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. 2018 Apr 10;69(12):3141–3155. doi: 10.1093/jxb/ery138

Fig. 2.

Fig. 2.

Cultures of S. sclerotiorum on PDA plates with leaf extracts from OsPGIP2 transgenic and wild-type lines. (A) Images of S. sclerotiorum inoculated on PDA plates treated with either leaf extracts (50%) or a mock solution at 36 h post-infection (hpi). Scale bars are 4 cm. (B) Statistical analysis of the diffusion diameter of S. sclerotiorum on PDA plates treated with either leaf extracts (50%) or a mock solution at 36 hpi. Data are means from three biological replicates (±SD) (n=3). Significant differences were determined by one-way ANOVA: ***P<0.001, **P<0.01, *P<0.05. 7-5WT and T45WT are wild-type controls. (C) Hyphal growth of S. sclerotiorum on PDA plates treated with either OsPGIP2 transgenic leaf extracts (50%) or a mock solution at 36 hpi. Scale bars are 1 mm.