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In vivo localization of antibodies raised against Eimeria maxima wall forming bodies during sexual intracellular development

Published online by Cambridge University Press:  30 July 2014

SONJA FRÖLICH*
Affiliation:
The iThree Institute, The School of Medical and Molecular Biosciences, The University of Technology Sydney, PO Box 123, Broadway, Sydney, New South Wales 2007, Australia
ANNISHA SHAHPAREE
Affiliation:
The iThree Institute, The School of Medical and Molecular Biosciences, The University of Technology Sydney, PO Box 123, Broadway, Sydney, New South Wales 2007, Australia
VALERIE C. WASINGER
Affiliation:
Bioanalytical Mass Spectrometry Facility, Mark Wainwright Analytical Centre, The University of New South Wales, Sydney, NSW 2052, Australia
MICHAEL WALLACH
Affiliation:
The iThree Institute, The School of Medical and Molecular Biosciences, The University of Technology Sydney, PO Box 123, Broadway, Sydney, New South Wales 2007, Australia
*
* Corresponding author: The iThree Institute, The School of Medical and Molecular Biosciences, The University of Technology Sydney, PO Box 123, Broadway NSW 2007, Australia. E-mail: [email protected]

Summary

Apicomplexan parasites cause devastating diseases in humans and livestock. Previously we demonstrated that antibodies targeting transmissible forms of the apicomplexan parasite, Eimeria, are effective at reducing parasite shedding thus preventing the transmission of the disease. However, the mechanisms responsible have not been fully defined. Moreover, there is no direct evidence that the parasite-specific IgG antibodies can reach the parasite developing in the enterocytes of the infected chicken host. This study summarizes our efforts using host immunity, parasite proteomics and 3D microscopy to provide a step forward in our understanding of how this immune response works. Eimeria maxima is an important pathogen of poultry and used as a surrogate for a number of human pathogens including Toxoplasma and Plasmodium. Our studies demonstrate that immunization with the purified wall forming bodies (WFBs) results in a production of parasite-specific IgG antibodies, which have the ability to reach in situ gametocytes in the intestinal lumen and permeate the enterocyte/parasite membranes in order to bind to the cytoplasmic Type 1 and Type 2 WFBs. This raises the intriguing possibility that via this process antibodies block the development of Eimeria maxima in vivo.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2014 

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