Evidence map›Paper›PMID 36269466›Full record

ArticleGlycoconjugate journal2023

Pseudomonas syringae DC3000 infection increases glucosylated N-glycans in Arabidopsis thaliana.

Gernot Beihammer, Andrea Romero-Pérez, Daniel Maresch, Rudolf Figl, Réka Mócsai, Clemens Grünwald-Gruber, Friedrich Altmann, Els J M Van Damme, Richard Strasser

Open access · hybridAbstract read
In one paragraph

Article in Glycoconjugate journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 2 institutions in 2 countries.

Gernot BeihammerInstitute of Plant Biotechnology and Cell Biology, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria.
Andrea Romero-PérezLaboratory of Biochemistry and Glycobiology, Department of Biotechnology, Ghent University, Ghent, Belgium.
Daniel MareschInstitute of Biochemistry, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna, Austria.
Rudolf FiglInstitute of Biochemistry, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna, Austria.
Réka MócsaiInstitute of Biochemistry, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna, Austria.
Clemens Grünwald-GruberInstitute of Biochemistry, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna, Austria.
Friedrich AltmannInstitute of Biochemistry, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna, Austria.
Els J M Van DammeLaboratory of Biochemistry and Glycobiology, Department of Biotechnology, Ghent University, Ghent, Belgium.
Richard StrasserInstitute of Plant Biotechnology and Cell Biology, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria. Richard.strasser@boku.ac.at.ORCID http://orcid.org/0000-0001-8764-6530
BOKU University · ATGhent University · BE

Funding

Austrian Science Fund FWF I 2417Austrian Science Fund FWF W 1224
6 · The paper itself

Abstract

Studying the interaction between the hemibiotrophic bacterium Pseudomonas syringae pv. tomato DC3000 and Arabidopsis thaliana has shed light onto the various forms of mechanisms plants use to defend themselves against pathogen attack. While a lot of emphasis has been put on investigating changes in protein expression in infected plants, only little information is available on the effect infection plays on the plants N-glycan composition. To close this gap in knowledge, total N-glycans were enriched from P. syringae DC3000-infected and mock treated Arabidopsis seedlings and analyzed via MALDI-TOF-MS. Additionally, fluorescently labelled N-glycans were quantified via HPLC-FLD. N-glycans from infected plants were overall less processed and displayed increased amounts of oligomannosidic N-glycans. As multiple peaks for certain oligomannosidic glycoforms were detected upon separation via liquid chromatography, a porous graphitic carbon (PGC)-analysis was conducted to separate individual N-glycan isomers. Indeed, multiple different N-glycan isomers with masses of two N-acetylhexosamine residues plus 8, 9 or 10 hexoses were detected in the infected plants which were absent in the mock controls. Treatment with jack bean α-mannosidase resulted in incomplete removal of hexoses from these N-glycans, indicating the presence of glucose residues. This hints at the accumulation of misfolded glycoproteins in the infected plants, likely because of endoplasmic reticulum (ER) stress. In addition, poly-hexose structures susceptible to α-amylase treatment were found in the DC3000-infected plants, indicating alterations in starch metabolism due to the infection process.

Indexed as

ArabidopsisGlycoproteinsPolysaccharidesProtein Processing, Post-TranslationalPseudomonas syringaeGlycoproteinsPolysaccharidesER stressGlycanGlycosylationMisfolded glycoproteinsPlant-pathogen interactionPosttranslational modification

Identifiers

PMID36269466
PMCPMC9925501
OpenAlexW4306973430

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.