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Short Communication

NtSWEET1 promotes tobacco resistance to Fusarium oxysporum-induced root rot disease

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Article: 1970940 | Received 03 Jul 2021, Accepted 17 Aug 2021, Published online: 24 Aug 2021

Figures & data

Figure 1. Fusarium oxysporum infection–mediated gene expression analysis. The base of a N. tabacum seedling was sampled 0, 6, 12, and 24 h after inoculation with F. oxysporum. F. oxysporum infection–mediated NtSUC4 (a), NtSTP12 (b), NtHEX6 (c), NtSWEET1 (d), NtSWEET3b (e), and NtSWEET12 (d) patterns of expression were analyzed using qRT-PCR. The mRNA levels in the samples were normalized against those of Actin mRNA. Data are the means ± SE (n = 3), and the experiments were repeated at least three times. Different letters indicate significant differences between groups (P < 0.05). qRT-PCR, Quantitative real-time reverse transcriptase–PCR; SE, standard error

Figure 1. Fusarium oxysporum infection–mediated gene expression analysis. The base of a N. tabacum seedling was sampled 0, 6, 12, and 24 h after inoculation with F. oxysporum. F. oxysporum infection–mediated NtSUC4 (a), NtSTP12 (b), NtHEX6 (c), NtSWEET1 (d), NtSWEET3b (e), and NtSWEET12 (d) patterns of expression were analyzed using qRT-PCR. The mRNA levels in the samples were normalized against those of Actin mRNA. Data are the means ± SE (n = 3), and the experiments were repeated at least three times. Different letters indicate significant differences between groups (P < 0.05). qRT-PCR, Quantitative real-time reverse transcriptase–PCR; SE, standard error

Figure 2. NtSWEET1 function and its role in defense of tobacco against root rot. (a) Hexose transport activity of NtSWEET1 was analyzed in the EBY4000 yeast strain. NtSWEET1 -transformed cells were grown on YNB media that contained 2% glucose, fructose, galactose, or maltose. Empty (pDRf1) vector and AtSWEET1 were used as the negative and positive controls, respectively. (b) Localization of NtSWEET1-GFP or free GFP was analyzed in tobacco leaves. The left and right channels indicate GFP and light image, respectively. (c) Wild-type (WT) and NtSWEET1 RNAi (#1 and #2) plants were inoculated with F. oxysporum. (d) Disease index of plants shown in (c) was calculated (n > 15). (e) Expression level of NtSWEET1 in the WT and NtSWEET1 RNAi plants (#1 and #2). Different letters indicate significant differences between groups (P < 0.05). DIC, Differential interference contrast; GFP, green fluorescent protein; WT, wild-type; YNB, yeast nitrogen base media

Figure 2. NtSWEET1 function and its role in defense of tobacco against root rot. (a) Hexose transport activity of NtSWEET1 was analyzed in the EBY4000 yeast strain. NtSWEET1 -transformed cells were grown on YNB media that contained 2% glucose, fructose, galactose, or maltose. Empty (pDRf1) vector and AtSWEET1 were used as the negative and positive controls, respectively. (b) Localization of NtSWEET1-GFP or free GFP was analyzed in tobacco leaves. The left and right channels indicate GFP and light image, respectively. (c) Wild-type (WT) and NtSWEET1 RNAi (#1 and #2) plants were inoculated with F. oxysporum. (d) Disease index of plants shown in (c) was calculated (n > 15). (e) Expression level of NtSWEET1 in the WT and NtSWEET1 RNAi plants (#1 and #2). Different letters indicate significant differences between groups (P < 0.05). DIC, Differential interference contrast; GFP, green fluorescent protein; WT, wild-type; YNB, yeast nitrogen base media

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