Social Evolution: How ants send signals in saliva
Ant colonies are complex systems in which each ant fulfills a specific role to help the whole colony survive. The ants in a colony develop into distinct types known as castes to perform these roles. In colonies of leaf cutter ants, for example, small “worker” ants usually care for the larvae and the fungus the colony feeds on, while larger worker ants leave the nest to forage for new leaves to grow the fungus on. Other species, such as the silver ant, possess a soldier caste that has huge mouthparts dedicated to fighting. Finally, most colonies have one or several “queen” ants that focus on reproduction. It is important that the colony has the right numbers of each caste: if too many ants develop into soldiers, for example, the colony will starve, while a colony with too many foragers cannot take care of its larvae.
Genetic cues, environmental cues like food or the size of the colony, or a combination of both, can determine the caste that an individual will become (for a review see Schwander et al., 2010). Adult ants are able to influence the caste fate of larvae by changing the types of food they provide, by producing chemicals known as pheromones, and by regulating the temperature of the chamber the larvae live in (Wheeler, 1991). Now, in eLife, Laurent Keller and Richard Benton of the University of Lausanne and colleagues – including Adria LeBoeuf as first author – report on a new way in which adult ants can alter how larvae develop (LeBoeuf et al., 2016).
Juvenile hormone regulates development and reproduction in insects and also appears to affect caste fate in ants (Wheeler, 1986; Wheeler and Nijhout, 1981; Rajakumar et al., 2012; Nijhout, 1994). When the larvae of an ant called Pheidole bicarinata were exposed to increased amounts of a molecule that is very similar to juvenile hormone, most of them became soldiers instead of workers (Wheeler and Nijhout, 1981). However, it was not clear how the levels of this hormone were regulated in larvae.
Like most other social insects, adult ants feed their larvae by transferring fluid (saliva) mouth-to-mouth in a process called trophallaxis. LeBoeuf et al. – who are based at institutes in Switzerland, the US, Brazil, Japan and the UK – used mass spectroscopy and RNA sequencing to identify the molecules present in the saliva of the Florida carpenter ant (Camponotus floridanus). They found that, in addition to nutrients, ant saliva also contains juvenile hormone and other molecules including proteins, microRNAs and cuticular hydrocarbons (Figure 1). Furthermore, the amount of juvenile hormone transferred by trophallaxis is high enough to affect how the larvae develop.
Alongside juvenile hormone, some other molecules in the saliva may also be acting as chemical signals: for example, it is known that cuticular hydrocarbons help ants to discriminate nestmates from non-nestmates (Hefetz, 2007). Furthermore, many of the proteins LeBeouf et al. identified in carpenter ants are involved in regulating the growth, development and behavior of other social insects.
This study is the first to show that trophallaxis can circulate juvenile hormone and other proteins that might be involved in larval development and caste fate around the colony. It also suggests that the ants exchange other hormones that we did not previously know were involved in communication between individuals: these hormones include hexamerin, which is known to be involved in caste fate in social insects (Zhou et al., 2007). The next challenge will be to find out whether trophallaxis really plays an active role in regulating caste fate. One way to test this idea would be to remove all the soldiers from the colony and observe whether this changes the amount of different hormones present in ant saliva as the colony attempts to replace the soldiers. Adult ants are best placed to know the needs of the colony, so it makes sense that they use several strategies to guarantee that the colony produces the right mix of castes.
References
-
The evolution of hydrocarbon pheromone parsimony in ants (Hymenoptera: Formicidae) - interplay of colony odor uniformity and odor idiosyncrasyMyrmecological News 10:59–68.
-
Nature versus nurture in social insect caste differentiationTrends in Ecology & Evolution 25:275–282.https://doi.org/10.1016/j.tree.2009.12.001
-
Developmental and physiological determinants of caste in social hymenoptera: Evolutionary implicationsThe American Naturalist 128:13–34.https://doi.org/10.1086/284536
-
The developmental basis of worker caste polymorphism in antsThe American Naturalist 138:1218–1238.https://doi.org/10.1086/285279
Article and author information
Author details
Publication history
Copyright
© 2016, Knaden
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
-
- 1,970
- views
-
- 224
- downloads
-
- 0
- citations
Views, downloads and citations are aggregated across all versions of this paper published by eLife.
Download links
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)
Further reading
-
- Evolutionary Biology
- Genetics and Genomics
Evolutionary arms races can arise at the contact surfaces between host and viral proteins, producing dynamic spaces in which genetic variants are continually pursued. However, the sampling of genetic variation must be balanced with the need to maintain protein function. A striking case is given by protein kinase R (PKR), a member of the mammalian innate immune system. PKR detects viral replication within the host cell and halts protein synthesis to prevent viral replication by phosphorylating eIF2α, a component of the translation initiation machinery. PKR is targeted by many viral antagonists, including poxvirus pseudosubstrate antagonists that mimic the natural substrate, eIF2α, and inhibit PKR activity. Remarkably, PKR has several rapidly evolving residues at this interface, suggesting it is engaging in an evolutionary arms race, despite the surface’s critical role in phosphorylating eIF2α. To systematically explore the evolutionary opportunities available at this dynamic interface, we generated and characterized a library of 426 SNP-accessible nonsynonymous variants of human PKR for their ability to escape inhibition by the model pseudosubstrate inhibitor K3, encoded by the vaccinia virus gene K3L. We identified key sites in the PKR kinase domain that harbor K3-resistant variants, as well as critical sites where variation leads to loss of function. We find K3-resistant variants are readily available throughout the interface and are enriched at sites under positive selection. Moreover, variants beneficial against K3 were also beneficial against an enhanced variant of K3, indicating resilience to viral adaptation. Overall, we find that the eIF2α-binding surface of PKR is highly malleable, potentiating its evolutionary ability to combat viral inhibition.
-
- Ecology
- Evolutionary Biology
Seasonal polyphenism enables organisms to adapt to environmental challenges by increasing phenotypic diversity. Cacopsylla chinensis exhibits remarkable seasonal polyphenism, specifically in the form of summer-form and winter-form, which have distinct morphological phenotypes. Previous research has shown that low temperature and the temperature receptor CcTRPM regulate the transition from summer-form to winter-form in C. chinensis by impacting cuticle content and thickness. However, the underling neuroendocrine regulatory mechanism remains largely unknown. Bursicon, also known as the tanning hormone, is responsible for the hardening and darkening of the insect cuticle. In this study, we report for the first time on the novel function of Bursicon and its receptor in the transition from summer-form to winter-form in C. chinensis. Firstly, we identified CcBurs-α and CcBurs-β as two typical subunits of Bursicon in C. chinensis, which were regulated by low temperature (10 °C) and CcTRPM. Subsequently, CcBurs-α and CcBurs-β formed a heterodimer that mediated the transition from summer-form to winter-form by influencing the cuticle chitin contents and cuticle thickness. Furthermore, we demonstrated that CcBurs-R acts as the Bursicon receptor and plays a critical role in the up-stream signaling of the chitin biosynthesis pathway, regulating the transition from summer-form to winter-form. Finally, we discovered that miR-6012 directly targets CcBurs-R, contributing to the regulation of Bursicon signaling in the seasonal polyphenism of C. chinensis. In summary, these findings reveal the novel function of the neuroendocrine regulatory mechanism underlying seasonal polyphenism and provide critical insights into the insect Bursicon and its receptor.