Chitin synthase-deficient mutant of Fusarium oxysporum elicits tomato plant defence response and protects against wild-type infection

Molecular Plant Pathology

Volumn 11, Issue 4, 2010, Pages 479-493

  Pareja Jaime, Yolanda ^a   Martín Urdíroz, Magdalena ^a   Roncero, María Isabel González ^a   González Reyes, José Antonio ^a   Roldán, María Del Carmen Ruiz ^a  

^a UNIVERSITY OF CÓRDOBA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CHITIN SYNTHASE; CHITINASE;

ARTICLE; ATOMIC FORCE MICROSCOPY; ENZYMOLOGY; FLUORESCENCE MICROSCOPY; FUSARIUM; GENETICS; IMMUNOLOGY; METABOLISM; MICROBIOLOGY; PLANT DISEASE; TOMATO; TRANSMISSION ELECTRON MICROSCOPY; DEFICIENCY;

CHITIN SYNTHASE; CHITINASE; FUSARIUM; LYCOPERSICON ESCULENTUM; MICROSCOPY, ATOMIC FORCE; MICROSCOPY, ELECTRON, TRANSMISSION; MICROSCOPY, FLUORESCENCE; PLANT DISEASES;

FUSARIUM OXYSPORUM; FUSARIUM OXYSPORUM F. SP. LYCOPERSICI; LYCOPERSICON ESCULENTUM;

EID: 77954181811     PISSN: 14646722     EISSN: 13643703     Source Type: Journal    
DOI: 10.1111/j.1364-3703.2010.00624.x     Document Type: Article

References (38)

1. Alabouvette C, Olivain C, Steinberg C. Biological control of plant diseases: the European situation. Eur. J. Plant Pathol. 2006, 114:329-341.
2. Alabouvette C, Olivain C, Migheli Q, Steinberg C. Microbiological control of soil-borne phytopathogenic fungi with special emphasis on wilt-inducing Fusarium oxysporum. New Phytol. 2009, 184:529-544.
3. Armstrong GM, Armstrong JK. Formae speciales and races of Fusarium oxysporum causing wilt diseases. Fusarium: Disease, Biology, and Taxonomy 1981, 391-399. Nelson PE, Tousson TACook RJ. In, eds), University Park, PA, State University Press
4. Benhamou N, Garand C. Cytological analysis of defense-related mechanisms induced in pea root tissues in response to colonization by nonpathogenic Fusarium oxysporum Fo47. Phytopathology 2001, 91:730-740.
5. Bestwick CS, Brown IR, Bennett MHR, Mansfield JW. Localization of hydrogen peroxide accumulation during the hypersensitive reaction of lettuce cells to Pseudomonas syringae pv phaseolicola. Plant Cell 1997, 9:209-221.
6. Campbell RE, Tour O, Palmer AE, Steinbach PA, Baird GS, Zacharias DA, Tsien RY. A monomeric red fluorescent protein. Proc. Natl. Acad. Sci. USA 2002, 99:7877-7882.
7. Caracuel Z, Martinez-Rocha AL, Di Pietro A, Madrid MP, Roncero MIG. Fusarium oxysporum gas1 encodes a putative β-1,3-glucanosyltransferase required for virulence on tomato plants. Mol. Plant-Microbe Interact. 2005, 18:1140-1147.
8. Dalisay RF, Kuc JA. Persistence of induced resistance and enhanced peroxidase and chitinase activities in cucumber plants. Physiol. Mol. Plant Pathol. 1995, 47:315-327.
9. Danhash N, Wagemakers CA, van Kan JA, de Wit PJ. Molecular characterization of four chitinase cDNAs obtained from Cladosporium fulvum-infected tomato. Plant Mol. Biol. 1993, 22:1017-1029.
10. Di Pietro A, Roncero MIG. Cloning, expression, and role in pathogenicity of pg1 encoding the major extracellular endopolygalacturonase of the vascular wilt pathogen Fusarium oxysporum. Mol. Plant-Microbe. Interact. 1998, 11:91-98.
11. Di Pietro A, Garcia-Maceira FI, Meglecz E, Roncero MIG. A MAP kinase of the vascular wilt fungus Fusarium oxysporum is essential for root penetration and pathogenesis. Mol. Microbiol. 2001, 39:1140-1152.
12. Di Pietro A, Madrid MP, Caracuel Z, Delgado-Jarana J, Roncero MIG. Fusarium oxysporum: exploring the molecular arsenal of a vascular wilt fungus. Mol. Plant Pathol. 2003, 4:315-326.
13. Di Pietro A, Roncero MIG, Ruiz-Roldan MC. From tools of survival to weapons of destruction: role of cell wall-degrading enzymes in plant infection. The Mycota V: Plant Relationships 2009, 181-200. Deising H, In, ed.), Heidelberg, Berlin, Springer Verlag
14. Duijff BJ, Pouhair D, Olivain C, Alabouvette C, Lemanceau P. Implication of systemic induced resistance in the suppression of fusarium wilt of tomato by Pseudomonas fluorescens WCS417r and by nonpathonic Fusarium oxysporum Fo47. Eur. J. Plant Pathol. 1998, 104:903-910.
15. Fravel D, Olivain C, Alabouvette C. Fusarium oxysporum and its biocontrol. New Phytol. 2002, 157:493-502.
16. Freeman S, Rodriguez RJ. Genetic conversion of a fungal plant pathogen to a nonpathogenic, endophytic mutualist. Science 1993, 260:75-78.
17. Freeman S, Zveibil A, Vintal H, Maymon M. Isolation on nonpathogenic mutants of Fusarium oxysporum f. sp. melonis for biological control of Fusarium wilt in cucurbits. Phytopathology 2001, 92:164-168.
18. Fuchs J-G, Moënne-Loccoz Y, Défago G. Nonpathogenic Fusarium oxysporum strain Fo47 induces resistance to Fusarium wilt in tomato. Plant Dis. 1997, 81:492-496.
19. Heath MC. Plant resistance to fungi. Can. J. Plant Pathol. 1996, 18:469-475.
20. Hedley PE, Machray GC, Davies HV, Burch L, Waugh R. Potato (Solanum tuberosum) invertase-encoding cDNAs and their differential expression. Gene 1994, 145:211-214.
21. Huertas-Gonzalez MD, Ruiz-Roldan MC, Di Pietro A, Roncero MIG. Cross protection provides evidence for race-specific avirulence factors in Fusarium oxysporum. Physiol. Mol. Plant Pathol. 1999, 54:63-72.
22. Kavroulakis N, Ntougias S, Zervakis GI, Ehaliotis C, Haralampidis K, Papadopoulou KK. Role of ethylene in the protection of tomato plants against soil-borne fungal pathogens conferred by an endophytic Fusarium solani strain. J. Exp. Bot. 2007, 58:3853-3864.
23. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 2001, 25:402-408.
24. Madrid MP, Di Pietro A, Roncero MI. Class V chitin synthase determines pathogenesis in the vascular wilt fungus Fusarium oxysporum and mediates resistance to plant defence compounds. Mol. Microbiol. 2003, 47:257-266.
25. Martin-Urdiroz M, Roncero MI, Gonzalez-Reyes JA, Ruiz-Roldan C. ChsVb, a class VII chitin synthase involved in septation, is critical for pathogenicity in Fusarium oxysporum. Eukaryot. Cell 2008, 7:112-121.
26. Olivain C, Trouvelot S, Binet MN, Cordier C, Pugin A, Alabouvette C. Colonization of flax roots and early physiological responses of flax cells inoculated with pathogenic and nonpathogenic strains of Fusarium oxysporum. Appl. Environ. Microbiol. 2003, 69:5453-5462.
27. Panina Y, Fravel DR, Baker CJ, Shcherbakova LA. Biocontrol and plant pathogenic Fusarium oxysporum-induced changes in phenolic compounds in tomato leaves and roots. J. Phytopathol. 2007, 155:475-481.
28. Postma J, Luttikholt AJG. Colonization of carnation stems by a nonpathogenic isolate of Fusarium oxysporum and its effect on Fusarium oxysporum f. sp. dianthi. Can. J. Bot 1996, 74:1841-1851.
29. Redman RS, Freeman S, Clifton DR, Morrel J, Brown G, Rodriguez RJ. Biochemical analysis of plant protection afforded by a nonpathogenic endophytic mutant of Colletotrichum magna. Plant Physiol. 1999a, 119:795-804.
30. Redman RS, Ranson JC, Rodriguez RJ. Conversion of the pathogenic fungus Colletotrichum magna to a nonpathogenic, endophytic mutualist by gene disruption. Mol. Plant-Microbe Interact 1999b, 12:969-975.
31. Shaner NC, Campbell RE, Steinbach PA, Giepmans BN, Palmer AE, Tsien RY. Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein. Nat. Biotechnol. 2004, 22:1567-1572.
32. Shih MC, Heinrich P, Goodman HM. Cloning and chromosomal mapping of nuclear genes encoding chloroplast and cytosolic glyceraldehyde-3-phosphate-dehydrogenase from Arabidopsis thaliana. Gene 1991, 104:133-138.
33. Soulie MC, Perino C, Piffeteau A, Choquer M, Malfatti P, Cimerman A, Kunz C, Boccara M, Vidal-Cros A. Botrytis cinerea virulence is drastically reduced after disruption of chitin synthase class III gene (Bcchs3a). Cell. Microbiol. 2006, 8:1310-1321.
34. van Kan JA, Joosten MH, Wagemakers CA, van den Berg-Velthuis GC, de Wit PJ. Differential accumulation of mRNAs encoding extracellular and intracellular PR proteins in tomato induced by virulent and avirulent races of Cladosporium fulvum. Plant Mol. Biol. 1992, 20:513-527.
35. Wattad C, Freeman S, Dinoor A, Prusky D. A nonpathogenic mutant of Colletotrichum magna is deficient in extracellular secretion of pectate lyase. Mol. Plant-Microbe Interact. 1995, 8:621-626.
36. Weber I, Assmann D, Thines E, Steinberg G. Polar localizing class V myosin chitin synthases are essential during early plant infection in the plant pathogenic fungus Ustilago maydis. Plant Cell 2006, 18:225-242.
37. Werner S, Sugui JA, Steinberg G, Deising HB. A chitin synthase with a myosin-like motor domain is essential for hyphal growth, appressorium differentiation, and pathogenicity of the maize anthracnose fungus Colletotrichum graminicola. Mol. Plant-Microbe Interact. 2007, 20:1555-1567.
38. Yang L, Ukil L, Osmani A, Nahm F, Davies J, De Souza CP, Dou X, Perez-Balaguer A, Osmani SA. Rapid production of gene replacement constructs and generation of a green fluorescent protein-tagged centromeric marker in Aspergillus nidulans. Eukaryot. Cell 2004, 3:1359-1362.