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Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees

The honeybee gut microbiome is thought to be important for bee health, but the role of the individual members is poorly understood. Here, we present closed genomes and associated mobilomes of 102 Apilactobacillus kunkeei isolates obtained from the honey crop (foregut) of honeybees sampled from beehi...

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Autores principales: Dyrhage, Karl, Garcia-Montaner, Andrea, Tamarit, Daniel, Seeger, Christian, Näslund, Kristina, Olofsson, Tobias C, Vasquez, Alejandra, Webster, Matthew T, Andersson, Siv G E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648514/
https://www.ncbi.nlm.nih.gov/pubmed/36263788
http://dx.doi.org/10.1093/gbe/evac153
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author Dyrhage, Karl
Garcia-Montaner, Andrea
Tamarit, Daniel
Seeger, Christian
Näslund, Kristina
Olofsson, Tobias C
Vasquez, Alejandra
Webster, Matthew T
Andersson, Siv G E
author_facet Dyrhage, Karl
Garcia-Montaner, Andrea
Tamarit, Daniel
Seeger, Christian
Näslund, Kristina
Olofsson, Tobias C
Vasquez, Alejandra
Webster, Matthew T
Andersson, Siv G E
author_sort Dyrhage, Karl
collection PubMed
description The honeybee gut microbiome is thought to be important for bee health, but the role of the individual members is poorly understood. Here, we present closed genomes and associated mobilomes of 102 Apilactobacillus kunkeei isolates obtained from the honey crop (foregut) of honeybees sampled from beehives in Helsingborg in the south of Sweden and from the islands Gotland and Åland in the Baltic Sea. Each beehive contained a unique composition of isolates and repeated sampling of similar isolates from two beehives in Helsingborg suggests that the bacterial community is stably maintained across bee generations during the summer months. The sampled bacterial population contained an open pan-genome structure with a high genomic density of transposons. A subset of strains affiliated with phylogroup A inhibited growth of the bee pathogen Melissococcus plutonius, all of which contained a 19.5 kb plasmid for the synthesis of the antimicrobial compound kunkecin A, while a subset of phylogroups B and C strains contained a 32.9 kb plasmid for the synthesis of a putative polyketide antibiotic. This study suggests that the mobile gene pool of A. kunkeei plays a key role in pathogen defense in honeybees, providing new insights into the evolutionary dynamics of defensive symbiont populations.
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spelling pubmed-96485142022-11-14 Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees Dyrhage, Karl Garcia-Montaner, Andrea Tamarit, Daniel Seeger, Christian Näslund, Kristina Olofsson, Tobias C Vasquez, Alejandra Webster, Matthew T Andersson, Siv G E Genome Biol Evol Research Article The honeybee gut microbiome is thought to be important for bee health, but the role of the individual members is poorly understood. Here, we present closed genomes and associated mobilomes of 102 Apilactobacillus kunkeei isolates obtained from the honey crop (foregut) of honeybees sampled from beehives in Helsingborg in the south of Sweden and from the islands Gotland and Åland in the Baltic Sea. Each beehive contained a unique composition of isolates and repeated sampling of similar isolates from two beehives in Helsingborg suggests that the bacterial community is stably maintained across bee generations during the summer months. The sampled bacterial population contained an open pan-genome structure with a high genomic density of transposons. A subset of strains affiliated with phylogroup A inhibited growth of the bee pathogen Melissococcus plutonius, all of which contained a 19.5 kb plasmid for the synthesis of the antimicrobial compound kunkecin A, while a subset of phylogroups B and C strains contained a 32.9 kb plasmid for the synthesis of a putative polyketide antibiotic. This study suggests that the mobile gene pool of A. kunkeei plays a key role in pathogen defense in honeybees, providing new insights into the evolutionary dynamics of defensive symbiont populations. Oxford University Press 2022-10-20 /pmc/articles/PMC9648514/ /pubmed/36263788 http://dx.doi.org/10.1093/gbe/evac153 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dyrhage, Karl
Garcia-Montaner, Andrea
Tamarit, Daniel
Seeger, Christian
Näslund, Kristina
Olofsson, Tobias C
Vasquez, Alejandra
Webster, Matthew T
Andersson, Siv G E
Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees
title Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees
title_full Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees
title_fullStr Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees
title_full_unstemmed Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees
title_short Genome Evolution of a Symbiont Population for Pathogen Defense in Honeybees
title_sort genome evolution of a symbiont population for pathogen defense in honeybees
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648514/
https://www.ncbi.nlm.nih.gov/pubmed/36263788
http://dx.doi.org/10.1093/gbe/evac153
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