Evidence map›Paper›PMID 25615440›Full record

ArticleThe ISME journal2015

Chemotaxis by natural populations of coral reef bacteria.

Jessica Tout, Thomas C Jeffries, Katherina Petrou, Gene W Tyson, Nicole S Webster, Melissa Garren, Roman Stocker, Peter J Ralph, Justin R Seymour

Open access · bronzeAbstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
9.7field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 85 citations in OpenAlex.

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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 4 institutions in 2 countries.

Jessica ToutPlant Functional Biology and Climate Change Cluster, University of Technology Sydney, Sydney, New South Wales, Australia.
Thomas C JeffriesPlant Functional Biology and Climate Change Cluster, University of Technology Sydney, Sydney, New South Wales, Australia.
Katherina PetrouPlant Functional Biology and Climate Change Cluster, University of Technology Sydney, Sydney, New South Wales, Australia.
Gene W TysonAustralian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, University of Queensland, St Lucia, Queensland, Australia.
Nicole S WebsterAustralian Institute of Marine Science, Townsville, Queensland, Australia.
Melissa GarrenDepartment of Civil and Environmental Engineering, Ralph M. Parsons Laboratory, Massachusetts Institute of Technology, Cambridge, MA, USA.
Roman StockerDepartment of Civil and Environmental Engineering, Ralph M. Parsons Laboratory, Massachusetts Institute of Technology, Cambridge, MA, USA.
Peter J RalphPlant Functional Biology and Climate Change Cluster, University of Technology Sydney, Sydney, New South Wales, Australia.
Justin R SeymourPlant Functional Biology and Climate Change Cluster, University of Technology Sydney, Sydney, New South Wales, Australia.
University of Technology Sydney · AUParsons (United States) · USAustralian Institute of Marine Science · AUUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Corals experience intimate associations with distinct populations of marine microorganisms, but the microbial behaviours underpinning these relationships are poorly understood. There is evidence that chemotaxis is pivotal to the infection process of corals by pathogenic bacteria, but this evidence is limited to experiments using cultured isolates under laboratory conditions. We measured the chemotactic capabilities of natural populations of coral-associated bacteria towards chemicals released by corals and their symbionts, including amino acids, carbohydrates, ammonium and dimethylsulfoniopropionate (DMSP). Laboratory experiments, using a modified capillary assay, and in situ measurements, using a novel microfabricated in situ chemotaxis assay, were employed to quantify the chemotactic responses of natural microbial assemblages on the Great Barrier Reef. Both approaches showed that bacteria associated with the surface of the coral species Pocillopora damicornis and Acropora aspera exhibited significant levels of chemotaxis, particularly towards DMSP and amino acids, and that these levels of chemotaxis were significantly higher than that of bacteria inhabiting nearby, non-coral-associated waters. This pattern was supported by a significantly higher abundance of chemotaxis and motility genes in metagenomes within coral-associated water types. The phylogenetic composition of the coral-associated chemotactic microorganisms, determined using 16S rRNA amplicon pyrosequencing, differed from the community in the seawater surrounding the coral and comprised known coral associates, including potentially pathogenic Vibrio species. These findings indicate that motility and chemotaxis are prevalent phenotypes among coral-associated bacteria, and we propose that chemotaxis has an important role in the establishment and maintenance of specific coral-microbe associations, which may ultimately influence the health and stability of the coral holobiont.

Indexed as

Coral ReefsAnimalsAnthozoaBacteriaChemotactic FactorsChemotaxisDNA, BacterialMetagenomePhylogenyRNA, Ribosomal, 16SSeawaterSulfonium CompoundsVibrioChemotactic FactorsdimethylpropiothetinDNA, BacterialRNA, Ribosomal, 16SSulfonium Compounds

Identifiers

PMID25615440
PMCPMC4511932
OpenAlexW2133103356

What OpenQuestion holds

Textmetadata
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.