Evidence map›Paper›PMID 41320831›Full record

ArticleGenome biology and evolution2025

Comparative Genomics Reveals Multipartite Genomes Undergoing Loss in the Fungal Endosymbiotic Genus Mycetohabitans.

Bhuwan Abbot, Sara Field, Lauren Carneal, Richard Allen White, Andra Buchan, Caroline West, Laira Lee, Morgan Elizabeth Carter

Abstract read
In one paragraph

Article in Genome biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Phylogenetically diverse MucoralesMicrobial genomics · 2026
    Article
  2. Review
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

8 authors.

Bhuwan AbbotDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0009-0002-4879-2150
Sara FieldDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0009-0004-4724-4202
Lauren CarnealDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0009-0000-6423-0137
Richard Allen WhiteDepartment of Bioinformatics and Genomics, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0000-0002-6292-5936
Andra BuchanDepartment of Bioinformatics and Genomics, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0009-0000-9388-4068
Caroline WestDepartment of Bioinformatics and Genomics, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0000-0001-8578-5174
Laira LeeNorth Carolina School of Science and Mathematics - Morganton, Morganton, NC 28655, USA.ORCID 0009-0006-5843-329X
Morgan Elizabeth CarterDepartment of Biological Sciences, The University of North Carolina at Charlotte, Charlotte, NC 28223, USA.ORCID 0000-0001-5639-2013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endosymbiotic bacteria extensively impact phenotypes of their eukaryotic hosts, while experiencing dramatic changes to their own genome as they become more host-restricted in lifestyle. Understanding the trajectory of such a genome has largely been done through the study of animal-associated bacteria, especially insect endosymbionts. Yet, endofungal bacteria provide another natural experimental model for investigating how microbial genomes change when living inside of a host cell. Mycetohabitans spp. are culturable bacterial endosymbionts of the Mucoromycota fungus Rhizopus microsporus. To investigate the genome dynamics resulting from the endohyphal nature of this emerging model genus, we long-read sequenced and assembled new complete genomes to combine with previous assemblies, creating a global dataset of 28 complete Mycetohabitans genomes. All genomes were between 3.3 and 3.9 Mbp in size and were multipartite, structured into two conserved replicons with some strains having an additional plasmid. Based on evolutionary rate and gene content analysis of the different replicons, we termed the two major ones a chromosome and chromid. The differential presence of a third, mobilome-rich plasmid in some strains and the proliferation of transposable elements provide putative mechanisms for recombination or gene loss. The conservation of intact prophage and putative toxin-antitoxin systems and extensive enrichment of secondary metabolite clusters in the Mycetohabitans genomes highlight the dynamic nature of this reducing genome. With fungal-bacterial symbioses becoming increasingly apparent phenomena, lessons learned from this symbiosis will inform our understanding of bacterial adaptation to novel hosts and the process of microbe-microbe coevolution.

Indexed as

Genome, FungalRhizopusSymbiosisEvolution, MolecularGenome, BacterialGenomicsPhylogenychromidendofungalpangenomepseudogeneRhizopustransposable elements

Identifiers

PMID41320831
PMCPMC12696581

What Socratic holds

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Registered trials

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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 Socratic graph.