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Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles

The phylum Apicomplexa comprises human pathogens such as Plasmodium but is also an under-explored hotspot of evolutionary diversity central to understanding the origins of parasitism and non-photosynthetic plastids. We generated single-cell transcriptomes for all major apicomplexan groups lacking la...

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Autores principales: Janouškovec, Jan, Paskerova, Gita G, Miroliubova, Tatiana S, Mikhailov, Kirill V, Birley, Thomas, Aleoshin, Vladimir V, Simdyanov, Timur G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733595/
https://www.ncbi.nlm.nih.gov/pubmed/31418692
http://dx.doi.org/10.7554/eLife.49662
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author Janouškovec, Jan
Paskerova, Gita G
Miroliubova, Tatiana S
Mikhailov, Kirill V
Birley, Thomas
Aleoshin, Vladimir V
Simdyanov, Timur G
author_facet Janouškovec, Jan
Paskerova, Gita G
Miroliubova, Tatiana S
Mikhailov, Kirill V
Birley, Thomas
Aleoshin, Vladimir V
Simdyanov, Timur G
author_sort Janouškovec, Jan
collection PubMed
description The phylum Apicomplexa comprises human pathogens such as Plasmodium but is also an under-explored hotspot of evolutionary diversity central to understanding the origins of parasitism and non-photosynthetic plastids. We generated single-cell transcriptomes for all major apicomplexan groups lacking large-scale sequence data. Phylogenetic analysis reveals that apicomplexan-like parasites are polyphyletic and their similar morphologies emerged convergently at least three times. Gregarines and eugregarines are monophyletic, against most expectations, and rhytidocystids and Eleutheroschizon are sister lineages to medically important taxa. Although previously unrecognized, plastids in deep-branching apicomplexans are common, and they contain some of the most divergent and AT-rich genomes ever found. In eugregarines, however, plastids are either abnormally reduced or absent, thus increasing known plastid losses in eukaryotes from two to four. Environmental sequences of ten novel plastid lineages and structural innovations in plastid proteins confirm that plastids in apicomplexans and their relatives are widespread and share a common, photosynthetic origin.
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spelling pubmed-67335952019-09-11 Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles Janouškovec, Jan Paskerova, Gita G Miroliubova, Tatiana S Mikhailov, Kirill V Birley, Thomas Aleoshin, Vladimir V Simdyanov, Timur G eLife Evolutionary Biology The phylum Apicomplexa comprises human pathogens such as Plasmodium but is also an under-explored hotspot of evolutionary diversity central to understanding the origins of parasitism and non-photosynthetic plastids. We generated single-cell transcriptomes for all major apicomplexan groups lacking large-scale sequence data. Phylogenetic analysis reveals that apicomplexan-like parasites are polyphyletic and their similar morphologies emerged convergently at least three times. Gregarines and eugregarines are monophyletic, against most expectations, and rhytidocystids and Eleutheroschizon are sister lineages to medically important taxa. Although previously unrecognized, plastids in deep-branching apicomplexans are common, and they contain some of the most divergent and AT-rich genomes ever found. In eugregarines, however, plastids are either abnormally reduced or absent, thus increasing known plastid losses in eukaryotes from two to four. Environmental sequences of ten novel plastid lineages and structural innovations in plastid proteins confirm that plastids in apicomplexans and their relatives are widespread and share a common, photosynthetic origin. eLife Sciences Publications, Ltd 2019-08-16 /pmc/articles/PMC6733595/ /pubmed/31418692 http://dx.doi.org/10.7554/eLife.49662 Text en © 2019, Janouškovec 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 Evolutionary Biology
Janouškovec, Jan
Paskerova, Gita G
Miroliubova, Tatiana S
Mikhailov, Kirill V
Birley, Thomas
Aleoshin, Vladimir V
Simdyanov, Timur G
Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
title Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
title_full Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
title_fullStr Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
title_full_unstemmed Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
title_short Apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
title_sort apicomplexan-like parasites are polyphyletic and widely but selectively dependent on cryptic plastid organelles
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733595/
https://www.ncbi.nlm.nih.gov/pubmed/31418692
http://dx.doi.org/10.7554/eLife.49662
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