Skip to main content
. 2016 Jun 1;6:27078. doi: 10.1038/srep27078

Figure 2. Plant phenotyping and molecular analysis of SlRPT4 silenced tomato plants.

Figure 2

(A) phenotype of experimental tomato plants. ToLCNDV tolerant cultivar H-88-78-1 plants were infiltrated with Agrobacterium containing the TRV:SlRPT4 construct (HSlRPT4). Subsequent to SlRPT4 silencing process, ToLCNDV infection was performed. The photographs of the plants were taken at 7, 14, 21 and 28 days post inoculation (dpi). HSlRPT4, SlRPT4 silenced H-88-78-1; HTRV:00, vector infiltrated control plant; HTRV:00+T vector infiltrated control plant infected with ToLCNDV; HSlRPT4+T, SlRPT4 silenced H-88-78-1 infected with ToLCNDV; HT, cultivar H-88-78-1agroinfiltrated with ToLCNDV. Level of viral DNA in HT (ToLCNDV infected cultivar H-88-78-1) and HTRV:SlRPT4+T (SlRPT4 silenced H-88-78-1 infected with ToLCNDV) at different dpi. (B) Southern blot of tomato genomic DNA from all experimental plants were hybridized with ToLCNDV-coat protein gene specific probe. Replicative forms of ToLCNDV genome are designate as open circular (OC), linear (Lin), supercoiled (SC) and single strand (SS). TRV:00 infiltrated H-88-78-1 was taken as a mock control. Ethidium bromide stained DNA from each experiments were shown as equivalent loading. (C) Relative accumulation of viral DNA in the samples HT and HSlRPT4+T at different time points. Data depicts means ± SD of three independent experiments (n = 3); *P < 0.05; **P < 0.01; ***P < 0.001.