Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula

Colditz, F.; Braun, H. P.; Jacquet, C.; Niehaus, Karsten; Krajinski, F.

Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula

Colditz F, Braun HP, Jacquet C, Niehaus K, Krajinski F (2005)
Plant Molecular Biology 59(3): 387-406.

Zeitschriftenaufsatz | Veröffentlicht | Englisch

Download

Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!

DOI

https://doi.org/10.1007/s11103-005-0184-z

Autor*in

Colditz, F.; Braun, H. P.; Jacquet, C.; Niehaus, Karsten^UniBi; Krajinski, F.

Einrichtung

Fakultät für Biologie > Proteom- und Metabolomforschung
Centrum für Biotechnologie > Arbeitsgruppe K. Niehaus

Abstract / Bemerkung

To investigate the molecular mechanisms underlying susceptibility of legumes to the root pathogen Aphanomyces euteiches (oomycota), comparative proteomic studies have been carried out. In a first approach, we have analysed two Medicago truncatula lines of the French CORE collection (F83.005-5 (R2002) and F83.005-9 (R2002)), which showed either increased or decreased susceptibility to A. euteiches as compared to the widely adopted line A17. Several proteins were identified to be differentially induced after pathogen challenge in the two M. truncatula accessions with altered disease susceptibility, whereof proteins with increased abundances in the more resistant line F83.005-9 could be involved in mechanisms that lead to an improved disease resistance. Among these proteins, we identified two proteasome alpha subunits, which might be involved in defense response. To broaden our studies on A. euteiches-tolerance of M. truncatula, we investigated two other phenomena that lead to an either increased A. euteiches-resistance or to an enhanced susceptibility. The topic of an enhanced plant resistance to A. euteiches was studied in plants showing a bioprotective effect of a pre-established arbuscular mycorrhiza (AM) symbiosis. Evaluation of root fresh weights and pathogen spreading in the root system clearly indicate that mycorrhizal plants show increased A. euteiches-resistance as compared to non-mycorrhizal plants. Proteome analyses revealed the induction of similar protein patterns as in the M. truncatula accessions with comparatively high resistance level to A. euteiches. In a third approach, increased A. euteiches susceptibility was effected by exogenous abscisic acid (ABA) application prior to root infection. Evaluation of the abundance levels of a group of pathogenesis related class 10 (PR10)-like proteins, which were previously identified to be regulated after A. euteiches infection, revealed a correlation between the abundance levels of these proteins and the A. euteiches infection level or severity.

Stichworte

Aphanomyces euteiches; ABA; proteasome; PR10; proteomics; Medicago truncatula

Erscheinungsjahr

2005

Zeitschriftentitel

Plant Molecular Biology

Band

Ausgabe

Seite(n)

387-406

ISSN

0167-4412

eISSN

1573-5028

Page URI

https://pub.uni-bielefeld.de/record/1601792

Zitieren

Colditz F, Braun HP, Jacquet C, Niehaus K, Krajinski F. Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula. Plant Molecular Biology. 2005;59(3):387-406.

Colditz, F., Braun, H. P., Jacquet, C., Niehaus, K., & Krajinski, F. (2005). Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula. Plant Molecular Biology, 59(3), 387-406. https://doi.org/10.1007/s11103-005-0184-z

Colditz, F., Braun, H. P., Jacquet, C., Niehaus, Karsten, and Krajinski, F. 2005. “Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula”. Plant Molecular Biology 59 (3): 387-406.

Colditz, F., Braun, H. P., Jacquet, C., Niehaus, K., and Krajinski, F. (2005). Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula. Plant Molecular Biology 59, 387-406.

Colditz, F., et al., 2005. Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula. Plant Molecular Biology, 59(3), p 387-406.

F. Colditz, et al., “Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula”, Plant Molecular Biology, vol. 59, 2005, pp. 387-406.

Colditz, F., Braun, H.P., Jacquet, C., Niehaus, K., Krajinski, F.: Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula. Plant Molecular Biology. 59, 387-406 (2005).

Colditz, F., Braun, H. P., Jacquet, C., Niehaus, Karsten, and Krajinski, F. “Proteomic profiling unravels insights into the molecular background underlying increased Aphanomyces euteiches tolerance of Medicago truncatula”. Plant Molecular Biology 59.3 (2005): 387-406.

34 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Proteomics analysis of Medicago truncatula response to infection by the phytopathogenic bacterium Ralstonia solanacearum points to jasmonate and salicylate defence pathways.
Yamchi A, Ben C, Rossignol M, Zareie SR, Mirlohi A, Sayed-Tabatabaei BE, Pichereaux C, Sarrafi A, Rickauer M, Gentzbittel L., Cell Microbiol 20(4), 2018
PMID: 29084417

Molecular and cellular control of cell death and defense signaling in pepper.
Choi HW, Choi HW, Hwang BK., Planta 241(1), 2015
PMID: 25252816

Proteomic investigation of response to FORL infection in tomato roots.
Mazzeo MF, Cacace G, Ferriello F, Puopolo G, Zoina A, Ercolano MR, Siciliano RA., Plant Physiol Biochem 74(), 2014
PMID: 24262994

Comparison of systemic and local interactions between the arbuscular mycorrhizal fungus Funneliformis mosseae and the root pathogen Aphanomyces euteiches in Medicago truncatula.
Zhang H, Franken P., Mycorrhiza 24(6), 2014
PMID: 24419810

The alternative Medicago truncatula defense proteome of ROS-defective transgenic roots during early microbial infection.
Kiirika LM, Schmitz U, Colditz F., Front Plant Sci 5(), 2014
PMID: 25101099

NFP, a LysM protein controlling Nod factor perception, also intervenes in Medicago truncatula resistance to pathogens.
Rey T, Nars A, Bonhomme M, Bottin A, Huguet S, Balzergue S, Jardinaud MF, Bono JJ, Cullimore J, Dumas B, Gough C, Jacquet C., New Phytol 198(3), 2013
PMID: 23432463

From callus to embryo: a proteomic view on the development and maturation of somatic embryos in Cyclamen persicum.
Rode C, Lindhorst K, Braun HP, Winkelmann T., Planta 235(5), 2012
PMID: 22127736

Phoma medicaginis stimulates the induction of the octadecanoid and phenylpropanoid pathways in Medicago truncatula.
Kamphuis LG, Williams AH, Küster H, Trengove RD, Singh KB, Oliver RP, Ellwood SR., Mol Plant Pathol 13(6), 2012
PMID: 22212347

Silencing of the Rac1 GTPase MtROP9 in Medicago truncatula stimulates early mycorrhizal and oomycete root colonizations but negatively affects rhizobial infection.
Kiirika LM, Bergmann HF, Schikowsky C, Wimmer D, Korte J, Schmitz U, Niehaus K, Colditz F., Plant Physiol 159(1), 2012
PMID: 22399646

Protein arginine methylation modulates light-harvesting antenna translation in Chlamydomonas reinhardtii.
Blifernez O, Wobbe L, Niehaus K, Kruse O., Plant J 65(1), 2011
PMID: 21175895

Proteomics and functional analyses of pepper abscisic acid-responsive 1 (ABR1), which is involved in cell death and defense signaling.
Choi DS, Hwang BK., Plant Cell 23(2), 2011
PMID: 21335377

Expression of coordinately regulated defence response genes and analysis of their role in disease resistance in Medicago truncatula.
Samac DA, Peñuela S, Schnurr JA, Hunt EN, Foster-Hartnett D, Vandenbosch KA, Gantt JS., Mol Plant Pathol 12(8), 2011
PMID: 21726379

Hydrogen peroxide scavenging mechanisms are components of Medicago truncatula partial resistance to Aphanomyces euteiches
Djébali N, Mhadhbi H, Lafitte C, Dumas B, Esquerré-Tugayé MT, Aouani ME, Jacquet C., Eur J Plant Pathol 131(4), 2011
PMID: IND44685738

Differential gel electrophoresis (DIGE) to quantitatively monitor early symbiosis- and pathogenesis-induced changes of the Medicago truncatula root proteome.
Schenkluhn L, Hohnjec N, Niehaus K, Schmitz U, Colditz F., J Proteomics 73(4), 2010
PMID: 19895911

Proteomic studies of phytopathogenic fungi, oomycetes and their interactions with hosts
Bhadauria V, Banniza S, Wang LX, Wei YD, Peng YL., Eur J Plant Pathol 126(1), 2010
PMID: IND44296653

Real-time PCR Suggests that Aphanomyces euteiches is Associated with Reduced Amounts of Phytophthora medicaginis in Alfalfa that is Co-inoculated with Both Pathogens
, Journal of phytopathology. 158(2), 2010
PMID: IND44311057

Model legumes contribute to faba bean breeding
Rispail Nicolas, Kaló Péter, Kiss GyörgyB, Ellis THNoel, Gallardo Karine, Thompson RichardD, Prats Elena, Larrainzar Estibaliz, Ladrera Ruben, González EstherM, Arrese-Igor Cesar, Ferguson BrettJ, Gresshoff PeterM, Rubiales Diego., Field Crops Res 115(3), 2010
PMID: IND44316555

Faba bean breeding for disease resistance
Sillero JosefinaC, Villegas-Fernández AngelM, Thomas Jane, Rojas-Molina MariaM, Emeran AmeroA, Fernández-Aparicio Mónica, Rubiales Diego., Field Crops Res 115(3), 2010
PMID: IND44316559

A study on the susceptibility of the model legume plant Medicago truncatula to the soil-borne pathogen Fusarium oxysporum
Ramírez-Suero M, Khanshour A, Martinez Y, Rickauer M., Eur J Plant Pathol 126(4), 2010
PMID: IND44336452

Proteomics of plant pathogenic fungi.
González-Fernández R, Prats E, Jorrín-Novo JV., J Biomed Biotechnol 2010(), 2010
PMID: 20589070

Proteomic analysis of Medicago truncatula root plastids.
Daher Z, Recorbet G, Valot B, Robert F, Balliau T, Potin S, Schoefs B, Dumas-Gaudot E., Proteomics 10(11), 2010
PMID: 20336678

Comparative proteomic studies of root-microbe interactions.
Mathesius U., J Proteomics 72(3), 2009
PMID: 19152841

Pathogenesis and stress related, as well as metabolic proteins are regulated in tomato stems infected with Ralstonia solanacearum.
Dahal D, Heintz D, Van Dorsselaer A, Braun HP, Wydra K., Plant Physiol Biochem 47(9), 2009
PMID: 19482482

Are plants in the field already induced? Implications for practical disease control
Walters DaleR., Crop Prot 28(6), 2009
PMID: IND44195406

Differential expression proteomics to investigate responses and resistance to Orobanche crenata in Medicago truncatula.
Castillejo MA, Maldonado AM, Dumas-Gaudot E, Fernández-Aparicio M, Susín R, Diego R, Jorrín JV., BMC Genomics 10(), 2009
PMID: 19575787

Recent Advances in Medicago truncatula Genomics.
Ané JM, Zhu H, Frugoli J., Int J Plant Genomics 2008(), 2008
PMID: 18288239

Two alternative recessive quantitative trait loci influence resistance to spring black stem and leaf spot in Medicago truncatula.
Kamphuis LG, Lichtenzveig J, Oliver RP, Ellwood SR., BMC Plant Biol 8(), 2008
PMID: 18366746

Silencing of PR-10-like proteins in Medicago truncatula results in an antagonistic induction of other PR proteins and in an increased tolerance upon infection with the oomycete Aphanomyces euteiches.
Colditz F, Niehaus K, Krajinski F., Planta 226(1), 2007
PMID: 17237953

Medicago truncatula root nodule proteome analysis reveals differential plant and bacteroid responses to drought stress.
Larrainzar E, Wienkoop S, Weckwerth W, Ladrera R, Arrese-Igor C, González EM., Plant Physiol 144(3), 2007
PMID: 17545507

Recent advances in legume-microbe interactions: recognition, defense response, and symbiosis from a genomic perspective.
Samac DA, Graham MA., Plant Physiol 144(2), 2007
PMID: 17556521

Root rot disease of legumes caused by Aphanomyces euteiches.
Gaulin E, Jacquet C, Bottin A, Dumas B., Mol Plant Pathol 8(5), 2007
PMID: 20507520

Recycling or regulation? The role of amino-terminal modifying enzymes.
Walling LL., Curr Opin Plant Biol 9(3), 2006
PMID: 16597508

Endophyte or parasite--what decides?
Kogel KH, Franken P, Hückelhoven R., Curr Opin Plant Biol 9(4), 2006
PMID: 16713330

Annual Medicago: from a model crop challenged by a spectrum of necrotrophic pathogens to a model plant to explore the nature of disease resistance.
Tivoli B, Baranger A, Sivasithamparam K, Barbetti MJ., Ann Bot 98(6), 2006
PMID: 16803846

51 References

Daten bereitgestellt von Europe PubMed Central.

Abscisic acid determines basal susceptibility of tomato to Botrytis cinerea and suppresses salicylic acid-dependent signaling mechanisms.
Audenaert K, De Meyer GB, Hofte MM., Plant Physiol. 128(2), 2002
PMID: 11842153

Proteome analysis and identification of symbiosis-related proteins from Medicago truncatula Gaertn. by two-dimensional electrophoresis and mass spectrometry.
Bestel-Corre G, Dumas-Gaudot E, Poinsot V, Dieu M, Dierick JF, van TD, Remacle J, Gianinazzi-Pearson V, Gianinazzi S., Electrophoresis 23(1), 2002
PMID: 11824612

Bødker, Mycorrhiza 8(), 1998

Plant proteome analysis.
Canovas FM, Dumas-Gaudot E, Recorbet G, Jorrin J, Mock HP, Rossignol M., Proteomics 4(2), 2004
PMID: 14760698

Proteomic approach: identification of Medicago truncatula proteins induced in roots after infection with the pathogenic oomycete Aphanomyces euteiches.
Colditz F, Nyamsuren O, Niehaus K, Eubel H, Braun HP, Krajinski F., Plant Mol. Biol. 55(1), 2004
PMID: 15604668

Medicago truncatula--a model in the making!
Cook DR., Curr. Opin. Plant Biol. 2(4), 1999
PMID: 10459004

Cryptogein affects expression of alpha3, alpha6 and beta1 20S proteasome subunits encoding genes in tobacco.
Dahan J, Etienne P, Petitot AS, Houot V, Blein JP, Suty L., J. Exp. Bot. 52(362), 2001
PMID: 11520884

Interaction between vesicular-arbuscular mycorrhizal fungi and plant pathogens.
Dehne HW., Phytopathology 72(8), 1982
PMID: IND82102446

Dixon, 1992

Djordjevic, Mol. Plant–Microbe Interact. 16(), 2003

Correlation between protein and mRNA abundance in yeast.
Gygi SP, Rochon Y, Franza BR, Aebersold R., Mol. Cell. Biol. 19(3), 1999
PMID: 10022859

Hagedorn, 1989

Harrison, Mol. Plant–Microbe Interact. 6(), 1993

Integrated plant proteomics — putting the green genomes to work
Heazlewood JL, Millar AH., Funct. Plant Biol. 30(5), 2003
PMID: IND44640409

Salicylic acid-independent induction of pathogenesis-related protein transcripts by sugars is dependent on leaf developmental stage.
Herbers K, Meuwly P, Metraux JP, Sonnewald U., FEBS Lett. 397(2-3), 1996
PMID: 8955355

Hoagland, Calif. Agric. Exp. Stud. Circ. 347(), 1950

Solubilization of plant membrane proteins for analysis by two-dimensional gel electrophoresis.
Hurkman WJ, Tanaka CK., Plant Physiol. 81(3), 1986
PMID: 16664906

Proteome reference maps of Medicago truncatula embryogenic cell cultures generated from single protoplasts.
Imin N, De Jong F, Mathesius U, van Noorden G, Saeed NA, Wang XD, Rose RJ, Rolfe BG., Proteomics 4(7), 2004
PMID: 15221745

Insight on segregation distortions in two intraspecific crosses between annual species of Medicago (Leguminosae).
Jenczewski E, Gherardi M, Bonnin I, Prosperi JM, Olivieri I, Huguet T., Theor. Appl. Genet. 94(5), 1997
PMID: IND20604210

Molecular cloning and characterization of a novel Jasmonate inducible pathogenesis-related class 10 protein gene, JIOsPR10, from rice (Oryza sativa L.) seedling leaves.
Jwa NS, Kumar Agrawal G, Rakwal R, Park CH, Prasad Agrawal V., Biochem. Biophys. Res. Commun. 286(5), 2001
PMID: 11527396

Activation of the programmed cell death pathway by inhibition of proteasome function in plants.
Kim M, Ahn JW, Jin UH, Choi D, Paek KH, Pai HS., J. Biol. Chem. 278(21), 2003
PMID: 12637532

Kjøller, Mycorrhiza 6(), 1996

Interactions between pea root-inhabiting fungi examined using signature fatty acids.
Larsen J, Bodker L., New Phytol. 149(3), 2001
PMID: IND23032309

Levenfors, Eur. J. Plant Pathol. 109(), 2003

Modulation of an RNA-binding protein by abscisic-acid-activated protein kinase.
Li J, Kinoshita T, Pandey S, Ng CK, Gygi SP, Shimazaki K, Assmann SM., Nature 418(6899), 2002
PMID: 12181571

Inhibition of the plastidic ATP/ADP transporter protein primes potato tubers for augmented elicitation of defense responses and enhances their resistance against Erwinia carotovora.
Linke C, Conrath U, Jeblick W, Betsche T, Mahn A, During K, Neuhaus HE., Plant Physiol. 129(4), 2002
PMID: 12177473

Lo, Mol. Plant–Microbe Interact. 12(), 1999

Characterization of a gene family encoding abscisic acid- and environmental stress-inducible proteins of alfalfa.
Luo M, Liu JH, Mohapatra S, Hill RD, Mohapatra SS., J. Biol. Chem. 267(22), 1992
PMID: 1379227

Establishment of a root proteome reference map for the model legume Medicago truncatula using the expressed sequence tag database for peptide mass fingerprinting.
Mathesius U, Keijzers G, Natera SH, Weinman JJ, Djordjevic MA, Rolfe BG., Proteomics 1(11), 2001
PMID: 11922602

McGee, Mol. Plant–Microbe Interact. 14(), 2001

Abscisic acid influences the susceptibility of Arabidopsis thaliana to Pseudomonas syringae pv. tomato and Peronospora parasitica
Mohr PG, Cahill DM., Funct. Plant Biol. 30(4), 2003
PMID: IND44640407

High sequence similarity between a ribonuclease from ginseng calluses and fungus-elicited proteins from parsley indicates that intracellular pathogenesis-related proteins are ribonucleases.
Moiseyev GP, Beintema JJ, Fedoreyeva LI, Yakovlev GI., Planta 193(3), 1994
PMID: 7764876

Proteome analysis of cultivar-specific interactions between Rhizobium leguminosarum biovar trifolii and subterranean clover cultivar Woogenellup.
Morris AC, Djordjevic MA., Electrophoresis 22(3), 2001
PMID: 11258772

Transcriptional profiling of Medicago truncatula roots after infection wtih Aphanomyces euteiches (oomycota) identifies novel genes upregulated during this pathogenic interaction.
Nyamsuren O, Colditz F, Rosendahl S, Tamasloukht MB, Bekel T, Meyer F, Kuester H, Franken P, Krajinski F., Physiol. Mol. Plant Pathol. 63(1), 2003
PMID: IND43743021

Soft rot susceptibility of potatoes with high reducing sugar content.
Otazu V, Secor GA., Phytopathology 71(3), 1981
PMID: IND81033865

Pathogenesis-related protein 10 isolated from hot pepper functions as a ribonuclease in an antiviral pathway.
Park CJ, Kim KJ, Shin R, Park JM, Shin YC, Paek KH., Plant J. 37(2), 2004
PMID: 14690503

Peart, PNAS 99(), 2002

AUTHOR UNKNOWN, 0

Prospéri, Grain Legumes 28(), 2000

Prospéri, 2001

Endoproteolytic activities in pea roots inoculated with arbuscular mycorrhizal fungus Glomus mosseae and/or Aphanomyces euteiches in relation to bioprotection.
Slezack S, Dumas-Gaudot E, Rosendahl S, Kjoller R, Paynot M, Negrel J, Gianinazzi S., New Phytol. 142(3), 1999
PMID: IND22029973

Preferential induction of 20S proteasome subunits during elicitation of plant defense reactions: towards the characterization of "plant defense proteasomes".
Suty L, Lequeu J, Lancon A, Etienne P, Petitot AS, Blein JP., Int. J. Biochem. Cell Biol. 35(5), 2003
PMID: 12672456

In planta histochemical staining of fungal alkaline phosphatase activity for analysis of efficient arbuscular mycorrhizal infections.
Tisserant B, Gianinazzi-Pearson V, Gianinazzi S, Gollote A., Mycol. Res. 97(2), 1993
PMID: IND93024576

Torregrosa, Mol. Plant–Microbe Interact. 17(), 2004

AUTHOR UNKNOWN, 0

VandenBosch, Plant Physiol. 131(), 2003

Vandemark, Arch. Phytol. Plant Prot. 37(), 2004

Mapping the proteome of barrel medic (Medicago truncatula).
Watson BS, Asirvatham VS, Wang L, Sumner LW., Plant Physiol. 131(3), 2003
PMID: 12644662

Abscisic Acid Suppression of Phenylalanine Ammonia-Lyase Activity and mRNA, and Resistance of Soybeans to Phytophthora megasperma f.sp. glycinea.
Ward EW, Cahill DM, Bhattacharyya MK., Plant Physiol. 91(1), 1989
PMID: 16667002

AUTHOR UNKNOWN, 0

Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology.
Winkel-Shirley B., Plant Physiol. 126(2), 2001
PMID: 11402179

Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB