Construction of a New Fusion Protein Vector Associated to Fibronectin Binding Protein A and Clumping Factor A Derived from Staphylococcus aureus NCTC8325 | ||
| Iranian Journal of Basic Medical Sciences | ||
| مقاله 3، دوره 12، شماره 1، فروردین 2009، صفحه 18-24 اصل مقاله (298.63 K) | ||
| نوع مقاله: Original Article | ||
| شناسه دیجیتال (DOI): 10.22038/ijbms.2009.5129 | ||
| نویسندگان | ||
| Jamshid Faghri* 1؛ Kamran Pooshang Bagheri1؛ Delavar Shahbaz Zadeh2؛ Rahmatolah Yazdani1؛ Hamid Mirmohammad Sadeghi3؛ Sharareh Moghim1 | ||
| 1Department of Bacteriology and Virology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran | ||
| 2Department of Biotechnology, Pasteur Institute of Iran, Tehran, Iran | ||
| 3Department of Biotechnology, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran | ||
| چکیده | ||
| Objective(s) Staphylococcus aureus is a leading cause of many nosocomial and community acquired infections. According to many reports, antibiotic therapy can not guarantee the eradication of S. aureus infections. Thus designing an adhesin based vaccine could restrain the S. aureus infections. This study designed for construction of a new fusion protein vaccine against S. aureus infections based on adhesin molecules fibronectin binding protein A (FnBPA) and clumping factor A (ClfA). Materials and Methods Bioinformatic experiments were performed using Oligo analyzer and DNAMAN softwares. The fragments corresponding to fnbA binding domain and a C-terminal fragment from clfA were amplified from S. aureus NCTC8325 genomic DNA. Purified PCR products and the vector, pET15b, were digested with Nco\ and BamHI. The digested PCR products were hybridized together and then ligated to digested vector. Finally incomplete construct was assembled by Taq DNA polymerase. To quick confirmation of cloning procedure the new construct designated pfnbA-clfA was digested with Ncol and BamHI. To further verification, the product was sent for sequencing. Results The data based on bioinformatic analysis showed no homology between fusion protein and human proteins. Digestion of new vector with Ncol and BamHI confirmed the ligation of fusion protein sequence into pET15b. Sequencing results verified the integrity of target sequences. Conclusion This study is the first effort to construct a new fusion protein vector based on S. aureus adhesins using a new design. This project is being continued to study the expression and biological activity of the fusion protein in a cell culture model. | ||
| کلیدواژهها | ||
| Cell adhesion molecules؛ Fusion protein vaccine؛ Staphylococcus aureus | ||
| مراجع | ||
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