Evidence map›Paper›PMID 25980449›Full record

ArticleEnvironmental microbiology2016

Changes in secondary metabolic profiles of Microcystis aeruginosa strains in response to intraspecific interactions.

Enora Briand, Myriam Bormans, Muriel Gugger, Pieter C Dorrestein, William H Gerwick

Open access · greenAbstract read
In one paragraph

Article in Environmental microbiology, 2016. 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
7.3field-weighted citation impact, top 3% 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, 78 citations in OpenAlex.

  1. Review
  2. Article
  3. Secondary metabolism ofApplied and environmental microbiology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Metabolomics Applied to Cyanobacterial Toxins and Natural Products.Advances in experimental medicine and biology · 2023
    Review
  8. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 5 institutions in 2 countries.

Enora BriandUMR CNRS 6553 ECOBIO, University of Rennes 1, 35042, Rennes Cedex, France.
Myriam BormansUMR CNRS 6553 ECOBIO, University of Rennes 1, 35042, Rennes Cedex, France.
Muriel GuggerCollection of Cyanobacteria, Institut Pasteur, 75724, Paris, France.
Pieter C DorresteinCollaborative Mass Spectrometry Innovation Center, University of California San Diego, La Jolla, CA, 92093, USA.
William H GerwickCenter for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA, 92093, USA.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRScripps Institution of Oceanography · USUniversité de Rennes · FRUniversity of California San Diego · US

Funding

Unified Computation Tools for Natural Products ResearchR01GM107550 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COTTRELL, GARRISON W, GERWICK, WILLIAM HENRY · 2013 to 2025
$8.2M
NIGMS NIH HHS GM107550NIGMS NIH HHS R01 GM107550
6 · The paper itself

Abstract

The cyanobacteria Microcystis proliferate in freshwater ecosystems and produce bioactive compounds including the harmful toxins microcystins (MC). These secondary metabolites play an important role in shaping community composition through biotic interactions although their role and mode of regulation are poorly understood. As natural cyanobacterial populations include producing and non-producing strains, we tested if the production of a range of peptides by coexisting cells could be regulated through intraspecific interactions. With an innovative co-culturing chamber together with advanced mass spectrometry (MS) techniques, we monitored the growth and compared the metabolic profiles of a MC-producing as well as two non-MC-producing Microcystis strains under mono- and co-culture conditions. In monocultures, these strains grew comparably; however, the non-MC-producing mutant produced higher concentrations of cyanopeptolins, aerucyclamides and aeruginosins than the wild type. Physiological responses to co-culturing were reflected in a quantitative change in the production of the major peptides. Using a MS/MS-based molecular networking approach, we identified new analogues of known classes of peptides as well as new compounds. This work provides new insights into the factors that regulate the production of MC and other secondary metabolites in cyanobacteria, and suggests interchangeable or complementary functions allowing bloom-forming cyanobacteria to efficiently colonize and dominate in fluctuating aquatic environments.

Indexed as

Coculture TechniquesEcosystemFresh WaterMetabolomeMicrocystinsMicrocystisOligopeptidesPeptides, CyclicTandem Mass SpectrometrymicrocystinMicrocystinsOligopeptidesPeptides, Cyclic

Identifiers

PMID25980449
PMCPMC5083810
OpenAlexW1838271312

What OpenQuestion holds

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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.