Evidence map›Paper›PMID 31898475›Full record

ArticleBMC genomics2020

A detailed in silico analysis of secondary metabolite biosynthesis clusters in the genome of the broad host range plant pathogenic fungus Sclerotinia sclerotiorum.

Carolyn Graham-Taylor, Lars G Kamphuis, Mark C Derbyshire

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
12.0field-weighted citation impact, top 1% 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

17 citing papers in PubMed, 49 citations in OpenAlex.

  1. Functional Characterization of Two Adjacent Oxygenase Genes,Journal of fungi (Basel, Switzerland) · 2026
    Article
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  6. Fungal Effectoromics: A World in Constant Evolution.International journal of molecular sciences · 2022
    Review
  7. Review
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  9. The NecrotrophFrontiers in plant science · 2022
    Article
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  11. Article
  12. Review
  13. Article
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  16. Article
  17. Understanding Host-Pathogen Interactions inPlants (Basel, Switzerland) · 2020
    Review
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

3 authors at 1 institution in 1 country.

Carolyn Graham-TaylorCentre for Crop and Disease Management, School of Molecular and Life Sciences, Curtin University, Bentley, Perth, Western Australia, Australia.
Lars G KamphuisCentre for Crop and Disease Management, School of Molecular and Life Sciences, Curtin University, Bentley, Perth, Western Australia, Australia.
Mark C DerbyshireCentre for Crop and Disease Management, School of Molecular and Life Sciences, Curtin University, Bentley, Perth, Western Australia, Australia. mark.derbyshire@curtin.edu.au.
Curtin University · AU

Funding

Grains Research and Development Corporation CUR00023
6 · The paper itself

Abstract

backgroundThe broad host range pathogen Sclerotinia sclerotiorum infects over 400 plant species and causes substantial yield losses in crops worldwide. Secondary metabolites are known to play important roles in the virulence of plant pathogens, but little is known about the secondary metabolite repertoire of S. sclerotiorum. In this study, we predicted secondary metabolite biosynthetic gene clusters in the genome of S. sclerotiorum and analysed their expression during infection of Brassica napus using an existing transcriptome data set. We also investigated their sequence diversity among a panel of 25 previously published S. sclerotiorum isolate genomes.

resultsWe identified 80 putative secondary metabolite clusters. Over half of the clusters contained at least three transcriptionally coregulated genes. Comparative genomics revealed clusters homologous to clusters in the closely related plant pathogen Botrytis cinerea for production of carotenoids, hydroxamate siderophores, DHN melanin and botcinic acid. We also identified putative phytotoxin clusters that can potentially produce the polyketide sclerin and an epipolythiodioxopiperazine. Secondary metabolite clusters were enriched in subtelomeric genomic regions, and those containing paralogues showed a particularly strong association with repeats. The positional bias we identified was borne out by intraspecific comparisons that revealed putative secondary metabolite genes suffered more presence / absence polymorphisms and exhibited a significantly higher sequence diversity than other genes.

conclusionsThese data suggest that S. sclerotiorum produces numerous secondary metabolites during plant infection and that their gene clusters undergo enhanced rates of mutation, duplication and recombination in subtelomeric regions. The microevolutionary regimes leading to S. sclerotiorum secondary metabolite diversity have yet to be elucidated. Several potential phytotoxins documented in this study provide the basis for future functional analyses.

Indexed as

AscomycotaBiosynthetic PathwaysBrassica napusComputer SimulationGenome, FungalHost-Pathogen InteractionsHost SpecificityPlant DiseasesRecombination, GeneticSecondary MetabolismTelomereBiosynthetic gene clusterBotcinic acidGene lossGenomic comparisonMelaninNecrotrophPhytotoxinPseudogenisationSubtelomere

Identifiers

PMID31898475
PMCPMC6941272
OpenAlexW2998848358

What OpenQuestion holds

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LicenceCC BY
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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.