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. 2026 Mar 25;43(1):17–25. doi: 10.5511/plantbiotechnology.25.0922a

Figure 2. Infection of Dianthus plants by wtALSV. (A) Dianthus seedling grown on soil. Yellow arrowheads indicated expanded true leaves in which gold particles were bombarded. Bar=10 mm. (B) wtALSV-infected plants at 30 days after post inoculation. Number of true leaves 2 to 8 were harvested and used for RNA extraction. Bar=20 mm. (C) RT-PCR assay of wtALSV infection to leaves of Dianthus ‘Telstar Picotee’ and ‘Telstar Crimson’. The 2 to 8 indicated the number of true leaves. An arrow indicates DNA products (360 bp). (D) Whole flower, gynoecium and sepal of ‘Telstar Crimson’ plants. Bars=10 mm. (E) RT-PCR assay of wtALSV infection to flower organs of ‘Telstar Crimson’ plants.

Figure 2. Infection of Dianthus plants by wtALSV. (A) Dianthus seedling grown on soil. Yellow arrowheads indicated expanded true leaves in which gold particles were bombarded. Bar=10 mm. (B) wtALSV-infected plants at 30 days after post inoculation. Number of true leaves 2 to 8 were harvested and used for RNA extraction. Bar=20 mm. (C) RT-PCR assay of wtALSV infection to leaves of Dianthus ‘Telstar Picotee’ and ‘Telstar Crimson’. The 2 to 8 indicated the number of true leaves. An arrow indicates DNA products (360 bp). (D) Whole flower, gynoecium and sepal of ‘Telstar Crimson’ plants. Bars=10 mm. (E) RT-PCR assay of wtALSV infection to flower organs of ‘Telstar Crimson’ plants.