Evidence map›Paper›PMID 39575835›Full record

ArticleThe Plant journal : for cell and molecular biology2025

Laser dissection-assisted phloem transcriptomics highlights the metabolic and physiological changes accompanying clubroot disease progression in oilseed rape.

Sara Blicharz, Karolina Stefanowicz, William Truman, Aneta Basińska-Barczak, Deeksha Singh, Anna Kasprzewska, Nuria de Diego, Ondřej Vrobel, Sanja Ćavar Zeljković, Petr Tarkowski and 1 more

Abstract read
In one paragraph

Article in The Plant journal : for cell and molecular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

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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

11 authors.

Sara Blicharz *Institute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.
Karolina Stefanowicz *Institute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.
William TrumanInstitute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.ORCID 0000-0002-9840-2539
Aneta Basińska-BarczakInstitute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.
Deeksha SinghInstitute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.
Anna KasprzewskaInstitute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.
Nuria de DiegoCzech Advanced Technology and Research Institute (CATRIN), Palacký University Olomouc, Olomouc, Czech Republic.
Ondřej VrobelCzech Advanced Technology and Research Institute (CATRIN), Palacký University Olomouc, Olomouc, Czech Republic.ORCID 0000-0002-3074-6810
Sanja Ćavar ZeljkovićCzech Advanced Technology and Research Institute (CATRIN), Palacký University Olomouc, Olomouc, Czech Republic.
Petr TarkowskiCzech Advanced Technology and Research Institute (CATRIN), Palacký University Olomouc, Olomouc, Czech Republic.ORCID 0000-0002-7581-7686
Robert MalinowskiInstitute of Plant Genetics Polish Academy of Sciences, ul. Strzeszyńska 34, Poznań, 60-479, Poland.ORCID 0000-0001-5199-877X

Funding

National Science Centre Poland
6 · The paper itself

Abstract

Plasmodiophora brassicae, a soil-borne biotroph, establishes galls as strong physiological sinks on Brassicaceae plants including Brassica napus and Arabidopsis thaliana. We compare transcriptional profiles of phloem dissected from leaf petioles and hypocotyls of healthy and infected B. napus plants. Our results highlight how pathogenesis accompanies phloem-mediated defence responses whilst exerting a strong influence on carbon-nitrogen (C-N) economy. We observe transcriptional changes indicating decreased aliphatic glucosinolate biosynthesis, fluctuating jasmonic acid responses, altered amino acid (AA) and nitrate transport, carbohydrate metabolism and modified cytokinin responses. Changes observed in phloem-dissected from upper versus lower plant organs point to phloem as a conduit in mediating C-N repartitioning, nutrition-related signalling and cytokinin dynamics over long distances during clubroot disease. To assess changes in physiology, we measured AAs, sugars and cytokinins, in phloem exudates from B. napus plants. Despite the decrease in most AA and sucrose levels, isopentyl-type cytokinins increased within infected plants. Furthermore, we employed Arabidopsis for visualising promoter activities of B. napus AA and N transporter orthologues and tested the impact of disrupted cytokinin transport during P. brassicae-induced gall formation using Atabcg14 mutants. Our physiological and microscopy studies show that the host developmental reaction to P. brassicae relies on cytokinin and is accompanied by intense nitrogen and carbon repartitioning. Overall, our work highlights the systemic aspects of host responses that should be taken into account when studying clubroot disease.

Indexed as

ArabidopsisBrassica napusGene Expression Regulation, PlantPhloemPlant DiseasesPlasmodiophoridaAmino AcidsCarbonCyclopentanesCytokininsGlucosinolatesNitrogenOxylipinsPlant LeavesTranscriptomeAmino AcidsCarbonCyclopentanesCytokininsGlucosinolatesjasmonic acidNitrogenOxylipinsBrassica napusclubrootlaser dissection transcriptomicsoilseed rapephloemPlasmodiophora brassicae

Identifiers

PMID39575835
PMCPMC11703547

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Registered trials

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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.