Volatiles emitted by herbivore-attacked plants (senders) can enhance defenses in neighboring plants (receivers), however, the temporal dynamics of this phenomenon remain poorly studied. Using a custom-built, high-throughput proton transfer reaction time-of-flight mass spectrometry (PTR-ToF-MS) system, we explored temporal patterns of volatile transfer and responses between herbivore-attacked and undamaged maize plants. We found that continuous exposure to natural blends of herbivore-induced volatiles results in clocked temporal response patterns in neighboring plants, characterized by an induced terpene burst at the onset of the second day of exposure. This delayed burst is not explained by terpene accumulation during the night, but coincides with delayed jasmonate accumulation in receiver plants. The delayed burst occurs independent of day:night light transitions and cannot be fully explained by sender volatile dynamics. Instead, it is the result of a stress memory from volatile exposure during the first day and secondary exposure to bioactive volatiles on the second day. Our study reveals that prolonged exposure to natural blends of stress-induced volatiles results in a response that integrates priming and direct induction into a distinct and predictable temporal response pattern. This provides an answer to the long-standing question of whether stress volatiles predominantly induce or prime plant defenses in neighboring plants, by revealing that they can do both in sequence.
Keywords: defense priming; ecology; herbivory; plant biology; plant defense; plant-plant interactions; spodoptera exigua; volatile organic compounds; zea mays.
Most plants are anchored to the soil by roots and need to be able to defend themselves from insects and other animal pests while remaining stationary. One way plants achieve this is to emit chemicals known as herbivore-induced plant volatiles (HIPVs) into the air when they are under attack to attract other animals that are natural enemies of the pest. Certain HIPVs also prime other nearby plants (known as ‘receivers’) to be ready for an attack, or even pre-emptively activate defense responses in the plant before they encounter the pest. However, it remains unclear how the temporal patterns of HIPVs emitted from attacked plants affect how receiver plants respond to these chemicals, and how day-to-night light fluctuations impact this transfer of chemical information. To investigate this question, Waterman et al. exposed maize plants to a common pest caterpillar called Spodoptera exigua. Individual infested maize plants (referred to as ‘senders’) were placed in transparent glass chambers that were linked by a narrow tube to a second glass chamber containing a receiver plant that had not encountered caterpillars. The team used a mass spectrometry approach to measure the HIPVs emitted by the sender plants and the responses of the receivers in real-time. The experiments found that within the first few hours of exposure to HIPVs, receiver plants had a small burst of defense activity that was followed by a far stronger burst several hours later. The second burst coincided with the accumulation of plant hormones called jasmonates in the receiver plants, and was not controlled by fluctuations in light levels. This suggests that HIPVs first prime and then subsequently induce defense responses in other plants in a manner that is independent of the patterns of day and night. In the future, these findings may be used to aid in the diagnosis and monitoring of pest outbreaks in crop fields. They will also help us to better understand how plants communicate and the impact of this communication on their environment.
© 2023, Waterman et al.