Convergent reductive evolution and host adaptation in Mycoavidus bacterial endosymbionts of Mortierellaceae fungi.

Fungal bacterial interactions Gene loss Host-specificity Secondary metabolism

Journal

Fungal genetics and biology : FG & B
ISSN: 1096-0937
Titre abrégé: Fungal Genet Biol
Pays: United States
ID NLM: 9607601

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 13 04 2023
revised: 06 09 2023
accepted: 11 09 2023
pubmed: 17 9 2023
medline: 17 9 2023
entrez: 16 9 2023
Statut: ppublish

Résumé

Intimate associations between fungi and intracellular bacterial endosymbionts are becoming increasingly well understood. Phylogenetic analyses demonstrate that bacterial endosymbionts of Mucoromycota fungi are related either to free-living Burkholderia or Mollicutes species. The so-called Burkholderia-related endosymbionts or BRE comprise Mycoavidus, Mycetohabitans and Candidatus Glomeribacter gigasporarum. These endosymbionts are marked by genome contraction thought to be associated with intracellular selection. However, the conclusions drawn thus far are based on a very small subset of endosymbiont genomes, and the mechanisms leading to genome streamlining are not well understood. The purpose of this study was to better understand how intracellular existence shapes Mycoavidus and BRE functionally at the genome level. To this end we generated and analyzed 14 novel draft genomes for Mycoavidus living within the hyphae of Mortierellomycotina fungi. We found that our novel Mycoavidus genomes were significantly reduced compared to free-living Burkholderiales relatives. Using a genome-scale phylogenetic approach including the novel and available existing genomes of Mycoavidus, we show that the genus is an assemblage composed of two independently derived lineages including three well supported clades of Mycoavidus. Using a comparative genomic approach, we shed light on the functional implications of genome reduction, documenting shared and unique gene loss patterns between the three Mycoavidus clades. We found that many endosymbiont isolates demonstrate patterns of vertical transmission and host-specificity, but others are present in phylogenetically disparate hosts. We discuss how reductive evolution and host specificity reflect convergent adaptation to the intrahyphal selective landscape, and commonalities of eukaryotic endosymbiont genome evolution.

Identifiants

pubmed: 37716699
pii: S1087-1845(23)00069-5
doi: 10.1016/j.fgb.2023.103838
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103838

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kevin Amses (K)

Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97333, USA.

Alessandro Desiró (A)

Department of Plant Soil and Microbial Sciences, Michigan State University, East Lansing MI 48824, USA.

Abigail Bryson (A)

Department of Plant Soil and Microbial Sciences, Michigan State University, East Lansing MI 48824, USA.

Igor Grigoriev (I)

United States Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; Department of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720, USA.

Stephen Mondo (S)

United States Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; Department of Agricultural Biology, Colorado State University, Fort Collins, CO, USA.

Anna Lipzen (A)

United States Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Kurt LaButti (K)

United States Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Robert Riley (R)

United States Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Vasanth Singan (V)

United States Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Paris Salazar-Hamm (P)

Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97333, USA.

Jason King (J)

Department of Agricultural Biology, Colorado State University, Fort Collins, CO, USA.

Elizabeth Ballou (E)

School of Biosciences, University of Sheffield, Western Bank S10 2TN, UK.

Teresa Pawlowska (T)

MRC Centre for Medical Mycology, University of Exeter, Exeter EX4 4QD, UK.

Rasheed Adeleke (R)

School of Integrative Plant Science, Cornell University, Ithaca, NY 14853-5904, USA; Unit for Environmental Sciences and Management, North-West University, Potchefstroom, Private bag X6001, 2520, South Africa.

Gregory Bonito (G)

Department of Plant Soil and Microbial Sciences, Michigan State University, East Lansing MI 48824, USA.

Jessie Uehling (J)

Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97333, USA. Electronic address: Jessie.Uehling@OregonState.edu.

Classifications MeSH