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Development of monoclonal antibodies against the myxosporean, ceratomyxa shasta, and characterization of the salmonid host response

ScholarsArchive at Oregon State University

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Title Development of monoclonal antibodies against the myxosporean, ceratomyxa shasta, and characterization of the salmonid host response
Names Bartholomew, Jerri Lee (creator)
Fryer, John L. (advisor)
Date Issued 1988-11-11 (iso8601)
Note Graduation date: 1989
Abstract Monoclonal antibodies (Mabs) were produced against the
myxosporean parasite, Ceratomyxa shasta, and were characterized
by indirect immunofluorescent techniques, western blot analysis,
and immunoelectron microscopy. The resulting Mabs reacted
specifically with the trophozoite and sporoblast stages of the
parasite, but not with the mature spore, indicating that certain
antigens are stage-specific. Two of the Mabs produced also reacted
with trout white blood cells as evidenced by indirect fluorescent
antibody techniques (IFAT) and Western blot analysis. Further
characterization of these cross-reacting antibodies showed that they
were directed against carbohydrate epitopes on both the parasite
and trout immunoglobulin heavy chain. One hybridoma produced
antibodies of high specificity for prespore stages of C. shasta.
Ultrastructural analysis of the parasite using immunogold labeling
showed that the Mab specifically bound antigen located in the
cytoplasm of the trophozoites.
The C. shasta-specific antibodies produced by monoclonal
technology, standard histological methods, and scanning electron
microscopy were used to investigate the host response of Sa lmo
gairdneri against infection by the parasite. In infected fish the
parasite was first observed in the mucosal epithelium of the
posterior intestine using IFAT. As the trophozoites proliferated, the
infection spread anteriorally and into the submucosa, muscularis,
and serosa of the intestine. Hepatic tissues were also infected early
in the disease process. In the terminal stages of the infection,
trophozoites had penetrated the stomach, pyloric caeca, pancreas,
and adipose tissues and were also observed in the blood and
kidney. In fish refractory to infection, the parasite was observed in
the lumen of the intestine. Examination of infection in a moribound
fish by scanning electron microscopy showed extensive destruction
of the mucosal folds of the posterior intestine. Although a vigorous
tissue response was evident in infected tissues, trout antibodies
specific for the parasite were not detected by either Western blot
analysis or IFAT.
The distribution of the infective stage of C. shasta in the
Columbia River basin was also investigated. The range of the
parasite was extended in the Columbia River to its confluence with
the Snake River and in the Snake River to Oxbow Dam.
Genre Thesis/Dissertation
Topic Salmonidae -- Parasites
Identifier http://hdl.handle.net/1957/40514

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