Abstract

Social animals display a wide range of behavioural defences against infectious diseases, some of which increase social contacts with infectious individuals (e.g. mutual grooming), while others decrease them (e.g. social exclusion). These defences often rely on the detection of infectious individuals, but this can be achieved in several ways that are difficult to differentiate. Here, we combine non-pathogenic immune challenges with automated tracking in colonies of the clonal raider ant to ask whether ants can detect the immune status of their social partners and to quantify their behavioural responses to this perceived infection risk. We first show that a key behavioural response elicited by live pathogens (allogrooming) can be qualitatively recapitulated by immune challenges alone. Automated scoring of interactions between all colony members reveals that this behavioural response increases the network centrality of immune-challenged individuals through a general increase in physical contacts. These results show that ants can detect the immune status of their nest-mates and respond with a general ‘caring’ strategy, rather than avoidance, towards social partners that are perceived to be infectious. Finally, we find no evidence that changes in cuticular hydrocarbon profiles drive these behavioural effects.

Highlights

  • We combine non-pathogenic immune challenges with automated tracking in colonies of the clonal raider ant to ask whether ants can detect the immune status of their social partners and to quantify their behavioural responses to this perceived infection risk

  • Social animals are vulnerable to infectious diseases because spatial proximity, frequent social interactions and shared resources can facilitate the spread of pathogens [1,2,3]

  • We focus on cuticular hydrocarbons (CHCs), non-volatile compounds carried on the body surface that plays a key role in social insect communication [47]

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Summary

Introduction

Social animals are vulnerable to infectious diseases because spatial proximity, frequent social interactions and shared resources can facilitate the spread of pathogens [1,2,3]. Received grooming (in seconds) was analysed using a Tweedie generalized linear mixed model (GLMM, function glmmTMB from package glmmTMB) with treatment (pathogen- versus sham-exposed), time post-exposure (a nine-level factor), and their interaction as fixed factors, and individual nested in colony as a random factor. To evaluate determinants of individual behaviour (isolation, activity, mean speed) and node parameters (eigenvector centrality, strength, skewness), linear mixed-effects models (LMM) were fitted (function lme from package nlme) with treatment (immune-challenged versus control-injected), time post-injection (9-level factor), and their interaction as fixed effects, and individual nested in colony as a random factor (to account for the non-independence of ants from the same colony [61]). A permutational multivariate analysis of variance using Bray–Curtis Distance Matrices (ADONIS) was performed to analyse the effects of the treatment (immune-challenged versus control-injected versus naive), the social environment (alone versus in group) and their interaction on CHC profiles. To identify the individual compounds that differed between groups, a random forest analysis was performed [64]

Results
Discussion
15. Geffre AC et al 2020 Honey bee virus causes
Methods
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