Plant Pathology Seminar Series “Mechanisms of plant defense to fungal pathogens” Lu Liu Unlike animals that are mobile and have a somatic adaptive immune system, plants respond to fungal pathogen infection by innate defenses (Jones and Dangl 2006). The epidermal cell layer of aerial plant parts, often covered in a waxy cuticle, is the first line of defense against invading fungi. Besides that, plants are able to recognize pathogen-derived elicitor molecules that trigger a number of induced defenses in plants since fungal pathogens can degrade the cuticle and penetrate the epidermis. Microbial elicitors constitute a broad array of compounds, including different oligosaccharides, lipids, peptides, and proteins (Montesano et al. 2003). Plants also generate endogenous elicitors due to the damage caused by microbes, which are, therefore, called damage-associated molecular patterns (DAMPs) (Wu et al. 2014). At the same time, plants encode hundreds of receptors to recognize different types of elicitors and activate signaling pathways (Okmen and Doehlemann 2014). Once the immunity system is activated, a series of defense responses occur, including plant cell wall strengthening, secondary metabolite production, reactive oxygen species (ROS) production, defense-related protein synthesis, and hypersensitive reaction (HR) (Howell and Davis 2005; Huckelhoven 2007; Zhang et al. 2012). It has been suggested that effective defense against biotrophic fungi largely relies on programmed cell death (PCD) in the host. In contrast, PCD benefits the development of necrotrophic fungal pathogens (Glazebrook 2005; Qiu et al. 2015; Vargas et al. 2012). Understanding plant defense mechanisms at the molecular level can help us better manipulate plant resistance and develop disease management strategies. 4:10 pm | Monday, November 2 | Johnson Hall 343 Plant Pathology 515, Fall, 2015 References: Dangl, J and Jones, J. 2001. Plant pathogens and integrated defense responses to infection. Nature 411:826 – 833. Glazebrook, J. 2005. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu. Rev. Phytopathol. 43: 205-27. Howel, J., and Davis M. 2005. Plant defense mechanisms against fungal pathogens: polygalacturonase inhibitor proteins. Can. J. Plant Pathol. 27: 5-15. Huckelhoven, R. 2007. Cell wall-associated mechanisms of disease resistance and susceptibility. Annu. Rev. Phytopathol. 45:101-27. Jones, J., and Dangl, J. 2006. The plant immune system. Nature 444:324-329. Montesano, M., Brader, G., and Palva, E. 2003. Pathogen derived elicitors: searching for receptors in plants. Mol. Plant Pathol. 4: 73-79. Okmen, B., and Doehlemann, G. 2014. Inside plant: biotrophic strategies to modulate host immunity and metabolism. Curr. Opin. Plant Biol. 20: 19-25. Qiu, W., Feechan, A., and Dry, I. 2015. Current understanding of grapevine defense mechanisms against the biotrophic fungus (Erysiphe necator), the causal agent of powdery mildew disease. Hortic. Res. 2: 15020. Vargas, W., Martin, J., Rech, G., Rivera, L., Benito, E., Diaz-Minguez, J., Thon, M., and Sukno, S. 2012. Plant defense mechanisms are activated during biotrophic and necrotrophic development of Colletotricum graminicolain maize. Plant Physiol. 158: 1342-1358. Wu, S., Shan, L., and He, P. 2014. Microbial signature-triggered plant defense responses and early signaling mechanisms. Plant Sci. 228: 118-126. Zhang, H., Wang, C., Cheng, Y., Chen, X., Han, Q., Huang, L., Wei, G., and Kang, Z. 2012. Histological and cytological characterization of adult plant resistance to wheat stripe rust. Plant Cell Rep. 31: 2121-2137.
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