Original Article
Over view of Septoria Diseases on Different Crops and its Management
Year: 2020 | Month: September | Volume 13 | Issue 3
1.Arraiano, L.S. and Brown, J.K.M. 2017. Sources of resistance and susceptibility to Septoria tritici blotch of wheat. Mol. Plant Pathol., 18: 276–292.
View at Google Scholar2.Benedict, W.G. 1971. Differential effect of light intensity on the infection of wheat by Septoria tritici Desm. under controlled environmental conditions. Physiological Plant Pathology, 1: 55-66.
View at Google Scholar3.Blum, L.E.B. and Lin, M.T. 1991. Potencial de Trichoderma e Pseudomonas fluorescentes para o controle do tombamento de mudas causado por Cylindrocladium spp. Fitopatologia Brasileira, Brasília, 16(1): 71-74.
View at Google Scholar4.Caldwell, R.M. and Narvaes, I. 1960. Losses to winter wheat from infection by Septoria tritici. Phytopathology, 50: 630.
View at Google Scholar5.Cooke, B.M. and Jones, D.G. 1970. The effect of near-ultraviolet irradiation and agar medium on the sporulation of Septoria nodorum and S. tritici. Transactions of the British Mycological Society, 54: 221-226.
View at Google Scholar6.Chakraborty, S. andNewton, A.C. 2011. Climate change, plant diseases and food security: an overview. Plant Pathol. 60: 2–14.
View at Google Scholar7.Cook, R.J. and Baker, K.F. 1983. The nature and practice of biological control of plant pathogens. St Paul: APS, pp. 539.
View at Google Scholar8.Dean, R., Van-Kan, J.A.L., Pretorius, Z.A., Hammond-Kosack, K.E., Di Pietro, A., Spanu, P.D., Rudd, J.J., Dickman, M., Kahmann, R. and Ellis, J. et al. 2012. The top 10 fungal pathogens in molecular plant pathology. Mol. Plant Pathol., 13: 414–430.
View at Google Scholar9.Djerbi, M., Kerlan, C. and Bompeix, G. 1974. Observations sur la morphogen~se et la cytology des fructifications du Septoria tritici Rob. et Desm. Annales de l’Institut National de la Recherche Agronomique de Tunisie, 47(3): 56.
View at Google Scholar10.Estep, L.K., Torriani, S.F.F. and Zala, M. et al. 2015. Emergence and early evolution of fungicide resistance in North American populations of Zymoseptoria tritici. Plant Pathology, 64(4): 961–971.
View at Google Scholar11.Eyal, Z. 1999. The Septoria/Stagonospora blotch diseases of wheat: past, present, and future. In: M. van Ginkel, A. McNabb and J. Krupinsky (eds): Septoria and Stagonospora diseases of cereals: a compilation of global research. CIMMYT, Mexico, pp. 177–182.
View at Google Scholar12.Fisher, M.C., Henk, D.A., Briggs, C.J., Brownstein, J.S., Madoff, L.C., McCraw, S.L. and Gurr, S.J. 2012. Emerging fungal threats to animal, plant and ecosystem health. Nature. 484: 186–194.
View at Google Scholar13.Fisher, N.L., Burgess, L.W., Toussoun, T.A. and Nelson, R.E. 1982. Carnation leaves as a substrate and for preserving cultures of Fusarium species. Phytopathology, 72: 151-153.
View at Google Scholar14.Haghdel, M. and Banihashemi, Z. 2005. Survival and host range of Mycosphaerella graminicola the causal agent of Septoria leaf blotch of wheat. Iranian Journal of Plant Pathology, 41: 613–630.
View at Google Scholar15.Hayes, L.E., Sackett, K.E., Anderson, N.P., Flowers, M.D. and Mundt, C.C. 2016. Evidence of selection for fungicide resistance in Zymoseptoria tritici populations on wheat in western Oregon. Plant Disease, 100(2): 483–489.
View at Google Scholar16.Hilu, H.M. and Bever, W.M. 1957. Inoculation, oversummering and suscept-pathogen relationship of Septoria tritici on Triticum species. Phytopathology, 47: 474–480.
View at Google Scholar17.Holliday, P. 1989. A Dictionary of Plant Pathology. Cambridge University Press, Cambridge, UK, pp. 560.
View at Google Scholar18.Kovalenko, S.N. 1976. The role of the dates of showing of winter wheat in the reduction of the development of Septoria leaf spot under the conditions of the Forest-steppe in the USSR. Nauch Trudy USKA, 161: 123-125.
View at Google Scholar19.Lee, N.P. and Jones, D.G. 1974. Rapid method for spore production in three Septoria species. Transactions of the British Mycological Society, 62: 208-211.
View at Google Scholar20.Lee, W.S., Rudd, J.J., Hammond-Kosack, K.E. and Kanyuka, K. 2014. Mycosphaerella graminicola LysM effector-mediated stealth pathogenesis subverts recognition through both CERK1 and CEBiP homologues in wheat. Mol. Plant Microbe Interact., 27: 236–243.
View at Google Scholar21.McDonald, B.A. and Mundt, C.C. 2016. How knowledge of pathogen population biology informs management of Septoria tritici blotch. Phytopathology, 106(9): 948–955.
View at Google Scholar22.Ors, M., Randoux, B., Siah, A., Couleaud, G., Maumené, C., Sahmer, K., Reignault, P., Halama, P. and Selim, S.A. 2019. Plant nutrient-and microbial protein-based resistance inducer elicits wheat cultivar-dependent resistance against Zymoseptoria tritici. Phytopathology, 109: 2033–2045.
View at Google Scholar23.Pierobom, C.R. 1983. Studies on pycnidial and ascocarpic fungi which cause leaf spots in wheat in Washington. Ph.D. Thesis, Washington State University, Pullman, Washington.
View at Google Scholar24.Priest, M.J. 2006. Fungi of Australia: Septoria. ABRS, Canberra, CSIRO Publishing, Melbourne, Australia, pp. 268.
View at Google Scholar25.Rawat, S., Ali, S., Mittra, B.. and Grover, A. 2017. Expression analysis of chitinase upon challenge inoculation to Alternaria wounding and defense inducers in Brassica juncea. Biotechnol. Rep., 13: 72–79.
View at Google Scholar26.Rudd, J.J., Kanyuka, K.. and Hassani-Pak, K et al. 2015. Transcriptome and metabolite profiling of the infection cycle of Zymoseptoria tritici on wheat reveals a biphasic interaction with plant immunity involving differential pathogen chromosomal contributions and a variation on the hemibiotrophic lifestyle definition. Plant physiology, 167: 1158-1185.
View at Google Scholar27.Savary, S. , Willocquet, L., Pethybridge, S.J., Esker, P. and McRoberts, N. and Nelson, A. 2019. The global burden of pathogens and pests on major food crops. Nature Ecology & Evolution, 3(3): 430–439.
View at Google Scholar28.Shaw, M.W. and Royle, D.J. 1987. Spatial distributions of Septoria nodorum and S. tritici within crops of winter wheat. Plant Pathology, 36: 84-94.
View at Google Scholar29.Shen, Q., Liu, L., Wang, L. and Wang, Q. 2018. Indole primes plant defense against necrotrophic fungal pathogen infection. PLoS ONE, 13(11): e0207607.
View at Google Scholar30.Shirin, S., Mohammad, R., Heshmatolah, A., Rasoul, Z. and Hassan-Reza, E. 2009. Studies on the host range of Septoria species on cereals and some wild grasses in Iran. Phytopathol. Mediterr., 48: 422-429.
View at Google Scholar31.Sprague, R. 1950. Some leaf spot fungi on western Gramineae. Mycologia, 42: 758–777.
View at Google Scholar32.Tateda, C., Zhang, Z., Shrestha, J., Jelenska, J., Chinchilla, D. and Greenberg, J.T. 2014. Salicylic acid regulates Arabidopsis microbial pattern receptor kinase levels and signaling. Plant Cell, 26: 4171–4187.
View at Google Scholar33.Tokeshi, H. and Carvalho, P.C.T. 1980. doenças do tomateiro – Lycopersicum esculentum mill. In: galli, f. Manual de fitopatologia - doenças das plantas cultivadas. São paulo: agronômica ceres, 2(35): 511-532.
View at Google Scholar34.Torriani, S.F.F., Melichar, J.P.E., Mills, C., Pain, N., Sierotzki, H. and Courbot, M. 2015. Zymoseptoria tritici: a major threat to wheat production, integrated approaches to control. Fungal Genetics and Biology, 79: 8–12.
View at Google Scholar35.Valeria, S., Chiara, P., Valentina, F., Marzia, B., Slaven, Z., Fabrizio, Q., Mauro, F., Marco, Z., Babak, M., Massimo, R. and Angela L. 2020. Tramesan elicits durum wheat defense against the Septoria disease complex. Biomolecules, 10: 608.
View at Google Scholar37.Yates, S., Mikaberidze, A. and Krattinger, S.G. et al. 2019. Precision Phenotyping Reveals Novel Loci for Quantitative Resistance to Septoria tritici Blotch. Plant phenomics, 1: 1-11.
View at Google Scholar38.Zelikovitch, N. and Eyal, Z. 1989. Maintenance of virulence of Septoria tritici cultures. Mycological Research, 92: 361-364.
View at Google Scholar39.Zhan, J., Pettway, R.E. and McDonald, B.A. 2003. The global genetic structure of the wheat pathogen Mycosphaerella graminicola is characterized by high nuclear diversity, low mitochondrial diversity, regular recombination, and gene flow. Fungal Genetics and Biology, 38(3): 286–297.
View at Google Scholar