Host Active Defense Responses Occur within 24 Hours after Pathogen Inoculation in the Rice Blast System

Rice Science

Volumn 14, Issue 4, 2007, Pages 302-310

  WANG, Zhong hua ^a   JIA, Yu lin ^b   LIN, Hui ^c   INTERN, Adair ^c   VALENT, Barbara ^d   RUTGER, J Neil ^b  

^a ZHEJIANG WANLI UNIVERSITY   (China)

^b USDA ARS Dale Bumpers National Rice Research Center   (United States)

^c UNIVERSITY OF ARKANSAS   (United States)

^d KANSAS STATE UNIVERSITY   (United States)

Author keywords

cytology; defense; disease resistance; lesion mimic mutant; rice (Oryza sativa)

Indexed keywords

FUNGI; MAGNAPORTHE GRISEA; ORYZA SATIVA;

EID: 42949099768     PISSN: 16726308     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1672-6308(08)60009-8     Document Type: Article

References (41)

1. Bent A. Plant disease resistance genes: Function meets structure. Plant Cell 8 (1996) 1757-1771
2. Martin G., Bogdanove A., and Sesser G. Understanding functions of plant disease resistance proteins. Ann Rev Plant Biol 54 (2003) 1-5
3. Silue D., Nottenghem J., and Thorreau D. Evidence for a gene-for-gene relationship in the Oryza sativa-Magnaporthe grisea pathosystem. Phytopathology 82 (1992) 577-580
4. Valent B. The rice blast fungus, Magnaporthe grisea. In: Carroll G., and Tudzynoski P. (Eds). The Mycota V: Plant Relationships. Part B (1997), Springer-Verlag, Heidelberg, Berlin 37-54
5. Jia Y., Valent B., and Lee F. Determination of host resistance responses to Magnaporthe grisea on detached rice leaves using a spot inoculation method. Plant Dis 87 (2003) 129-133
6. Talbot N. On the trail of a cereal killer: Exploring the biology of Magnaporthe grisea. Annu Rev Microbiol 57 (2003) 177-202
7. Jia Y., McAdams S., Bryan G., Hershey H., and Valent B. Direct interaction of resistance gene and avirulence gene products confers rice blast resistance. EMBO J 19 (2000) 4004-4014
8. Orbach M., Farrall L., Sweigard J., Chumley F., and Valent B. A telomeric avirulence gene determines efficacy for the rice blast resistance gene Pi-ta. Plant Cell 12 (2000) 2019-2032
9. Hammond-Kosack K., and Jones J. Resistance gene- dependent plant defense responses. Plant Cell 8 (1996) 1773-1791
10. Yang Y., Shah J., and Klessig D. Signal perception and transduction in plant defense responses. Genes Dev 11 (1997) 1621-1639
11. Dixon R., Harrison M., and Lamb C. Early events in the activation of plant defense responses. Annu Rev Phytopath 32 (1994) 479-501
12. Jia Y., and Martin G. Rapid transcript accumulation of pathogenesis- related genes during an incompatible interaction in bacterial speck disease-resistant tomato plants. Plant Mol Biol 40 (1999) 455-465
13. Dietrich R., Richberg M., Schmidt R., Dean C., and Dangl J. A novel zinc-finger protein is encoded by the Arabidopsis LSD1 gene and functions as a negative regulator of plant cell death. Cell 88 (1997) 685-694
14. Greenberg J., and Ausubel F. Arabidopsis mutants compromised for the control of cellular damage during pathogenesis and aging. Plant J 4 (1993) 327-342
15. Greenberg J., Guo A., Klessig D., and Ausubel F. Programmed cell death in plants: A pathogen-triggered response activated coordinately with multiple defense functions. Cell 77 (1994) 551-563
16. Marchetti M., Bollich C., and Uecker F. Spontaneous occurrence of the Sekiguchi lesion in two American rice lines: Its induction, inheritance, and utilization. Phytopathology 73 (1983) 603-606
17. Neuffer M., and Calvert O. Dominant disease lesion mimics in Maize. J Heredity 66 (1975) 265-270
18. Takahashi A., Kawasaki T., Henmi K., Shii K., Kodama O., Satoh H., and Shimamoto K. Lesion mimic mutants of rice with alterations in early signaling events of defense. Plant J 17 (1999) 535-545
19. Walbot V. Maize mutants for the 21st century. Plant Cell 3 (1991) 851-856
20. Yin Z., Chen J., Goh M., Leung H., Khush G., and Wang G. Characterizing rice lesion mimic mutants and identifying a mutant with broad spectrum resistance to rice blast and bacterial blight. Mol Plant-Microbe Interact 13 (2000) 869-876
21. Kim S., Ahn I., and Lee Y. Analysis of genes expressed during rice-Magnaporthe grisea interaction. Mol Plant-Microbe Interact 14 (2001) 1340-1346
22. Simmons C., Litts J., Huang N., and Rodriguez R. Structure of a rice beta-glucanase gene regulated by ethylene, cytokinin, wounding, salicylic acid and fungal elicitors. Plant Mol Biol 18 (1992) 33-45
23. Xiong L., Lee M., Qi M., and Yang Y. Identification of defense- related rice genes by suppression subtractive hybridization and differential screening. Mol Plant-Microbe Interact 14 (2001) 685-692
24. Xu Y., Zhu Q., Panbangred W., Shirasu K., and Lamb C. Regulation, expression and function of a new basic chitinase gene in rice (Oryza sativa L.). Plant Mol Biol 30 (1996) 387-401
25. Zhu Q., Dabi T., Beeche A., Yamamoto R., Lawton M., and Lamb C. Cloning and properties of a rice gene encoding phenylalanine ammonia-lyase. Plant Mol Biol 29 (1995) 535-550
26. Zhu Q., and Lamb C. Isolation and characterization of a rice gene encoding a basic chitinase. Mol Gen Genet 226 (1991) 289-296
27. Correll J., Harp T., Guerber J., Zeigler R., Liu B., Cartwright R., and Lee F. Characterization of Pyricularia grisea in the United States using independent genetic and molecular markers. Phytopathology 90 (2000) 1396-1404
28. Bryan G., Wu K., Farrall L., Jia Y., Hershey H., McAdams S., Faulk K., Donaldson G., Tarchini R., and Valent B. A single amino acid difference distinguishes resistant and susceptible alleles of the rice blast resistance gene Pi-ta. Plant Cell 12 (2000) 2033-2045
29. Jia Y. Registration of Katy lesion mimic mutant 1. Crop Sci 45 (2005) 1675
30. Counce P., Keisling T., and Mitchell A. A uniform adaptive and objective system for describing rice development. Crop Sci 40 (2000) 436-443
31. Valent B., Farrall L., and Chumley F. Magnaporthe grisea genes for pathogenicity and virulence identified through a series of backcrosses. Genetics 127 (1991) 87-101
32. Ausubel F., Brent R., Kingston R., Moore D., Smith J., Sideman J., and Estrual K. Protocols in Molecular Biology (1987), John Wiley and Sons, New York
33. Kim S., Cho K., Yu S., Kim S., Hong J., Han C., Bae D., Nam M., and Kang K. Proteomic analysis of differentially expressed proteins induced by rice blast fungus and elicitor in suspension-cultured rice cells. Proxemics 3 (2003) 2368-2378
34. Bhatia Y., Misra S., and Bisaria V. Microbial β-glucosidases: Cloning, properties and applications. Critic Rev Biotech 22 (2002) 375-407
35. Jia Y., Rutger J., Wang Z., Singh P., Martin R., and Pinson S. Development and characterization of rice mutant populations for functional genomics of host-parasite interactions. Phytopathology 94 (suppl) (2004) S47
36. Buschges R., Hollricher K., Panstruga R., Simons G., Wolter M., Frijters A., van Daelen R., van der Lee T., Diergaarde P., Groenendijk J., Topsch S., Vos P., Salmini F., and Schulze-Lefert P. A novel control element of plant pathogen resistance. Cell 88 (1997) 596-705
37. Jarosch B., Kogel K., and Schaffrath U. The ambivalence of the barley Mlo locus: Mutations conferring resistance against powdery mildew (Blumeria graminis f. sp. hordei) enhance susceptibility to the rice blast fungus Magnaporthe grisea. Mol Plant-Microbe Interact 12 (1999) 508-514
38. Hu G., Yalpani N., Briggs S., and Johal G. A prophyrin pathway impairment is responsible for the phenotype of a dominant disease lesion mimic mutant of maize. Plant Cell 10 (1998) 531-536
39. Heath M., Howard R., Valent B., and Chumley F. Ultrastructural interactions of one strain of Magnaporthe grisea with goosegrass and weeping lovegrass. Can J Bot 70 (1992) 779-787
40. Koga H. Cytological aspects of infection by rice blast fungus Pyricularia oryzae. In: Sreenivasaprasad S., and Johnson R. (Eds). Major Fungal Disease of Rice: Recent Advances (2001), Kluwer Academic, Dordrech
41. Collmer A., Badel J., Deng W., Fouts D., Ramos A., Rehm A., Anderson D., Scheneewind O., van Dijk K., and Alfano J. Pseudomonas syringae Hrp type III secretion system and effector proteins. Proc Natl Acad Sci USA 97 (2000) 8770-8777