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
-
- 1,971
- 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
-
- Cancer Biology
- Evolutionary Biology
In growing cell populations such as tumours, mutations can serve as markers that allow tracking the past evolution from current samples. The genomic analyses of bulk samples and samples from multiple regions have shed light on the evolutionary forces acting on tumours. However, little is known empirically on the spatio-temporal dynamics of tumour evolution. Here, we leverage published data from resected hepatocellular carcinomas, each with several hundred samples taken in two and three dimensions. Using spatial metrics of evolution, we find that tumour cells grow predominantly uniformly within the tumour volume instead of at the surface. We determine how mutations and cells are dispersed throughout the tumour and how cell death contributes to the overall tumour growth. Our methods shed light on the early evolution of tumours in vivo and can be applied to high-resolution data in the emerging field of spatial biology.
-
- Evolutionary Biology
Spatial patterns in genetic diversity are shaped by individuals dispersing from their parents and larger-scale population movements. It has long been appreciated that these patterns of movement shape the underlying genealogies along the genome leading to geographic patterns of isolation by distance in contemporary population genetic data. However, extracting the enormous amount of information contained in genealogies along recombining sequences has, until recently, not been computationally feasible. Here we capitalize on important recent advances in genome-wide gene-genealogy reconstruction and develop methods to use thousands of trees to estimate per-generation dispersal rates and to locate the genetic ancestors of a sample back through time. We take a likelihood approach in continuous space using a simple approximate model (branching Brownian motion) as our prior distribution of spatial genealogies. After testing our method with simulations we apply it to Arabidopsis thaliana. We estimate a dispersal rate of roughly 60km2 per generation, slightly higher across latitude than across longitude, potentially reflecting a northward post-glacial expansion. Locating ancestors allows us to visualize major geographic movements, alternative geographic histories, and admixture. Our method highlights the huge amount of information about past dispersal events and population movements contained in genome-wide genealogies.