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Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides

Eukaryotic microbes have three primary mechanisms for obtaining nutrients and energy: phagotrophy, photosynthesis and osmotrophy. Traits associated with the latter two functions arose independently multiple times in the eukaryotes. The Fungi successfully coupled osmotrophy with filamentous growth, a...

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Autores principales: Leonard, Guy, Labarre, Aurélie, Milner, David S., Monier, Adam, Soanes, Darren, Wideman, Jeremy G., Maguire, Finlay, Stevens, Sam, Sain, Divya, Grau-Bové, Xavier, Sebé-Pedrós, Arnau, Stajich, Jason E., Paszkiewicz, Konrad, Brown, Matthew W., Hall, Neil, Wickstead, Bill, Richards, Thomas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795050/
https://www.ncbi.nlm.nih.gov/pubmed/29321239
http://dx.doi.org/10.1098/rsob.170184
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author Leonard, Guy
Labarre, Aurélie
Milner, David S.
Monier, Adam
Soanes, Darren
Wideman, Jeremy G.
Maguire, Finlay
Stevens, Sam
Sain, Divya
Grau-Bové, Xavier
Sebé-Pedrós, Arnau
Stajich, Jason E.
Paszkiewicz, Konrad
Brown, Matthew W.
Hall, Neil
Wickstead, Bill
Richards, Thomas A.
author_facet Leonard, Guy
Labarre, Aurélie
Milner, David S.
Monier, Adam
Soanes, Darren
Wideman, Jeremy G.
Maguire, Finlay
Stevens, Sam
Sain, Divya
Grau-Bové, Xavier
Sebé-Pedrós, Arnau
Stajich, Jason E.
Paszkiewicz, Konrad
Brown, Matthew W.
Hall, Neil
Wickstead, Bill
Richards, Thomas A.
author_sort Leonard, Guy
collection PubMed
description Eukaryotic microbes have three primary mechanisms for obtaining nutrients and energy: phagotrophy, photosynthesis and osmotrophy. Traits associated with the latter two functions arose independently multiple times in the eukaryotes. The Fungi successfully coupled osmotrophy with filamentous growth, and similar traits are also manifested in the Pseudofungi (oomycetes and hyphochytriomycetes). Both the Fungi and the Pseudofungi encompass a diversity of plant and animal parasites. Genome-sequencing efforts have focused on host-associated microbes (mutualistic symbionts or parasites), providing limited comparisons with free-living relatives. Here we report the first draft genome sequence of a hyphochytriomycete ‘pseudofungus’; Hyphochytrium catenoides. Using phylogenomic approaches, we identify genes of recent viral ancestry, with related viral derived genes also present on the genomes of oomycetes, suggesting a complex history of viral coevolution and integration across the Pseudofungi. H. catenoides has a complex life cycle involving diverse filamentous structures and a flagellated zoospore with a single anterior tinselate flagellum. We use genome comparisons, drug sensitivity analysis and high-throughput culture arrays to investigate the ancestry of oomycete/pseudofungal characteristics, demonstrating that many of the genetic features associated with parasitic traits evolved specifically within the oomycete radiation. Comparative genomics also identified differences in the repertoire of genes associated with filamentous growth between the Fungi and the Pseudofungi, including differences in vesicle trafficking systems, cell-wall synthesis pathways and motor protein repertoire, demonstrating that unique cellular systems underpinned the convergent evolution of filamentous osmotrophic growth in these two eukaryotic groups.
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spelling pubmed-57950502018-02-05 Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides Leonard, Guy Labarre, Aurélie Milner, David S. Monier, Adam Soanes, Darren Wideman, Jeremy G. Maguire, Finlay Stevens, Sam Sain, Divya Grau-Bové, Xavier Sebé-Pedrós, Arnau Stajich, Jason E. Paszkiewicz, Konrad Brown, Matthew W. Hall, Neil Wickstead, Bill Richards, Thomas A. Open Biol Research Eukaryotic microbes have three primary mechanisms for obtaining nutrients and energy: phagotrophy, photosynthesis and osmotrophy. Traits associated with the latter two functions arose independently multiple times in the eukaryotes. The Fungi successfully coupled osmotrophy with filamentous growth, and similar traits are also manifested in the Pseudofungi (oomycetes and hyphochytriomycetes). Both the Fungi and the Pseudofungi encompass a diversity of plant and animal parasites. Genome-sequencing efforts have focused on host-associated microbes (mutualistic symbionts or parasites), providing limited comparisons with free-living relatives. Here we report the first draft genome sequence of a hyphochytriomycete ‘pseudofungus’; Hyphochytrium catenoides. Using phylogenomic approaches, we identify genes of recent viral ancestry, with related viral derived genes also present on the genomes of oomycetes, suggesting a complex history of viral coevolution and integration across the Pseudofungi. H. catenoides has a complex life cycle involving diverse filamentous structures and a flagellated zoospore with a single anterior tinselate flagellum. We use genome comparisons, drug sensitivity analysis and high-throughput culture arrays to investigate the ancestry of oomycete/pseudofungal characteristics, demonstrating that many of the genetic features associated with parasitic traits evolved specifically within the oomycete radiation. Comparative genomics also identified differences in the repertoire of genes associated with filamentous growth between the Fungi and the Pseudofungi, including differences in vesicle trafficking systems, cell-wall synthesis pathways and motor protein repertoire, demonstrating that unique cellular systems underpinned the convergent evolution of filamentous osmotrophic growth in these two eukaryotic groups. The Royal Society 2018-01-10 /pmc/articles/PMC5795050/ /pubmed/29321239 http://dx.doi.org/10.1098/rsob.170184 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Leonard, Guy
Labarre, Aurélie
Milner, David S.
Monier, Adam
Soanes, Darren
Wideman, Jeremy G.
Maguire, Finlay
Stevens, Sam
Sain, Divya
Grau-Bové, Xavier
Sebé-Pedrós, Arnau
Stajich, Jason E.
Paszkiewicz, Konrad
Brown, Matthew W.
Hall, Neil
Wickstead, Bill
Richards, Thomas A.
Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides
title Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides
title_full Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides
title_fullStr Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides
title_full_unstemmed Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides
title_short Comparative genomic analysis of the ‘pseudofungus’ Hyphochytrium catenoides
title_sort comparative genomic analysis of the ‘pseudofungus’ hyphochytrium catenoides
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795050/
https://www.ncbi.nlm.nih.gov/pubmed/29321239
http://dx.doi.org/10.1098/rsob.170184
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