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Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae

Class Ascetosporea (Rhizaria; Endomyxa) comprises many parasites of invertebrates. Within this group, recent group‐specific environmental DNA (eDNA) studies have contributed to the establishment of the new order Mikrocytida, a new phylogeny and characterization of Paramyxida, and illuminated the div...

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Autores principales: Ward, Georgia M., Neuhauser, Sigrid, Groben, René, Ciaghi, Stefan, Berney, Cédric, Romac, Sarah, Bass, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173291/
https://www.ncbi.nlm.nih.gov/pubmed/29336517
http://dx.doi.org/10.1111/jeu.12501
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author Ward, Georgia M.
Neuhauser, Sigrid
Groben, René
Ciaghi, Stefan
Berney, Cédric
Romac, Sarah
Bass, David
author_facet Ward, Georgia M.
Neuhauser, Sigrid
Groben, René
Ciaghi, Stefan
Berney, Cédric
Romac, Sarah
Bass, David
author_sort Ward, Georgia M.
collection PubMed
description Class Ascetosporea (Rhizaria; Endomyxa) comprises many parasites of invertebrates. Within this group, recent group‐specific environmental DNA (eDNA) studies have contributed to the establishment of the new order Mikrocytida, a new phylogeny and characterization of Paramyxida, and illuminated the diversity and distribution of haplosporidians. Here, we use general and lineage‐specific PCR primers to investigate the phylogenetic “gap” between haplosporidians and their closest known free‐living relatives, the testate amoeba Gromia and reticulate amoeba Filoreta. Within this gap are Paradinium spp. parasites of copepods, which we show to be highly diverse and widely distributed in planktonic and benthic samples. We reveal a robustly supported radiation of parasites, ENDO‐3, comprised of Paradinium and three further clades (ENDO‐3a, ENDO‐3b and SPP). A further environmental group, ENDO‐2, perhaps comprising several clades, branches between this radiation and the free‐living amoebae. Early diverging haplosporidians were also amplified, often associated with bivalves or deep‐sea samples. The general primer approach amplified an overlapping set of novel lineages within ENDO‐3 and Haplosporida, whereas the group‐specific primer strategy, targeted to amplify from the earliest known divergent haplosporidians to Gromia, generated greater sequence diversity across part of this phylogenetic range.
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spelling pubmed-61732912018-10-05 Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae Ward, Georgia M. Neuhauser, Sigrid Groben, René Ciaghi, Stefan Berney, Cédric Romac, Sarah Bass, David J Eukaryot Microbiol Original Articles Class Ascetosporea (Rhizaria; Endomyxa) comprises many parasites of invertebrates. Within this group, recent group‐specific environmental DNA (eDNA) studies have contributed to the establishment of the new order Mikrocytida, a new phylogeny and characterization of Paramyxida, and illuminated the diversity and distribution of haplosporidians. Here, we use general and lineage‐specific PCR primers to investigate the phylogenetic “gap” between haplosporidians and their closest known free‐living relatives, the testate amoeba Gromia and reticulate amoeba Filoreta. Within this gap are Paradinium spp. parasites of copepods, which we show to be highly diverse and widely distributed in planktonic and benthic samples. We reveal a robustly supported radiation of parasites, ENDO‐3, comprised of Paradinium and three further clades (ENDO‐3a, ENDO‐3b and SPP). A further environmental group, ENDO‐2, perhaps comprising several clades, branches between this radiation and the free‐living amoebae. Early diverging haplosporidians were also amplified, often associated with bivalves or deep‐sea samples. The general primer approach amplified an overlapping set of novel lineages within ENDO‐3 and Haplosporida, whereas the group‐specific primer strategy, targeted to amplify from the earliest known divergent haplosporidians to Gromia, generated greater sequence diversity across part of this phylogenetic range. John Wiley and Sons Inc. 2018-02-02 2018 /pmc/articles/PMC6173291/ /pubmed/29336517 http://dx.doi.org/10.1111/jeu.12501 Text en © 2018 The Authors Journal of Eukaryotic Microbiology published by Wiley Periodicals, Inc. on behalf of International Society of Protistologists This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ward, Georgia M.
Neuhauser, Sigrid
Groben, René
Ciaghi, Stefan
Berney, Cédric
Romac, Sarah
Bass, David
Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae
title Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae
title_full Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae
title_fullStr Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae
title_full_unstemmed Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae
title_short Environmental Sequencing Fills the Gap Between Parasitic Haplosporidians and Free‐living Giant Amoebae
title_sort environmental sequencing fills the gap between parasitic haplosporidians and free‐living giant amoebae
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173291/
https://www.ncbi.nlm.nih.gov/pubmed/29336517
http://dx.doi.org/10.1111/jeu.12501
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