期刊
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES
卷 14, 期 -, 页码 E166-E170出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ijid.2009.12.009
关键词
FepA; Immunity; Iron; Siderophore
资金
- Biotechnology Council of the I.R. Iran
- Shahed University, Tehran, Iran
Objectives: Ferric siderophore complexes are produced by most bacteria to acquire iron, a vital element. These complexes are transported across the outer membrane by receptor proteins commonly known as FepA (ferric enterobactin protein). In this study we attempted to evaluate the immunogenicity of the membrane protein FepA, aiming at inhibition of iron uptake to protect invasion of the host by the bacterium. Methods: The genomic fepA gene was amplified from Escherichia coli O157:H7. The PCR product was ligated into pET28a and was then expressed in E. coli BL21(DE3). The recombinant protein purified by nickel-nitrilotriacetic acid (Ni-NTA) affinity chromatography was injected into BALB/C mice to induce immunity. Antibody titer was determined by ELISA. Mouse groups were challenged with various doses of E. coli O157: H7, Shigella flexneri, Klebsiella pneumoniae, and Salmonella typhi to study immune response. Results: An 85-kDa recombinant protein was expressed and purified. Immunogenicity of the recombinant protein was determined by injecting BALB/C mice. The antibody produced therein could efficiently recognize and bind ferric enterobactin binding protein. Immunized mice challenged with higher doses of selected bacteria survived. Conclusions: Significant recognition by the antibody of ferric enterobactin binding protein may lead to its application in the restriction of Enterobacteriaceae propagation. (C) 2010 International Society for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
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