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

Apoplast Bacterial wilt Dynamic gene expression Effectors Metabolism RNAseq Ralstonia solanacearum T3SS Virulence factors Xylem

Journal

BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258

Informations de publication

Date de publication:
09 Mar 2021
Historique:
received: 21 09 2020
accepted: 19 02 2021
entrez: 22 3 2021
pubmed: 23 3 2021
medline: 15 5 2021
Statut: epublish

Résumé

Ralstonia 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. We 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. This 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.

Sections du résumé

BACKGROUND BACKGROUND
Ralstonia 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.
RESULTS RESULTS
We 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.
CONCLUSIONS CONCLUSIONS
This 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.

Identifiants

pubmed: 33750302
doi: 10.1186/s12864-021-07457-w
pii: 10.1186/s12864-021-07457-w
pmc: PMC7941725
doi:

Substances chimiques

Virulence Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

170

Subventions

Organisme : Ministerio de Economía y Competitividad
ID : PID2019-108595RB-I00
Organisme : Ministerio de Economía y Competitividad
ID : FPU
Organisme : Ministerio de Economía y Competitividad
ID : PID2019-108595RB-I00
Organisme : Generalitat de Catalunya
ID : FI
Organisme : "la Caixa" Foundation
ID : INPhINIT
Organisme : Universitat de Barcelona (ES)
ID : APIF
Organisme : Ministério da Ciência, Tecnologia e Inovação
ID : CNPq senior researcher fellowship
Organisme : Ministério da Ciência, Tecnologia e Inovação
ID : 2019/05287-2

Références

Plant Physiol. 2009 Aug;150(4):1656-64
pubmed: 19458111
Front Plant Sci. 2017 Nov 07;8:1899
pubmed: 29163618
J Bacteriol. 2000 Dec;182(23):6659-66
pubmed: 11073909
Mol Plant Pathol. 2016 Aug;17(6):890-902
pubmed: 26609568
mBio. 2012 Aug 31;3(4):
pubmed: 22807564
New Phytol. 2011 Dec;192(4):976-87
pubmed: 21902695
Microbiology (Reading). 2001 Dec;147(Pt 12):3215-29
pubmed: 11739754
Mol Plant Microbe Interact. 2005 Dec;18(12):1296-305
pubmed: 16478049
Bioinformatics. 2015 Jan 15;31(2):166-9
pubmed: 25260700
Microb Biotechnol. 2013 Nov;6(6):614-20
pubmed: 23617636
Sci Rep. 2016 Jun 03;6:27058
pubmed: 27257085
Mol Plant Microbe Interact. 2004 Jun;17(6):686-95
pubmed: 15195951
PLoS Pathog. 2006 Aug;2(8):e82
pubmed: 16933989
mBio. 2016 Apr 12;7(2):e00359-16
pubmed: 27073091
Mol Plant Microbe Interact. 2018 Jan;31(1):175-184
pubmed: 28840786
Proc Natl Acad Sci U S A. 2013 Jan 29;110(5):E425-34
pubmed: 23319638
FEMS Microbiol Lett. 2009 Jun;295(2):238-44
pubmed: 19456869
New Phytol. 2010 Sep;187(4):920-8
pubmed: 20673287
Plant Pathol J. 2020 Feb;36(1):43-53
pubmed: 32089660
Mol Plant Microbe Interact. 2000 Mar;13(3):259-67
pubmed: 10707351
Mol Cell Proteomics. 2018 Jun;17(6):1112-1125
pubmed: 29523767
Mol Plant Microbe Interact. 2018 Jul;31(7):750-765
pubmed: 29460676
J Bacteriol. 2014 Mar;196(5):949-60
pubmed: 24363343
Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):E3055-E3064
pubmed: 29531038
J Exp Bot. 2002 May;53(372):1367-76
pubmed: 11997382
Microbiology (Reading). 2009 Apr;155(Pt 4):1192-1202
pubmed: 19332821
Mol Plant Microbe Interact. 1992 Mar-Apr;5(2):187-93
pubmed: 1617200
J Bacteriol. 1990 Oct;172(10):5742-9
pubmed: 2211508
Appl Environ Microbiol. 1997 Mar;63(3):844-50
pubmed: 16535550
OMICS. 2012 May;16(5):284-7
pubmed: 22455463
Genome Biol. 2014;15(12):550
pubmed: 25516281
Nucleic Acids Res. 2008 Jun;36(10):3420-35
pubmed: 18445632
J Bacteriol. 1995 Mar;177(5):1259-67
pubmed: 7868600
Annu Rev Microbiol. 2002;56:289-314
pubmed: 12142488
Mol Plant Microbe Interact. 2012 Jul;25(7):941-53
pubmed: 22414437
Sci Rep. 2016 Feb 17;6:21121
pubmed: 26884212
Nature. 1964 Apr 18;202:313-4
pubmed: 14167811
mSphere. 2020 Mar 4;5(2):
pubmed: 32132161
Mol Microbiol. 1999 Jan;31(1):237-51
pubmed: 9987125
Appl Environ Microbiol. 2007 Nov;73(22):7210-7
pubmed: 17873071
Mol Plant Microbe Interact. 2014 Mar;27(3):277-85
pubmed: 24283938
Curr Opin Microbiol. 2009 Feb;12(1):44-52
pubmed: 19144559
Mol Microbiol. 2002 Oct;46(2):427-37
pubmed: 12406219
Stand Genomic Sci. 2016 Jan 15;11:7
pubmed: 26779304
J Exp Bot. 2020 Mar 25;71(6):2157-2171
pubmed: 32211785
Nat Methods. 2012 Mar 04;9(4):357-9
pubmed: 22388286
Plant Dis. 2011 Oct;95(10):1292-1301
pubmed: 30731700
Front Microbiol. 2013 Nov 20;4:349
pubmed: 24312090
Bioinformation. 2007 May 20;2(1):5-7
pubmed: 18084642
BMC Genomics. 2013 Dec 06;14:859
pubmed: 24314259
PeerJ. 2016 Jan 05;4:e1549
pubmed: 26788428
Mol Plant Pathol. 2013 Sep;14(7):651-62
pubmed: 23718203
mBio. 2017 Sep 26;8(5):
pubmed: 28951474
FEBS Lett. 2005 Apr 11;579(10):2077-81
pubmed: 15811321
Annu Rev Phytopathol. 1991;29:65-87
pubmed: 18479193
J Bacteriol. 2006 May;188(10):3697-708
pubmed: 16672623
Annu Rev Phytopathol. 2012;50:67-89
pubmed: 22559068
mBio. 2015 Mar 17;6(2):e02471
pubmed: 25784703
Bioinformatics. 2017 Sep 15;33(18):2938-2940
pubmed: 28645171
Front Microbiol. 2020 Jul 30;11:1683
pubmed: 32849353
FEMS Microbiol Rev. 2010 Mar;34(2):107-33
pubmed: 19925633
FEMS Microbiol Rev. 2015 Jan;39(1):17-46
pubmed: 25100612
Clin Microbiol Rev. 2007 Oct;20(4):535-49
pubmed: 17934073
Phytopathology. 2002 Oct;92(10):1142-8
pubmed: 18944225
J Biol Chem. 2016 Mar 25;291(13):6813-30
pubmed: 26823466
PLoS One. 2014 Jan 31;9(1):e87312
pubmed: 24498070
PLoS One. 2015 Oct 07;10(10):e0139090
pubmed: 26445498
Mol Plant Microbe Interact. 2009 Jul;22(7):773-82
pubmed: 19522559
J Bacteriol. 2009 May;191(10):3424-8
pubmed: 19060134
J Bacteriol. 1993 Oct;175(19):6169-78
pubmed: 8407789
Front Plant Sci. 2017 Mar 20;8:370
pubmed: 28373879
Mol Plant Pathol. 2018 Jan;19(1):129-142
pubmed: 27768829
Microbiology (Reading). 2012 Aug;158(Pt 8):2107-2116
pubmed: 22609750
Cell Host Microbe. 2020 Oct 7;28(4):548-557.e7
pubmed: 32735848

Auteurs

R de Pedro-Jové (R)

Department of Genetics, University of Barcelona, Barcelona, Catalonia, Spain.
Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain.

M Puigvert (M)

Department of Genetics, University of Barcelona, Barcelona, Catalonia, Spain.
Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain.

P Sebastià (P)

Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain.

A P Macho (AP)

Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, 201602, China.

J S Monteiro (JS)

Departamento de Bioquímica, Universidade de São Paulo, São Paulo, Brazil.

N S Coll (NS)

Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain.

J C Setúbal (JC)

Departamento de Bioquímica, Universidade de São Paulo, São Paulo, Brazil.

M Valls (M)

Department of Genetics, University of Barcelona, Barcelona, Catalonia, Spain. marcvalls@ub.edu.
Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain. marcvalls@ub.edu.

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Classifications MeSH