Cargando…

Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis

Insect–bacterial symbioses are ubiquitous, but there is still much to uncover about how these relationships establish, persist and evolve. The tsetse endosymbiont Sodalis glossinidius displays intriguing metabolic adaptations to its microenvironment, but the process by which this relationship evolve...

Descripción completa

Detalles Bibliográficos
Autores principales: Hall, Rebecca J., Thorpe, Stephen, Thomas, Gavin H., Wood, A. Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478623/
https://www.ncbi.nlm.nih.gov/pubmed/32543366
http://dx.doi.org/10.1099/mgen.0.000378
_version_ 1783580093623304192
author Hall, Rebecca J.
Thorpe, Stephen
Thomas, Gavin H.
Wood, A. Jamie
author_facet Hall, Rebecca J.
Thorpe, Stephen
Thomas, Gavin H.
Wood, A. Jamie
author_sort Hall, Rebecca J.
collection PubMed
description Insect–bacterial symbioses are ubiquitous, but there is still much to uncover about how these relationships establish, persist and evolve. The tsetse endosymbiont Sodalis glossinidius displays intriguing metabolic adaptations to its microenvironment, but the process by which this relationship evolved remains to be elucidated. The recent chance discovery of the free-living species of the genus Sodalis , Sodalis praecaptivus , provides a serendipitous starting point from which to investigate the evolution of this symbiosis. Here, we present a flux balance model for S. praecaptivus and empirically verify its predictions. Metabolic modelling is used in combination with a multi-objective evolutionary algorithm to explore the trajectories that S. glossinidius may have undertaken from this starting point after becoming internalized. The order in which key genes are lost is shown to influence the evolved populations, providing possible targets for future in vitro genetic manipulation. This method provides a detailed perspective on possible evolutionary trajectories for S. glossinidius in this fundamental process of evolutionary and ecological change.
format Online
Article
Text
id pubmed-7478623
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-74786232020-09-09 Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis Hall, Rebecca J. Thorpe, Stephen Thomas, Gavin H. Wood, A. Jamie Microb Genom Research Article Insect–bacterial symbioses are ubiquitous, but there is still much to uncover about how these relationships establish, persist and evolve. The tsetse endosymbiont Sodalis glossinidius displays intriguing metabolic adaptations to its microenvironment, but the process by which this relationship evolved remains to be elucidated. The recent chance discovery of the free-living species of the genus Sodalis , Sodalis praecaptivus , provides a serendipitous starting point from which to investigate the evolution of this symbiosis. Here, we present a flux balance model for S. praecaptivus and empirically verify its predictions. Metabolic modelling is used in combination with a multi-objective evolutionary algorithm to explore the trajectories that S. glossinidius may have undertaken from this starting point after becoming internalized. The order in which key genes are lost is shown to influence the evolved populations, providing possible targets for future in vitro genetic manipulation. This method provides a detailed perspective on possible evolutionary trajectories for S. glossinidius in this fundamental process of evolutionary and ecological change. Microbiology Society 2020-06-16 /pmc/articles/PMC7478623/ /pubmed/32543366 http://dx.doi.org/10.1099/mgen.0.000378 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
spellingShingle Research Article
Hall, Rebecca J.
Thorpe, Stephen
Thomas, Gavin H.
Wood, A. Jamie
Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis
title Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis
title_full Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis
title_fullStr Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis
title_full_unstemmed Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis
title_short Simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus Sodalis
title_sort simulating the evolutionary trajectories of metabolic pathways for insect symbionts in the genus sodalis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478623/
https://www.ncbi.nlm.nih.gov/pubmed/32543366
http://dx.doi.org/10.1099/mgen.0.000378
work_keys_str_mv AT hallrebeccaj simulatingtheevolutionarytrajectoriesofmetabolicpathwaysforinsectsymbiontsinthegenussodalis
AT thorpestephen simulatingtheevolutionarytrajectoriesofmetabolicpathwaysforinsectsymbiontsinthegenussodalis
AT thomasgavinh simulatingtheevolutionarytrajectoriesofmetabolicpathwaysforinsectsymbiontsinthegenussodalis
AT woodajamie simulatingtheevolutionarytrajectoriesofmetabolicpathwaysforinsectsymbiontsinthegenussodalis