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Teseo, S.

Publications and source records attributed to Teseo, S..

2 recordsLinked to original sources

The scent of symbiosis: gut bacteria affect social interactions in leafcutting ants

Animal gut microbiota affect host physiology and behaviour. In eusocial Hymenoptera, where colony-level integrity is preserved via a nestmate discrimination system based on cuticular hydrocarbon mixtures, microorganismal effects may influence social dynamics. Although nestmate recognition has undergone a thorough exploration during the last four decades, few studies have investigated the putative role of gut microbes. Here we integrate metagenomic, chemical and behavioural approaches to test whether gut microbes affect nestmate recognition in Acromyrmex echinatior leaf-cutting ants. Treating workers with a sterile diet or with antibiotics resulted in a substantial alteration of their gut microbial communities. In pairwise social interactions, untreated vs. antibiotic-treated nestmates behaved more aggressively than other nestmate and non-nestmate pairs, suggesting that the suppression of microbes indirectly alters chemical social cues and triggers aggressive behaviour. Chemical analyses on treated individuals revealed a decrease in the abundance of two metapleural gland antifungal compounds, and we confirmed the correspondence between aggression levels and chemical profile differences. Feeding microbiota-remodelled ants with conspecific faecal droplets partially restored the original bacterial communities. Furthermore, non-nestmates fed with faecal droplets from different colonies were unusually aggressive compared to pairs fed with faecal droplets from the same colony. This suggests that chemicals derived from microbial strains may shape nestmate recognition, opening novel questions about the role of microorganisms in the evolution of social behaviour.

evolutionary biology

Reduced foraging investment as an adaptation to patchy food sources: a phasic army ant simulation

Colonies of several ant species within the subfamily Dorylinae alternate stereotypical discrete phases of foraging and reproduction. Such phasic cycles are thought to be adaptive because they minimize the amount of foraging and the related costs, and at the same time enhance the colony-level ability to rely on patchily distributed food sources. In order to investigate these hypotheses, we use here a simple computational approach to study the population dynamics of two species of virtual ant colonies that differ quantitatively in their foraging investment. One species, which we refer to as \"phasic\", forages only half of the time, mirroring the phasic activity of some army ants; the other \"non-phasic\" species forages instead all the time. We show that, when foraging costs are relatively high, populations of phasic colonies grow on average faster than non-phasic populations, outcompeting them in mixed populations. Interestingly, such tendency becomes more consistent as food becomes more difficult to find but locally abundant. According to our results, reducing the foraging investment, for example by adopting a phasic lifestyle, can result in a reproductive advantage, but only in specific conditions. We thus suggest phasic colony cycles to have emerged together with the doryline specialization in feeding on the brood of other eusocial insects, a resource that is hard to obtain but highly abundant if available.

animal behavior and cognition