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Clinical and Diagnostic Laboratory Immunology, Sep 1995, 524-530, Vol 2, No. 5
JM Bumstead, PP Dunn and FM Tomley
An immunoblotting technique was used to identify lymphostimulatory antigens
within sized polypeptide fractions of Eimeria maxima sporozoites. Six
fractions contained polypeptides that specifically stimulated the
proliferation of immune lymphocytes in an in vitro assay, and polyclonal
antisera were made in rabbits against these fractions. cDNA clones,
isolated with antisera against a lymphostimulatory fraction of around 70
kDa, were found to encode four different antigens including a classical
hsp70, a molecule homologous to an endoplasmic reticulum chaperonin
(BiP/GRP), and a calcium- dependent serine/threonine protein kinase that
appears homologous to a recently described molecule from Plasmodium
falciparum. The protein kinase cDNA clone was overexpressed in Escherichia
coli, and the recombinant antigen was found to induce both antibody and
lymphoproliferative responses in chickens when administered subcutaneously.
Thus, immunoblotting, in combination with in vitro lymphoproliferation
assays, can be used as an initial screen for the identification of
lymphostimulatory antigens from a complex pool of polypeptides, and a
combination of cDNA cloning, expression, and immunization allows assessment
of the lymphostimulatory activity of individual polypeptides. These studies
should facilitate further evaluation of antigens that are potential
candidates for inclusion in a recombinant vaccine against poultry
coccidiosis.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Nitrocellulose immunoblotting for identification and molecular gene cloning of Eimeria maxima antigens that stimulate lymphocyte proliferation
Institute for Animal Health, Compton, Newbury, Berkshire, United Kingdom.
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