Literaturdatenbank
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Wendland, L. D., Klein, P. A., Jacobson, E. R., & Brown, M. B. (2010). Mycoplasma agassizii strain variation and distinct host antibody responses explain differences between enzyme-linked immunosorbent assays and western blot assays. Clinical and vaccine immunology, 17(11), 1739–1745.
Added by: Admin (06 Jan 2014 18:23:14 UTC) |
| Resource type: Journal Article BibTeX citation key: Wendland2010 View all bibliographic details  |
Categories: General Keywords: Bakterien - bacteria, Gopherus agassizii, Gopherus polyphemus, Schildkröten - turtles + tortoises, Testudinidae, Veterinärmedizin - veterinary medicine Creators: Brown, Jacobson, Klein, Wendland Collection: Clinical and vaccine immunology |
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| Abstract |
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Testudinidae The precarious status of desert (Gopherus agassizii) and gopher (G. polyphemus) tortoises has resulted in conservation efforts that now include health assessment as an important component of management decision-making. Mycoplasmal upper respiratory tract disease (URTD) is one of very few diseases in chelonians for which comprehensive and rigorously validated diagnostic tests exist. In this study, serum samples obtained from eight Gopherus tortoises documented at necropsy to (i) be enzyme-linked immunosorbent assay (ELISA) seropositive using the PS6 antigen, (ii) be infected with Mycoplasma agassizii as indicated by direct isolation of the pathogen from the respiratory surfaces, and (iii) have histological lesions of mycoplasmal URTD were used to evaluate four distinct clinical isolates of M. agassizii as antigens for ELISA and Western blot analyses. Each animal sample reacted in the Western blot with its homologous M. agassizii strain, but recognition of heterologous M. agassizii strains was variable. Further, individual animals varied significantly with respect to the specific proteins recognized by the humoral immune response. An additional 114 Gopherus serum samples were evaluated using ELISA antigens prepared from the four distinct M. agassizii strains; A405 values were significantly correlated (r2 goodness of fit range, 0.708 to 0.771; P < 0.0001) for all antigens tested. The results confirm that strain variation is responsible for the observed differences between Western blot binding patterns. Thus, reliance on a single M. agassizii strain as an antigen in Western blot assays may provide false-negative results. This could have adverse consequences for the well-being of these environmentally sensitive hosts if false-negative animals were relocated to sites consisting of true-negative populations.
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