Microscopic and biochemical evidence of differentially virulent field isolates of Diplocarpon rosae causing black spot disease of roses

Plant Physiology and Biochemistry

Volumn 48, Issue 2-3, 2010, Pages 167-175

  Gachomo, Emma W ^a   Kotchoni, Simeon O ^b  

^a SOUTH DAKOTA STATE UNIVERSITY   (United States)

^b PURDUE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGEN PEROXIDE; REACTIVE OXYGEN METABOLITE; VEGETABLE PROTEIN;

ARTICLE; ASCOMYCETES; CLIMATE; COMPARATIVE STUDY; ENZYMOLOGY; FUNGAL MORPHOLOGY; INNATE IMMUNITY; ISOLATION AND PURIFICATION; METABOLISM; MICROBIOLOGY; PATHOGENICITY; PLANT DISEASE; PLANT LEAF; ROSE; TROPIC CLIMATE; VIRULENCE;

ASCOMYCOTA; CLIMATE; FUNGAL STRUCTURES; HYDROGEN PEROXIDE; IMMUNITY, INNATE; PLANT DISEASES; PLANT LEAVES; PLANT PROTEINS; REACTIVE OXYGEN SPECIES; ROSA; TROPICAL CLIMATE; VIRULENCE;

DIPLOCARPON ROSAE; ROSA;

EID: 77649182621     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2010.01.003     Document Type: Article

References (48)

1. Almagro L., Gómez Ros L.V., Belchi-Navarro S., Bru R., Ros Barcelo A., and Pedreño M.A. Class III peroxidises in plant defence reactions. Plant Exp. Bot. 60 (2009) 377-390
2. Black W.A., Byrne D.H., and Pemberton H.B. Field study of black spot resistance in rose. HortScience 29 (1994) 525
3. Blechert O., and Debener T. Morphological characterization of the interaction between Diplocarpon rosae and various rose species. Plant Pathol. 54 (2005) 82-90
4. Boller T. Biochemical analysis of chitinases and β-1,3-glucanases. In: Gurr S.J., McPherson M.J., and Bowles D.J. (Eds). Molecular Plant Pathology: a Practical Approach (1992), Oxford University Press, UK 23-30
5. Byrne D.H., Black W., Ma Y., and Pemberton H.B. The use of amphidiploidy in the development of black spot resistant rose germplasm. Acta Hort 424 (1996) 269-272
6. Cahill D.M., and McComb J.A. A comparison of changes in phenylalanine ammonia lyase activity, lignin and phenolic synthesis in the roots of Eucalyptus calopyhlla (field resistant) and E. marginata (susceptible) when infected with Phytophthora cinnamomi. Physiol. Mol. Plant Pathol. 40 (1992) 315-332
7. Campbell W.J., and Ogren W.L. Electron transport through photosystem I stimulates light activation of rubilose bisphosphate carboxylase/oxygenase (rubisco) by rubisco activase. Plant Physiol. 94 (1990) 479-484
8. Cohen I., Knopf J.A., Irimovitch V., and Shapira M. A proposed mechanism for the inhibitory effects of oxidative stress on rubisco assembly and its subunit expression. Plant Physiol. 137 (2005) 738-746
9. Cui Y., Magill J., Frederiksen R., and Magill C. Chalcone synthase and phenylalanine ammonia lyase mRNA following exposure of sorghum seedlings to three fungal pathogens. Physiol. Mol. Plant Pathol. 49 (1996) 187-199
10. Dann E.K., Meuwly P., Métraux J.P., and Deverall B.J. The effect of pathogen inoculation or chemical treatment on activities of chitinase and ß-1,3-glucanase and accumulation of salicylic acid in leaves of green bean, Phaseolus vulgaris L. Physiol. Mol. Plant Pathol. 49 (1996) 307-319
11. Daugrois J.H., Lafitte C., Barthe J.P., and Touze A. Induction of ß-1,3-glucanase and chitinase activity in compatible and incompatible interactions between Colletotrichum Lindemuthianum and bean cultivars. J. Phytopathol. 130 (1990) 225-234
12. Debener T., Drewes-Alvarez R., and Rockstroch K. Identification of five physiological races of blackspot, Diplocarpon rosae Wolf, on roses. Plant Breed. 117 (1998) 267-270
13. Fecht-Christoffers M.M., Braun H.-P., Lemaitre-Guillier C., VanDorsselaer A., and Horst W.J. Effect of manganese toxicity on the proteome of the leaf apoplast in cowpea. Plant Physiol. 133 (2003) 1935-1946
14. Gachomo E.W. Studies of the Life Cycle of Diplocarpon Rosae Wolf on Roses and the Effectiveness of Fungicides on Pathogenesis (2005), Cuvillier Verlag, Goettingen, Germany. 3-86537-460-3
15. Gachomo E.W., and Kotchoni S.O. Detailed description of developmental growth stages of Diplocarpon rosae in Rosa: a core building block for efficient disease management. Ann. Appl. Biol. 151 (2007) 233-243
16. Gordon L.Kh. Functional characteristics of adaptive aging of detached wheat roots. Fiziol. Biokhim. Kul't. Rast. 24 (1992) 128-133
17. In: Greppin H., Penel C., and Gaspar T. (Eds). Molecular and Physiological Aspects of Plant Peroxidases (1986), University of Geneva, Switzerland
18. Hahlbrock K., and Ragg H. Light-induced changes of enzyme activities in parsley cell suspension cultures. Arch. Biochem. Biophys. 166 (1975) 41-46
19. Horst R.K. Black spot. Compendium of Rose Diseases (1983), APS Press, Minnesota, USA 7-11
20. Hwang B.K., Sunwoo J.Y., Kim Y.J., and Kim B.S. Accumulation of ß-1,3-glucanase and chitinase isoforms, and salicylic acid in the DL-ß amino-n-butyric acid-induced resistance response of pepper stems to Phytophthora capsici. Physiol. Mol. Plant Pathol. 51 (1997) 305-322
21. 2 in transgenic rice leads to cell death and enhanced resistance to both bacterial and fungal pathogens. Transgenic Res. 12 (2003) 577-586
22. Kirch H.-H., Schlingensiepen S., Kotchoni O.S., Ramanjulu S., and Bartels D. Detailed expression analysis of selected genes of the aldehyde dehydrogenase (ALDH) gene superfamily in Arabidopsis thaliana. Plant Mol. Biol. 57 (2005) 315-332
23. Klotz K.L., Liu T.T.Y., Liu L., and Lagrimini L.M. Expression of the tobacco anionic peroxidase gene is tissue-specific and developmentally regulated. Plant Mol. Biol. 36 (1998) 509-520
24. Kotchoni O.S., and Gachomo W.E. The reactive oxygen species network pathways: an essential prerequisite for perception of pathogen attack and the acquired disease resistance in plants. J. Biosci. 31 (2006) 389-404
25. Kotchoni O.S., Kuhns C., Ditzer A., Kirch H.-H., and Bartels D. Over-expression of different aldehyde dehydrogenase genes in Arabidopsis thaliana confers tolerance to abiotic stress and protects plants against lipid peroxidation and oxidative stress. Plant Cell Environ. 29 (2006) 1033-1048
26. Kovtun Y., Chlu W.L., Tena G., and Shen J. Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants. Proc. Natl. Acad. Sci. U S A 97 (2000) 2940-2945
27. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 681-685
28. Livingstone D.M., Hampton J.L., Phipps P.M., and Grabau E.A. Enhanced resistance to Sclerotinia minor in peanut by expressing a barley oxalate oxidase gene. Plant Physiol. 137 (2005) 1354-1362
29. Lu H., and Higgins V.J. The effect of hydrogen peroxide on the viability of tomato cells and of the fungal pathogen Cladosporium fulvum. Physiol. Mol. Plant Pathol. 54 (1999) 131-143
30. Ma Y., Byrne D.H., and Chen J. Amphidiploid induction from diploid rose interspecific hybrids. HortScience 32 (1997) 292-295
31. Mäder M., and Amberg-Fisher V. Role of peroxidase in lignification of tobacco cells: I. Oxidation of nicotinamide adenine dinucleotide and formation of hydrogen peroxide by cell wall peroxidase. Plant Physiol. 70 (1982) 1128-1131
32. Malolepsza U. Spatial and temporal variation of reactive oxygen species and antioxidant enzymes in o-hydroxyethylorutin-treated tomato leaves inoculated with Botrytis cinerea. Plant Pathol. 54 (2005) 317-324
33. Marin-Navarro J., and Moreno J. Modification of the proteolytic fragmentation pattern upon oxidation of cysteines from ribulose 1,5-bisphosphate carboxilase/oxygenase. Biochem. J. 42 (2003) 14930-14938
34. 2 plays different roles in determining penetration failure in three diverse plant-fungal interactions. Plant J. 29 (2002) 257-268
35. Mittler R., Vanderauwera S., Gollery M., and Van Breusegem F. Reactive oxygen gene network of plants. Trends Plant Sci. 9 (2004) 490-498
36. Molano J., Duran A., and Cabib E. A rapid and sensitive assay for chitinase using tritiated chitin. Anal. Biochem. 83 (1977) 648-656
37. C. Obinger, U. Burner, R. Ebermann, C. Pene, H. Greppin. Plant peroxidases: biochemistry and physiology. IV International Symposium 1996. Proceedings University of Agriculture, Vienna and University of Geneva, Switzerland (1996).
38. Passardi F., Cosio C., Penel C., and Dunand C. Peroxidases have more functions than a swiss army knife. Plant Cell Rep. 24 (2005) 255-265
39. Ryder M.H., and Jones D.A. Biological control of crown gall. In: Hornby D. (Ed). Biological Control of Soil-borne Plant Pathogens (1990), CAB International, Wallingford 45-63
40. Schweizer P., Christofel A., and Dudler R. Transient expression of members of the germin-like gene family in epidermal cells of wheat confers disease resistance. Plant J. 20 (1999) 541-552
41. Smith I.M., Dunez J., Lelliott R.A., Phillips D.H., and Archer S.A. European Handbook of Plant Diseases (1988), Blackwell Scientific Publications, Oxford
42. Suo Y., and Leung D.W.M. Elevation of extracellular _β-1,3-glucanase and chitinase activities in rose in response to treatment with acibenzolar-S-methyl and infection by D. rosae. J. Plant Physiol. 158 (2001) 971-976
43. Swamy M., Siegers G.M., Minguet S., Wollscheid B., and Schamel W.W.A. Blue native polyacrylamide gel electrophoresis (BN-PAGE) for the identification and analysis of multiprotein complexes. Sci. STKE 345 (2006) p14
44. 2 accumulation in papillae and hypersensitive response during the barley-powdery mildew interaction. Plant J. 11 (1997) 1187-1194
45. Van Loon L.C., and Van Strien E.A. The families of pathogenesis-related proteins, their activities, and comparative analysis of PR-1 type proteins. Physiol. Mol. Plant Pathol. 55 (1999) 85-97
46. 4 plant Flaveria bidentis reduces rubisco carbamylation and leaf photosynthesis. Plant Physiol. 137 (2005) 747-755
47. Von Tiedemann A. Evidence for a primary role of active oxygen species in induction of host cell death during infection of bean leaves with Botrytis cinerea. Physiol. Mol. Plant Pathol. 50 (1997) 151-166
48. Zehr B., Savin T., and Hall R.A. One step low background Coomasie staining procedure for polyacrylamide gels. Anal. Biochem. 182 (1989) 157-159