Effects of galU mutation on Pseudomonas syringae-plant interactions

Molecular Plant-Microbe Interactions

Volumn 23, Issue 9, 2010, Pages 1184-1196

  Deng, Wen Ling ^a   Lin, Yuan Chun ^a   Lin, Rong Hwa ^a,b   Wei, Chia Fong ^a   Huang, Yi Chiao ^a   Peng, Hwei Ling ^b   Huang, Hsiou Chen ^a  

^a NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

^b NATIONAL CHIAO TUNG UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

FLAGELLIN; HYDROGEN PEROXIDE; LIPOPOLYSACCHARIDE; URIDINE TRIPHOSPHATE GLUCOSE 1 PHOSPHATE URIDYLYLTRANSFERASE;

ARTICLE; BIOFILM; GENETICS; GROWTH, DEVELOPMENT AND AGING; HOST PATHOGEN INTERACTION; METABOLISM; MICROBIOLOGY; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PHYSIOLOGY; PSEUDOMONAS SYRINGAE; TOBACCO;

BIOFILMS; FLAGELLIN; HOST-PATHOGEN INTERACTIONS; HYDROGEN PEROXIDE; LIPOPOLYSACCHARIDES; MOLECULAR SEQUENCE DATA; MUTATION; PSEUDOMONAS SYRINGAE; TOBACCO; UTP-GLUCOSE-1-PHOSPHATE URIDYLYLTRANSFERASE;

ANIMALIA; BACTERIA (MICROORGANISMS); PSEUDOMONAS SYRINGAE; PSEUDOMONAS SYRINGAE PV. SYRINGAE;

EID: 77955523024     PISSN: 08940282     EISSN: None     Source Type: Journal    
DOI: 10.1094/MPMI-23-9-1184     Document Type: Article

References (59)

1. Abramovitch, R. B., Kim, Y. J., Chen, S., Dickman, M. B., and Martin, G. B. 2003. Pseudomonas type III effector AvrPtoB induces plant disease susceptibility by inhibition of host programmed cell death. EMBO (Eur. Mol. Biol. Organ.) J. 22:60-69.
2. Altschul, S. F., Madden, T. L., Schaffer, A. A., Zhang, J., Zhang, Z., Miller, W., and Lipman, D. J. 1997. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res. 25:3389-3402.
3. Ames, G. F., Spudich, E. N., and Nikaido, H. 1974. Protein composition of outer membrane of Salmonella typhimurium: Effect of lipopolysaccharide mutations. J. Bacteriol. 117:406-416.
4. Beattie, G. A., and Lindow, S. E. 1994. Epiphytic fitness of phytopathogenic bacteria: Physiological adaptations for growth and survival. Pages 1-27 in: Bacterial Pathogenesis of Plants and Animals-Molecular and Cellular Mechanisms. Vol.192. J. L. Dangl, ed. Springer-Verlag, Berlin.
5. Bedini, E., De Castro, C., Erbs, G., Mangoni, L., Dow, J. M., Newman, M. A., Parrilli, M., and Unverzagt, C. 2005. Structure-dependent modulation of a pathogen response in plants by synthetic O-antigen polysaccharides. J. Am. Chem. Soc. 127:2414-2416.
6. Brede, G., Fjaervik, E., and Valla, S. 1991. Nucleotide sequence and expression analysis of the Acetobacter xylinum uridine diphosphoglucose pyrophosphorylase gene. J. Bacteriol. 173:7042-7045.
7. Brown, I., Mansfield, J., and Bonas, U. 1995. hrp Genes in Xanthomonas campestris pv. vesticatoria determine ability to suppress papilla deposition in pepper mesophyll cells. Mol. Plant-Microbe Interact. 8:825-836.
8. Chang, H. Y., Lee, J. H., Deng, W. L., Fu, T. F., and Peng, H. L. 1996. Virulence and outer membrane properties of a galU mutant of Klebsiella pneumoniae CG43. Microb. Pathog. 20:255-261.
9. Chang, H.-Y., Huang, H.-C., Lee, J.-H., and Peng, H.-L. 1999. Characterization of a putative Pseudomonas UDP-glucose pyrophosphorylase. Proc. Natl. Sci. Counc. R.O.C. (B) 23:74-84.
10. Collmer, A., Badel, J. L., Charkowski, A. O., Deng, W.-L., Fouts, D. E., Ramos, A. R., Rehm, A. H., Anderson, D. M., Schneewind, O., van Dijk, K., and Alfano, J. R. 2000. Pseudomonas syringae Hrp type III secretion system and effector proteins. Proc. Natl. Acad. Sci. U.S.A. 97:8770-8777.
11. DebRoy, S., Thilmony, R., Kwack, Y. B., Nomura, K., and He, S. Y. 2004. A family of conserved bacterial effectors inhibits salicylic acid-mediated basal immunity and promotes disease necrosis in plants. Proc. Natl. Acad. Sci. U.S.A. 101:9927-9932.
12. Deng, W. L., Preston, G., Collmer, A., Chang, C. J., and Huang, H. C. 1998. Characterization of the hrpC and hrpRS operons of Pseudomonas syringae pathovars syringae, tomato, and glycinea and analysis of the ability of hrpF, hrpG, hrcC, hrpT, and hrpV mutants to elicit the hypersensitive response and disease in plants. J. Bacteriol. 180:4523-4531.
13. Desaki, Y., Miya, A., Venkatesh, B., Tsuyumu, S., Yamane, H., Kaku, H., Minami, E., and Shibuya, N. 2006. Bacterial lipopolysaccharides induce defense responses associated with programmed cell death in rice cells. Plant Cell Physiol. 47:1530-1540.
14. Djordjevic, D., Wiedmann, M., and McLandsborough, L. A. 2002. Microtiter plate assay for assessment of Listeria monocytogenes biofilm formation. Appl. Environ. Microbiol. 68:2950-2958.
15. Dow, J. M., Newman, M. A., and von Roepenack, E. 2000. The induction and modulation of plant defense responses by bacterial liposaccharides. Annu. Rev. Phytopathol. 38:241-261.
16. Dubray, G., and Bezard, G. 1982. A highly sensitive periodic acid-silver stain for 1,2-diol groups of glycoproteins and polysaccharides in polyacrylamide gels. Anal. Biochem. 119:325-329.
17. Duggleby, R. G., Peng, H. L., and Chang, H. Y. 1996. An improved assay for UDP glucose pyrophosphorylase and other enzymes that have nucleotide products. Experientia 52:568-572.
18. Finlay, B. B., and McFadden, G. 2006. Anti-immunology: Evasion of the host immune system by bacterial and viral pathogens. Cell 124:767-782.
19. Goldman, R. C., and Leive, L. 1987. Electrophoretic separation of liposaccharide monomers differing in polysaccharide length. Methods Enzymol. 138:267-275.
20. Goodman, R. M., and Novacky, A. J. 1994. The hypersensitive reaction in plants to pathogens. The American Phytopathological Society, St. Paul, MN, U.S.A.
21. Hauck, P., Thilmony, R., and He, S. Y. 2003. A Pseudomonas syringae type III effector suppresses cell wall-based extracellular defense in susceptible Arabidopsis plants. Proc. Natl. Acad. Sci. U.S.A. 100:8577-8582.
22. He, P., Shan, L., and Sheen, J. 2007. Elicitation and suppression of microbeassociated molecular pattern-triggered immunity in plant-microbe interactions. Cell. Microbiol. 9:1385-1396.
23. He, S. Y., Huang, H. C., and Collmer, A. 1993. Pseudomonas syringae pv. syringae harpinPss: A protein that is secreted via the Hrp pathway and elicits the hypersensitive response in plants. Cell 73:1255-1266.
24. Huang, H. C., Schuurink, R., Denny, T. P., Atkinson, M. M., Baker, C. J., Yucel, I., Hutcheson, S. W., and Collmer, A. 1988. Molecular cloning of a Pseudomonas syringae pv. syringae gene cluster that enables Pseudomonas fluorescens to elicit the hypersensitive response in tobacco plants. J. Bacteriol. 170:4748-4756.
25. Huang, H. C., Lin, R. H., Chang, C. J., Collmer, A., and Deng, W. L. 1995. The complete hrp gene cluster of Pseudomonas syringae pv. syringae 61 includes two blocks of genes required for harpinPss secretion that are arranged colinearly with Yersinia ysc homologs. Mol. Plant-Microbe Interact. 8:733-746.
26. Huynh, T. V., Dahlbeck, D., and Staskawicz, B. J. 1989. Bacterial blight of soybean: Regulation of a pathogen gene determining host cultivar specificity. Science 245:1374-1377.
27. Jayaswal, R. K., Bressan, R. A., and Handa, A. K. 1985. Effects of a mutation that eliminates UDP glucose-pyrophosphorylase on the pathogenicity of Erwinia carotovora subsp. carotovora. J. Bacteriol. 164:473-476.
28. Jones, J. D., and Dangl, J. L. 2006. The plant immune system. Nature 444:323-329.
29. Keen, N. T., Tamaki, S., Kobayashi, D., and Trollinger, D. 1988. Improved broad-host-range plasmids for DNA cloning in gram-negative bacteria. Gene 70:191-197.
30. Klement, Z., Bozso, Z., Ott, P. G., Kecskes, M. L., and Rudolph, K. 1999. Symptomless resistant response instead of the hypersensitive reaction in tobacco leaves after infiltration of heterologous pathovars of Pseudomonas syringae. J. Phytopathol. 147:467-475.
31. Klement, Z., Bozso, Z., Kecskes, M. L., Besenyei, E., Arnold, C., and Ott, P. G. 2003. Local early induced resistance of plants as the first line of defence against bacteria. Pest Manage. Sci. 59:465-474.
32. Komeda, Y., Icho, T., and Iino, T. 1977. Effects of galU mutation on flagellar formation in Escherichia coli. J. Bacteriol. 129:908-915.
33. Koplow, J., and Goldfine, H. 1974. Alteration in the outer membrane of the cell envelope of heptose-deficient mutants of Escherichia coli. J. Bacteriol. 117:527-543.
34. Kovach, M. E., Elzer, P. H., Hill, D. S., Robertson, G. T., Farris, M. A., Roop II, R. M., and Peterson, K. M. 1995. Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene 166:175-176.
35. Leeman, M., van Pelt, J. A., den Ouden, F. M., Heinsbroek, M., Bakker, P. A. H. M., and Schippers, B. 1995. Induction of systemic resistance against Fusarium wilt of radish by lipopolysaccharides of Pseudomonas fluorescens. Phytopathology 85:1021-1027.
36. Miller, S. I., Ernst, R. K., and Bader, M. W. 2005. LPS, TLR4 and infectious disease diversity. Nat. Rev. Microbiol. 3:36-46.
37. Mishina, T. E., and Zeier, J. 2007. Pathogen-associated molecular pattern recognition rather than development of tissue necrosis contributes to bacterial induction of systemic acquired resistance in Arabidopsis. Plant J. 50:500-513.
38. Mudgett, M. B. 2005. New insights to the function of phytopathogenic bacterial Type III effectors in plants. Annu. Rev. Plant Biol. 56:509-531.
39. Nesper, J., Lauriano, C. M., Klose, K. E., Kapfhammer, D., Kraiss, A., and Reidl, J. 2001. Characterization of Vibrio cholerae O1 El for galU and galE mutants: Influence on lipopolysaccharide structure, colonization, and biofilm formation. Infect. Immun. 69:435-445.
40. Newman, M. A., Daniels, M. J., and Dow, J. M. 1997. The activity of lipid A and core components of bacterial lipopolysaccharides in the prevention of the hypersensitive response in pepper. Mol. Plant-Microbe Interact. 10:926-928.
41. Newman, M. A., Dow, J. M., and Daniels, M. J. 2001. Bacterial liposaccharides and plant-pathogen interactions. Eur. J. Plant Pathol. 107:95-102.
42. Newman, M. A., von Roepenack-Lahaye, E., Parr, A., Daniels, M. J., and Dow, J. M. 2002. Prior exposure to lipopolysaccharide potentiates expression of plant defenses in response to bacteria. Plant J. 29:487-495.
43. Ott, P. G., Varga, G. J., Szatmari, A., Bozso, Z., Klement, E., Medzihradszky, K. F., Besenyei, E., Czelleng, A., and Klement, Z. 2006. Novel extracellular chitinases rapidly and specifically induced by general bacterial elicitors and suppressed by virulent bacteria as a marker of early basal resistance in tobacco. Mol. Plant-Microbe Interact. 19:161-172.
44. Priebe, G. P., Dean, C. R., Zaidi, T., Meluleni, G. J., Coleman, F. T., Coutinho, Y. S., Noto, M. J., Urban, T. A., Pier, G. B., and Goldberg, J. B. 2004. The galU gene of Pseudomonas aeruginosa is required for corneal infection and efficient systemic spread following pneumonia but not for infection confined to the lung. Infect. Immun. 72:4224-4232.
45. Reitz, M., Rudolph, K., Schroder, I., Hoffmann-Hergarten, S., Hallmann, J., and Sikora, R. A. 2000. Lipopolysaccharides of Rhizobium etli strain G12 act in potato roots as an inducing agent of systemic resistance to infection by the cyst nematode Globodera pallida. Appl. Environ. Microbiol. 66:3515-3518.
46. Sambrook, J., Fritsch, E. F., and Maniatis, T. 1989. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, U.S.A.
47. Sandlin, R. C., Lampel, K. A., Keasler, S. P., Goldberg, M. B., Stolzer, A. L., and Maurelli, A. T. 1995. Avirulence of rough mutants of Shigella flexneri: Requirement of O antigen for correct unipolar localization of IcsA in the bacterial outer membrane. Infect. Immun. 63:229-237.
48. Schechter, L. M., Roberts, K. A., Jamir, Y., Alfano, J. R., and Collmer, A. 2004. Pseudomonas syringae type III secretion system targeting signals and novel effectors studied with a Cya translocation reporter. J. Bacteriol. 186:543-555.
49. Schulman, H., and Kennedy, E. P. 1977. Identification of UDP-glucose as intermediate in the biosynthesis of the membrane-derived oligosaccharides of Escherichia coli. J. Biol. Chem. 252:6299-6303.
50. Schwessinger, B., and Zipfel, C. 2008. News from the frontline: Recent insights into PAMP-triggered immunity in plants. Curr. Opin. Plant Biol. 11:389-395.
51. Silipo, A., Molinaro, A., Sturiale, L., Dow, J. M., Erbs, G., Lanzetta, R., Newman, M. A., and Parrilli, M. 2005. The elicitation of plant innate immunity by lipooligosaccharide of Xanthomonas campestris. J. Biol. Chem. 280:33660-33668.
52. Taguchi, F., Shimizu, R., Inagaki, Y., Toyoda, K., Shiraishi, T., and Ichinose, Y. 2003. Post-translational modification of flagellin determines the specificity of HR induction. Plant Cell Physiol. 44:342-349.
53. Taguchi, F., Shibata, S., Suzuki, T., Ogawa, Y., Aizawa, S., Takeuchi, K., and Ichinose, Y. 2008. Effects of glycosylation on swimming ability and flagellar polymorphic transformation in Pseudomonas syringae pv. tabaci 6605. J. Bacteriol. 190:764-768.
54. Underwood, W., Zhang, S., and He, S. Y. 2007. The Pseudomonas syringae type III effector tyrosine phosphatase HopAO1 suppresses innate immunity in Arabidopsis thaliana. Plant J. 52:658-672.
55. Van Wees, S. C., Pieterse, C. M., Trijssenaar, A., Van't Westende, Y. A., Hartog, F., and Van Loon, L. C. 1997. Differential induction of systemic resistance in Arabidopsis by biocontrol bacteria. Mol. Plant-Microbe Interact. 10:716-724.
56. Wandersman, C., and Letoffe, S. 1993. Involvement of lipopolysaccharide in the secretion of Escherichia coli -haemolysin and Erwinia chrysanthemi proteases. Mol. Microbiol. 7:141-150.
57. Wei, C. F., Deng, W. L., and Huang, H. C. 2005. A chaperone-like HrpG protein acts as a suppressor of HrpV in regulation of the Pseudomonas syringae pv. syringae type III secretion system. Mol. Microbiol. 57:520-536.
58. West, N. P., Sansonetti, P., Mounier, J., Exley, R. M., Parsot, C., Guadagnini, S., Prevost, M. C., Prochnicka-Chalufour, A., Delepierre, M., Tanguy, M., and Tang, C. M. 2005. Optimization of virulence functions through glucosylation of Shigella LPS. Science 307:1313-1317.
59. Zeidler, D., Zahringer, U., Gerber, I., Dubery, I., Hartung, T., Bors, W., Hutzler, P., and Durner, J. 2004. Innate immunity in Arabidopsis thaliana: Lipopolysaccharides activate nitric oxide synthase (NOS) and induce defense genes. Proc. Natl. Acad. Sci. U.S.A. 101:15811-15816.