Evidence map›Paper›PMID 26978374›Full record

ArticleMarine drugs2016

Deep Subseafloor Fungi as an Untapped Reservoir of Amphipathic Antimicrobial Compounds.

Marion Navarri, Camille Jégou, Laurence Meslet-Cladière, Benjamin Brillet, Georges Barbier, Gaëtan Burgaud, Yannick Fleury

Abstract read
In one paragraph

Article in Marine drugs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

7 authors.

Marion NavarriLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. marion.navarri@univ-brest.fr.
Camille JégouLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. camille.jegou@univ-brest.fr.
Laurence Meslet-CladièreLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. laurence.meslet@univ-brest.fr.
Benjamin BrilletLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. benjamin.brillet@univ-brest.fr.
Georges BarbierLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. georges.barbier@univ-brest.fr.
Gaëtan BurgaudLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. gaetan.burgaud@univ-brest.fr.
Yannick FleuryLaboratoire de Biodiversité et d'Ecologie Microbienne (EA 3882), Université de Brest, Technopole Brest Iroise, 29280 Plouzané, France. yannick.fleury@univ-brest.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The evolving global threat of antimicrobial resistance requires a deep renewal of the antibiotic arsenal including the isolation and characterization of new drugs. Underexplored marine ecosystems may represent an untapped reservoir of novel bioactive molecules. Deep-sea fungi isolated from a record-depth sediment core of almost 2000 m below the seafloor were investigated for antimicrobial activities. This antimicrobial screening, using 16 microbial targets, revealed 33% of filamentous fungi synthesizing bioactive compounds with activities against pathogenic bacteria and fungi. Interestingly, occurrence of antimicrobial producing isolates was well correlated with the complexity of the habitat (in term of microbial richness), as higher antimicrobial activities were obtained at specific layers of the sediment core. It clearly highlights complex deep-sea habitats as chemical battlefields where synthesis of numerous bioactive compounds appears critical for microbial competition. The six most promising deep subseafloor fungal isolates were selected for the production and extraction of bioactive compounds. Depending on the fungal isolates, antimicrobial compounds were only biosynthesized in semi-liquid or solid-state conditions as no antimicrobial activities were ever detected using liquid fermentation. An exception was made for one fungal isolate, and the extraction procedure designed to extract amphipathic compounds was successful and highlighted the amphiphilic profile of the bioactive metabolites.

Indexed as

Anti-Bacterial AgentsAntifungal AgentsBacteriaFungiGeologic SedimentsSeawaterAnti-Bacterial AgentsAntifungal Agentsamphipathic compoundsantimicrobial metabolitesdeep subseafloor fungisolid-state fermentation

Identifiers

PMID26978374
PMCPMC4820304

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.