Identification and analysis of immunodominant antigens for ELISA-based detection of Theileria annulata

Bilgic, H. B., Karagenc, T., Bakırc, S., Shiels, B. , Tait, A., Kinnaird, J., Eren, H. and Weir, W. (2016) Identification and analysis of immunodominant antigens for ELISA-based detection of Theileria annulata. PLoS ONE, 11(6), e0156645. (doi: 10.1371/journal.pone.0156645) (PMID:27270235) (PMCID:PMC4896419)

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Abstract

Tropical or Mediterranean theileriosis, caused by the protozoan parasite Theileria annulata, remains an economically important bovine disease in North Africa, Southern Europe, India, the Middle East and Asia. The disease affects mainly exotic cattle and imposes serious constraints upon livestock production and breed improvement programmes. While microscopic and molecular methods exist which are capable of detecting T. annulata during acute infection, the identification of animals in the carrier state is more challenging. Serological tests, which detect antibodies that react against parasite-encoded antigens, should ideally have the potential to identify carrier animals with very high levels of sensitivity and specificity. However, assays developed to date have suffered from a lack of sensitivity and/or specificity and it is, therefore, necessary to identify novel parasite antigens, which can be developed for this purpose. In the present study, genes encoding predicted antigens were bioinformatically identified in the T. annulata genome. These proteins, together with a panel of previously described antigens, were assessed by western blot analysis for immunoreactivity, and this revealed that four novel candidates and five previously described antigens were recognised by immune bovine serum. Using a combination of immunoprecipitation and mass spectrophotometric analysis, an immunodominant protein (encoded by TA15705) was identified as Ta9, a previously defined T cell antigen. Western blotting revealed another of the five proteins in the Ta9 family, TA15710, also to be an immunodominant protein. However, validation by Enzyme-Linked Immunosorbent Assay indicated that due to either allelic polymorphism or differential immune responses of individual hosts, none of the novel candidates can be considered ideal for routine detection of T. annulata-infected/carrier animals.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Shiels, Professor Brian and Tait, Professor Andy and Weir, Professor Willie and Kinnaird, Dr Jane
Authors: Bilgic, H. B., Karagenc, T., Bakırc, S., Shiels, B., Tait, A., Kinnaird, J., Eren, H., and Weir, W.
College/School:College of Medical Veterinary and Life Sciences > School of Biodiversity, One Health & Veterinary Medicine
Journal Name:PLoS ONE
Publisher:Public Library of Science
ISSN:1932-6203
ISSN (Online):1932-6203
Published Online:07 June 2016
Copyright Holders:Copyright © 2016 Bilgic et al.
First Published:First published in PLoS ONE 11(6):e0156645
Publisher Policy:Reproduced under a Creative Commons License

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Project CodeAward NoProject NamePrincipal InvestigatorFunder's NameFunder RefLead Dept
392992An integrated approach for the development of sustainable methods to control tropical theileriosisAndrew TaitWellcome Trust (WELLCOME)075820/A/04/ZSCHOOL OF VETERINARY MEDICINE