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Cofer, T. M.

Publications and source records attributed to Cofer, T. M..

3 recordsLinked to original sources

High-resolution kinetics of herbivore-induced plant volatile transfer reveal tightly clocked responses in neighboring plants

Volatiles emitted by herbivore-attacked plants (senders) can enhance defenses in neighboring plants (receivers), with important consequences for community dynamics. 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.

plant biology↗

The Arabidopsis thaliana carboxylesterase AtCXE12 converts volatile (Z)-3-hexenyl acetate to (Z)-3-hexenol

The green leaf volatiles (Z)-3-hexenal, (Z)-3-hexenol, and (Z)-3-hexenyl acetate are produced by nearly all plants in response to wounding and insect attack, can be transferred between plants, metabolized, and act as defense cues. If and how plant leaves convert exogenous (Z)-3-hexenyl acetate to (Z)-3-hexenol is unknown. We show that Arabidopsis leaves rapidly convert exogenous (Z)-3-hexenyl acetate to (Z)-3-hexenol. Inhibitor and fractionation experiments identified the carboxylesterases AtCXE5 and AtCXE12 as likely contributors to (Z)-3-hexenyl acetate esterase activity in Arabidopsis leaves. Heterologous expression of AtCXE5 and AtCXE12 revealed that both enzymes hydrolyze (Z)-3-hexenyl acetate to (Z)-3-hexenol in vitro, and assays using T-DNA insertion mutant plants showed that AtCXE12 significantly contributes to the conversion of (Z)-3-hexenyl acetate to (Z)-3-hexenol in planta. Lastly, we found that leaves from several other plant species possess (Z)-3-hexenyl acetate esterase activity, as well as homologs of AtCXE5 and AtCXE12 from Arabidopsis. Collectively, our study provides a better understanding of green leaf volatile biosynthesis and conversion dynamics, necessary for unraveling the potential functions of these compounds.

plant biology↗

Immature leaves are the dominant volatile (Z)-3-hexenyl acetate sensing organs of maize

Plants perceive herbivory induced volatiles and respond to them by upregulating their defenses. So far, the organs responsible for volatile perception remain poorly described. Here, we show that responsiveness to the herbivory induced green leaf volatile (Z)-3-hexenyl acetate (HAC) in terms of volatile emission, transcriptional regulation and defense hormone activation is largely constrained to younger maize leaves. Older leaves are much less sensitive to HAC. In a given leaf, responsiveness to HAC is high at immature developmental stages and drops off rapidly during maturation. Responsiveness to the non-volatile elicitor ZmPep3 shows an opposite pattern, demonstrating that hyposmia is not driven by defective canonical defense signaling. Neither stomatal conductance nor leaf cuticle composition explain the unresponsiveness of older leaves to HAC, suggesting perception mechanisms upstream of canonical defense signaling as driving factors. Finally, we show that hyposmia in older leaves is not restricted to HAC, and extends to the full blend of herbivory induced volatiles. In conclusion, our work identifies immature maize leaves as dominant stress volatile sensing organs. The tight spatiotemporal control of volatile perception may facilitate within-plant defense signaling to protect young leaves, and may allow plants with complex architectures to explore the dynamic odor landscapes at the outer periphery of their shoots.

plant biology↗