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The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis

Almost all Lumbricid earthworms (Oligochaeta: Lumbricidae) harbor extracellular species-specific bacterial symbionts of the genus Verminephrobacter (Betaproteobacteria) in their nephridia. The symbionts have a beneficial effect on host reproduction and likely live on their host's waste products...

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Autores principales: Lund, Marie B., Kjeldsen, Kasper U., Schramm, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975124/
https://www.ncbi.nlm.nih.gov/pubmed/24734029
http://dx.doi.org/10.3389/fmicb.2014.00128
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author Lund, Marie B.
Kjeldsen, Kasper U.
Schramm, Andreas
author_facet Lund, Marie B.
Kjeldsen, Kasper U.
Schramm, Andreas
author_sort Lund, Marie B.
collection PubMed
description Almost all Lumbricid earthworms (Oligochaeta: Lumbricidae) harbor extracellular species-specific bacterial symbionts of the genus Verminephrobacter (Betaproteobacteria) in their nephridia. The symbionts have a beneficial effect on host reproduction and likely live on their host's waste products. They are vertically transmitted and presumably associated with earthworms already at the origin of Lumbricidae 62–136 million years ago. The Verminephrobacter genomes carry signs of bottleneck-induced genetic drift, such as accelerated evolutionary rates, low codon usage bias, and extensive genome shuffling, which are characteristic of vertically transmitted intracellular symbionts. However, the Verminephrobacter genomes lack AT bias, size reduction, and pseudogenization, which are also common genomic hallmarks of vertically transmitted, intracellular symbionts. We propose that the opportunity for genetic mixing during part of the host—symbiont life cycle is the key to evade drift-induced genome erosion. Furthermore, we suggest the earthworm-Verminephrobacter association as a new experimental system for investigating host-microbe interactions, and especially for understanding genome evolution of vertically transmitted symbionts in the presence of genetic mixing.
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spelling pubmed-39751242014-04-14 The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis Lund, Marie B. Kjeldsen, Kasper U. Schramm, Andreas Front Microbiol Microbiology Almost all Lumbricid earthworms (Oligochaeta: Lumbricidae) harbor extracellular species-specific bacterial symbionts of the genus Verminephrobacter (Betaproteobacteria) in their nephridia. The symbionts have a beneficial effect on host reproduction and likely live on their host's waste products. They are vertically transmitted and presumably associated with earthworms already at the origin of Lumbricidae 62–136 million years ago. The Verminephrobacter genomes carry signs of bottleneck-induced genetic drift, such as accelerated evolutionary rates, low codon usage bias, and extensive genome shuffling, which are characteristic of vertically transmitted intracellular symbionts. However, the Verminephrobacter genomes lack AT bias, size reduction, and pseudogenization, which are also common genomic hallmarks of vertically transmitted, intracellular symbionts. We propose that the opportunity for genetic mixing during part of the host—symbiont life cycle is the key to evade drift-induced genome erosion. Furthermore, we suggest the earthworm-Verminephrobacter association as a new experimental system for investigating host-microbe interactions, and especially for understanding genome evolution of vertically transmitted symbionts in the presence of genetic mixing. Frontiers Media S.A. 2014-03-28 /pmc/articles/PMC3975124/ /pubmed/24734029 http://dx.doi.org/10.3389/fmicb.2014.00128 Text en Copyright © 2014 Lund, Kjeldsen and Schramm. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Lund, Marie B.
Kjeldsen, Kasper U.
Schramm, Andreas
The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
title The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
title_full The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
title_fullStr The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
title_full_unstemmed The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
title_short The earthworm—Verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
title_sort earthworm—verminephrobacter symbiosis: an emerging experimental system to study extracellular symbiosis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975124/
https://www.ncbi.nlm.nih.gov/pubmed/24734029
http://dx.doi.org/10.3389/fmicb.2014.00128
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