Individual heterogeneity can influence the dynamics of infectious diseases in wildlife and humans alike. Thus, recent work has sought to identify behavioural characteristics that contribute disproportionately to individual variation in pathogen acquisition (super-receiving) or transmission (super-spreading). However, it remains unknown whether the same behaviours enhance both acquisition and transmission, a scenario likely to result in explosive epidemics. Here, we examined this possibility in an ecologically relevant host-pathogen system: house finches and their bacterial pathogen, Mycoplasma gallisepticum, which causes severe conjunctivitis. We examined behaviours likely to influence disease acquisition (feeder use, aggression, social network affiliations) in an observational field study, finding that the time an individual spends on bird feeders best predicted the risk of conjunctivitis. To test whether this behaviour also influences the likelihood of transmitting M. gallisepticum, we experimentally inoculated individuals based on feeding behaviour and tracked epidemics within captive flocks. As predicted, transmission was fastest when birds that spent the most time on feeders initiated the epidemic. Our results suggest that the same behaviour underlies both pathogen acquisition and transmission in this system and potentially others. Identifying individuals that exhibit such behaviours is critical for disease management.

Anthropogenic food provisioning of wildlife can alter the frequency of contacts among hosts and between hosts and environmental sources of pathogens. Despite the popularity of garden bird feeding, few studies have addressed how feeders influence host contact rates and disease dynamics. We experimentally manipulated feeder density in replicate aviaries containing captive, pathogen-naive, groups of house finches () and continuously tracked behaviours at feeders using radio-frequency identification devices. We then inoculated one bird per group with (Mg), a common bacterial pathogen for which feeders are fomites of transmission, and assessed effects of feeder density on house finch behaviour and pathogen transmission. We found that pathogen transmission was significantly higher in groups with the highest density of bird feeders, despite a significantly lower rate of intraspecific aggressive interactions relative to the low feeder density groups. Conversely, among naive group members that never showed signs of disease, we saw significantly higher concentrations of Mg-specific antibodies in low feeder density groups, suggesting that birds in low feeder density treatments had exposure to subclinical doses of Mg. We discuss ways in which the density of garden bird feeders could play an important role in mediating the intensity of Mg epidemics.This article is part of the theme issue 'Anthropogenic resource subsidies and host-parasite dynamics in wildlife'.

In social organisms, immune-mediated behavioural changes (sickness behaviours) can both influence and respond to social dynamics. We tested whether social status in house finches (Haemorhous mexicanus) modulates the acute phase response or aggressive interactions with flockmates. We treated subordinate or dominant finches within captive flocks with lipopolysaccharide (LPS) to stimulate an acute phase response (APR), and quantified mass loss, activity, foraging behaviours, and agonistic interactions. Subordinate finches lost more mass than dominants in response to LPS, but social status did not influence the expression of sickness behaviours (activity and foraging) upon LPS injection. LPS-injected subordinate birds experienced reduced aggression from mid-ranking but not dominant flockmates, indicating status-mediated effects of sickness behaviour on agonistic interactions. Our results suggest that social status in house finches influences one component of the APR (mass loss) and can interact with the APR to modulate intraspecific agonistic interactions in ways likely relevant for disease transmission.

Despite the ubiquity of parasites and pathogens, behavioral and physiological responses to infection vary widely across individuals. Although such variation can have pronounced effects on population-level processes, including the transmission of infectious disease, the study of individual responses to infection in free-living animals remains a challenge. To fully understand the causes and consequences of heterogeneous responses to infection, research in ecoimmunology and disease-ecology must incorporate minimally invasive techniques to track individual animals in natural settings. Here, we review how several technologies, collectively termed remote biomonitoring, enable the collection of data on behavioral and physiological responses to infection in small, free-living animals. Specifically, we focus on the use of radiotelemetry and radio-frequency identification to study fever, sickness-behaviors (including lethargy and anorexia), and rates of inter-individual contact in the wild, all of which vary widely across individuals and impact the spread of pathogens within populations. In addition, we highlight future avenues for field studies of these topics using emerging technologies such as global positioning system tracking and tri-axial accelerometry. Through the use of such remote biomonitoring techniques, researchers can gain valuable insights into why responses to infection vary so widely and how this variation impacts the spread and evolution of infectious diseases.

Animal personality has been linked to individual variation in both stress physiology and social behaviors, but few studies have simultaneously examined covariation between personality traits, stress hormone levels, and behaviors in free-living animals. We investigated relationships between exploratory behavior (one aspect of animal personality), stress physiology, and social and foraging behaviors in wild house finches (Haemorhous mexicanus). We conducted novel environment assays after collecting samples of baseline and stress-induced plasma corticosterone concentrations from a subset of house finches. We then fitted individuals with Passive Integrated Transponder tags and monitored feeder use and social interactions at radio-frequency identification equipped bird feeders. First, we found that individuals with higher baseline corticosterone concentrations exhibit more exploratory behaviors in a novel environment. Second, more exploratory individuals interacted with more unique conspecifics in the wild, though this result was stronger for female than for male house finches. Third, individuals that were quick to begin exploring interacted more frequently with conspecifics than slow-exploring individuals. Finally, exploratory behaviors were unrelated to foraging behaviors, including the amount of time spent on bird feeders, a behavior previously shown to be predictive of acquiring a bacterial disease that causes annual epidemics in house finches. Overall, our results indicate that individual differences in exploratory behavior are linked to variation in both stress physiology and social network traits in free-living house finches. Such covariation has important implications for house finch ecology, as both traits can contribute to fitness in the wild.