Cloning, Expression, and Antigenicity of 14 Proteins from Campylobacter jejuni

被引:5
作者
Zhang, Maojun [1 ,2 ]
Meng, Fanliang [1 ,2 ]
Cao, Fangfang [1 ,2 ,3 ]
Qiao, Bo [1 ,2 ,4 ]
Liu, Guodong [1 ,2 ,5 ]
Liu, Hongying [1 ,2 ]
Zhou, Yizhuang [1 ,2 ,6 ]
Dong, Haiyan [1 ,2 ]
Gu, Yixin [1 ,2 ]
Xiao, Di [1 ,2 ]
Zhang, Yongchan [1 ,2 ]
Zhang, Jianzhong [1 ,2 ]
机构
[1] Chinese Ctr Dis Control & Prevent, Natl Inst Communicable Dis Control & Prevent, Beijing 102206, Peoples R China
[2] Chinese Ctr Dis Control & Prevent, State Key Lab Infect Dis Prevent & Control, Beijing 102206, Peoples R China
[3] Peking Union Med Coll, Sch Publ Hlth, Beijing 100021, Peoples R China
[4] Zhengzhou Univ, Coll Publ Hlth, Zhengzhou, Henan, Peoples R China
[5] Beijing Municipal Ctr Dis Control & Prevent, Beijing, Peoples R China
[6] BGI, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
GUILLAIN-BARRE-SYNDROME; OUTER-MEMBRANE PROTEIN; ACID EXTRACT; INFECTION; IDENTIFICATION; IMMUNOGENICITY; ASSOCIATION; ANTIBODIES; CHINA; MICE;
D O I
10.1089/fpd.2011.1122
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Fourteen Campylobacter jejuni genes-porA, cadF, omp18, dnaK, flaC, peb1, peb2, peb3, peb4, ahpC, groEL, tuF, hipO, and Cj0069-were cloned and expressed in Escherichia coli BL21. The recombinant proteins were purified on histidine (His) and glutathione S-transferase (GST) trap columns using the AKTA Explorer 100 System. Recombinant proteins were visualized using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and identified using matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The antigenicities of these recombinant proteins were assessed by Western blotting and enzyme-linked immunosorbent assays with anti-C. jejuni immune rabbit sera. Four recombinant proteins, including rGST-PorA, rHis-CadF, rGST-GroEL, and rGST-TuF, demonstrated reactions with both anti-serum and preimmune serum, while rHis-DnaK, rGST-FlaC, rGST-PEB2, rGST-PEB3, rGST-PEB4, and rGST-HipO showed variable antigenicity characteristics to the anti-sera derived from different C. jejuni strains. rHis-Omp18, rHis-PEB1, and rGST-AhpC demonstrated universal and specific antigenities with the entire anti-sera panel tested in this present study, while recombinant rGST-Cj0069 and rHis-DnaK did not react with any of the anti-C. jejuni sera tested. In conclusion, rGST-AhpC may be useful as a potential serodiagnostic antigen for C. jejuni infection.
引用
收藏
页码:706 / 712
页数:7
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