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. 2022 Dec 23;13:929478. doi: 10.3389/fpls.2022.929478

Table 4.

Data from the detached leaf assay on infected citrus (grapefruit) and apple (Red Delicious) leaves measuring the effect of a 0.8-1ml peptide solution at 25 μM concentration.

Treatment DNA RNA
CLas clearance from infected citrus leaves
Water (control) 23.99 ± 0.020 (9.4 × 105 ± 0.051) 26.04 ± 0.020 (7.4 × 105 ± 0.071)
UGK-17 31.44 ± 0.013 (9.2 × 103 ± 0.210) 33.30 ± 0.026 (7.0 × 102 ± 0.310)
UGK-9 23.07 ± 0.009 (10.3 × 105 ± 019) 24.56 ± 0.019 (8.8 × 105 ± 0.053)
UGK-13 28.05 ± 0.012 (5.5 × 104 ± 0.065) 31.12 ± 0.011 (7.7 × 103 ± 0.065)
30P-3 29.08 ± 0.018 (2.3 × 104 ± 0.122) 31.80 ± 0.028 (6.8 × 103 ± 0.190)
Erwinia amylovora clearance from infected apple leaves
Water (control) 28.73 ± 0.590 (5.6 × 104 ± 0.07) 28.91 ± 0.990 (5.4 × 104 ± 0.051)
UGK-17 34.46 ± 0.028 (400 ± 0.31) 34.10 ± 0.560 (700 ± 0.210)
UGK-9 35.66 ± 1.43 (~102) 32.62 ± 0.570 (4.7 × 103 ± 0.019)
UGK-13 35.78 ± 2.98 (~102) 34.44 ± 0.620 (300 ± 0.065)
30P-3 36.50 ± 0.89 (~102) 31.54 ± 0.018 (7.8 × 103 ± 0.122)

The levels of bacteria in the DNA/RNA extracted from the infected leaves were measured using qPCR, which provided the Ct values for the amplicon generated by the CLas- and E. amylovora-specific primers. The colony-forming units (cfu) of the bacterial load were computed using the cfu vs. Ct standard curve (Bao et al., 2020; Salm and Geider, 2004).

CLas, Candidatus Liberibacter asiaticus.