Evidence map›Paper›PMID 40467487›Full record

ArticleMicrobes and environments2025

Marked Genome Reduction Driven by a Parasitic Lifestyle: Two Complete Genomes of Endosymbiotic Bacteria Possibly Hosted by a Dinoflagellate.

Takuro Nakayama, Ryo Harada, Akinori Yabuki, Mami Nomura, Kogiku Shiba, Kazuo Inaba, Yuji Inagaki

Abstract read
In one paragraph

Article in Microbes and environments, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Takuro NakayamaCenter for Computational Sciences, University of Tsukuba.
Ryo HaradaFaculty of Medicine, Dalhousie University.
Akinori YabukiResearch Institute for Global Change (RIGC), Japan Agency for Marine-Earth Science and Technology (JAMSTEC).
Mami NomuraFaculty of Science, Yamagata University.
Kogiku ShibaShimoda Marine Research Center, University of Tsukuba.
Kazuo InabaShimoda Marine Research Center, University of Tsukuba.
Yuji InagakiCenter for Computational Sciences, University of Tsukuba.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteria with endosymbiotic lifestyles often show marked genome reduction. While the shrinkage of genomes in intracellular symbionts of animals, including parasitic bacteria, has been extensively exami-ned, less is known about symbiotic bacteria associated with single-celled eukaryotes. We herein report the genomes of two novel gammaproteobacterial lineages, RS3 and XS4, identified as putative parasitic endosymbionts of the dinoflagellate Citharistes regius. Phylogenetic ana-lyses suggest that RS3 and XS4 belong to the family Fastidiosibacteraceae within the order Beggiatoales, forming independent lineages therein. The genomes of RS3 and XS4 are 529 and 436‍ ‍kbp in size, respectively, revealing marked reductions from related bacterial genomes. XS4, which has a very reduced genome with a low GC content, uses a different genetic code, in which UGA assigned tryptophan. The small genomes of RS3 and XS4 encode a limited number of proteins, retaining only approximately 20% of the predicted ancestral proteome. Metabolic reconstruction suggests that RS3 and XS4 are parasitic symbionts that are heavily dependent on their host for essential metabolites. Furthermore, we found that the ancestor of both genomes likely acquired an ADP:ATP antiporter gene via horizontal gene transfer, an event that may have enabled their evolution as energy parasites by facilitating the acquisition of ATP from their host. These results on novel bacteria with highly reduced genomes expand our understanding of the phylogenetic and genomic diversities of endosymbiotic bacteria in protists.

Indexed as

DinoflagellidaGammaproteobacteriaGenome, BacterialSymbiosisBase CompositionGene Transfer, HorizontalGenome SizePhylogenyFastidiosibacteraceaeGammaproteobacteriagenome reductionparasitismphylogenomics

Identifiers

PMID40467487
PMCPMC12213064

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.