Evidence map›Paper›PMID 33750302›Full record

ArticleBMC genomics2021

Dynamic expression of Ralstonia solanacearum virulence factors and metabolism-controlling genes during plant infection.

R de Pedro-Jové, M Puigvert, P Sebastià, A P Macho, J S Monteiro, N S Coll, J C Setúbal, M Valls

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
10.6field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 66 citations in OpenAlex.

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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

8 authors at 4 institutions in 3 countries.

R de Pedro-Jové *Department of Genetics, University of Barcelona, Barcelona, Catalonia, Spain.
M Puigvert *Department of Genetics, University of Barcelona, Barcelona, Catalonia, Spain.
P Sebastià *Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain.
A P MachoShanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, 201602, China.
J S MonteiroDepartamento de Bioquímica, Universidade de São Paulo, São Paulo, Brazil.
N S CollCentre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain.
J C SetúbalDepartamento de Bioquímica, Universidade de São Paulo, São Paulo, Brazil.
M VallsDepartment of Genetics, University of Barcelona, Barcelona, Catalonia, Spain. marcvalls@ub.edu.
Center for Research in Agricultural Genomics · ESUniversidade de São Paulo · BRCenter for Excellence in Molecular Plant Sciences · CNUniversitat de Barcelona · ES

Funding

Generalitat de Catalunya FI"la Caixa" Foundation INPhINITMinistério da Ciência, Tecnologia e Inovação 2019/05287-2Ministério da Ciência, Tecnologia e Inovação CNPq senior researcher fellowshipMinisterio de Economía y Competitividad FPUMinisterio de Economía y Competitividad PID2019-108595RB-I00Universitat de Barcelona (ES) APIF
6 · The paper itself

Abstract

backgroundRalstonia solanacearum is the causal agent of bacterial wilt, a devastating plant disease responsible for serious economic losses especially on potato, tomato, and other solanaceous plant species in temperate countries. In R. solanacearum, gene expression analysis has been key to unravel many virulence determinants as well as their regulatory networks. However, most of these assays have been performed using either bacteria grown in minimal medium or in planta, after symptom onset, which occurs at late stages of colonization. Thus, little is known about the genetic program that coordinates virulence gene expression and metabolic adaptation along the different stages of plant infection by R. solanacearum.

resultsWe performed an RNA-sequencing analysis of the transcriptome of bacteria recovered from potato apoplast and from the xylem of asymptomatic or wilted potato plants, which correspond to three different conditions (Apoplast, Early and Late xylem). Our results show dynamic expression of metabolism-controlling genes and virulence factors during parasitic growth inside the plant. Flagellar motility genes were especially up-regulated in the apoplast and twitching motility genes showed a more sustained expression in planta regardless of the condition. Xylem-induced genes included virulence genes, such as the type III secretion system (T3SS) and most of its related effectors and nitrogen utilisation genes. The upstream regulators of the T3SS were exclusively up-regulated in the apoplast, preceding the induction of their downstream targets. Finally, a large subset of genes involved in central metabolism was exclusively down-regulated in the xylem at late infection stages.

conclusionsThis is the first report describing R. solanacearum dynamic transcriptional changes within the plant during infection. Our data define four main genetic programmes that define gene pathogen physiology during plant colonisation. The described expression of virulence genes, which might reflect bacterial states in different infection stages, provides key information on the R. solanacearum potato infection process.

Indexed as

Ralstonia solanacearumSolanum lycopersicumPlant DiseasesVirulenceVirulence FactorsVirulence FactorsApoplastBacterial wiltDynamic gene expressionEffectorsMetabolismRalstonia solanacearumRNAseqT3SSVirulence factorsXylem

Identifiers

PMID33750302
PMCPMC7941725
OpenAlexW3138462712

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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.