and mycelial fragment was applied for non-sporulating fungi. Conidia of fungi were harvested from 14-days old culture. A PDB-based 14-days old colony of non-sporulating fungi, filtered, washed with sterilized water then mixed with sterilized water and blended with medium speed for two minutes. Both are assessed the density by direct count with a haemacytometer under light microscope with 10 x 10 magnification. Both types of suspension were adjusted to 10 4 cfu/mL. Inoculation was done twice, first by seed treatment, second by propagules spraying. Before treatment the seed was treated with hot water at 52?C for 20 minutes to eliminate possible existing fungi on and inside the seeds. Seeds of chili cv