Evidence map›Paper›PMID 34620932›Full record

ArticleScientific reports2021

Apoplastic effector candidates of a foliar forest pathogen trigger cell death in host and non-host plants.

Lukas Hunziker, Mariana Tarallo, Keiko Gough, Melissa Guo, Cathy Hargreaves, Trevor S Loo, Rebecca L McDougal, Carl H Mesarich, Rosie E Bradshaw

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Genome-Wide Characterization of Effector Protein-Encoding Genes inJournal of fungi (Basel, Switzerland) · 2023
    Article
  4. Targeted Gene Mutations in the Forest PathogenPlants (Basel, Switzerland) · 2022
    Article
  5. Chromosome-level assembly of theFrontiers in microbiology · 2022
    Article
  6. Article
  7. 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

9 authors at 3 institutions in 2 countries.

Lukas Hunziker *Centre for Crop and Disease Management, Curtin University, Bentley, Perth, 6102, Australia.
Mariana Tarallo *Bio-Protection Research Centre, School of Fundamental Sciences, Massey University, Palmerston North, 4474, New Zealand.
Keiko GoughScion, New Zealand Forest Research Institute Ltd, Rotorua, 3010, New Zealand.
Melissa GuoBio-Protection Research Centre, School of Fundamental Sciences, Massey University, Palmerston North, 4474, New Zealand.
Cathy HargreavesScion, New Zealand Forest Research Institute Ltd, Rotorua, 3010, New Zealand.
Trevor S LooBio-Protection Research Centre, School of Fundamental Sciences, Massey University, Palmerston North, 4474, New Zealand.
Rebecca L McDougalScion, New Zealand Forest Research Institute Ltd, Rotorua, 3010, New Zealand.
Carl H MesarichBio-Protection Research Centre, School of Agriculture and Environment, Massey University, Palmerston North, 4474, New Zealand.
Rosie E BradshawBio-Protection Research Centre, School of Fundamental Sciences, Massey University, Palmerston North, 4474, New Zealand. R.E.Bradshaw@massey.ac.nz.
Massey University · NZFuture Forests Research · NZCurtin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Forests are under threat from pests, pathogens, and changing climate. A major forest pathogen worldwide is the hemibiotroph Dothistroma septosporum, which causes dothistroma needle blight (DNB) of pines. While D. septosporum uses effector proteins to facilitate host infection, it is currently unclear whether any of these effectors are recognised by immune receptors to activate the host immune system. Such information is needed to identify and select disease resistance against D. septosporum in pines. We predicted and investigated apoplastic D. septosporum candidate effectors (DsCEs) using bioinformatics and plant-based experiments. We discovered DsCEs that trigger cell death in the angiosperm Nicotiana spp., indicative of a hypersensitive defence response and suggesting their recognition by immune receptors in non-host plants. In a first for foliar forest pathogens, we developed a novel protein infiltration method to show that tissue-cultured pine shoots can respond with a cell death response to a DsCE, as well as to a reference cell death-inducing protein. The conservation of responses across plant taxa suggests that knowledge of pathogen-angiosperm interactions may also be relevant to pathogen-gymnosperm interactions. These results contribute to our understanding of forest pathogens and may ultimately provide clues to disease immunity in both commercial and natural forests.

Indexed as

AscomycotaCell DeathDisease ResistanceHost-Pathogen InteractionsNicotianaPinusPlant Diseases

Identifiers

PMID34620932
PMCPMC8497623
OpenAlexW3202162328

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.