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Comparative genomic analysis and phylogenetic position of Theileria equi

BACKGROUND: Transmission of arthropod-borne apicomplexan parasites that cause disease and result in death or persistent infection represents a major challenge to global human and animal health. First described in 1901 as Piroplasma equi, this re-emergent apicomplexan parasite was renamed Babesia equ...

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Autores principales: Kappmeyer, Lowell S, Thiagarajan, Mathangi, Herndon, David R, Ramsay, Joshua D, Caler, Elisabet, Djikeng, Appolinaire, Gillespie, Joseph J, Lau, Audrey OT, Roalson, Eric H, Silva, Joana C, Silva, Marta G, Suarez, Carlos E, Ueti, Massaro W, Nene, Vishvanath M, Mealey, Robert H, Knowles, Donald P, Brayton, Kelly A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505731/
https://www.ncbi.nlm.nih.gov/pubmed/23137308
http://dx.doi.org/10.1186/1471-2164-13-603
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author Kappmeyer, Lowell S
Thiagarajan, Mathangi
Herndon, David R
Ramsay, Joshua D
Caler, Elisabet
Djikeng, Appolinaire
Gillespie, Joseph J
Lau, Audrey OT
Roalson, Eric H
Silva, Joana C
Silva, Marta G
Suarez, Carlos E
Ueti, Massaro W
Nene, Vishvanath M
Mealey, Robert H
Knowles, Donald P
Brayton, Kelly A
author_facet Kappmeyer, Lowell S
Thiagarajan, Mathangi
Herndon, David R
Ramsay, Joshua D
Caler, Elisabet
Djikeng, Appolinaire
Gillespie, Joseph J
Lau, Audrey OT
Roalson, Eric H
Silva, Joana C
Silva, Marta G
Suarez, Carlos E
Ueti, Massaro W
Nene, Vishvanath M
Mealey, Robert H
Knowles, Donald P
Brayton, Kelly A
author_sort Kappmeyer, Lowell S
collection PubMed
description BACKGROUND: Transmission of arthropod-borne apicomplexan parasites that cause disease and result in death or persistent infection represents a major challenge to global human and animal health. First described in 1901 as Piroplasma equi, this re-emergent apicomplexan parasite was renamed Babesia equi and subsequently Theileria equi, reflecting an uncertain taxonomy. Understanding mechanisms by which apicomplexan parasites evade immune or chemotherapeutic elimination is required for development of effective vaccines or chemotherapeutics. The continued risk of transmission of T. equi from clinically silent, persistently infected equids impedes the goal of returning the U. S. to non-endemic status. Therefore comparative genomic analysis of T. equi was undertaken to: 1) identify genes contributing to immune evasion and persistence in equid hosts, 2) identify genes involved in PBMC infection biology and 3) define the phylogenetic position of T. equi relative to sequenced apicomplexan parasites. RESULTS: The known immunodominant proteins, EMA1, 2 and 3 were discovered to belong to a ten member gene family with a mean amino acid identity, in pairwise comparisons, of 39%. Importantly, the amino acid diversity of EMAs is distributed throughout the length of the proteins. Eight of the EMA genes were simultaneously transcribed. As the agents that cause bovine theileriosis infect and transform host cell PBMCs, we confirmed that T. equi infects equine PBMCs, however, there is no evidence of host cell transformation. Indeed, a number of genes identified as potential manipulators of the host cell phenotype are absent from the T. equi genome. Comparative genomic analysis of T. equi revealed the phylogenetic positioning relative to seven apicomplexan parasites using deduced amino acid sequences from 150 genes placed it as a sister taxon to Theileria spp. CONCLUSIONS: The EMA family does not fit the paradigm for classical antigenic variation, and we propose a novel model describing the role of the EMA family in persistence. T. equi has lost the putative genes for host cell transformation, or the genes were acquired by T. parva and T. annulata after divergence from T. equi. Our analysis identified 50 genes that will be useful for definitive phylogenetic classification of T. equi and closely related organisms.
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spelling pubmed-35057312012-11-26 Comparative genomic analysis and phylogenetic position of Theileria equi Kappmeyer, Lowell S Thiagarajan, Mathangi Herndon, David R Ramsay, Joshua D Caler, Elisabet Djikeng, Appolinaire Gillespie, Joseph J Lau, Audrey OT Roalson, Eric H Silva, Joana C Silva, Marta G Suarez, Carlos E Ueti, Massaro W Nene, Vishvanath M Mealey, Robert H Knowles, Donald P Brayton, Kelly A BMC Genomics Research Article BACKGROUND: Transmission of arthropod-borne apicomplexan parasites that cause disease and result in death or persistent infection represents a major challenge to global human and animal health. First described in 1901 as Piroplasma equi, this re-emergent apicomplexan parasite was renamed Babesia equi and subsequently Theileria equi, reflecting an uncertain taxonomy. Understanding mechanisms by which apicomplexan parasites evade immune or chemotherapeutic elimination is required for development of effective vaccines or chemotherapeutics. The continued risk of transmission of T. equi from clinically silent, persistently infected equids impedes the goal of returning the U. S. to non-endemic status. Therefore comparative genomic analysis of T. equi was undertaken to: 1) identify genes contributing to immune evasion and persistence in equid hosts, 2) identify genes involved in PBMC infection biology and 3) define the phylogenetic position of T. equi relative to sequenced apicomplexan parasites. RESULTS: The known immunodominant proteins, EMA1, 2 and 3 were discovered to belong to a ten member gene family with a mean amino acid identity, in pairwise comparisons, of 39%. Importantly, the amino acid diversity of EMAs is distributed throughout the length of the proteins. Eight of the EMA genes were simultaneously transcribed. As the agents that cause bovine theileriosis infect and transform host cell PBMCs, we confirmed that T. equi infects equine PBMCs, however, there is no evidence of host cell transformation. Indeed, a number of genes identified as potential manipulators of the host cell phenotype are absent from the T. equi genome. Comparative genomic analysis of T. equi revealed the phylogenetic positioning relative to seven apicomplexan parasites using deduced amino acid sequences from 150 genes placed it as a sister taxon to Theileria spp. CONCLUSIONS: The EMA family does not fit the paradigm for classical antigenic variation, and we propose a novel model describing the role of the EMA family in persistence. T. equi has lost the putative genes for host cell transformation, or the genes were acquired by T. parva and T. annulata after divergence from T. equi. Our analysis identified 50 genes that will be useful for definitive phylogenetic classification of T. equi and closely related organisms. BioMed Central 2012-11-09 /pmc/articles/PMC3505731/ /pubmed/23137308 http://dx.doi.org/10.1186/1471-2164-13-603 Text en Copyright ©2012 Kappmeyer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kappmeyer, Lowell S
Thiagarajan, Mathangi
Herndon, David R
Ramsay, Joshua D
Caler, Elisabet
Djikeng, Appolinaire
Gillespie, Joseph J
Lau, Audrey OT
Roalson, Eric H
Silva, Joana C
Silva, Marta G
Suarez, Carlos E
Ueti, Massaro W
Nene, Vishvanath M
Mealey, Robert H
Knowles, Donald P
Brayton, Kelly A
Comparative genomic analysis and phylogenetic position of Theileria equi
title Comparative genomic analysis and phylogenetic position of Theileria equi
title_full Comparative genomic analysis and phylogenetic position of Theileria equi
title_fullStr Comparative genomic analysis and phylogenetic position of Theileria equi
title_full_unstemmed Comparative genomic analysis and phylogenetic position of Theileria equi
title_short Comparative genomic analysis and phylogenetic position of Theileria equi
title_sort comparative genomic analysis and phylogenetic position of theileria equi
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505731/
https://www.ncbi.nlm.nih.gov/pubmed/23137308
http://dx.doi.org/10.1186/1471-2164-13-603
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