Evidence map›Paper›PMID 40488422›Full record

ArticleGenetics2025

Polygenic strategies for host-specific and general virulence of Botrytis cinerea across diverse eudicot hosts.

Céline Caseys, Daniel J Kliebenstein

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Combined generalist and host-specific transcriptional strategies enable host generalism in the fungal pathogenProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Molecular Breeding for Fungal Resistance in Common Bean.International journal of molecular sciences · 2025
    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

2 authors.

Céline CaseysDepartment of Plant Sciences, University of California, Davis, CA 95616, USA.ORCID 0000-0003-4187-9018
Daniel J KliebensteinDepartment of Plant Sciences, University of California, Davis, CA 95616, USA.ORCID 0000-0001-5759-3175

Funding

NSF IOS 2020754USDA 2019-05709
6 · The paper itself

Abstract

Diverse qualitative and quantitative genetic architectures can successfully enable fungal virulence and host range. To model the quantitative genetic architecture of a generalist pathogen with an extensive host range, we conducted a genome-wide association study (GWAS) of the lesion area of Botrytis cinerea across 8 hosts. This revealed that it was possible to partition the virulence, as defined by the lesion area, common across all hosts from host-specific virulence. All traits showed that a large proportion of the Botrytis genome likely contributes to fungal lesion development on leaves with small effect sizes. The candidate genes are evenly spread across the core chromosomes with no indication of bipartite genomic architecture. The GWAS-identified polymorphisms and genes show that B. cinerea relies on genetic variants across hundreds of genes for growing on diverse hosts, with most genes influencing relatively few hosts. When pathogen genes were associated with multiple hosts, they were associated with unrelated rather than related host species. Comparative genomics further suggested that the GWAS-identified genes are largely syntenic with other specialist Botrytis species and not unique to B. cinerea. Overall, as shown in Arabidopsis thaliana, B. cinerea's generalist behavior is derived from the sum of the genome-wide genetic variation acting within gene networks that differentially coordinate the interaction with diverse hosts.

Indexed as

BotrytisHost-Pathogen InteractionsMultifactorial InheritancePlant DiseasesGenome, FungalGenome-Wide Association StudyHost SpecificityPolymorphism, Single NucleotideVirulenceBotrytis cinereacropsfungal virulencefungigeneralist pathogenGWAShost–pathogen interactionhost rangequantitative genetics

Identifiers

PMID40488422
PMCPMC12239214

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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.