Cargando…
Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum”
BACKGROUND: ‘Chlorochromatium aggregatum’ is a phototrophic consortium, a symbiosis that may represent the highest degree of mutual interdependence between two unrelated bacteria not associated with a eukaryotic host. ‘Chlorochromatium aggregatum’ is a motile, barrel-shaped aggregate formed from a s...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053972/ https://www.ncbi.nlm.nih.gov/pubmed/24267588 http://dx.doi.org/10.1186/gb-2013-14-11-r127 |
_version_ | 1782320479624757248 |
---|---|
author | Liu, Zhenfeng Müller, Johannes Li, Tao Alvey, Richard M Vogl, Kajetan Frigaard, Niels-Ulrik Rockwell, Nathan C Boyd, Eric S Tomsho, Lynn P Schuster, Stephan C Henke, Petra Rohde, Manfred Overmann, Jörg Bryant, Donald A |
author_facet | Liu, Zhenfeng Müller, Johannes Li, Tao Alvey, Richard M Vogl, Kajetan Frigaard, Niels-Ulrik Rockwell, Nathan C Boyd, Eric S Tomsho, Lynn P Schuster, Stephan C Henke, Petra Rohde, Manfred Overmann, Jörg Bryant, Donald A |
author_sort | Liu, Zhenfeng |
collection | PubMed |
description | BACKGROUND: ‘Chlorochromatium aggregatum’ is a phototrophic consortium, a symbiosis that may represent the highest degree of mutual interdependence between two unrelated bacteria not associated with a eukaryotic host. ‘Chlorochromatium aggregatum’ is a motile, barrel-shaped aggregate formed from a single cell of ‘Candidatus Symbiobacter mobilis”, a polarly flagellated, non-pigmented, heterotrophic bacterium, which is surrounded by approximately 15 epibiont cells of Chlorobium chlorochromatii, a non-motile photolithoautotrophic green sulfur bacterium. RESULTS: We analyzed the complete genome sequences of both organisms to understand the basis for this symbiosis. Chl. chlorochromatii has acquired relatively few symbiosis-specific genes; most acquired genes are predicted to modify the cell wall or function in cell-cell adhesion. In striking contrast, ‘Ca. S. mobilis’ appears to have undergone massive gene loss, is probably no longer capable of independent growth, and thus may only reproduce when consortia divide. A detailed model for the energetic and metabolic bases of the dependency of ‘Ca. S. mobilis’ on Chl. chlorochromatii is described. CONCLUSIONS: Genomic analyses suggest that three types of interactions lead to a highly sophisticated relationship between these two organisms. Firstly, extensive metabolic exchange, involving carbon, nitrogen, and sulfur sources as well as vitamins, occurs from the epibiont to the central bacterium. Secondly, ‘Ca. S. mobilis’ can sense and move towards light and sulfide, resources that only directly benefit the epibiont. Thirdly, electron cycling mechanisms, particularly those mediated by quinones and potentially involving shared protonmotive force, could provide an important basis for energy exchange in this and other symbiotic relationships. |
format | Online Article Text |
id | pubmed-4053972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40539722014-06-12 Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” Liu, Zhenfeng Müller, Johannes Li, Tao Alvey, Richard M Vogl, Kajetan Frigaard, Niels-Ulrik Rockwell, Nathan C Boyd, Eric S Tomsho, Lynn P Schuster, Stephan C Henke, Petra Rohde, Manfred Overmann, Jörg Bryant, Donald A Genome Biol Research BACKGROUND: ‘Chlorochromatium aggregatum’ is a phototrophic consortium, a symbiosis that may represent the highest degree of mutual interdependence between two unrelated bacteria not associated with a eukaryotic host. ‘Chlorochromatium aggregatum’ is a motile, barrel-shaped aggregate formed from a single cell of ‘Candidatus Symbiobacter mobilis”, a polarly flagellated, non-pigmented, heterotrophic bacterium, which is surrounded by approximately 15 epibiont cells of Chlorobium chlorochromatii, a non-motile photolithoautotrophic green sulfur bacterium. RESULTS: We analyzed the complete genome sequences of both organisms to understand the basis for this symbiosis. Chl. chlorochromatii has acquired relatively few symbiosis-specific genes; most acquired genes are predicted to modify the cell wall or function in cell-cell adhesion. In striking contrast, ‘Ca. S. mobilis’ appears to have undergone massive gene loss, is probably no longer capable of independent growth, and thus may only reproduce when consortia divide. A detailed model for the energetic and metabolic bases of the dependency of ‘Ca. S. mobilis’ on Chl. chlorochromatii is described. CONCLUSIONS: Genomic analyses suggest that three types of interactions lead to a highly sophisticated relationship between these two organisms. Firstly, extensive metabolic exchange, involving carbon, nitrogen, and sulfur sources as well as vitamins, occurs from the epibiont to the central bacterium. Secondly, ‘Ca. S. mobilis’ can sense and move towards light and sulfide, resources that only directly benefit the epibiont. Thirdly, electron cycling mechanisms, particularly those mediated by quinones and potentially involving shared protonmotive force, could provide an important basis for energy exchange in this and other symbiotic relationships. BioMed Central 2013 2013-11-22 /pmc/articles/PMC4053972/ /pubmed/24267588 http://dx.doi.org/10.1186/gb-2013-14-11-r127 Text en Copyright © 2013 Liu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Liu, Zhenfeng Müller, Johannes Li, Tao Alvey, Richard M Vogl, Kajetan Frigaard, Niels-Ulrik Rockwell, Nathan C Boyd, Eric S Tomsho, Lynn P Schuster, Stephan C Henke, Petra Rohde, Manfred Overmann, Jörg Bryant, Donald A Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” |
title | Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” |
title_full | Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” |
title_fullStr | Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” |
title_full_unstemmed | Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” |
title_short | Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “Chlorochromatium aggregatum” |
title_sort | genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium “chlorochromatium aggregatum” |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053972/ https://www.ncbi.nlm.nih.gov/pubmed/24267588 http://dx.doi.org/10.1186/gb-2013-14-11-r127 |
work_keys_str_mv | AT liuzhenfeng genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT mullerjohannes genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT litao genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT alveyrichardm genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT voglkajetan genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT frigaardnielsulrik genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT rockwellnathanc genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT boyderics genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT tomsholynnp genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT schusterstephanc genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT henkepetra genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT rohdemanfred genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT overmannjorg genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum AT bryantdonalda genomicanalysisrevealskeyaspectsofprokaryoticsymbiosisinthephototrophicconsortiumchlorochromatiumaggregatum |