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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6733595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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