Tuesday, October 17, 2023

Unlocking nature's silent conversations: Real-time visualization of plant-plant communications through airborne volatiles

SAITAMA UNIVERSITY

Figure 1: Plant-plant communication between damaged plants and intact neighboring plants — IMAGE:
PLANTS RELEASE VOCS INTO THE ATMOSPHERE WHEN DAMAGED BY INSECTS. INTACT NEIGHBORING PLANTS SENSE VOCS AND ACTIVATE PRE-EMPTIVE DEFENSE RESPONSES AGAINST THE INSECTS.
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CREDIT: MASATSUGU TOYOTA/SAITAMA UNIVERSITY

Saitama, Japan: Plants emit volatile organic compounds (VOCs) into the atmosphere upon mechanical damages or insect attacks. Undamaged neighboring plants sense the released VOCs as danger cues to activate defense responses against upcoming threats (Figure 1). This phenomenon of airborne communication among plants through VOCs was first documented in 1983 and has since been observed in more than 30 different plant species. However, the molecular mechanisms underlying VOC perception to defense induction remain unclear.

Unveiling the Invisible Conversation

The team, led by Professor Masatsugu Toyota (Saitama University, Japan), visualized plant-plant communications via VOCs in real time and revealed how VOCs are taken up by plants, initiating Ca2+-dependent defense responses against future threats.

This groundbreaking research will be published in Nature Communications on October 17, 2023. Yuri Aratani and Takuya Uemura led the work as a Ph.D. student and a postdoctoral researcher, respectively, in Toyota’s lab and collaborated with Professor Kenji Matsui at Yamaguchi University, Japan.

“We constructed equipment to pump VOCs emitted from plants fed by caterpillars onto undamaged neighboring plants and combined it with a wild-field, real-time fluorescent imaging system,” says Toyota. This innovative setup visualized bursts of fluorescence spreading in a mustard plant Arabidopsis thaliana after exposure to VOCs emitted from the insect-damaged plants (Figure 2; Video 1). The plants create fluorescent protein sensors for intracellular Ca2+ and therefore, changes in intracellular Ca2+ concentration can be monitored by observing changes in fluorescence.

“In addition to insect attacks, VOCs released from manually smashed leaves induced Ca2+ signals in undamaged neighboring plants,” says Toyota (Video 2).

To identify what type of VOCs induced Ca2+ signals in plants, Toyota’s team of scientists investigated various VOCs known to induce defense responses in plants. They found that two VOCs, (Z)-3-hexenal (Z-3-HAL) and (E)-2-hexenal (E-2-HAL), both six-carbon aldehydes, induce Ca2+ signals in Arabidopsis (Figure 3; Video 3). Z-3-HAL and E-2-HAL are airborne chemicals with grassy smells and are known as green leaf volatiles (GLVs) emitted from mechanically- and herbivore-damaged plants.

Exposing Arabidopsis to Z-3-HAL and E-2-HAL resulted in the upregulation of defense-related genes. To understand the relationship between the Ca2+ signals and the defense responses, they treated Arabidopsis with the Ca2+ channel inhibitor, LaCl3 and the Ca2+ chelating agent, EGTA. These chemicals suppressed both the Ca2+ signals and the induction of defense-related genes, providing evidence that Arabidopsis perceives GLVs and activates defense responses in a Ca2+-dependent manner.

Guard Cells: The Gateway to Awareness

They also identified which specific cells exhibited the Ca2+ signals in response to GLVs by engineering transgenic plants expressing the fluorescent protein sensors exclusively in guard, mesophyll, or epidermal cells. Upon Z-3-HAL exposure, Ca2+ signals were generated in guard cells within approximately 1 minute and then in mesophyll cells, whereas epidermal cells generated Ca2+ signals more slowly (Video 4). Guard cells are bean-shaped cells on plant surfaces and form stomata, small pores that connect inner tissues and the atmosphere.

“Plants do not possess a “nose”, but stomata serve as a plant gateway mediating rapid GLV entry into interspaces in leaf tissues,” says Toyota. In fact, they found that pretreating with abscisic acid (ABA), one of the phytohormones known for its ability to close stomata, reduced Ca2+ responses in wild-type leaves. On the other hand, mutants with impaired ABA-induced stomatal closures maintained normal Ca2+ signals in leaves even when treated with ABA.

“We have finally unveiled the intricate story of when, where, and how plants respond to airborne 'warning messages' from their threatened neighbors,” he says. “This ethereal communication network, hidden from our view, plays a pivotal role in safeguarding neighboring plants from imminent threats in a timely manner,” he adds.

This pioneering research not only deepens our appreciation for the astonishing world of plants but also underscores the remarkable ways in which nature has equipped them to thrive and adapt in the face of adversity. The profound implications of these findings resonate far beyond the boundaries of plant science, offering a glimpse into the intricate tapestry of life on Earth.

Left panel: Equipment for exposing intact Arabidopsis to VOCs emitted by insect-damaged plants (dashed arrow). Right panel: Ca2+ signals (yellow arrowheads, 600 and 1200 s) were induced by VOCs released from insect-damaged plants (dashed arrow).