Early responses of Arabidopsis thaliana to infection by Verticillium longisporum

Physiological and Molecular Plant Pathology

Volumn 74, Issue 5-6, 2010, Pages 419-427

  Tischner, Rudolf ^a   Koltermann, Michael ^a   Hesse, Holger ^b   Plath, Magda ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b MAX PLANCK INSTITUTE OF MOLECULAR PLANT PHYSIOLOGY   (Germany)

Author keywords

Arabidopsis thaliana; Early responses; Gene expression; Verticillium longisporum

Indexed keywords

ARABIDOPSIS; ARABIDOPSIS THALIANA; VERTICILLIUM DAHLIAE VAR. LONGISPORUM;

EID: 77956428424     PISSN: 08855765     EISSN: 10961178     Source Type: Journal    
DOI: 10.1016/j.pmpp.2010.06.004     Document Type: Article

References (48)

1. Heinz R., Lee S.W., Saparno A., Nazar R.N., Robb J. Cyclical systemic colonization in Verticillium-infected tomato. Physiol Mol Plant Pathol 1998, 52:385-396.
2. Presley J.T., Carns H.R., Taylor E.E., Schnatho W.C. Movement of conidia of Verticillium albo-atrum in cotton plants. Phytopathology 1966, 56:375-382.
3. Zeise K., von Tiedemann A. Host specialization among vegetative compatibility groups of Verticillium dahliae in relation to V. longisporum. J Phytopathol 2002, 150:112-119.
4. Steventon L.A., Okori P., Dixelius C. An investigation of the susceptibility of Arabidopsis thaliana to isolates of two species of Verticillium. J Phytopathol 2001, 149:395-401.
5. Veronese P., Narasimhan M.L., Stevenson R.A., Zhu J.K., Weller S., Subbarao-Bressan R.A. Identification of a locus controlling Verticillium disease symptom response in Arabidopsis thaliana. Plant J 2003, 35:574-587.
6. Nachmias A., Buchner V., Krikun J. Comparison of protein-lipopolylsaccharide complexes produced by pathogenic and non-pathogenic strains of Verticillium dahliae Kleb. from potato. Physiol Plant Pathol 1982, 20:213-221.
7. Zeidler D., Zaehringer U., Gerber I., Dubery I., Hartung T., Bors W., et al. Innate immunity in Arabidopsis thaliana: lipopolysaccharides activate nitric oxide synthase (NOS) and induce defense genes. PNAS (USA) 2004, 101:15811-15816.
8. Baker C.J., Orlandi E.W., Mock N.M. Harpin, an elicitor of the hypersensitive response in tobacco caused by Erwinia amylovora, elicits active oxygen production in suspension cells. Plant Physiol 1993, 102:1341-1344.
9. De Torres M., Sanchez P., Fernandez-Delmond I., Grant M. Expression profiling of the host response to bacterial infection: the transition from basal to induced defense responses in RPM1-mediated resistance. Plant J 2003, 33:665-676.
10. van Wees S.C., Chang H.S., Zhu T., Glazebrook J. Characterization of the early responses of Arabidopsis to Alternaria brassicicola infection using expression profiling. Plant Physiol 2003, 132:606-617.
11. Wang R.C., Tischner R., Gutiérrez R.A., Hoffman M., Xing X., Chen M., et al. Genomic analysis of the nitrate response using a nitrate reductase-null mutant of Arabidopsis. Plant Physiol 2004, 136:2512-2522.
12. Larsson C. Plasma membranes. Modern methods of plant analysis, new series 1985, vol. 1:85-104. Springer, Berlin. H.F. Likens, J.F. Jacksons (Eds.).
13. Johansson F., Olbe M., Sommarin M., Larsson C. Brij 58, a polyoxyethylene acyl ether, creates membrane vesicles of uniform sidedness. A new tool to obtain inside-out (cytoplasmic side out) plasma membrane vesicles. Plant J 1995, 7:165-173.
14. Quail P.H. Plant cell fractionation. Ann Rev Plant Physiol 1979, 30:425-484.
15. Wessel D., Flügge U.I. A method for the quantitative recovery of protein in dilute solutions in the presence of detergents and lipids. Anal Biochem 1984, 138:141-143.
16. Leikert J.F., Rathel T.R., Muller C., Vollmar A.M., Dirsch V.M. Reliable in vitro measurement of nitric oxide released from endothelial cells using low concentrations of the fluorescent probe 4,5-diaminofluorescein. FEBS Let 2001, 506:131-134.
17. Tusher V.G., Tibshirani R., Chu G. Significance analysis of microarrays applied to the ionizing radiation response. Proc Natl Acad Sci USA 2001, 98:5116-5121.
18. Usadel B., Nagel A., Thimm O., Redestig H., Blaesing O.E., Palacious-Rojas N., et al. Extension of the visualization tool MapMan to allow statistical analysis of arrays, display of co-responding genes and comparison with known responses. Plant Physiol 2005, 138:1195-1204.
19. Okubara P.A., Paulitz T.C. Root defense responses to fungal pathogens: a molecular perspective. Plant Soil 2005, 274:215-226.
20. Gust A.A., Biswas R., Lenz H.D., Rauhut T., Ranf S., Kemmerling B., et al. Bacteria derived peptidoglycans constitute pathogen-associated molecular patterns triggering innate immunity in Arabidopsis. J Biol Chem 2007, 282:32338-32348.
21. De Wit P.J.G.M. How plants recognize pathogens and defend themselves. Cell Mol Life Sci 2007, 64:2726-2732.
22. Gachon C., Saindrenan P. Real-time PCR monitoring of fungal development in Arabidopsis thaliana infected by Alternaria brassicicola and Botrytis cinerea. Plant Physiol Biochem 2004, 42:367-371.
23. Floryszak-Wieczorek J., Arasimowicz M., Milczarek G., Jelen H., Jackowiak H. Only an early nitric oxide burst and the following wave of secondary nitric oxide generation enhanced effective defence responses of pelargonium to a necrotrophic pathogen. New Phytol 2007, 175:718-730.
24. Wendehenne D., Durner J., Klessig D.F. Nitric oxide: a new player in plant signalling and defence responses. Curr Opin Plant Biol 2004, 7:449-455.
25. Nürnberger T., Scheel D. Signal transmission in the plant immune response. Trends Plant Sci 2001, 6:372-379.
26. Kim J., Shiu S.H., Thoma S., Li W.H., Patterson S.E. Patterns of expansion and expression divergence in the plant polygalacturonase gene family. Genome Biol. 2006, 7:R87.
27. Kende H., Bradford K.J., Brummell D.A., Cho H., Cosgrove D.J., Fleming A.J., et al. Nomenclature for members of the expansin superfamily of genes and proteins. Plant Mol Biol 2004, 55:311-314.
28. Fraser C., Rider L., Chapple C. An expression and bioinformatics analysis of the Arabidopsis serine carboxypeptidase-like gene family. Plant Physiol 2005, 138:1136-1148.
29. Dessau subdomains M., Halimi Y., Erez T., Chomsky-Hecht O., Chamovitz D.A. The Arabidopsis COP9 signalosome subunit 7 is a model PCI domain protein with involved in COP9 signalosome assembly. Plant Cell 2008, 20:2815-2834.
30. Belenghi B., Acconica F., Trovato M., Perazolli M., Bocedi A., Polticelli F., et al. AtCVYS1, a cystatin from Arabidopsis thaliana, suppresses hypersentive cell death. Eur J Biochem 2003, 270:2593-2604.
31. Jorda' L., Coego A., Conejero V., Vera P. A genomic cluster containing four differentially regulated subtilisin-like processing protease genes is in tomato plants. J Biol Chem 1999, 274:2360-2365.
32. Eulgem T. Regulation of the Arabidopsis defense transcriptome. Trends Plant Sci. 2005, 10:71-79.
33. Kalde M., Barth M., Somssich I.E., Lippok B. Members of the Arabidopsis WRKY group III transcription factors are part of different plant defense signaling pathways. Mol Plant-Microbe Interact 2003, 16:295-305.
34. Xu X., Chen C., Fan B., Chen Z. Physical and functional interactions between pathogen-induced Arabidopsis WRKY18, WRKY40, and WRKY60 transcription factors. Plant Cell 2006, 18:1310-1326.
35. Yanhui C., Xiaoyuan Y., Kun H., Meihua L., Jigang L., Zhaofeng G., et al. The MYB transcription factor superfamily of Arabidopsis: expression analysis and phylogenetic comparison with the rice MYB family. Plant Mol Biol 2006, 60:107-124.
36. Sun S., Yu J.P., Chen F., Zhao T.J., Fang X.H., Li Y.Q., et al. TINY, a dehydration-responsive element (DRE)-binding protein-like transcription factor connecting the DRE- and ethylene-responsive element-mediated signaling pathways in Arabidopsis. J Biol Chem 2008, 283:6261-6271.
37. Chen H.M., Pan J.S., Zhao X.X., Zhou J.M., Cai R. Reporter-based screen for Arabidopsis mutants compromised in nonhost resistance. Chinese Sci Bull 2008, 53:1027-1034.
38. Chen K., Fan B., Du L., Chen Z. Activation of hypersensitive cell death by pathogen-induced receptor- like protein kinases from Arabidopsis. Plant Mol Biol. 2004, 56:271-283.
39. Roy S., Gilliham M., Berger B., Essah P., Cheffings C., Miller A., et al. Investigating glutamate receptor-like gene co-expression in Arabidopsis thaliana. Plant Cell Environ 2008, 31:861-871.
40. Vanderbeld B., Snedden W.A. Developmental and stimulus-induced expression patterns of Arabidopsis calmodulin-like CML37, CLM38 and CLM39. Plant Mol Biol 2007, 64:683-697.
41. Thevissen K., Ghazi A., De Samblanx G., Brownlee C., Osborn R.W., Broekaert W.F. Fungal membrane responses induced by plant defensins and thionins. J Biol Chem 1996, 271:15018-15025.
42. Wormuth D., Heiber I., Shaikali J., Kandlbinder A., Baier M., Dietz K.J. Redox regulation and antioxidative defence in Arabidopsis leaves viewed from a systems biology perspective. J Biotechnol 2007, 129:229-248.
43. Charng Y., Liu H., Liu N., Chi W., Wang C., Chang S., et al. A heat-inducible transcription factor, HsfA2, is required for extension of acquired thermotolerance in Arabidopsis. Plant Physiol 2007, 143:251-262.
44. Espinoza C., Medina C., Somerville S., Arce-Johnson P. Senescence- associated genes induced during compatible viral interactions with grapevine and Arabidopsis. J Exp Bot 2007, 58:3197-3212.
45. Zhang X., Wollenweber B., Jiang D., Liu F., Zhao J. Water deficits and heat shock effects on photosynthesis of transgenic Arabidopsis thaliana constitutively expressing ABP9, a bZIP transcription factor. J Exp Bot 2008, 59:839-848.
46. Carter C., Graham R.A., Thornburg R.W. Arabidopsis thaliana contains a large family of germin-like proteins: characterization of cDNA and genomic sequences encoding 12 unique family members. Plant Mol Biol 1998, 38:929-943.
47. Medina J., Ballesteros M.L., Salinas J. Phylogenetic and functional analysis of Arabidopsis RCI2 genes. J Exp Bot 2007, 58:4333-4346.
48. Knoth C., Eulgem T. The oomycete response gene LURP1 is required for defense against Hyaloperonospora parasitica in Arabidopsis thaliana. Plant J 2008, 55:53-64.