Evidence map›Paper›PMID 30426643›Full record

ArticleMolecular plant pathology2019

Contribution of cell wall peroxidase- and NADPH oxidase-derived reactive oxygen species to Alternaria brassicicola-induced oxidative burst in Arabidopsis.

Evelin Kámán-Tóth, Tamás Dankó, Gábor Gullner, Zoltán Bozsó, László Palkovics, Miklós Pogány

Open access · hybridAbstract read
In one paragraph

Article in Molecular plant pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.7field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 60 citations in OpenAlex.

  1. Comparative Secretome Profiling ofPlants (Basel, Switzerland) · 2026
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  8. Differential gene expression in ripe mango fruit (Frontiers in fungal biology · 2025
    Article
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  11. Review
  12. Review
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  15. Proteomic Analysis of Proteins Related to Defense Responses inInternational journal of molecular sciences · 2023
    Article
  16. Article
  17. Reactive oxygen species signalling in plant stress responses.Nature reviews. Molecular cell biology · 2022
    Review
  18. Review
  19. Article
  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 4 institutions in 1 country.

Evelin Kámán-TóthPlant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1022, Budapest, Herman Ottó út 15, Hungary.
Tamás DankóPlant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1022, Budapest, Herman Ottó út 15, Hungary.
Gábor GullnerPlant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1022, Budapest, Herman Ottó út 15, Hungary.
Zoltán BozsóPlant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1022, Budapest, Herman Ottó út 15, Hungary.
László PalkovicsSzent István University, Faculty of Horticultural Science, H-1118, Budapest, Villányi út 29-43, Hungary.
Miklós PogányPlant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1022, Budapest, Herman Ottó út 15, Hungary.
Centre for Agricultural Research · HUHungarian Academy of Sciences · HUMagyar Agrár- és Élettudományi Egyetem · HUPlant Protection Institute · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell wall peroxidases and plasma membrane-localized NADPH oxidases are considered to be the main sources of the apoplastic oxidative burst in plants attacked by microbial pathogens. In spite of this established doctrine, approaches attempting a comparative, side-by-side analysis of the functions of extracellular reactive oxygen species (ROS) generated by the two enzymatic sources are scarce. Previously, we have reported the role of Arabidopsis NADPH oxidase RBOHD (respiratory burst oxidase homologue D) in plants challenged with the necrotrophic fungus Alternaria brassicicola. Here, we present results on the activity of apoplastic class III peroxidases PRX33 (At3g49110) and PRX34 (At3g49120) investigated in the same Arabidopsis-Alternaria pathosystem. ROS generated by Arabidopsis peroxidases PRX33 and PRX34 increase the necrotic symptoms and colonization success of A. brassicicola. In addition, the knockdown of PRX33 and PRX34 transcript levels leads to a reduced number of host cells showing an extracellular burst of ROS after inoculation with A. brassicicola. Our results also reveal an age-dependent transcript distribution of ROS-producing peroxidase and NADPH oxidase enzymes, and some potential new components of the RBOHD, PRX33 and PRX34 signalling networks.

Indexed as

AlternariaArabidopsisArabidopsis ProteinsCell WallGene Expression Regulation, PlantNADPH OxidasesPeroxidaseReactive Oxygen SpeciesArabidopsis ProteinsNADPH-oxidase, ArabidopsisNADPH OxidasesPeroxidaseReactive Oxygen SpeciesAlternariaArabidopsiscell wall peroxidaseERECTAJAR1NHO1VIGS

Identifiers

PMID30426643
PMCPMC6637864
OpenAlexW2900497255

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.