Immunology
Masoud Reza Seyfi Abad Shapouri; Mohammad Rashno; Pezhman Mahmoodi; Mahshid Ariya
Volume 9, Issue 1 , March 2018, , Pages 67-72
Abstract
Monoclonal antibodies (MAbs) are invaluable molecules which have several advantages over polyclonal immunoglobulins (Igs) including consistency and higher specificity and hence can be used in biological researches, diagnosis and treatment of diseases. The present study was conducted to produce monoclonal ...
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Monoclonal antibodies (MAbs) are invaluable molecules which have several advantages over polyclonal immunoglobulins (Igs) including consistency and higher specificity and hence can be used in biological researches, diagnosis and treatment of diseases. The present study was conducted to produce monoclonal antibody against chicken IgG.TheIgG molecules were purified from chicken serum and used as antigens to immunize several mice. Thereafter, a well-immunized mouse was chosen and used for fusion process. After production of hybridoma cells, several rounds of cloning were carried out and produced MAbs were examined by various immunological assays including enzyme-linked immunosorbent assay (ELISA) and western and dot blotting. Assessment of grown hybridomas indicated that only one clone (5B8) has produced desired MAb against chicken IgG. Meanwhile, using an indirect ELISA, it was shown that this MAb successfully recognizes chicken IgG molecules attached to influenza virus nucleoprotein. Evaluation of cross reactivity of MAb 5B8 with several avian serum samples revealed that this molecule specifically identifies chicken antibody molecules. However, it also recognized turkey antibodies with less affinity. In addition to research applications like isolation and purification of chicken and turkey IgG molecules, such a MAb can be applied to design and development of various immunoassays (e.g. ELISA) in these avian species.
Immunology
Masood Reza Seyfi Abad Shapouri; Maryam Ekhtelat; Masood Ghorbanpoor Najaf Abadi; Mohsen Lotfi; Mohamad Rashno
Volume 7, Issue 3 , September 2016, , Pages 247-253
Abstract
Bovine Viral Diarrhea virus (BVDV) is an important viral pathogen of cattle causing several clinical syndromes. There are usually no pathognomonic clinical signs of BVDV infection. Diagnostic investigations therefore rely on serological detection and virus isolation. Nonstructural protein 3 (NS3) as ...
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Bovine Viral Diarrhea virus (BVDV) is an important viral pathogen of cattle causing several clinical syndromes. There are usually no pathognomonic clinical signs of BVDV infection. Diagnostic investigations therefore rely on serological detection and virus isolation. Nonstructural protein 3 (NS3) as immunogenic protein of BVDV is genetically and antigenically conserved among different isolates. This protein is therefore a candidate antigen for developing ELISA for serological studies. The aim of this study was to produce monoclonal antibody (MAb) against recombinant NS3 protein. For this purpose, the recombinant MBP-NS3 protein was expressed into expression vector pMalc2x in E. coli and purified using amylose resin chromatography column and the purified protein used as antigen in MAb production. After immunizing Balb/c mice with the recombinant antigen, the mouse showing highest titer of anti-NS3 antibody by indirect ELISA was selected for fusion. Spleen cells of the immunized mouse were fused with SP2/0 myeloma cells using polyethylene glycol. The cells in fusion mix were re-suspended in HAT medium and distributed in 96-well plates. Then culture supernatants of primary clones were screened by indirect ELISA. The positive clones after three times cloning, were selected and the reactivity of the monoclonal antibodies with recombinant and natural antigens was established by Western blotting. Based on these results, it appears that the specific monoclonal antibodies produced against NS3 recombinant antigen may be suitable for developing BVDV laboratory diagnostic assays.
