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A novel antigen from Anaplasma marginale: characterization, expression and preliminary evaluation of the recombinant
Michelle Hope1, George Riding, Moira Menzies
1Cooperative Research Center for Vaccine Technology and CSIRO Livestock Industries, Queensland Biosciences Precinct, 306 Carmody Road, QLD 4067, St. Lucia, Australia. shelly.hope@csiro.au
Abstract:
Through a process of protein fractionation and vaccination we previously identified four native antigens that confer a degree of protection against challenge with Anaplasma marginale. One of these, Ana 29 has been successfully cloned and sequenced using degenerate primers designed to N-terminal and internal peptide sequences. The full-length gene codes for a protein with a theoretical molecular weight of 27 kDa and pI 8.6. The sequence is highly conserved, showing 99% identity between two Australian and an American isolate of A. marginale. The gene sequences from these isolates also share 99% identity with the strain of Anaplasma centrale used in the commercial Australian vaccine. Protein prediction algorithms suggest the native protein is an integral membrane protein. This protein has been over-expressed and purified from Escherichia coli and used in vaccination trials in cattle using two adjuvants. The initial results from the trial show a significant level of protection was obtained with one adjuvant; in comparison, the second adjuvant slightly aggravated the disease. Preliminary data suggests a good correlation between the induction of an IgG2 response and protection.
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