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Histopathology of Seed-Borne Infections - Applied Research Center ...

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Location <strong>of</strong> Fungal Hyphae in <strong>Seed</strong>s 1375.5.4.1.5 CercosporaCercospora species cause serious diseases <strong>of</strong> Arachis hypogaea, Glycine max, andBeta vulgaris. Cercospora kekuchii and C. sojina cause purple seed stain and seeddiscoloration <strong>of</strong> soybean, respectively. Ilyas et al. (1975) found hyphae <strong>of</strong> C. kekuchiiconfined to the seed coat, but Singh and Sinclair (1985, 1986) observed theiroccurrence in the seed coat, endosperm, and embryo. Singh and Sinclair (1985),using symptomatic seeds with gray to brown discoloration <strong>of</strong> the seed coat as wellas cotyledons (collected from uninoculated and artificially inoculated plants byC. sojina), found that the pathogen colonized the seed coat tissues (Figure 5.16A),the space between the seed coat and embryo, and, rarely, the hypocotyl-radicle region<strong>of</strong> the embryo. Abundant hyphae occurred in the hilar region including tracheid bar(Figure 5.16B).Rastogi, Singh, and Singh (1998c) found hyphae <strong>of</strong> C. traversiana in the seedcoat and tissues <strong>of</strong> the hilar region in moderately infected seeds <strong>of</strong> Trigonella foenumgraecum.Abundant hyphae occurred in the seed coat, endosperm, and embryo inseverely infected seeds. Singh (1991) has reported the presence <strong>of</strong> conidia <strong>of</strong>C. personata in the shells <strong>of</strong> groundnut, but there is no histopathological evidencefor this.5.5.4.1.6 BotrytisBotrytis anthophila, which causes anther mold <strong>of</strong> Trifolium pratense (red clover),reduces pollen fertility and also seed formation. Bondarzew (1914) and Silow (1933)reported systemic infection <strong>of</strong> plants. The infection originated from intraseminalmycelium, particularly present in the hourglass cells <strong>of</strong> the seed coat. Using seedsincubated on agar for 3 to 5 days, Bennum (1972) observed predominantly intercellularand rarely intracellular mycelium in the seed coat and hilar region — remnants<strong>of</strong> funiculus, tracheid bar, and aerenchyma (stellate parenchyma) — but not in theembryo.Botrytis fabae occurs in the seed coat, cotyledons, and embryonal axis in infectedseeds <strong>of</strong> Vicia faba. Hyphae are present in the seed coat <strong>of</strong> all the infected seeds,but these occur in 40% <strong>of</strong> cotyledons and 20% <strong>of</strong> embryonic axes (Harrison, 1978).Van der Spek (1965) has reported Botrytis cinerea in the cells <strong>of</strong> seed coat in flax.5.5.4.1.7 PyriculariaPyricularia oryzae causes the most destructive and widely distributed blast diseasein rice. Chung and Lee (1983) have reported infection <strong>of</strong> P. oryzae within the tissues<strong>of</strong> the glumes, rachilla, pedicel, palea, lemma, and pericarp. In heavily infectedseeds, the mycelium penetrates the aleurone layer and peripheral layers <strong>of</strong> theendosperm. The affected layers <strong>of</strong> endosperm turn dark brown. The embryos arefree <strong>of</strong> infection. Earlier, Suzuki (1930, 1934) had reported that seeds from earsartificially inoculated before, during, and after the flowering period, carried thefungal hyphae in the endosperm and embryo.The seeds <strong>of</strong> Eleusine coracona infected by Pyricularia grisea are asymptomaticand symptomatic (discolored). The discolored seeds exhibited two to three timeshigher infection than the asymptomatic seeds. Pericarp <strong>of</strong> all the infected seeds had

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