Evidence map›Paper›PMID 25205095›Full record

ArticlemBio2014

The plant pathogen Xanthomonas campestris pv. campestris exploits N-acetylglucosamine during infection.

Alice Boulanger, Claudine Zischek, Martine Lautier, Stevie Jamet, Pauline Rival, Sébastien Carrère, Matthieu Arlat, Emmanuelle Lauber

Open access · goldAbstract read
In one paragraph

Article in mBio, 2014. 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
6.1field-weighted citation impact, top 4% 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, 34 citations in OpenAlex.

  1. Review
  2. Pathogens (Basel, Switzerland) · 2026
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  5. Efficacy ofMicrobiology spectrum · 2025
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  6. Synergistic antibacterial activity ofFrontiers in microbiology · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. A plant growth-promoting bacteriaFrontiers in plant science · 2022
    Article
  11. Proteome Analysis of Walnut Bacterial Blight Disease.International journal of molecular sciences · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

8 authors at 3 institutions in 1 country.

Alice BoulangerINRA, Laboratoire des Interactions Plantes-Microorganismes, UMR 441, Castanet-Tolosan, France CNRS, Laboratoire des Interactions Plantes-Microorganismes, UMR 2594, Castanet-Tolosan, France.
Claudine Zischek
Martine Lautier
Stevie JametINRA, Laboratoire des Interactions Plantes-Microorganismes, UMR 441, Castanet-Tolosan, France CNRS, Laboratoire des Interactions Plantes-Microorganismes, UMR 2594, Castanet-Tolosan, France.
Pauline RivalINRA, Laboratoire des Interactions Plantes-Microorganismes, UMR 441, Castanet-Tolosan, France CNRS, Laboratoire des Interactions Plantes-Microorganismes, UMR 2594, Castanet-Tolosan, France.
Sébastien Carrère
Matthieu Arlat
Emmanuelle Lauberelauber@toulouse.inra.fr.
Centre National de la Recherche Scientifique · FRLaboratoire des Interactions Plantes Micro-Organismes · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledN-Acetylglucosamine (GlcNAc), the main component of chitin and a major constituent of bacterial peptidoglycan, is present only in trace amounts in plants, in contrast to the huge amount of various sugars that compose the polysaccharides of the plant cell wall. Thus, GlcNAc has not previously been considered a substrate exploited by phytopathogenic bacteria during plant infection. Xanthomonas campestris pv. campestris, the causal agent of black rot disease of Brassica plants, expresses a carbohydrate utilization system devoted to GlcNAc exploitation. In addition to genes involved in GlcNAc catabolism, this system codes for four TonB-dependent outer membrane transporters (TBDTs) and eight glycoside hydrolases. Expression of all these genes is under the control of GlcNAc. In vitro experiments showed that X. campestris pv. campestris exploits chitooligosaccharides, and there is indirect evidence that during the early stationary phase, X. campestris pv. campestris recycles bacterium-derived peptidoglycan/muropeptides. Results obtained also suggest that during plant infection and during growth in cabbage xylem sap, X. campestris pv. campestris encounters and metabolizes plant-derived GlcNAc-containing molecules. Specific TBDTs seem to be preferentially involved in the consumption of all these plant-, fungus- and bacterium-derived GlcNAc-containing molecules. This is the first evidence of GlcNAc consumption during infection by a phytopathogenic bacterium. Interestingly, N-glycans from plant N-glycosylated proteins are proposed to be substrates for glycoside hydrolases belonging to the X. campestris pv. campestris GlcNAc exploitation system. This observation extends the range of sources of GlcNAc metabolized by phytopathogenic bacteria during their life cycle. IMPORTANCE: Despite the central role of N-acetylglucosamine (GlcNAc) in nature, there is no evidence that phytopathogenic bacteria metabolize this compound during plant infection. Results obtained here suggest that Xanthomonas campestris pv. campestris, the causal agent of black rot disease on Brassica, encounters and metabolizes GlcNAc in planta and in vitro. Active and specific outer membrane transporters belonging to the TonB-dependent transporters family are proposed to import GlcNAc-containing complex molecules from the host, from the bacterium, and/or from the environment, and bacterial glycoside hydrolases induced by GlcNAc participate in their degradation. Our results extend the range of sources of GlcNAc metabolized by this phytopathogenic bacterium during its life cycle to include chitooligosaccharides that could originate from fungi or insects present in the plant environment, muropeptides leached during peptidoglycan recycling and bacterial lysis, and N-glycans from plant N-glycosylated proteins present in the plant cell wall as well as in xylem sap.

Indexed as

AcetylglucosamineBrassicaCell WallComputational BiologyMembrane Transport ProteinsMutationPeptidoglycanPhenotypePlant DiseasesPlant ProteinsPlasmidsPromoter Regions, GeneticXanthomonas campestrisXylemAcetylglucosamineMembrane Transport ProteinsPeptidoglycanPlant Proteins

Identifiers

PMID25205095
PMCPMC4173781
OpenAlexW2117121448

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.