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Isolation and characterization of a leukocytolytic factor from Aeromonas salmonicida

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Field Value
Title Isolation and characterization of a leukocytolytic factor from Aeromonas salmonicida
Names Fuller, David Wallace (creator)
Fryer, J. L. (advisor)
Date Issued 1974-11-05 (iso8601)
Note Graduation date: 1975
Abstract The purpose of this study was to find what effect temperature
and immunization has on the phagocytic activity of fish leukocytes
against certain disease causing bacteria. Also proposed was the
isolation and characterization of a leukocytolytic factor produced by
one of these bacteria, Aeromonas salmonicida.
Investigations revealed that temperature had no significant effect
on the phagocytic activity of leukocytes from either immunized or
nonimmunized rainbow trout toward Aeromonas salmonicida and
Vibrio anquillarum. Leukocytes from rainbow trout immunized with
killed A. salmonicida vaccine showed a significantly higher phagocytic
activity than those from nonimmunized rainbow trout toward A.
salmonicida at 12°C and 23°C, but not at 7°C and 18°C. The phagocytic
activity of the leukocytes from rainbow trout immunized with
killed V. anguillarum vaccine was significantly higher against V.
anguillarum at 70, 120, 180, and 230C.
A material characterized as a glycoprotein was isolated from
the supernatant of a broth culture of A. salmonicida by combinations
of ammonium sulfate and ethanol precipitations followed by DEAE
chromatography. A virulent strain of A. salmonicida produced more
of this substance than an avirulant strain. This material was demonstrated
to be cytolytic to rainbow trout leukocytes, and salmon and
steelhead embryo cell cultures. An affinity for cell membranes was
indicated by a hemagglutinating activity with sheep erythrocytes.
Intravenous injection of the material into rainbow trout caused marked
leukopenia followed by leukocytosis with an ultimate return of total
white cell counts to normal. Simultaneous intraperitoneal injections
of the material with one LD₅₀ of A. salmonicida greatly increased
the susceptibility of the host to the organism, indicating that this is
a virulence factor.
The ratio of protein, as assayed by the Lowry method, to
hexose, as assayed by the anthrone method, was consistently between
0.35 and 0.45 with small amounts of amino sugars noted. No lipids
were detected by the assay methods used. The material was demonstrated
to be antigenic and appeared to have a molecular weight of
between 100, 000 and 300, 000 as indicated by ultrafiltration methods.
Electron micrographs revealed aggregates of oval or egg-shaped
particles measuring approximately 40 nm by 25 to 30 nm per particle. It was determined that the leukocytolytic factor is not the endotoxin
produced by this bacterium.
Genre Thesis/Dissertation
Topic Leucocytes
Identifier http://hdl.handle.net/1957/44129

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