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. 2021 Oct 11;10(10):1025. doi: 10.3390/biology10101025

Table 3.

Pathogenicity of 15 seed-borne fungus species isolated *.

Fungus Pre-Emergence
Damping Off ** (%)
Post-Emergence
Damping Off ** (%)
Survival ** (%)
Control (fungus-free) 1.0 e 0.0 d 99.0 a
Alternaria alternata 2.5 e 0.0 d 97.5 ab
Bipolaris austrostipae 7.5 c–e 7.5 a–d 75.0 c–f
B. cynodontis 25.0 a 12.5 ab 62.5 f
B. sorokiniana 12.5 b–e 2.5 cd 85.0 a–e
B. tetramera 17.5 a–c 5.0 b–d 77.5 c–f
Cladosporium anthropophilum 15.0 a–d 2.5 cd 82.5 b–e
Curvularia mebaldsii 15.0 a–d 0.0 d 85.0 a–e
Exerohilum rostratum 15.0 a–d 0.0 d 85.0 a–e
Fusarium chlamydosporum 17.5 a–c 10.0 a–c 72.5 d–f
F. equiseti 20.0 ab 10.0 a–c 70.0 ef
F. fujikuroi 12.5 b–e 5.0 b–d 82.5 b–e
F. oxysporum 2.5 e 0.0 d 97.5 ab
F. proliferatum 22.5 ab 15.0 a 65.0 f
F. verticillioides 5.0 de 5.0 b–d 90.0 a–c
Stemphylium globuliferum 7.5 c–e 5.0 b–d 87.5 a–d

* The seed-borne fungi isolated were tested for their pathogenicity using a soil infestation technique with fungus growing on sterilized sorghum–sand medium (1:1) at 10% moisture for 15 d at 26 ± 2 °C. Pots (25 cm-diameter) filled with sterilized soil were individually infested with the fungal inocula at 0.3%, mixed thoroughly, and watered with tap water and kept moistened for one week before planting. In each pot, 10 surface-sterilized wheat grains were sown. For each fungus, 10 pots (replicates) were used. All pots were arranged in a completely randomized way and kept for two months in a greenhouse. The pots were observed daily for grain germination, and the disease incidence was recorded. Each value is the mean of 10 replicates (pots), values within a column followed by the same letter(s) are not significantly different according to Duncan’s multiple range test (p ≤ 0.05). ** Pre-emergence damping off = seed/seedling death before emergence; Post-emergence damping off = seedling death after emergence; survival = living plants two months after planting.