Role of plant stomata in bacterial invasion

Cellular Microbiology

Volumn 9, Issue 7, 2007, Pages 1621-1629

  Underwood, William ^a   Melotto, Maeli ^a   He, Sheng Yang ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIUM LIPOPOLYSACCHARIDE; CARBON DIOXIDE; CORONATINE; RAIN;

ADAPTATION; AIR TEMPERATURE; BACTERIAL PLANT DISEASE; BACTERIAL STRAIN; BACTERIAL VIRULENCE; CARBON DIOXIDE TRANSPORT; CELL PROTECTION; DISEASE PREDISPOSITION; HUMIDITY; INFECTION RISK; INNATE IMMUNITY; MICROBIAL ACTIVITY; NONHUMAN; PATHOGENESIS; PHOTOSYNTHESIS; PLANT CELL; PLANT LEAF; PLANT MORPHOLOGY; PLANT PATHOGEN INTERACTION; PLANT STOMA; PLANT TISSUE; PLANT WATER USE; PRIORITY JOURNAL; REGULATORY MECHANISM; RISK ASSESSMENT; RISK FACTOR; RISK REDUCTION; SHORT SURVEY; SIGNAL TRANSDUCTION; WATER LOSS;

ARABIDOPSIS; BACTERIA; IMMUNITY, NATURAL; LYCOPERSICON ESCULENTUM; PLANT DISEASES; PLANT EPIDERMIS; PLANT LEAVES; PLANTS; PSEUDOMONAS SYRINGAE; SIGNAL TRANSDUCTION;

BACTERIA (MICROORGANISMS);

EID: 34250782284     PISSN: 14625814     EISSN: 14625822     Source Type: Journal    
DOI: 10.1111/j.1462-5822.2007.00938.x     Document Type: Short Survey

References (59)

1. Ausubel, F.M. (2005) Are innate immune signaling pathways in plants and animals conserved? Nat Immunol 6: 973-979.
2. Beattie, G.A., and Lindow, S.E. (1995) The secret life of foliar bacterial pathogens on leaves. Annu Rev Phytopathol 33: 145-172.
3. Bender, C.L., Alarcon-Chaidez, F., and Gross, D.C. (1999) Pseudomonas syringae phytotoxins: Mode of action, regulation, and biosynthesis by peptide and polyketide synthetases. Microbiol Mol Biol Rev 63: 266-292.
4. + channels of Cf-9 transgenic tobacco guard cells as targets for Cladosporium fulvum Avr9 elicitor-dependent signal transduction. Plant J 19: 453-462.
5. Block, A., Schmelz, E., Jones, J.B., and Klee, H.J. (2005) Coronatine and salicylic acid: The battle between Arabidopsis and Pseudomonas for phytohormone control. Mol Plant Pathol 6: 79-83.
6. Boureau, T., Routtu, J., Roine, E., Taira, S., and Romantschuk, M. (2002) Localization of hrp A-induced Pseudomonas syringae pv. tomato DC3000 in infected tomato leaves. Mol Plant Pathol 3: 451-460.
7. Brooks, D.M., Hernández-Guzmán, G., Kloek, A.P., Alarcón-Chaidez, F., Sreedharan, A., Rangaswamy, V., et al. (2004) Identification and characterization of a well-defined series of coronatine biosynthetic mutants of Pseudomonas syringae pv. tomato DC3000. Mol Plant-Microbe Interact 17: 162-174.
8. Brooks, D.M., Bender, C.L., and Kunkel, B.N. (2005) The Pseudomonas syringae phytotoxin coronatine promotes virulence by overcoming salicylic acid-dependent defences in Arabidopsis thaliana. Mol Plant Pathol 6: 629-639.
9. Budde, I.P., and Ullrich, M.S. (2000) Interactions of Pseudomonas syringae pv. glycinea with host and nonhost plants in relation to temperature and phytotoxin synthesis. Mol Plant-Microbe Interact 9: 951-961.
10. Budde, I.P., Rohde, B.H., Bender, C.L., and Ullrich, M.S. (1998) Growth phase and temperature influence promoter activity, transcript abundance, and protein stability during biosynthesis of the Pseudomonas syringae phytotoxin coronatine. J Bacteriol 180: 1360-1367.
11. Chisholm, S.T., Coaker, G., Day, B., and Staskawicz, B.J. (2006) Host-microbe interactions: Shaping the evolution of the plant immune response. Cell 124: 803-814.
12. Cui, J., Bahrami, A.K., Pringle, E.G., Hernandez-Guzman, G., Bender, C.L., Pierce, N.E., and Ausubel, F.M. (2005) Pseudomonas syringae manipulates systemic plant defenses against pathogens and herbivores. Proc Natl Acad Sci USA 102: 1791-1796.
13. Devoto, A., Nieto-Rostro, M., Xie, D., Ellis, C., Harmston, R., Patrick, E., et al. (2002) COI1 links jasmonate signaling and fertility to the SCF ubiquitin-ligase complex in Arabidopsis. Plant J 32: 457-466.
14. Fan, L.M., Zhao, Z., and Assmann, S.M. (2004) Guard cells: A dynamic signaling model. Curr Opin Plant Biol 7: 537-546.
15. Felix, G., Duran, J.D., Volko, S., and Boller, T. (1999) Plants have a sensitive perception system for the most conserved domain of bacterial flagellin. Plant J 18: 265-276.
16. Feys, B.J.F., Benedetti, C.E., Penfold, C.N., and Turner, J.G. (1994) Arabidopsis mutants selected for resistance to the phytotoxin coronatine are male sterile, insensitive to methyl jasmonate, and resistant to a bacterial pathogen. Plant Cell 6: 751-759.
17. Glazebrook, J. (2005) Contrasting mechanisms of defense against biotrophic and nectrotrophic pathogens. Annu Rev Phytopathol 43: 205-227.
18. Glazebrook, J., Chen, W., Estes, B., Chang, H.S., Nawrath, C., Metraux, J.P., et al. (2003) Topology of the network integrating salicylate and jasmonate signal transduction derived from global expression phenotyping. Plant J 34: 217-228.
19. Gómez-Gómez, L., and Boller, T. (2000) FLS2: An LRR receptor-like kinase involved in the perception of the bacterial elicitor flagellin in Arabidopsis. Mol Cell 5: 1003-1011.
20. Greulich, F., Yoshihara, T., and Ichihara, A. (1995) Coronatine, a bacterial phytotoxin, acts as a stereospecific analog of jasmonate type signals in tomato cells and potato tissues. J Plant Physiol 147: 359-366.
21. Guimaraes, R.L., and Stotz, H.U. (2004) Oxalate production by Sclerotinia sclerotiorum deregulates guard cells during infection. Plant Physiol 136: 3703-3711.
22. He, P., Chintamanani, S., Chen, Z., Zhu, L., Kunkel, B.N., Alfano, J.R., et al. (2004) Activation of a COI1-dependent pathway in Arabidopsis by Pseudomonas syringae type III effectors and coronatine. Plant J 37: 589-602.
23. Hosy, E., Vavasseur, A., Mouline, K., Dreyer, I., Gaymard, F., Poree, F., et al. (2003) The Arabidopsis outward K+ channel GORK is involved in regulation of stomatal movements and plant transpiration. Proc Natl Acad Sci USA 100: 5549-5554.
24. Huang, J.-S. (1986) Ultrastructure of bacterial penetration in plants. Annu Rev Phytopathol 24: 141-157.
25. Hugouvieux, V., Barber, C.E., and Daniels, M.J. (1998) Entry of Xanthomonas campestris pv. campestris into hydathodes of Arabidopsis thaliana leaves: A system for studying early infection events in bacterial pathogenesis. Mol Plant-Microbe Interact 11: 537-543.
26. Ichihara, A., Shiraishi, K., Sato, H., Sakamura, S., Nishiyama, K., Sakai, R., et al. (1977) The structure of coronatine. J Am Chem Soc 99: 636-637.
27. 2+ sensor priming hypothesis. Curr Opin Plant Biol 9: 654-663.
28. Jones, J.D.G., and Dangl, J.L. (2006) The plant immune system. Nature 444: 323-329.
29. Kloek, A.P., Verbsky, M.L., Sharma, S.B., Schoelz, J.E., Vogel, J., Klessig, D.F., and Kunkel, B.N. (2001) Resistance to Pseudomonas syringae conferred by an Arabidopsis thaliana coronatine-insensitive (coi1) mutation occurs through two distinct mechanisms. Plant J 26: 509-522.
30. Klüsener, B., Young, J.J., Murata, Y., Allen, G.J., Mori, I.C., Hugouvieux, V., and Schroeder, J.I. (2002) Convergence of calcium signaling pathways of pathogenic elicitors and abscisic acid in Arabidopsis guard cells. Plant Physiol 130: 2152-2163.
31. Koda, Y., Takahashi, K., Kikuta, Y., Greulich, F., Toshima, H., and Ichihara, A. (1996) Similarities of the biological activities of coronatine and coronafacic acid to those of jasmonic acid. Phytochemistry 41: 93-96.
32. Kunkel, B.N., and Brooks, D.M. (2002) Cross talk between signaling pathways in pathogen defense. Curr Opin Plant Biol 5: 325-331.
33. Kunze, G., Zipfel, C., Robatzek, S., Niehaus, K., Boller, T., and Felix, G. (2004) The N terminus of bacterial elongation factor Tu elicits innate immunity in Arabidopsis plants. Plant Cell 16: 3496-3507.
34. Laurie-Berry, N., Joardar, V., Street, I.H., and Kunkel, B.N. (2006) The Arabidopsis thaliana JASMONATE INSENSITIVE 1 gene is required for suppression of salicylic acid-dependent defenses during infection by Pseudomonas syringae. Mol Plant-Microbe Interact 19: 789-800.
35. Lee, J.-S. (1998) The mechanism of stomatal closing by salicylic acid in Commelina communis L. J Plant Biol 41: 97-102.
36. Lee, S., Choi, H., Suh, S., Doo, I.-S., Oh, K.-Y., Choi, E.J., et al. (1999) Oligogalacturonic acid and chitosan reduce stomatal aperture by inducing the evolution of reactive oxygen species from guard cells of tomato and Commelina communis. Plant Physiol 121: 147-152.
37. Li, L., Zhao, Y., McCaig, B.C., Wingerd, B.A., Wang, J., Whalen, M.E., et al. (2004) The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development. Plant Cell 16: 126-143.
38. Lindow, S.E., and Brandl, M.T. (2003) Microbiology of the phyllosphere. Appl Environ Microbiol 69: 1875-1883.
39. Manthe, B., Schulz, M., and Schnable, H. (1992) Effects of salicylic acid on growth and stomatal movements on Vicia faba L. evidence for salicylic acid metabolism. J Chem Ecol 18: 1525-1539.
40. Marré, E. (1979) Fusicoccin: A tool in plant physiology. Annu Rev Plant Physiol 30: 273-288.
41. Melotto, M., Underwood, W., Koczan, J., Nomura, K., and He, S.Y. (2006) Plant stomata function in innate immunity against bacterial invasion. Cell 126: 969-980.
42. Mino, Y., Matsuchita, Y., and Sakai, R. (1987) Effect of coronatine on stomatal opening in leaves of broadbean and Italian ryegrass. Ann Phytopathol Soc Jpn 53: 53-55.
43. Mittal, S.M., and Davis, K.R. (1995) Role of the phytotoxin coronatine in the infection of Arabidopsis thaliana by Pseudomonas syringae pv. tomato. Mol Plant-Microbe Interact 8: 165-171.
44. Mori, I.C., Pinontoan, R., Kawano, T., and Muto, S. (2001) Involvement of superoxide generation in salicylic acid-induced stomatal closure in Vicia faba. Plant Cell Physiol 42: 1383-1388.
45. Mustilli, A.C., Merlot, S., Vavasseur, A., Fenzi, F., and Giraudat, J. (2002) Arabidopsis OST1 protein kinase mediates the regulation of stomatal aperture by abscisic acid and acts upstream of reactive oxygen species production. Plant Cell 12: 3089-3099.
46. Nomura, K., Melotto, M., and He, S.Y. (2005) Suppression of host defense in compatible plant-Pseudomonas syringae interactions. Curr Opin Plant Biol 8: 361-368.
47. Palmer, D.A., and Bender, C.L. (1993) Effects of environmental and nutritional factors on production of the polyketide phytotoxin coronatine by Pseudomonas syringae pv. glycinea. Appl Environ Microbiol 59: 1619-1623.
48. Palmer, D.A., and Bender, C.L. (1995) Ultrastructure of tomato leaf tissue treated with the pseudomonad phytotoxin coronatine and comparison with methyl jasmonate. Mol Plant-Microbe Interact 8: 683-692.
49. Parker, J.E., Barber, C.E., Fan, M.J., and Daniels, M.J. (1993) Interaction of Xanthomonas campestris with Arabidopsis thaliana: characterization of a gene from X. c. pv. raphani that confers avirulence to most A. thaliana accessions. Mol Plant-Microbe Interact 6: 216-224.
50. Reymond, P., and Farmer, E.E. (1998) Jasmonate and salicylate as global signals for defense gene expression. Curr Opin Plant Biol 1: 404-411.
51. Schroeder, J.I., Allen, G.J., Hugouvieux, V., Kwak, J.M., and Waner, D. (2001) Guard cell signal transduction. Annu Rev Plant Physiol Plant Mol Biol 52: 627-658.
52. Tamogami, S., and Kodama, O. (2000) Coronatine elicits phytoalexin production in rice leaves (Oryza sativa L.) in the same manner as jasmonic acid. Phytochem 54: 689-694.
53. Thilmony, R., Underwood, W., and He, S.Y. (2006) Genome-wide transcriptional analysis of the Arabidopsis thaliana interaction with the plant pathogen Pseudomonas syringae pv. tomato DC3000 and the human pathogen Escherichia coli O157:H7. Plant J 46: 34-53.
54. Ullrich, M., Penaloza-Vazquez, A., Bailey, A.M., and Bender, C.L. (1995) A modified two-component regulatory system is involved in temperature-dependent biosynthesis of the Pseudomonas syringae phytotoxin coronatine. J Bacteriol 177: 6160-6169.
55. Weiler, E., Kutchan, W.T.M., Gorba, T., Brodschelm, W., Neisel, U., and Bublitz, F. (1994) The Pseudomonas phytotoxin coronatine mimics octadecanoid signaling molecules of higher plants. FEBS Lett 345: 9-13.
56. Xu, L.H., Liu, F.Q., Lechner, E., Genschik, P., Crosby, W.L., Ma, H., et al. (2002) The SCF COI1 ubiquitin-ligase complexes are required for jasmonate response in Arabidopsis. Plant Cell 14: 1919-1935.
57. Zeidler, D., Zähringer, U., Gerber, I., Dubery, I., Hartung, T., Bors, W., et al. (2004) Innate immunity in Arabidopsis thaliana: lipopolysaccharides activate nitric oxide synthase (NOS) and induce defense genes. Proc Natl Acad Sci USA 101: 15811-15816.
58. Zhao, Y., Thilmony, R., Bender, C.L., Schaller, A., He, S.Y., and Howe, G.A. (2003) Virulence systems of Pseudomonas syringae pv. tomato promote bacterial speck disease in tomato by targeting the jasmonate signaling pathway. Plant J 36: 485-499.
59. Zipfel, C., Kunze, G., Chinchilla, D., Caniard, A., Jones, J.D., Boller, T., and Felix, G. (2006) Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium-mediated transformation. Cell 125: 749-760.