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The role of GPI-linked surface proteins in site-specific tropism of Eimeria parasites and the potential of these proteins for novel therapies.

Reference	BB/F002564/1
Principal Investigator / Supervisor	Professor Fiona Tomley
Co-Investigators / Co-Supervisors	Dr Chandrasekaran Subramaniam
Institution	The Pirbright Institute
Department	Div of Microbiology Compton
Funding type	Research
Value (£)	411,656
Status	Completed
Type	Research Grant
Start date	18/10/2007
End date	17/10/2010
Duration	36 months

Abstract

Eimeria parasites cause coccidiosis in a number of vertebrate hosts but are mainly a problem in the poultry industry where seven different species infect chickens and cause major economic and welfare problems. The seven species all colonise a distinct portion of the chicken intestines and moreover, immunity generated by infection is highly specific with recovered birds remaining totally susceptible to infection with the other six species. We have studied GPI-linked surface antigens (SAGs) of Eimeria tenella and have found that this parasite has two multi-gene families that encode 62 variant SAGs. The genes are clustered, along with a large number of pseudogenes, into tandem arrays within four chromosomal loci and expression of the genes is strictly developmentally regulated. Preliminary work on other species of Eimeria indicates that these too possess multiple SAGs that are related to, but distinct from, those of E. tenella. Since the SAGs are consitutively expressed on the parasite surface they are good candidates for interaction with host cells and we have shown that they have binding properties. We hypothesise that SAGs may play a role in determining the site tropism of Eimeria parasites within the chicken intestine and moreover that the strict developmental expression of SAGs may be a parasite adaptive mechanism by which later merozoite stages evade potent immune responses induced by the early sporozoite stage. We will test these ideas in this project by using parasite transgenesis to manipulate the E. tenella genome specifically to (i) express a dominant sporozoite E. maxima SAG in E. tenella, (ii) alter the strict developmental regulation of E. tenella SAG1 and (iii) attempt to knock out EtSAG1. The resultant trangenic parasites will be studied in vitro and in vivo to determine the phenotypic effects of SAG manipulation in terms of site of development, parasite growth and pathogenicity. Pilot immunisation experiments will also be carried out.

Summary

Microscopic single-celled parasites can cause many types of disease in man and domestic animals, some of them very serious. We are working on Eimeria parasites, which cause enteritis in domestic chickens that can lead to very high death rates if infections are not controlled. There are seven different species of Eimeria that infect chickens and each one of these grows in a different part of the chicken gut, rapidly producing many millions of new parasites that are excreted in the faeces and infect neighbouring birds. Birds that recover from infection develop natural immunity to the species they were infected with but unfortunately they remain fully susceptible to infections with the other six species. We have done a lot of work one species of the parasite, Eimeria tenella, and have discovered that the surface coat of the parasite, which is composed of molecules (proteins) that the host easily recognises, changes during the course of infection so that the later stages of the parasite no longer have the same coat as the early stages. We have also taken a brief look at the surface coats of some other species of Eimeria and find that are composed of related, but different, proteins to the coat of E. tenella. We think that the specific nature of the surface coat of each parasite may be important in determining which part of the gut each parasite goes to and that the variable nature of the coat between species may explain why host immunity is only effective against a single species at a time. We also think that having a coat that changes during infection may help the parasite to complete its own life cycle without being damaged too much by the host immunity that prevents reinfection. In this proposal we plan to carry out experiments to find out if we are on the right track with our thoughts First of all we will take a more detailed look at the surface coat of a second Eimeria parasite (Eimeria maxima) and once we know precisely which proteins it is composed of wewill begin to use genetic manipulation to do some 'coat swap' experiments. We will make the early stage of Eimeria tenella wear the coat of the early stage of Eimeria maxima and then determine whereabouts within the chicken gut this mixed parasite grows. We will also test whether chickens that have been infected with this mixed parasite develop immunity to just one or to both of the species and if the answer is to both species we will try to exploit the use of these surface coats as vaccines. We will also look at what happens if the later stages of Eimeria tenella are made to wear the same coat as the early stages, as we expect that chickens infected with this type of parasite are likely to suffer a much less severe infection that with a normal parasite and again this may be a way to produce a defined, attenuated vaccine.

Committee	Closed Committee - Animal Sciences (AS)
Research Topics	Animal Health, Immunology, Microbiology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	Industrial Partnership Award (IPA)

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