Barthelonids represent a deep-branching metamonad clade with mitochondrion-related organelles predicted to generate no ATP

Author:

Yazaki Euki1ORCID,Kume Keitaro2,Shiratori Takashi34,Eglit Yana56,Tanifuji Goro7,Harada Ryo4,Simpson Alastair G. B.56ORCID,Ishida Ken-ichiro34,Hashimoto Tetsuo34,Inagaki Yuji48ORCID

Affiliation:

1. Interdisciplinary Theoretical and Mathematical Sciences (iTHEMS), RIKEN, Wako, Saitama, Japan

2. Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan

3. Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan

4. Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan

5. Department of Biology, Dalhousie University, Halifax, Nova Scotia, Canada

6. Centre for Comparative Genomics and Evolutionary Bioinformatics, Dalhousie University, Halifax, Nova Scotia, Canada

7. Department of Zoology, National Museum of Nature and Science, Ibaraki, Japan

8. Center for Computational Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan

Abstract

We here report the phylogenetic position of barthelonids, small anaerobic flagellates previously examined using light microscopy alone. Barthelona spp. were isolated from geographically distinct regions and we established five laboratory strains. Transcriptomic data generated from one Barthelona strain (PAP020) were used for large-scale, multi-gene phylogenetic (phylogenomic) analyses. Our analyses robustly placed strain PAP020 at the base of the Fornicata clade, indicating that barthelonids represent a deep-branching metamonad clade. Considering the anaerobic/microaerophilic nature of barthelonids and preliminary electron microscopy observations on strain PAP020, we suspected that barthelonids possess functionally and structurally reduced mitochondria (i.e. mitochondrion-related organelles or MROs). The metabolic pathways localized in the MRO of strain PAP020 were predicted based on its transcriptomic data and compared with those in the MROs of fornicates. We here propose that strain PAP020 is incapable of generating ATP in the MRO, as no mitochondrial/MRO enzymes involved in substrate-level phosphorylation were detected. Instead, we detected a putative cytosolic ATP-generating enzyme (acetyl-CoA synthetase), suggesting that strain PAP020 depends on ATP generated in the cytosol. We propose two separate losses of substrate-level phosphorylation from the MRO in the clade containing barthelonids and (other) fornicates.

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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