Evidence map›Paper›PMID 26037118›Full record

ArticlemBio2015

Lifestyle evolution in cyanobacterial symbionts of sponges.

Ilia Burgsdorf, Beate M Slaby, Kim M Handley, Markus Haber, Jochen Blom, Christopher W Marshall, Jack A Gilbert, Ute Hentschel, Laura Steindler

Open access · goldAbstract read
In one paragraph

Article in mBio, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
14.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 123 citations in OpenAlex.

  1. Anoxia-adapted cyanobacteria in a marine blue hole.Applied and environmental microbiology · 2026
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  3. Rhamnose biosynthesis is not impaired by the deletion of putativeApplied and environmental microbiology · 2025
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  15. Bacteria Isolated From the Antarctic SpongeFrontiers in microbiology · 2021
    Article
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  18. Article
  19. Article
  20. Cultivation of Bacteria FromFrontiers in microbiology · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 4 countries.

Ilia BurgsdorfDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Beate M SlabyDepartment of Botany II, Julius-von-Sachs Institute for Biosciences, University of Würzburg, Würzburg, Germany.
Kim M HandleyDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, USA.
Markus HaberDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Jochen BlomBioinformatics and System Biology Justus-Liebig-University, Giessen, Giessen, Germany.
Christopher W MarshallArgonne National Laboratory, Institute for Genomic and Systems Biology, Argonne, Illinois, USA.
Jack A Gilbert
Ute HentschelDepartment of Botany II, Julius-von-Sachs Institute for Biosciences, University of Würzburg, Würzburg, Germany.
Laura SteindlerDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel lsteindler@univ.haifa.ac.il.
University of Haifa · ILUniversity of Würzburg · DEArgonne National Laboratory · USMarine Biological Laboratory · USUniversity of Chicago · USUniversity of Giessen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledThe "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. IMPORTANCE: While the Synechococcus/Prochlorococcus-type cyanobacteria are widely distributed in the world's oceans, a subgroup has established its niche within marine sponge tissues. Recently, the first genome of sponge-associated cyanobacteria, "Candidatus Synechococcus spongiarum," was described. The sequencing of three representatives of different clades within this cyanobacterial group has enabled us to investigate intraspecies diversity, as well as to give a more comprehensive understanding of the common symbiotic features that adapt "Ca. Synechococcus spongiarum" to its life within the sponge host.

Indexed as

Evolution, MolecularGenome, BacterialSymbiosisAnimalsBacteriophagesMethionineO AntigensPhotosystem II Protein ComplexPhylogenyPoriferaRNA, Ribosomal, 16SSequence AlignmentSequence Analysis, DNASynechococcusMethionineO AntigensPhotosystem II Protein ComplexRNA, Ribosomal, 16S

Identifiers

PMID26037118
PMCPMC4453008
OpenAlexW2101991850

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.