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Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites
BACKGROUND: Vector-borne apicomplexan parasites are a major cause of mortality and morbidity to humans and livestock globally. The most important disease syndromes caused by these parasites are malaria, babesiosis and theileriosis. Strategies for control often target parasite stages in the mammalian...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460460/ https://www.ncbi.nlm.nih.gov/pubmed/28583072 http://dx.doi.org/10.1186/s12864-017-3788-1 |
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author | Lempereur, Laetitia Larcombe, Stephen D. Durrani, Zeeshan Karagenc, Tulin Bilgic, Huseyin Bilgin Bakirci, Serkan Hacilarlioglu, Selin Kinnaird, Jane Thompson, Joanne Weir, William Shiels, Brian |
author_facet | Lempereur, Laetitia Larcombe, Stephen D. Durrani, Zeeshan Karagenc, Tulin Bilgic, Huseyin Bilgin Bakirci, Serkan Hacilarlioglu, Selin Kinnaird, Jane Thompson, Joanne Weir, William Shiels, Brian |
author_sort | Lempereur, Laetitia |
collection | PubMed |
description | BACKGROUND: Vector-borne apicomplexan parasites are a major cause of mortality and morbidity to humans and livestock globally. The most important disease syndromes caused by these parasites are malaria, babesiosis and theileriosis. Strategies for control often target parasite stages in the mammalian host that cause disease, but this can result in reservoir infections that promote pathogen transmission and generate economic loss. Optimal control strategies should protect against clinical disease, block transmission and be applicable across related genera of parasites. We have used bioinformatics and transcriptomics to screen for transmission-blocking candidate antigens in the tick-borne apicomplexan parasite, Theileria annulata. RESULTS: A number of candidate antigen genes were identified which encoded amino acid domains that are conserved across vector-borne Apicomplexa (Babesia, Plasmodium and Theileria), including the Pfs48/45 6-cys domain and a novel cysteine-rich domain. Expression profiling confirmed that selected candidate genes are expressed by life cycle stages within infected ticks. Additionally, putative B cell epitopes were identified in the T. annulata gene sequences encoding the 6-cys and cysteine rich domains, in a gene encoding a putative papain-family cysteine peptidase, with similarity to the Plasmodium SERA family, and the gene encoding the T. annulata major merozoite/piroplasm surface antigen, Tams1. CONCLUSIONS: Candidate genes were identified that encode proteins with similarity to known transmission blocking candidates in related parasites, while one is a novel candidate conserved across vector-borne apicomplexans and has a potential role in the sexual phase of the life cycle. The results indicate that a ‘One Health’ approach could be utilised to develop a transmission-blocking strategy effective against vector-borne apicomplexan parasites of animals and humans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3788-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5460460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54604602017-06-07 Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites Lempereur, Laetitia Larcombe, Stephen D. Durrani, Zeeshan Karagenc, Tulin Bilgic, Huseyin Bilgin Bakirci, Serkan Hacilarlioglu, Selin Kinnaird, Jane Thompson, Joanne Weir, William Shiels, Brian BMC Genomics Research Article BACKGROUND: Vector-borne apicomplexan parasites are a major cause of mortality and morbidity to humans and livestock globally. The most important disease syndromes caused by these parasites are malaria, babesiosis and theileriosis. Strategies for control often target parasite stages in the mammalian host that cause disease, but this can result in reservoir infections that promote pathogen transmission and generate economic loss. Optimal control strategies should protect against clinical disease, block transmission and be applicable across related genera of parasites. We have used bioinformatics and transcriptomics to screen for transmission-blocking candidate antigens in the tick-borne apicomplexan parasite, Theileria annulata. RESULTS: A number of candidate antigen genes were identified which encoded amino acid domains that are conserved across vector-borne Apicomplexa (Babesia, Plasmodium and Theileria), including the Pfs48/45 6-cys domain and a novel cysteine-rich domain. Expression profiling confirmed that selected candidate genes are expressed by life cycle stages within infected ticks. Additionally, putative B cell epitopes were identified in the T. annulata gene sequences encoding the 6-cys and cysteine rich domains, in a gene encoding a putative papain-family cysteine peptidase, with similarity to the Plasmodium SERA family, and the gene encoding the T. annulata major merozoite/piroplasm surface antigen, Tams1. CONCLUSIONS: Candidate genes were identified that encode proteins with similarity to known transmission blocking candidates in related parasites, while one is a novel candidate conserved across vector-borne apicomplexans and has a potential role in the sexual phase of the life cycle. The results indicate that a ‘One Health’ approach could be utilised to develop a transmission-blocking strategy effective against vector-borne apicomplexan parasites of animals and humans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3788-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-05 /pmc/articles/PMC5460460/ /pubmed/28583072 http://dx.doi.org/10.1186/s12864-017-3788-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lempereur, Laetitia Larcombe, Stephen D. Durrani, Zeeshan Karagenc, Tulin Bilgic, Huseyin Bilgin Bakirci, Serkan Hacilarlioglu, Selin Kinnaird, Jane Thompson, Joanne Weir, William Shiels, Brian Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites |
title | Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites |
title_full | Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites |
title_fullStr | Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites |
title_full_unstemmed | Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites |
title_short | Identification of candidate transmission-blocking antigen genes in Theileria annulata and related vector-borne apicomplexan parasites |
title_sort | identification of candidate transmission-blocking antigen genes in theileria annulata and related vector-borne apicomplexan parasites |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460460/ https://www.ncbi.nlm.nih.gov/pubmed/28583072 http://dx.doi.org/10.1186/s12864-017-3788-1 |
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