Genomic analysis reveals key aspects of prokaryotic symbiosis in the phototrophic consortium " Chlorochromatium aggregatum"

Zhenfeng Liu, Johannes Müller, Tao Li, Richard M. Alvey, Kajetan Vogl, Niels Ulrik Frigaard, Nathan C. Rockwell, Eric S. Boyd, Lynn P. Tomsho, Stephan C. Schuster, Petra Henke, Manfred Rohde, Jörg Overmann, Donald A. Bryant*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

35 Citations (Scopus)

Abstract

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.

Original languageEnglish
Article numberR127
JournalGenome Biology
Volume14
Issue number11
DOIs
Publication statusPublished - Nov 22 2013
Externally publishedYes

ASJC Scopus Subject Areas

  • Ecology, Evolution, Behavior and Systematics
  • Genetics
  • Cell Biology

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