Nematicidal activity of o-hydroxybenzaldehyde from common buckwheat methanol extract on Meloidogyne incognita.

The nematicidal activity of buckwheat (Fagopyrum esculentum Moench) on the root-knot nematode Meloidogyne incognita was tested. Dried plant methanol extract presented higher nematicidal activity than fresh plant extracts with an EC50 = 62.6 ± 26.0 and 40.8 ± 26.1 µg/ml after 48 and 72 hours of immersion, respectively. GC-MS analysis showed the presence of 17 aldehydes, with salicylaldehyde (o-hydroxybenzaldehyde) being the most abundant at 16%. Nematicidal activity of the latter refers to salicylaldehyde and other aldehydes with chemical similarities was then assessed. The most active aldehyde was o-hydroxybenzaldehyde followed by m-hydroxybenzaldehyde, p-hydroxybenzaldehyde and benzeneacetaldehyde with an EC50 of about 11.0 ± 1.0, 31.0 ± 22.0, 75.0 ± 23.0 and 168.1 ± 52.3 µg/ml after 1 day of immersion, respectively. Position 2 of the hydroxyl group in the benzene ring seems to be very important for the nematicidal activity, followed by positions 3 and 4. As a complementary experiment, synergistic activity was observed when we added o-hydroxybenzaldehyde to m-hydroxybenzaldehyde and to p-hydroxybenzaldehyde with an EC50 after 24 hours of immersion of 8.0 ± 2.5 and 6.1 ± 2.3 µg/ml, respectively. Antioxidant activity assessment showed that this latter is inversely proportional to nematicidal activity. Our results showed that F. esculentum and its major compound salicylaldehyde could be integrated into the pest management system.

Potent nematicidal activity of phenolic derivatives on Meloidogyne incognita.

The present study describes the nematicidal activity of ten selected phenolic derivatives using the root knot nematode, Meloidogyne incognita, model. Nematicidal activity was then correlated with the anti-oxidant power. The highest nematicidal activity was recorded for p-nitrophenol followed by m-nitrophenol, o-nitrophenol and p-bromophenol, with an EC50 after 1 day of immersion of about 0.70 ± 0.64, 8.14 ± 5.49, 15.79 ± 10.81 and 25.92 ± 11.37 µg/ml, respectively. The structure-activity relationship indicates that the nitro-group at position 4 on the phenolic ring (p-nitrophenol) is very important for nematicidal activity, followed by that at position 2 (o-nitrophenol) and position 3 (m-nitrophenol). p-Nitrophenol showed the highest nematicidal activity with the corresponding lowest anti-oxidant activity of about 97 ± 20 µg/ml. In conclusion, these findings suggest that phenolic derivatives could be considered as potent nematicidal agents and be integrated in the pest-management system.