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Clinical and Diagnostic Laboratory Immunology, 09 1995, 542-548, Vol 2, No. 5
U Gross, H Bormuth, C Gaissmaier, C Dittrich, V Krenn, W Bohne and DJ Ferguson
We previously reported the in vitro analysis of stage differentiation of
Toxoplasma gondii in murine bone marrow-derived macrophages. The purpose of
this study was to generate monoclonal rat antibodies that might be suitable
for investigating tachyzoite-bradyzoite interconversion in vivo with the
murine model. Immunization of Fischer rats with cysts of T. gondii NTE
resulted in the generation of seven monoclonal antibodies of the
immunoglobulin G2a, G2b, or M isotype, which were further characterized by
the immunoblot technique, immunofluorescence assay, immunohistology, and
immunoelectron microscopy. Immunoblots demonstrated specific reactivity of
five monoclonal antibodies with proteins with molecular masses of 40, 52,
55, 60, 64, 65, and 115 kDa. One antibody (CC2) appeared to recognize a
differently expressed antigen depending on the parasite stage, reacting
with a 40-kDa molecule in tachyzoites and a 115-kDa antigen in bradyzoites
and oocysts. Several other monoclonal antibodies were shown to be stage
specific and to react in immunofluorescence assays or in immunoblots with
either tachyzoites or bradyzoites. Kinetics of stage conversion in vitro
could be monitored by immunofluorescence with two of these monoclonal
antibodies. Preliminary immunohistological investigations of tissue
sections from infected mice demonstrated the possible usefulness of these
monoclonal antibodies for future in vivo studies on stage differentiation
of T. gondii in the murine system.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Monoclonal rat antibodies directed against Toxoplasma gondii suitable for studying tachyzoite-bradyzoite interconversion in vivo
Institute of Hygiene and Microbiology, University of Wurzburg, Germany.
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