Evidence map›Paper›PMID 28811531›Full record

ArticleScientific reports2017

The selective antifungal activity of Drosophila melanogaster metchnikowin reflects the species-dependent inhibition of succinate-coenzyme Q reductase.

Mohammad-Reza Bolouri Moghaddam, Thomas Gross, Annette Becker, Andreas Vilcinskas, Mohammad Rahnamaeian

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Proline-Rich Antimicrobial Peptides from Invertebrates.Molecules (Basel, Switzerland) · 2024
    Review
  5. Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Hemolymph of triatomines presents fungistatic activity againstThe journal of venomous animals and toxins including tropical diseases · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
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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

5 authors at 2 institutions in 1 country.

Mohammad-Reza Bolouri MoghaddamInstitute for Insect Biotechnology, Justus Liebig University of Giessen, Heinrich-Buff-Ring 26-32, D-35392, Giessen, Germany.
Thomas GrossInstitute of Botany, Justus Liebig University of Giessen, Heinrich-Buff-Ring 38, D-35392, Giessen, Germany.
Annette BeckerInstitute of Botany, Justus Liebig University of Giessen, Heinrich-Buff-Ring 38, D-35392, Giessen, Germany.ORCID 0000-0002-3229-2162
Andreas VilcinskasInstitute for Insect Biotechnology, Justus Liebig University of Giessen, Heinrich-Buff-Ring 26-32, D-35392, Giessen, Germany. andreas.vilcinskas@agrar.uni-giessen.de.
Mohammad RahnamaeianFraunhofer Institute for Molecular Biology and Applied Ecology, Department of Bioresources, Winchester Strasse 2, D-35394, Giessen, Germany. mohammad.rahnamaeian@uni-giessen.de.ORCID 0000-0001-5893-6037
Justus-Liebig-Universität Gießen · DEFraunhofer Institute for Molecular Biology and Applied Ecology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insect-derived antifungal peptides have a significant economic potential, particularly for the engineering of pathogen-resistant crops. However, the nonspecific antifungal activity of such peptides could result in detrimental effects against beneficial fungi, whose interactions with plants promote growth or increase resistance against biotic and abiotic stress. The antifungal peptide metchnikowin (Mtk) from Drosophila melanogaster acts selectively against pathogenic Ascomycota, including Fusarium graminearum, without affecting Basidiomycota such as the beneficial symbiont Piriformospora indica. Here we investigated the mechanism responsible for the selective antifungal activity of Mtk by using the peptide to probe a yeast two-hybrid library of F. graminearum cDNAs. We found that Mtk specifically targets the iron-sulfur subunit (SdhB) of succinate-coenzyme Q reductase (SQR). A functional assay based on the succinate dehydrogenase (SDH) activity of mitochondrial complex II clearly demonstrated that Mtk inhibited the SDH activity of F. graminearum mitochondrial SQR by up to 52%, but that the equivalent enzyme in P. indica was unaffected. A phylogenetic analysis of the SdhB family revealed a significant divergence between the Ascomycota and Basidiomycota. SQR is one of the key targets of antifungal agents and we therefore propose Mtk as an environmentally sustainable and more selective alternative to chemical fungicides.

Indexed as

AnimalsAntifungal AgentsAntimicrobial Cationic PeptidesCell LineDrosophila melanogasterDrosophila ProteinsElectron Transport Complex IIEnzyme InhibitorsMitochondriaPhylogenyRecombinant ProteinsAntifungal AgentsAntimicrobial Cationic PeptidesDrosophila ProteinsElectron Transport Complex IIEnzyme InhibitorsMtk protein, DrosophilaRecombinant Proteins

Identifiers

PMID28811531
PMCPMC5557811
OpenAlexW2742387892

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.