production of monoclonal antibody against recombinant polypeptide from the erns coding region of the bovine viral diarrhea virus

Authors

masood reza seyfi abad shapouri department of pathobiology, faculty of veterinary medicine, shahid chamran university of ahvaz, ahvaz, ir iran

maryam ekhtelat department of pharmacognosy, faculty of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; department of pharmacognosy, faculty of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel: +98-9161130232, fax: +98-6133333936

masood ghorbanpoor najaf abadi department of pathobiology, faculty of veterinary medicine, shahid chamran university of ahvaz, ahvaz, ir iran

pezhman mahmoodi koohi department of pathobiology, faculty of para veterinary science, bu-ali sina university, hamedan, ir iran

abstract

results based on our results, mab against recombinant erns was produced and reacted successfully with recombinant and natural antigens. conclusions with regards to the role of erns in the identification of pi animals, it appears that erns recombinant antigen and the specific monoclonal antibodies produced against it may be suitable for developing bvdv laboratory diagnostic assays. objectives erns as an immunogenic protein of bvdv, is genetically and antigenically conserved among different isolates and therefore, is a candidate antigen for development of the enzyme linked immunosorbent assay (elisa) for serological studies or identification of pi animals. the aim of this study was to produce a monoclonal antibody (mab) against recombinant erns. materials and methods for this purpose, recombinant maltose-binding protein (mbp)-erns protein was expressed in escherichia coli and purified using amylose resin chromatography column and used as an antigen in mab production. spleen cells of the immunized mice with the recombinant antigen were fused with sp2/0 myeloma cells. next, culture supernatants of primary clones of fused cells were screened by indirect elisa. after three rounds of cloning, the reactivity of the mabs with recombinant and natural antigen was established by western blotting. background bovine viral diarrhea (bvd) is an economically important cattle disease with a worldwide distribution. detection and elimination of animals persistently infected (pi) with bovine viral diarrhea virus (bvdv) is essential for the control of bvd and eradication of bvdv. there are usually no pathognomonic clinical signs of bvdv infection. diagnostic investigations therefore rely on laboratory-based detection of the virus, or virus-induced antigens or antibodies.

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Journal title:
jundishapur journal of microbiology

جلد ۸، شماره ۱۲، صفحات ۰-۰

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