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Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase

The mitochondrion of apicomplexan parasites is critical for parasite survival, although the full complement of proteins that localize to this organelle has not been defined. Here we undertake two independent approaches to elucidate the mitochondrial proteome of the apicomplexan Toxoplasma gondii. We...

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Autores principales: Seidi, Azadeh, Muellner-Wong, Linden S, Rajendran, Esther, Tjhin, Edwin T, Dagley, Laura F, Aw, Vincent YT, Faou, Pierre, Webb, Andrew I, Tonkin, Christopher J, van Dooren, Giel G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156079/
https://www.ncbi.nlm.nih.gov/pubmed/30204084
http://dx.doi.org/10.7554/eLife.38131
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author Seidi, Azadeh
Muellner-Wong, Linden S
Rajendran, Esther
Tjhin, Edwin T
Dagley, Laura F
Aw, Vincent YT
Faou, Pierre
Webb, Andrew I
Tonkin, Christopher J
van Dooren, Giel G
author_facet Seidi, Azadeh
Muellner-Wong, Linden S
Rajendran, Esther
Tjhin, Edwin T
Dagley, Laura F
Aw, Vincent YT
Faou, Pierre
Webb, Andrew I
Tonkin, Christopher J
van Dooren, Giel G
author_sort Seidi, Azadeh
collection PubMed
description The mitochondrion of apicomplexan parasites is critical for parasite survival, although the full complement of proteins that localize to this organelle has not been defined. Here we undertake two independent approaches to elucidate the mitochondrial proteome of the apicomplexan Toxoplasma gondii. We identify approximately 400 mitochondrial proteins, many of which lack homologs in the animals that these parasites infect, and most of which are important for parasite growth. We demonstrate that one such protein, termed TgApiCox25, is an important component of the parasite cytochrome c oxidase (COX) complex. We identify numerous other apicomplexan-specific components of COX, and conclude that apicomplexan COX, and apicomplexan mitochondria more generally, differ substantially in their protein composition from the hosts they infect. Our study highlights the diversity that exists in mitochondrial proteomes across the eukaryotic domain of life, and provides a foundation for defining unique aspects of mitochondrial biology in an important phylum of parasites.
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spelling pubmed-61560792018-09-25 Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase Seidi, Azadeh Muellner-Wong, Linden S Rajendran, Esther Tjhin, Edwin T Dagley, Laura F Aw, Vincent YT Faou, Pierre Webb, Andrew I Tonkin, Christopher J van Dooren, Giel G eLife Microbiology and Infectious Disease The mitochondrion of apicomplexan parasites is critical for parasite survival, although the full complement of proteins that localize to this organelle has not been defined. Here we undertake two independent approaches to elucidate the mitochondrial proteome of the apicomplexan Toxoplasma gondii. We identify approximately 400 mitochondrial proteins, many of which lack homologs in the animals that these parasites infect, and most of which are important for parasite growth. We demonstrate that one such protein, termed TgApiCox25, is an important component of the parasite cytochrome c oxidase (COX) complex. We identify numerous other apicomplexan-specific components of COX, and conclude that apicomplexan COX, and apicomplexan mitochondria more generally, differ substantially in their protein composition from the hosts they infect. Our study highlights the diversity that exists in mitochondrial proteomes across the eukaryotic domain of life, and provides a foundation for defining unique aspects of mitochondrial biology in an important phylum of parasites. eLife Sciences Publications, Ltd 2018-09-11 /pmc/articles/PMC6156079/ /pubmed/30204084 http://dx.doi.org/10.7554/eLife.38131 Text en © 2018, Seidi et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Seidi, Azadeh
Muellner-Wong, Linden S
Rajendran, Esther
Tjhin, Edwin T
Dagley, Laura F
Aw, Vincent YT
Faou, Pierre
Webb, Andrew I
Tonkin, Christopher J
van Dooren, Giel G
Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
title Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
title_full Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
title_fullStr Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
title_full_unstemmed Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
title_short Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
title_sort elucidating the mitochondrial proteome of toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156079/
https://www.ncbi.nlm.nih.gov/pubmed/30204084
http://dx.doi.org/10.7554/eLife.38131
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