A blend of volatile organic compounds (VOCs) emitted from plants induced by herbivory enables the priming of defensive
responses in neighboring plants. These effects may provide insights useful for pest control achieved with transgenic-plantemitted
volatiles. We therefore investigated, under both laboratory and greenhouse conditions, the priming of defense
responses in plants (lima bean and corn) by exposing them to transgenic-plant-volatiles (VOCos) including (E)-b-ocimene,
emitted from transgenic tobacco plants (NtOS2) that were constitutively overexpressing (E)-b-ocimene synthase. When lima
bean plants that had previously been placed downwind of NtOS2 in an open-flow tunnel were infested by spider mites,
they were more defensive to spider mites and more attractive to predatory mites, in comparison to the infested plants that
had been placed downwind of wild-type tobacco plants. This was similarly observed when the NtOS2-downwind maize
plants were infested with Mythimna separata larvae, resulting in reduced larval growth and greater attraction of parasitic
wasps (Cotesia kariyai). In a greenhouse experiment, we also found that lima bean plants (VOCos-receiver plants) placed
near NtOS2 were more attractive when damaged by spider mites, in comparison to the infested plants that had been placed
near the wild-type plants. More intriguingly, VOCs emitted from infested VOCos-receiver plants affected their conspecific
neighboring plants to prime indirect defenses in response to herbivory. Altogether, these data suggest that transgenicplant-
emitted volatiles can enhance the ability to prime indirect defenses via both plant-plant and plant-plant-plant
communications.
A blend of volatile organic compounds (VOCs) emitted from plants induced by herbivory enables the priming of defensiveresponses in neighboring plants. These effects may provide insights useful for pest control achieved with transgenic-plantemittedvolatiles. We therefore investigated, under both laboratory and greenhouse conditions, the priming of defenseresponses in plants (lima bean and corn) by exposing them to transgenic-plant-volatiles (VOCos) including (E)-b-ocimene,emitted from transgenic tobacco plants (NtOS2) that were constitutively overexpressing (E)-b-ocimene synthase. When limabean plants that had previously been placed downwind of NtOS2 in an open-flow tunnel were infested by spider mites,they were more defensive to spider mites and more attractive to predatory mites, in comparison to the infested plants thathad been placed downwind of wild-type tobacco plants. This was similarly observed when the NtOS2-downwind maizeplants were infested with Mythimna separata larvae, resulting in reduced larval growth and greater attraction of parasiticwasps (Cotesia kariyai). In a greenhouse experiment, we also found that lima bean plants (VOCos-receiver plants) placednear NtOS2 were more attractive when damaged by spider mites, in comparison to the infested plants that had been placednear the wild-type plants. More intriguingly, VOCs emitted from infested VOCos-receiver plants affected their conspecificneighboring plants to prime indirect defenses in response to herbivory. Altogether, these data suggest that transgenicplant-emitted volatiles can enhance the ability to prime indirect defenses via both plant-plant and plant-plant-plantcommunications.
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