Lifestyle Evolution in Cyanobacterial Symbionts of Sponges
The “Candidatus Synechococcus spongiarum” group includes different clades of cyanobacteria with high 16S rRNA sequence identity (~99%) and is the most abundant and widespread cyanobacterial symbiont of marine sponges. The first draft genome of a “Ca. Synechococcus spongiarum” group member was recent...
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American Society of Microbiology
2015
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pubmed-44530082015-06-11 Lifestyle Evolution in Cyanobacterial Symbionts of Sponges Burgsdorf, Ilia Slaby, Beate M. Handley, Kim M. Haber, Markus Blom, Jochen Marshall, Christopher W. Gilbert, Jack A. Hentschel, Ute Steindler, Laura Research Article The “Candidatus Synechococcus spongiarum” group includes different clades of cyanobacteria with high 16S rRNA sequence identity (~99%) and is the most abundant and widespread cyanobacterial symbiont of marine sponges. The first draft genome of a “Ca. Synechococcus spongiarum” group member was recently published, providing evidence of genome reduction by loss of genes involved in several nonessential functions. However, “Ca. Synechococcus spongiarum” includes a variety of clades that may differ widely in genomic repertoire and consequently in physiology and symbiotic function. Here, we present three additional draft genomes of “Ca. Synechococcus spongiarum,” each from a different clade. By comparing all four symbiont genomes to those of free-living cyanobacteria, we revealed general adaptations to life inside sponges and specific adaptations of each phylotype. Symbiont genomes shared about half of their total number of coding genes. Common traits of “Ca. Synechococcus spongiarum” members were a high abundance of DNA modification and recombination genes and a reduction in genes involved in inorganic ion transport and metabolism, cell wall biogenesis, and signal transduction mechanisms. Moreover, these symbionts were characterized by a reduced number of antioxidant enzymes and low-weight peptides of photosystem II compared to their free-living relatives. Variability within the “Ca. Synechococcus spongiarum” group was mostly related to immune system features, potential for siderophore-mediated iron transport, and dependency on methionine from external sources. The common absence of genes involved in synthesis of residues, typical of the O antigen of free-living Synechococcus species, suggests a novel mechanism utilized by these symbionts to avoid sponge predation and phage attack. American Society of Microbiology 2015-06-02 /pmc/articles/PMC4453008/ /pubmed/26037118 http://dx.doi.org/10.1128/mBio.00391-15 Text en Copyright © 2015 Burgsdorf et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
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Open Access Journal |
institution_category |
Foreign Institution |
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US National Center for Biotechnology Information |
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NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Burgsdorf, Ilia Slaby, Beate M. Handley, Kim M. Haber, Markus Blom, Jochen Marshall, Christopher W. Gilbert, Jack A. Hentschel, Ute Steindler, Laura |
spellingShingle |
Burgsdorf, Ilia Slaby, Beate M. Handley, Kim M. Haber, Markus Blom, Jochen Marshall, Christopher W. Gilbert, Jack A. Hentschel, Ute Steindler, Laura Lifestyle Evolution in Cyanobacterial Symbionts of Sponges |
author_facet |
Burgsdorf, Ilia Slaby, Beate M. Handley, Kim M. Haber, Markus Blom, Jochen Marshall, Christopher W. Gilbert, Jack A. Hentschel, Ute Steindler, Laura |
author_sort |
Burgsdorf, Ilia |
title |
Lifestyle Evolution in Cyanobacterial Symbionts of Sponges |
title_short |
Lifestyle Evolution in Cyanobacterial Symbionts of Sponges |
title_full |
Lifestyle Evolution in Cyanobacterial Symbionts of Sponges |
title_fullStr |
Lifestyle Evolution in Cyanobacterial Symbionts of Sponges |
title_full_unstemmed |
Lifestyle Evolution in Cyanobacterial Symbionts of Sponges |
title_sort |
lifestyle evolution in cyanobacterial symbionts of sponges |
description |
The “Candidatus Synechococcus spongiarum” group includes different clades of cyanobacteria with high 16S rRNA sequence identity (~99%) and is the most abundant and widespread cyanobacterial symbiont of marine sponges. The first draft genome of a “Ca. Synechococcus spongiarum” group member was recently published, providing evidence of genome reduction by loss of genes involved in several nonessential functions. However, “Ca. Synechococcus spongiarum” includes a variety of clades that may differ widely in genomic repertoire and consequently in physiology and symbiotic function. Here, we present three additional draft genomes of “Ca. Synechococcus spongiarum,” each from a different clade. By comparing all four symbiont genomes to those of free-living cyanobacteria, we revealed general adaptations to life inside sponges and specific adaptations of each phylotype. Symbiont genomes shared about half of their total number of coding genes. Common traits of “Ca. Synechococcus spongiarum” members were a high abundance of DNA modification and recombination genes and a reduction in genes involved in inorganic ion transport and metabolism, cell wall biogenesis, and signal transduction mechanisms. Moreover, these symbionts were characterized by a reduced number of antioxidant enzymes and low-weight peptides of photosystem II compared to their free-living relatives. Variability within the “Ca. Synechococcus spongiarum” group was mostly related to immune system features, potential for siderophore-mediated iron transport, and dependency on methionine from external sources. The common absence of genes involved in synthesis of residues, typical of the O antigen of free-living Synechococcus species, suggests a novel mechanism utilized by these symbionts to avoid sponge predation and phage attack. |
publisher |
American Society of Microbiology |
publishDate |
2015 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453008/ |
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1613230960473538560 |