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Factors mediating plastid dependency and the origins of parasitism in apicomplexans and their close relatives

Factors mediating plastid dependency and the origins of parasitism in apicomplexans and their close relatives
Factors mediating plastid dependency and the origins of parasitism in apicomplexans and their close relatives
Apicomplexans are a major lineage of parasites, including causative agents of malaria and toxoplasmosis. How such highly adapted parasites evolved from free-living ancestors is poorly understood, particularly because they contain nonphotosynthetic plastids with which they have a complex metabolic dependency. Here, we examine the origin of apicomplexan parasitism by resolving the evolutionary distribution of several key characteristics in their closest free-living relatives, photosynthetic chromerids and predatory colpodellids. Using environmental sequence data, we describe the diversity of these apicomplexan-related lineages and select five species that represent this diversity for transcriptome sequencing. Phylogenomic analysis recovered a monophyletic lineage of chromerids and colpodellids as the sister group to apicomplexans, and a complex distribution of retention versus loss for photosynthesis, plastid genomes, and plastid organelles. Reconstructing the evolution of all plastid and cytosolic metabolic pathways related to apicomplexan plastid function revealed an ancient dependency on plastid isoprenoid biosynthesis, predating the divergence of apicomplexan and dinoflagellates. Similarly, plastid genome retention is strongly linked to the retention of two genes in the plastid genome, sufB and clpC, altogether suggesting a relatively simple model for plastid retention and loss. Lastly, we examine the broader distribution of a suite of molecular characteristics previously linked to the origins of apicomplexan parasitism and find that virtually all are present in their free-living relatives. The emergence of parasitism may not be driven by acquisition of novel components, but rather by loss and modification of the existing, conserved traits.
0027-8424
10200-10207
Janouškovec, J
fbaa4a5d-872e-465b-b2c3-bb35df455cc6
Tikhonenkov, DV
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Burki, F
f0b7504b-e486-47c1-a648-d24a94641917
Howe, AT
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Kolísko, M
ed1d5859-cb65-4cfb-97d7-24c1c2394489
Mylnikov, AP
ba6dced3-1dcf-4879-aca5-36782fceee35
Keeling, PJ
fd51c2ef-1daa-442d-b186-71001aa7ca7d
Janouškovec, J
fbaa4a5d-872e-465b-b2c3-bb35df455cc6
Tikhonenkov, DV
a1c998c0-e960-4269-b711-70f098020d96
Burki, F
f0b7504b-e486-47c1-a648-d24a94641917
Howe, AT
9aa2ad2a-53b2-4fb4-a17d-0b3305f238a6
Kolísko, M
ed1d5859-cb65-4cfb-97d7-24c1c2394489
Mylnikov, AP
ba6dced3-1dcf-4879-aca5-36782fceee35
Keeling, PJ
fd51c2ef-1daa-442d-b186-71001aa7ca7d

Janouškovec, J, Tikhonenkov, DV, Burki, F, Howe, AT, Kolísko, M, Mylnikov, AP and Keeling, PJ (2015) Factors mediating plastid dependency and the origins of parasitism in apicomplexans and their close relatives. Proceedings of the National Academy of Sciences of the United States of America, 112 (33), 10200-10207. (doi:10.1073/pnas.1423790112).

Record type: Article

Abstract

Apicomplexans are a major lineage of parasites, including causative agents of malaria and toxoplasmosis. How such highly adapted parasites evolved from free-living ancestors is poorly understood, particularly because they contain nonphotosynthetic plastids with which they have a complex metabolic dependency. Here, we examine the origin of apicomplexan parasitism by resolving the evolutionary distribution of several key characteristics in their closest free-living relatives, photosynthetic chromerids and predatory colpodellids. Using environmental sequence data, we describe the diversity of these apicomplexan-related lineages and select five species that represent this diversity for transcriptome sequencing. Phylogenomic analysis recovered a monophyletic lineage of chromerids and colpodellids as the sister group to apicomplexans, and a complex distribution of retention versus loss for photosynthesis, plastid genomes, and plastid organelles. Reconstructing the evolution of all plastid and cytosolic metabolic pathways related to apicomplexan plastid function revealed an ancient dependency on plastid isoprenoid biosynthesis, predating the divergence of apicomplexan and dinoflagellates. Similarly, plastid genome retention is strongly linked to the retention of two genes in the plastid genome, sufB and clpC, altogether suggesting a relatively simple model for plastid retention and loss. Lastly, we examine the broader distribution of a suite of molecular characteristics previously linked to the origins of apicomplexan parasitism and find that virtually all are present in their free-living relatives. The emergence of parasitism may not be driven by acquisition of novel components, but rather by loss and modification of the existing, conserved traits.

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Published date: 25 February 2015

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Local EPrints ID: 457557
URI: http://eprints.soton.ac.uk/id/eprint/457557
ISSN: 0027-8424
PURE UUID: f19c6d17-cdcc-412f-88e9-f4deca5732d7
ORCID for J Janouškovec: ORCID iD orcid.org/0000-0001-6547-749X

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Date deposited: 13 Jun 2022 16:34
Last modified: 17 Mar 2024 04:11

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Contributors

Author: J Janouškovec ORCID iD
Author: DV Tikhonenkov
Author: F Burki
Author: AT Howe
Author: M Kolísko
Author: AP Mylnikov
Author: PJ Keeling

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