Extensive Polymorphism and Evidence of Immune Selection in a Highly Dominant Antigen Recognized by Bovine CD8 T Cells Specific for Theileria annulata

Author:

MacHugh Niall D.1,Weir William2,Burrells Alison1,Lizundia Regina3,Graham Simon P.45,Taracha Evans L.46,Shiels Brian R.2,Langsley Gordon3,Morrison W. Ivan1

Affiliation:

1. The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, United Kingdom

2. Parasitology Group, Division of Veterinary Infection and Immunity, Faculty of Veterinary Medicine, University of Glasgow, Bearsden Road, Glasgow G61 1QH, United Kingdom

3. Laboratory of Comparative Cell Biology of Apicomplexan Parasites, Department de Maladie Infectieuse, Institut Cochin, INSERM U567, CNRS, Faculte de Medicine Rene Descartes, UMR-S 8104, Paris 75104, France

4. The International Livestock Research Institute, P.O. Box 30709, Nairobi, Kenya

5. Present address: Virology Department, Veterinary Laboratories Agency, Addlestone KT15 3NB, United Kingdom.

6. Present address: Institute of Primate Research, P.O. Box 24481-00502, Karen, Kenya.

Abstract

ABSTRACT Although parasite strain-restricted CD8 T cell responses have been described for several protozoa, the precise role of antigenic variability in immunity is poorly understood. The tick-borne protozoan parasite Theileria annulata infects leukocytes and causes an acute, often fatal lymphoproliferative disease in cattle. Building on previous evidence of strain-restricted CD8 T cell responses to T. annulata , this study set out to identify and characterize the variability of the target antigens. Three antigens were identified by screening expressed parasite cDNAs with specific CD8 T cell lines. In cattle expressing the A10 class I major histocompatibility complex haplotype, A10-restricted CD8 T cell responses were shown to be focused entirely on a single dominant epitope in one of these antigens (Ta9). Sequencing of the Ta9 gene from field isolates of T. annulata demonstrated extensive sequence divergence, resulting in amino acid polymorphism within the A10-restricted epitope and a second A14-restricted epitope. Statistical analysis of the allelic sequences revealed evidence of positive selection for amino acid substitutions within the region encoding the CD8 T cell epitopes. Sequence differences in the A10-restricted epitope were shown to result in differential recognition by individual CD8 T cell clones, while clones also differed in their ability to recognize different alleles. Moreover, the representation of these clonal specificities within the responding CD8 T cell populations differed between animals. As well as providing an explanation for incomplete protection observed after heterologous parasite challenge of vaccinated cattle, these results have important implications for the choice of antigens for the development of novel subunit vaccines.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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