Fig. 1From: Fine mapping and identification of two NtTOM2A homeologs responsible for tobacco mosaic virus replication in tobacco (Nicotiana tabacum L.)Phenotypic characterization of two different cultivars that responded to tobacco mosaic virus (TMV) infection. a Plant phenotype of the susceptible cultivar K326 and resistant cultivar JT88 after infection with TMV-U1 and phosphate buffer saline (MOCK), respectively. Scale bar = 2 cm. b Disease index (DI) of the susceptible cultivar K326 and resistant cultivar JT88 investigated at 14 dpi. c TMV CP relative expression levels in apical non-inoculated leaves (AL) of two different cultivars detected by qRT-PCR. The tobacco actin gene used as an internal reference gene. d TMV accumulation levels in the inoculated leaves (IL) and apical non-inoculated leaves (AL). Virus contents detected by Western blot with an anti-TMV coat protein antibody. The target blot was cropped from the full-length original blot. dpi: days post inoculation, MOCK: mock-inoculated with phosphate buffer saline, TMV CP: TMV coat protein, β-ACTIN: anti-plant actin mouse monoclonal antibody. The data (Fig. 1b and 1c) are presented as means ± SDs of three biological replicates. Student t-tests were used to determine the significance of differences between K326 and JT88 (****P < 0.0001)Back to article page