Evidence map›Paper›PMID 29368587›Full record

ArticleBMC evolutionary biology2018

Widespread signatures of selection for secreted peptidases in a fungal plant pathogen.

Parvathy Krishnan, Xin Ma, Bruce A McDonald, Patrick C Brunner

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Frontiers in microbiology · 2024
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  6. Article
  7. Article
  8. Secretome Analysis for a New Strain of the Blackleg FungusJournal of fungi (Basel, Switzerland) · 2023
    Article
  9. Article
  10. Secretomic Insights into the Pathophysiology ofPathogens (Basel, Switzerland) · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Fungal evolution: cellular, genomic and metabolic complexity.Biological reviews of the Cambridge Philosophical Society · 2020
    Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Parvathy KrishnanPlant Pathology, Institute of Integrative Biology, ETH Zurich, Universitätstrasse 2, -8092, Zurich, CH, Switzerland.
Xin MaPlant Pathology, Institute of Integrative Biology, ETH Zurich, Universitätstrasse 2, -8092, Zurich, CH, Switzerland.
Bruce A McDonaldPlant Pathology, Institute of Integrative Biology, ETH Zurich, Universitätstrasse 2, -8092, Zurich, CH, Switzerland.
Patrick C BrunnerPlant Pathology, Institute of Integrative Biology, ETH Zurich, Universitätstrasse 2, -8092, Zurich, CH, Switzerland. patrick.brunner@usys.ethz.ch.
ETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFungal plant pathogens secrete a large arsenal of hydrolytic enzymes during the course of infection, including peptidases. Secreted peptidases have been extensively studied for their role as effectors. In this study, we combined transcriptomics, comparative genomics and evolutionary analyses to investigate all 39 secreted peptidases in the fungal wheat pathogen Zymoseptoria tritici and its close relatives Z. pseudotritici and Z. ardabiliae.

resultsRNA-seq data revealed that a majority of the secreted peptidases displayed differential transcription during the course of Z. tritici infection, indicative of specialization for different stages in the life cycle. Evolutionary analyses detected widespread evidence of adaptive evolution acting on at least 28 of the peptidases. A few peptidases displayed lineage-specific rates of molecular evolution, suggesting altered selection pressure in Z. tritici following host specialization on domesticated wheat. The peptidases belonging to MEROPS families A1 and G1 emerged as a particularly interesting group that may play key roles in host-pathogen co-evolution, host adaptation and pathogenicity. Sister genes in the A1 and G1 families showed accelerated substitution rates after gene duplications.

conclusionsThese results suggest widespread evolution of secreted peptidases leading to novel gene functions, consistent with predicted models of "escape from adaptive conflict" and "neo-functionalization". Our analyses identified candidate genes worthy of functional analyses that may encode effector functions, for example by suppressing plant defenses during the biotrophic phase of infection.

Indexed as

Selection, GeneticAscomycotaEvolution, MolecularGene Expression Regulation, EnzymologicGene Expression Regulation, FungalGenes, FungalPeptide HydrolasesPhylogenyPlant DiseasesTranscriptomeTriticumVirulencePeptide HydrolasesAdaptive evolutionEscape from adaptive conflict (EAC)Neo-functionalization (NEO-F)PeptidasesTranscriptomics

Identifiers

PMID29368587
PMCPMC5784588
OpenAlexW2794305444

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.