ArticleJournal of chemical ecology2017
What are the Mechanisms Behind a Parasite-Induced Decline in Nestmate Recognition in Ants?
Article in Journal of chemical ecology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
6 citing papers in PubMed, 9 citations in OpenAlex.
- Genetic Basis of Cuticular Hydrocarbon Variation in the Desert AntEcology and evolution · 2026Article
- Can Cuticular Hydrocarbons Be used as Chemotaxonomic Tool for Neosilba McAlpine (Diptera: Lonchaeidae)?Journal of chemical ecology · 2026Article
- Effect of Seasonal Variation on the Cuticular Chemical Composition of Atta laevigata (Smith 1858) (Hymenoptera: Formicidae).Journal of chemical ecology · 2025Article
- Non-lethal fungal infection could reduce aggression towards strangers in ants.Communications biology · 2023Article
- Chemically Insignificant Social Parasites Exhibit More Anti-Dehydration Behaviors than Their Hosts.Insects · 2021Article
- Extreme lifespan extension in tapeworm-infected ant workers.Royal Society open science · 2021Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
Social insects have developed sophisticated recognition skills to defend their nests against intruders. They do this by aggressively discriminating against non-nestmates with deviant cuticular hydrocarbon (CHC) signatures. Studying nestmate recognition can be challenging as individual insects do not only vary in their discriminatory abilities, but also in their motivation to behave aggressively. To disentangle the influence of signaling and behavioral motivation on nestmate recognition, we investigated the ant Temnothorax nylanderi, where the presence of tapeworm-infected nestmates leads to reduced nestmate recognition among uninfected workers. The parasite-induced decline in nestmate recognition could be caused by higher intra-colonial cue diversity as tapeworm-infected workers are known to exhibit a modified hydrocarbon signature. This in turn may broaden the neuronal template of their nestmates, leading to a higher tolerance towards alien conspecifics. To test this hypothesis, we exchanged infected ants between colonies and analyzed their impact on CHC profiles of uninfected workers. We demonstrate that despite frequent grooming, which should promote the transfer of recognition cues, CHC profiles of uninfected workers neither changed in the presence of tapeworm-infected ants, nor did it increase cue diversity among uninfected nestmates within or between colonies. However, CHC profiles were systematically affected by the removal of nestmates and addition of non-nestmates, independently from the ants' infection status. For example, when non-nestmates were present workers expressed more dimethyl alkanes and higher overall CHC quantities, possibly to achieve a better distinction from non-nestmates. Workers showed clear task-specific profiles with tapeworm-infected workers resembling more closely young nurses than older foragers. Our results show that the parasite-induced decline in nestmate recognition is not due to increased recognition cue diversity or altered CHC profiles of uninfected workers, but behavioral changes might explain tolerance towards intruders.
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Registered trials
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