Pheromones: The taste of togetherness

  1. Jonathan Trevorrow Clark
  2. Anandasankar Ray  Is a corresponding author
  1. University of California Riverside, United States
  2. the Institute for Integrative Genome Biology and the Interdisciplinary Neuroscience Program, University of California Riverside, United States

A wide range of organisms, including insects, can communicate with other organisms of the same species using sounds, signs and chemicals. The chemical cues emitted by organisms are called pheromones, and they trigger important behaviors like courtship, aggression, aggregation and aversion. The behavior produced by a pheromone depends on the chemical released and the social context in which it is detected.

Understanding how pheromones drive such powerful behaviors can be studied in depth in the fruit fly Drosophila melanogaster because its relatively simple nervous system makes it easy to investigate the neural circuits that detect and respond to these chemical signals. Several important principles have emerged from extensive studies of pheromone signaling in adult fruit flies, including an understanding of how pheromones are detected and how they can influence behavior in male and female flies in different ways. However, most of this work has focused on a pheromone called cis-vaccenyl acetate (van der Goes van Naters and Carlson, 2007). Now in eLife, Joshua Mast and colleagues from the Janelia Farm Research Campus, ETH Zürich and the US Department of Agriculture have used the chemosensory system of fruit fly larvae to identify new pheromones and the neurons that detect them (Mast et al., 2014).

D. melanogaster larvae have chemosensory (chemical detection) systems that are much simpler than those found in adults. This, along with the simple behavior of the larvae, makes them very suitable for studying pheromones. D. melanogaster larvae gather together on food sources, suggesting that they may produce pheromones that cause them to aggregate (Durisko et al., 2014). However, the identity of these pheromones remained a mystery.

Mast and co-workers now show that D. melanogaster larvae are attracted to surfaces on which other larvae of the same species have crawled, and have found that this behavior is caused by a chemical cue deposited by the larvae. Detecting this cue requires two ion channels, called pickpocket23 and pickpocket29, that are expressed in the neurons of the terminal organ, which is the main taste organ of a larva (Figure 1). Taste neurons expressing these two ion channels are also known to detect sex pheromones in adult D. melanogaster flies (Lu et al., 2012; Thistle et al., 2012; Toda et al., 2012). The simplicity of the larval neural circuits allowed Mast et al. to narrow down the possible neurons that could detect pheromones to a single pair of neurons (R58F10+) in the terminal organ. This finding also provides a foundation for future investigations into the precise regions of the brain to which this pair of neurons sends information.

Different species of fruit fly larvae use pheromones to either find or avoid one another.

(A) Mast et al. reveal that the attractive pheromones (Z)-5-tetradecenoic acid (Z-5-TA; gray dots) and (Z)-7-tetradecenoic acid (Z-7-TA; green dots) are secreted by the larvae of D. melanogaster and cause other larvae to gather together (top). The larvae of D. simulans produce these pheromones at lower levels, and are thought to produce an additional compound (red dots) that repels other larvae (bottom). (B) Dorsal view of the ‘head’ of a D. melanogaster larva. A single pair (green) of the 10 pairs of pickpocket23-expressing neurons (blue) extends into the terminal organ and detects Z-5-TA and Z-7-TA. This information is then relayed to a collection of neurons in the subesophageal zone (SEZ) of the brain (grey).

Next, Mast et al. used gas chromatography to separate the attractive chemicals deposited by the larvae, and then used mass spectrometry to identify a small number of compounds. Examining how the larvae responded to synthetic versions of each compound identified two rare fatty acids—(Z)-5-tetradecenoic acid and (Z)-7-tetradecenoic acid—as being responsible for attracting the larvae to each other. The pair of pickpocket23-expressing neurons in the terminal organ is able to detect both of these chemicals.

During courtship, pheromones are often used to signal that both participants are of the same species (Savarit et al., 1999; Ferveur, 2005). Generally, members of different Drosophila species will not court flies from other species because, it is thought, each species has a characteristic pheromone profile (Coyne et al., 1994). This species-specific effect is also partially seen in response to the pheromones that cause the larvae to aggregate: D. melanogaster larvae will gather together to form aggregates, but the larvae of a closely related species, Drosophila simulans, will not (Durisko et al., 2014).

Mast et al. reasoned that these differences in behavior could have several underlying causes. D. simulans may have lost sensitivity to the pheromones that D. melanogaster larvae find attractive, or may produce different pheromones—or a combination of these possibilities. Tests revealed that the lack of aggregation in D. simulans larvae is likely the result of the reduced production of both of the attractive D. melanogaster pheromones detected by Mast et al., as well as the production of an additional unknown repellant compound.

The differences in pheromone signaling between species are of great interest in evolutionary biology, as they could be key for establishing new species by preventing separate species breeding with each other (Cobb and Hallon, 1990; Ferveur, 2010). The demonstration by Mast et al. that the larvae of different, closely related, fly species produce different pheromones suggests that pheromones are able to influence social behavior even at that early developmental stage. Exactly how these pheromones evolved along with their receptor systems and circuits, and how they participate in species-specific adaptations, remain open questions for future investigation.

References

Article and author information

Author details

  1. Jonathan Trevorrow Clark

    Interdisciplinary Neuroscience Program, University of California Riverside, California, United States
    Competing interests
    No competing interests declared.
  2. Anandasankar Ray

    Entomology Department, the Institute for Integrative Genome Biology and the Interdisciplinary Neuroscience Program, University of California Riverside, California, United States
    For correspondence
    anand.ray@ucr.edu
    Competing interests
    AR: Founder and President of Sensorygen Inc. a flavor and fragrance research company for humans and arthropods.

Publication history

  1. Version of Record published: December 11, 2014 (version 1)

Copyright

© 2014, Clark and Ray

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 1,369
    views
  • 90
    downloads
  • 0
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Jonathan Trevorrow Clark
  2. Anandasankar Ray
(2014)
Pheromones: The taste of togetherness
eLife 3:e05490.
https://doi.org/10.7554/eLife.05490
  1. Further reading

Further reading

    1. Evolutionary Biology
    2. Microbiology and Infectious Disease
    Zachary H Williams, Alvaro Dafonte Imedio ... Welkin E Johnson
    Research Article

    HERV-K(HML-2), the youngest clade of human endogenous retroviruses (HERVs), includes many intact or nearly intact proviruses, but no replication competent HML-2 proviruses have been identified in humans. HML-2-related proviruses are present in other primates, including rhesus macaques, but the extent and timing of HML-2 activity in macaques remains unclear. We have identified 145 HML-2-like proviruses in rhesus macaques, including a clade of young, rhesus-specific insertions. Age estimates, intact ORFs, and insertional polymorphism of these insertions are consistent with recent or ongoing infectious activity in macaques. 106 of the proviruses form a clade characterized by an ~750 bp sequence between env and the 3' LTR, derived from an ancient recombination with a HERV-K(HML-8)-related virus. This clade is found in Old World monkeys (OWM), but not great apes, suggesting it originated after the ape/OWM split. We identified similar proviruses in white-cheeked gibbons; the gibbon insertions cluster within the OWM recombinant clade, suggesting interspecies transmission from OWM to gibbons. The LTRs of the youngest proviruses have deletions in U3, which disrupt the Rec Response Element (RcRE), required for nuclear export of unspliced viral RNA. We show that the HML-8 derived region functions as a Rec-independent constitutive transport element (CTE), indicating the ancestral Rec-RcRE export system was replaced by a CTE mechanism.

    1. Evolutionary Biology
    Deng Wang, Yaqin Qiang ... Jian Han
    Research Article

    Extant ecdysozoans (moulting animals) are represented by a great variety of soft-bodied or articulated organisms that may or may not have appendages. However, controversies remain about the vermiform nature (i.e. elongated and tubular) of their ancestral body plan. We describe here Beretella spinosa gen. et sp. nov. a tiny (maximal length 3 mm) ecdysozoan from the lowermost Cambrian, Yanjiahe Formation, South China, characterized by an unusual sack-like appearance, single opening, and spiny ornament. Beretella spinosa gen. et sp. nov has no equivalent among animals, except Saccorhytus coronarius, also from the basal Cambrian. Phylogenetic analyses resolve both fossil species as a sister group (Saccorhytida) to all known Ecdysozoa, thus suggesting that ancestral ecdysozoans may have been non-vermiform animals. Saccorhytids are likely to represent an early off-shot along the stem-line Ecdysozoa. Although it became extinct during the Cambrian, this animal lineage provides precious insight into the early evolution of Ecdysozoa and the nature of the earliest representatives of the group.