  影响  生化代谢  蛋白功能  结果  炎症反应  腹腔注射
文章编号:0001-6209(2008)07-0905-06
修稿时间:2007年12月27

HtpG protein of Shigella flexneri 2a strain 2457T evokes inflammatory response in mice
Xin Bu,Li Zhu,Xiankai Liu,Ge Zhao,Erling Feng,Jingfei Zhang,Jing Yuan and Hengliang Wang.HtpG protein of Shigella flexneri 2a strain 2457T evokes inflammatory response in mice[J].Acta Microbiologica Sinica,2008,48(7):905-910.
Authors:Xin Bu  Li Zhu  Xiankai Liu  Ge Zhao  Erling Feng  Jingfei Zhang  Jing Yuan and Hengliang Wang
Institution:1College of Food Science and Engineering, Northwest Agriculture & Forestry University, Yangling 712100, China;2Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China;Beijing Institute of Biotechnology, National Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China
Abstract:Objective] To analyze the function of htpG of S. flexneri 2a 2457T, we constructed an htpG deletion mutant and a recovery mutant. Methods] g-Red recombination system was used to construct an htpG deletion mutant of S. flexneri 2a 2457T. In addition, a recover mutant was obtained by introducing a low-copy plasmid containing one copy of htpG gene into the deletion mutant. Then, the growth curves of wild-type strain, deletion mutant and recover mutant were measured. Some of biochemical tests were also investigated. Furthermore, the Sereny tests were performed to evaluate the virulence of these strains. Results] No significant difference were observed among three strains. However, the titers of some inflammatory factors evoked by wild-type strain, deletion mutant and recovery mutant in intraperitoneal injected mice were quite different. Conclusion] These results suggest that the HtpG protein of Shigella flexneri 2a strain 2457T might be involved in the immunopathogenesis.
Keywords:Shigella flexneri 2a strain 2457T  HtpG  deletion mutant  inflammatory factor
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