Evidence map›Paper›PMID 26441923›Full record

ArticleFrontiers in microbiology2015

Whole genome resequencing of Botrytis cinerea isolates identifies high levels of standing diversity.

Susanna Atwell, Jason A Corwin, Nicole E Soltis, Anushryia Subedy, Katherine J Denby, Daniel J Kliebenstein

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
11.3field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 56 citations in OpenAlex.

  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
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  2. A multiplant transcriptomic atlas reveals conserved and lineage-specific defense architectures in response toProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Genetic and Genomic Analysis IdentifiesInternational journal of molecular sciences · 2025
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  10. The Adaptation ofJournal of fungi (Basel, Switzerland) · 2023
    Article
  11. Article
  12. Cells · 2023
    Review
  13. Article
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  15. International journal of molecular sciences · 2022
    Article
  16. Article
  17. Article
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  19. The Destructive Fungal PathogenPathogens (Basel, Switzerland) · 2020
    Review
  20. 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

6 authors at 2 institutions in 2 countries.

Susanna AtwellDepartment of Plant Sciences, University of California, Davis Davis, CA, USA.
Jason A CorwinDepartment of Plant Sciences, University of California, Davis Davis, CA, USA.
Nicole E SoltisDepartment of Plant Sciences, University of California, Davis Davis, CA, USA.
Anushryia SubedyDepartment of Plant Sciences, University of California, Davis Davis, CA, USA.
Katherine J DenbySchool of Life Sciences and Warwick Systems Biology Centre, University of Warwick Coventry, UK.
Daniel J KliebensteinDepartment of Plant Sciences, University of California, Davis Davis, CA, USA.
University of California, Davis · USUniversity of Warwick · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How standing genetic variation within a pathogen contributes to diversity in host/pathogen interactions is poorly understood, partly because most studied pathogens are host-specific, clonally reproducing organisms which complicates genetic analysis. In contrast, Botrytis cinerea is a sexually reproducing, true haploid ascomycete that can infect a wide range of diverse plant hosts. While previous work had shown significant genomic variation between two isolates, we proceeded to assess the level and frequency of standing variation in a population of B. cinerea. To begin measuring standing genetic variation in B. cinerea, we re-sequenced the genomes of 13 different isolates and aligned them to the previously sequenced T4 reference genome. In addition one of these isolates was resequenced from four independently repeated cultures. A high level of genetic diversity was found within the 13 isolates. Within this variation, we could identify clusters of genes with major effect polymorphisms, i.e., polymorphisms that lead to a predicted functional knockout, that surrounded genes involved in controlling vegetative incompatibility. The genotype at these loci was able to partially predict the interaction of these isolates in vegetative fusion assays showing that these loci control vegetative incompatibility. This suggests that the vegetative incompatibility loci within B. cinerea are associated with regions of increased genetic diversity. The genome re-sequencing of four clones from the one isolate (Grape) that had been independently propagated over 10 years showed no detectable spontaneous mutation. This suggests that B. cinerea does not display an elevated spontaneous mutation rate. Future work will allow us to test if, and how, this diversity may be contributing to the pathogen's broad host range.

Indexed as

Botrytis cinereadiversitygenome resequencingstanding genetic variationvegetative incompatibility loci

Identifiers

PMID26441923
PMCPMC4585241
OpenAlexW1897344135

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.