Evidence map›Paper›PMID 26528274›Full record

ArticleFrontiers in microbiology2015

VarR controls colonization and virulence in the marine macroalgal pathogen Nautella italica R11.

Melissa Gardiner, Neil D Fernandes, Dennis Nowakowski, Mark Raftery, Staffan Kjelleberg, Ling Zhong, Torsten Thomas, Suhelen Egan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  8. Exoproteome Analysis of the Seaweed PathogenFrontiers in microbiology · 2017
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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

8 authors at 2 institutions in 2 countries.

Melissa GardinerSchool of Biotechnology and Biomolecular Sciences, Centre for Marine Bio-Innovation, The University of New South Wales Sydney, NSW, Australia.
Neil D FernandesSchool of Biotechnology and Biomolecular Sciences, Centre for Marine Bio-Innovation, The University of New South Wales Sydney, NSW, Australia.
Dennis NowakowskiSchool of Biotechnology and Biomolecular Sciences, Centre for Marine Bio-Innovation, The University of New South Wales Sydney, NSW, Australia.
Mark RafteryBioanalytical Mass Spectrometry Facility, Mark Wainwright Analytical Centre, The University of New South Wales Sydney, NSW, Australia.
Staffan KjellebergSchool of Biotechnology and Biomolecular Sciences, Centre for Marine Bio-Innovation, The University of New South Wales Sydney, NSW, Australia ; Singapore Centre on Environmental Life Sciences Engineering, Nanyang Technological University, Singapore Singapore.
Ling ZhongBioanalytical Mass Spectrometry Facility, Mark Wainwright Analytical Centre, The University of New South Wales Sydney, NSW, Australia.
Torsten ThomasSchool of Biotechnology and Biomolecular Sciences, Centre for Marine Bio-Innovation, The University of New South Wales Sydney, NSW, Australia.
Suhelen EganSchool of Biotechnology and Biomolecular Sciences, Centre for Marine Bio-Innovation, The University of New South Wales Sydney, NSW, Australia.
UNSW Sydney · AUUniversity of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is increasing evidence to suggest that macroalgae (seaweeds) are susceptible to infectious disease. However, to date, little is known about the mechanisms that facilitate the colonization and virulence of microbial seaweed pathogens. One well-described example of a seaweed disease is the bleaching of the red alga Delisea pulchra, which can be caused by the bacterium Nautella italica R11, a member of the Roseobacter clade. This pathogen contains a unique luxR-type gene, varR, which we hypothesize controls its colonization and virulence. We show here that a varR knock-out strain is deficient in its ability to cause disease in D. pulchra and is defective in biofilm formation and attachment to a common algal polysaccharide. Moreover complementation of the varR gene in trans can restore these functions to the wild type levels. Proteomic analysis of bacterial cells in planktonic and biofilm growth highlight the potential importance of nitrogen scavenging, mobilization of energy reserves, and stress resistance in the biofilm lifestyle of N. italica R11. Moreover, we show that VarR regulates the expression of a specific subset of biofilm-associated proteins. Taken together these data suggest that VarR controls colonization and persistence of N. italica R11 on the surface of a macroalgal host and that it is an important regulator of virulence.

Indexed as

bacterial biofilmsDelisea pulchramacroalgaemicrobial interactionsquorum sensingseaweed diseasesolo LuxR-type regulator

Identifiers

PMID26528274
PMCPMC4602140
OpenAlexW2151380059

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.