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A Cell-surface Phylome for African Trypanosomes

The cell surface of Trypanosoma brucei, like many protistan blood parasites, is crucial for mediating host-parasite interactions and is instrumental to the initiation, maintenance and severity of infection. Previous comparisons with the related trypanosomatid parasites T. cruzi and Leishmania major...

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Autores principales: Jackson, Andrew P., Allison, Harriet C., Barry, J. David, Field, Mark C., Hertz-Fowler, Christiane, Berriman, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605285/
https://www.ncbi.nlm.nih.gov/pubmed/23556014
http://dx.doi.org/10.1371/journal.pntd.0002121
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author Jackson, Andrew P.
Allison, Harriet C.
Barry, J. David
Field, Mark C.
Hertz-Fowler, Christiane
Berriman, Matthew
author_facet Jackson, Andrew P.
Allison, Harriet C.
Barry, J. David
Field, Mark C.
Hertz-Fowler, Christiane
Berriman, Matthew
author_sort Jackson, Andrew P.
collection PubMed
description The cell surface of Trypanosoma brucei, like many protistan blood parasites, is crucial for mediating host-parasite interactions and is instrumental to the initiation, maintenance and severity of infection. Previous comparisons with the related trypanosomatid parasites T. cruzi and Leishmania major suggest that the cell-surface proteome of T. brucei is largely taxon-specific. Here we compare genes predicted to encode cell surface proteins of T. brucei with those from two related African trypanosomes, T. congolense and T. vivax. We created a cell surface phylome (CSP) by estimating phylogenies for 79 gene families with putative surface functions to understand the more recent evolution of African trypanosome surface architecture. Our findings demonstrate that the transferrin receptor genes essential for bloodstream survival in T. brucei are conserved in T. congolense but absent from T. vivax and include an expanded gene family of insect stage-specific surface glycoproteins that includes many currently uncharacterized genes. We also identify species-specific features and innovations and confirm that these include most expression site-associated genes (ESAGs) in T. brucei, which are absent from T. congolense and T. vivax. The CSP presents the first global picture of the origins and dynamics of cell surface architecture in African trypanosomes, representing the principal differences in genomic repertoire between African trypanosome species and provides a basis from which to explore the developmental and pathological differences in surface architectures. All data can be accessed at: http://www.genedb.org/Page/trypanosoma_surface_phylome.
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spelling pubmed-36052852013-04-03 A Cell-surface Phylome for African Trypanosomes Jackson, Andrew P. Allison, Harriet C. Barry, J. David Field, Mark C. Hertz-Fowler, Christiane Berriman, Matthew PLoS Negl Trop Dis Research Article The cell surface of Trypanosoma brucei, like many protistan blood parasites, is crucial for mediating host-parasite interactions and is instrumental to the initiation, maintenance and severity of infection. Previous comparisons with the related trypanosomatid parasites T. cruzi and Leishmania major suggest that the cell-surface proteome of T. brucei is largely taxon-specific. Here we compare genes predicted to encode cell surface proteins of T. brucei with those from two related African trypanosomes, T. congolense and T. vivax. We created a cell surface phylome (CSP) by estimating phylogenies for 79 gene families with putative surface functions to understand the more recent evolution of African trypanosome surface architecture. Our findings demonstrate that the transferrin receptor genes essential for bloodstream survival in T. brucei are conserved in T. congolense but absent from T. vivax and include an expanded gene family of insect stage-specific surface glycoproteins that includes many currently uncharacterized genes. We also identify species-specific features and innovations and confirm that these include most expression site-associated genes (ESAGs) in T. brucei, which are absent from T. congolense and T. vivax. The CSP presents the first global picture of the origins and dynamics of cell surface architecture in African trypanosomes, representing the principal differences in genomic repertoire between African trypanosome species and provides a basis from which to explore the developmental and pathological differences in surface architectures. All data can be accessed at: http://www.genedb.org/Page/trypanosoma_surface_phylome. Public Library of Science 2013-03-21 /pmc/articles/PMC3605285/ /pubmed/23556014 http://dx.doi.org/10.1371/journal.pntd.0002121 Text en © 2013 Jackson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jackson, Andrew P.
Allison, Harriet C.
Barry, J. David
Field, Mark C.
Hertz-Fowler, Christiane
Berriman, Matthew
A Cell-surface Phylome for African Trypanosomes
title A Cell-surface Phylome for African Trypanosomes
title_full A Cell-surface Phylome for African Trypanosomes
title_fullStr A Cell-surface Phylome for African Trypanosomes
title_full_unstemmed A Cell-surface Phylome for African Trypanosomes
title_short A Cell-surface Phylome for African Trypanosomes
title_sort cell-surface phylome for african trypanosomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605285/
https://www.ncbi.nlm.nih.gov/pubmed/23556014
http://dx.doi.org/10.1371/journal.pntd.0002121
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