biotic stress (Sclerotium delphinii) and hormone (MeJA) treatment transcriptome data

Sclerotium delphinii, named P1, was grown on the PDA medium for 6 days. Five 5 mm diameter agar blocks containing P1 mycelia were placed in 200 mL of PDB medium for 6 days. After diluting to half of the original concentration, it was used for the subsequent plant inoculation assay. The 4 months old D. catenatum clonal cultivar plantlets with the same growth state were selected and divided into ten groups, including CK, P1, MeJA (100 uM), and MeJA + P1 (MP1). After that, they were washed with sterile water and put into a sterile bottle filled with 0.25% ethanol solution (the solvent) or 100 uM MeJA. Among them, P1 and MP1 groups were evenly sprayed with 2 mL of mycelia suspensions (Mock with 0.25% ethanol solution). The leaves samples of D. catenatum plantlets treated with MeJA and P1 were collected for transcriptome sequencing at 1, 3, 12, and 24 hpi.