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Active Oxygen Species in Plant Defense against Pathogens
Open accessAbstract
Plant disease resistance to pathogens such as fungi, bacteria, and viruses often depends on whether the plant is able to recognize the pathogen early in the infection process. The recognition event leads to a rapid tissue necrosis at the site of infection, which is called the HR. The HR deprives the pathogen of nutrients and/or releases toxic molecules, thereby confining pathogen growth to a small region of the plant. This response provides resistance to the great majority of potential pathogens (nonhost or species resistance). For a given plant species, a much more limited number of true pathogens exhibit the ability to evade the host recognition system and grow extensively within the plant without evoking host necrosis at a11 or only after considerable delay. In this case, the plant exhibits susceptibility and the extensive growth of the successful pathogen can cause varying degrees of damage. However, certain races within pathogenic bacteria1 or funga1 species are recognized by certain cultivars or genotypes of the host plant species and the HR is triggered. These observations indicate that there is an ongqing evolution of the host plant's ability to recognize pathogen races that were previously unrecognized while the pathogen evolves to avoid recognition by a previously resistant host. Recognition of pathogens triggers a large range of inducible defense mechanisms that are believed to contribute to overall resistance in the plant. The mechanisms induced at the site of infection and associated with the HR include synthesis of antimicrobial compounds called phytoalexins, synthesis of hydrolytic enzymes that attack fungi and bacteria, and alterations in the synthesis of cell-wall structural proteins (for
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Citations
Cited by
H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response
Levine, A., Tenhaken, R., Dixon, R., & Lamb, C. (1994) · Cell · doi:10.1016/0092-8674(94)90544-4 · Cited by 2,766
Molecular Genetics of Plant Disease Resistance
Staskawicz, B. J., Ausubel, F. M., Baker, B. J., Ellis, J. G., & Jones, J. D. G. (1995) · Science · doi:10.1126/science.7732374 · Cited by 914
Initiation of Runaway Cell Death in an Arabidopsis Mutant by Extracellular Superoxide
Jabs, T., Dietrich, R. A., & Dangl, J. L. (1996) · Science · doi:10.1126/science.273.5283.1853 · Cited by 874
Death Don't Have No Mercy: Cell Death Programs in Plant-Microbe Interactions.
Dangl, J. L., Dietrich, R. A., & Richberg, M. H. (1996) · The Plant Cell · doi:10.1105/tpc.8.10.1793 · Cited by 873
Schützendübel, A., Schwanz, P., Teichmann, T., Gross, K., Langenfeld-Heyser, R., Godbold, D. L., & Polle, A. (2001) · Plant Physiology · doi:10.1104/pp.010318 · Cited by 746
Metadata
- Authors
- Mehdy, M. C.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 1994-06-01
- Volume
- 105
- Issue
- 2
- Pages
- 467-472
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2156371591
- Cited by
- 843
- References
- 0
- FWCI
- 75.12
- Type
- journal article
- Language
- en
- Open access
- green
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