You are here

Importance of Reactive Oxygen Species in Plants-Pathogens Interactions

Journal Name:

Publication Year:

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Plant pathogens have developed various independent and well-elaborated mech-anisms of penetrating and accessing plant cell contents. The production of reac-tive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen, the hydroxyperoxyl radical, the superoxide anion, hydrogen per-oxide, the hydroxyl radical and the closely related reactive nitrogen species, nitric oxide. There are profound differences between monocots and dicots as well as in the biology of biotrophic, hemibiotrophic and necrotrophic pathogens. ROS acts synergistically in a signal amplification to drive the hypersensitive reaction (HR) and the establishment of systemic defenses. The role of ROS in successful path-ogenesis, it is important to try to inhibit the cell death machinery selectively and simultaneously to monitor other defense and pathogenesis-related events. With the understanding of the molecular mechanisms underlying the localized activa-tion of the oxidative burst following perception of pathogen avirulence signals and key downstream responses including gene activation, cell death, and long-distance signaling, novel strategies will be developed for engineering enhanced protection against pathogens by manipulation of the oxidative burst and oxidant-mediated signal pathways. In this review, it is assessed the different roles of ROS in host–pathogen interactions with special emphasis on plant pathogens.
11
21

REFERENCES

References: 

Abdollahi H, Ghahremani Z (2011). The role of chloro-plasts in the interaction between Erwinia amylovora and host plants. Acta Horticulturae 896: 215-221.
Aist J R, Brushnell WR (1991). Invasion of plants by powdery mildew fungi, and cellular mechanisms of resistance; in: The fungal spore and disease interac-tion in plants and animals (eds) G T Cole and H C Hoch (New York: Plenum Press) pp 321–345
Albert FG, Benet LW, Anderson AJ (1986). Peroxidase associated with the root surface of Phaseols vulgaris. Canadian Journal of Botany 64: 573–578.
Alfano JR, Bauer DW, Milos TM Collmer A (1996). A. Analysis of the role of the Pseudomonas syringae pv. syringae HrpZ harpin in elicitation of the hyper-sensitive response in tobacco using functionally non-polar hrpZ deletion mutations, truncated HrpZ frag-ments, and hrmA mutations. Molecular Microbiol-ogy 19: 715–728.
Ali R, Ma W, Lemtiri-Chlieh, F, Tsaltas, D, Leng Q, von Bodman S (2007). Death don’t have no mercy and neither does calcium: Arabidopsis Cyclic Nucleotide Gated Channel 2 and innate immunity. The Plant Cell 19: 1081–1095.
Allan AC, Lapidot M, Culver JN, Fluhr R (2001). An early tobacco mosaic virus-induced oxidative burst in tobacco indicates extracellular perception of the virus coat protein. Plant Physiology 126: 97–108
Asada K (1999). The water–water cycle in chloroplasts: scavenging of active oxygens and dissipation of ex-cess photons. Annual Review of Plant Physiology Plant Molecular Biology 50:601–39
Asada K, Takahashi M (1987). “Production and scav-enging of active oxygen in photosynthesis,” in Pho-toinhibition: Topics of Photosynthesis, DJ Kyle, CB Osmond, CJ Arntzen, Eds., pp. 227-287, Elsevier, Amsterdam, 9th edition,
Baker CJ, Orlandi EW (1995). Active oxygen in plant pathogenesis. Annual Review of Phytopathology 33: 299– 321.
Bender CL, Stone HE, Sims JJ, Cooksey DA (1987). Re-duced pathogen fitness of Pseudomonas syringae pv. tomato Tn5 mutants defective in coronatine produc-tion. Physiological and Molecular Plant Pathology 30: 272–283.
Bindschedler L, Dewdney V, Blee J, Stone KA, Asai JM, Plotnikov T, (2006). Peroxidase-dependent apo-plastic oxidative burst in Arabidopsis required for pathogen resistance. The Plant Journal 47: 851–863.
21
KK Bastas / Selcuk J Agr Food Sci, 28(1):11-21
Bolwell GP, Wojtaszek P (1997). Mechanisms for the generation of reactive oxygen species in plant de-fence – a broad perspective. Physiological and Mo-lecular Plant Pathology 51: 347 – 366
Bolwell GP, Bindschedler LV, Blee KA, Butt VS, Da-vies DR, Gardner SL, Gerrish C, Minibayeva F (2002). The apoplastic oxidative burst in elicitor of the hypersensitive response produced by the plant pathogen Erwinia amylovora. Science 257: 85–88.
Bolwell GP, Davies DR, Gerrish C, Auh CK, Murphy TM (1998). Comparative biochemistry of the oxida-tive burst produced by rose and French bean cells re-veals two distinct mechanisms. Plant Physiology 116: 1379–1385.
Borsani O, Valpuesta V, Botella MA (2003). Develop-ing salt tolerance plants in a new century: a molecu-lar biology approach. Plant Cell Tissue Organ Cul-ture 73: 101–115
Bradley D, Kjellbom P, Lamb C (1992). Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: a novel, rapid defense re-sponse. Plant Cell 70: 21–30.
Britto D T, Kronzucker HJ (2001). Can unidirectional influx be measured in higher plants? A mathematical approach using parameters from efflux analysis; New Phytology 150 37–47
Brown I, Trethowan J, Kerry M, Mansfield J, Bolwell GP (1998). Localization of components of the oxida-tive cross-linking of glycoproteins and of callose synthesis in papillae formed duringthe interaction bet ween non-pathogenic strains of Xanthomonas campestris and French bean mesophyll cells. Plant Journal 15 333–343.

Thank you for copying data from http://www.arastirmax.com