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Infect. Immun., Jun 1996, 2151-2157, Vol 64, No. 6
TC Meng, ML Hetsko and FD Gillin
Although excystation is crucial to the initiation of infection by Giardia
lamblia, little is known about the regulation of this important process. We
have been able to reliably induce excystation in vitro by mimicking cyst
passage through the stomach and upper small intestine by the exposure of in
vitro-derived cysts to an acidic, reducing environment (stage I) followed
by protease treatment at a slightly alkaline pH (stage II). Preexposure of
cysts to polyclonal rabbit antiserum against purified cyst walls (PCWs) or
to wheat germ agglutinin (WGA) inhibited excystation by > 90%.
Adsorption of either ligand with PCWs eliminated inhibition, demonstrating
specificity for cyst wall epitopes. Inhibition by WGA was reversed by
either chitotriose or sialic acid, while inhibition by polyclonal
antibodies against PCWs (anti-PCW) was reversed only by sialic acid, which
also inhibited binding of both ligands to intact cysts and to cyst wall
antigens in immunoblots. Binding of anti-PCW did not affect acidification
of cyst cytoplasm during stage I. Exposure of cysts to anti-PCW and WGA
prior to, but not after, stage II was sufficient to inhibit excystation,
and inhibition could be partially reversed by increasing the protease
concentration during stage II. A 7- to 10-fold higher proportion of WGA-
and anti-PCW-treated cysts than control cysts remained intact after stage
II. Our results suggest that these ligands, which bind cyst wall epitopes,
inhibit excystation, most likely by interfering with proteolysis of cyst
wall glycoproteins during stage II.
Copyright © 1996, American Society for Microbiology
Inhibition of Giardia lamblia excystation by antibodies against cyst walls and by wheat germ agglutinin
Division of Infectious Diseases, Department of Medicine, University of California at San Diego Medical Center, 92103-8416, USA.
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