Cargando…

Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis

The hydrothermal vent mussel Bathymodiolus azoricus lives in an intimate symbiosis with two types of chemosynthetic Gammaproteobacteria in its gills: a sulfur oxidizer and a methane oxidizer. Despite numerous investigations over the last decades, the degree of interdependence between the three symbi...

Descripción completa

Detalles Bibliográficos
Autores principales: Ponnudurai, Ruby, Kleiner, Manuel, Sayavedra, Lizbeth, Petersen, Jillian M, Moche, Martin, Otto, Andreas, Becher, Dörte, Takeuchi, Takeshi, Satoh, Noriyuki, Dubilier, Nicole, Schweder, Thomas, Markert, Stephanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270565/
https://www.ncbi.nlm.nih.gov/pubmed/27801908
http://dx.doi.org/10.1038/ismej.2016.124
_version_ 1782501196221644800
author Ponnudurai, Ruby
Kleiner, Manuel
Sayavedra, Lizbeth
Petersen, Jillian M
Moche, Martin
Otto, Andreas
Becher, Dörte
Takeuchi, Takeshi
Satoh, Noriyuki
Dubilier, Nicole
Schweder, Thomas
Markert, Stephanie
author_facet Ponnudurai, Ruby
Kleiner, Manuel
Sayavedra, Lizbeth
Petersen, Jillian M
Moche, Martin
Otto, Andreas
Becher, Dörte
Takeuchi, Takeshi
Satoh, Noriyuki
Dubilier, Nicole
Schweder, Thomas
Markert, Stephanie
author_sort Ponnudurai, Ruby
collection PubMed
description The hydrothermal vent mussel Bathymodiolus azoricus lives in an intimate symbiosis with two types of chemosynthetic Gammaproteobacteria in its gills: a sulfur oxidizer and a methane oxidizer. Despite numerous investigations over the last decades, the degree of interdependence between the three symbiotic partners, their individual metabolic contributions, as well as the mechanism of carbon transfer from the symbionts to the host are poorly understood. We used a combination of proteomics and genomics to investigate the physiology and metabolism of the individual symbiotic partners. Our study revealed that key metabolic functions are most likely accomplished jointly by B. azoricus and its symbionts: (1) CO(2) is pre-concentrated by the host for carbon fixation by the sulfur-oxidizing symbiont, and (2) the host replenishes essential biosynthetic TCA cycle intermediates for the sulfur-oxidizing symbiont. In return (3), the sulfur oxidizer may compensate for the host's putative deficiency in amino acid and cofactor biosynthesis. We also identified numerous ‘symbiosis-specific' host proteins by comparing symbiont-containing and symbiont-free host tissues and symbiont fractions. These proteins included a large complement of host digestive enzymes in the gill that are likely involved in symbiont digestion and carbon transfer from the symbionts to the host.
format Online
Article
Text
id pubmed-5270565
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-52705652017-02-07 Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis Ponnudurai, Ruby Kleiner, Manuel Sayavedra, Lizbeth Petersen, Jillian M Moche, Martin Otto, Andreas Becher, Dörte Takeuchi, Takeshi Satoh, Noriyuki Dubilier, Nicole Schweder, Thomas Markert, Stephanie ISME J Original Article The hydrothermal vent mussel Bathymodiolus azoricus lives in an intimate symbiosis with two types of chemosynthetic Gammaproteobacteria in its gills: a sulfur oxidizer and a methane oxidizer. Despite numerous investigations over the last decades, the degree of interdependence between the three symbiotic partners, their individual metabolic contributions, as well as the mechanism of carbon transfer from the symbionts to the host are poorly understood. We used a combination of proteomics and genomics to investigate the physiology and metabolism of the individual symbiotic partners. Our study revealed that key metabolic functions are most likely accomplished jointly by B. azoricus and its symbionts: (1) CO(2) is pre-concentrated by the host for carbon fixation by the sulfur-oxidizing symbiont, and (2) the host replenishes essential biosynthetic TCA cycle intermediates for the sulfur-oxidizing symbiont. In return (3), the sulfur oxidizer may compensate for the host's putative deficiency in amino acid and cofactor biosynthesis. We also identified numerous ‘symbiosis-specific' host proteins by comparing symbiont-containing and symbiont-free host tissues and symbiont fractions. These proteins included a large complement of host digestive enzymes in the gill that are likely involved in symbiont digestion and carbon transfer from the symbionts to the host. Nature Publishing Group 2017-02 2016-11-01 /pmc/articles/PMC5270565/ /pubmed/27801908 http://dx.doi.org/10.1038/ismej.2016.124 Text en Copyright © 2017 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Ponnudurai, Ruby
Kleiner, Manuel
Sayavedra, Lizbeth
Petersen, Jillian M
Moche, Martin
Otto, Andreas
Becher, Dörte
Takeuchi, Takeshi
Satoh, Noriyuki
Dubilier, Nicole
Schweder, Thomas
Markert, Stephanie
Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis
title Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis
title_full Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis
title_fullStr Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis
title_full_unstemmed Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis
title_short Metabolic and physiological interdependencies in the Bathymodiolus azoricus symbiosis
title_sort metabolic and physiological interdependencies in the bathymodiolus azoricus symbiosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270565/
https://www.ncbi.nlm.nih.gov/pubmed/27801908
http://dx.doi.org/10.1038/ismej.2016.124
work_keys_str_mv AT ponnudurairuby metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT kleinermanuel metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT sayavedralizbeth metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT petersenjillianm metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT mochemartin metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT ottoandreas metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT becherdorte metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT takeuchitakeshi metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT satohnoriyuki metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT dubiliernicole metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT schwederthomas metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis
AT markertstephanie metabolicandphysiologicalinterdependenciesinthebathymodiolusazoricussymbiosis