Gammaherpesvirus reactivation can promote diseases or impair reproduction. Understanding reactivation patterns and associated risks of different stressors is therefore important. Nevertheless, outside the laboratory or captive environment, studies on the effects of stress on gammaherpesvirus reactivation in wild mammals are lacking. Here we used Mustelid gammaherpesvirus 1 (MusGHV-1) infection in European badgers (Meles meles) as a host–pathogen wildlife model to study the effects of a variety of demographic, physiological and environmental stressors on virus shedding in the genital tract. We collected 251 genital swabs from 150 free-ranging individuals across three seasons and screened them for the presence of MusGHV-1 DNA using PCR targeting the DNA polymerase gene. We explored possible links between MusGHV-1 DNA presence and seven variables reflecting stressors, using logistic regression analysis. The results reveal different sets of risk factors between juveniles and adults, likely reflecting primary infection and reactivation. In adults, virus shedding was more likely in badgers in poorer body condition and younger than 5 years or older than 7; while in juveniles, virus shedding is more likely in females and individuals in better body condition. However, living in social groups with more cubs was a risk factor for all badgers. We discuss possible explanations for these risk factors and their links to stress in badgers.

Diverse individual energy-budgeting tactics within wild populations provide resilience to natural fluctuations in food availability and expenditure costs. Although substantial heterogeneity in activity-related energy expenditure has been documented, few studies differentiate between responses to the environment and inter-individual differences stemming from life history, allometry, or somatic stores. Using tri-axial accelerometry, complemented by diet analysis, we investigated inter-individual within-season variation in overall dynamic body acceleration (ODBA; activity intensity measure) and “Activity” (above an ODBA threshold) in a high-density population of European badgers (Meles meles). Weather (including wind speed) affected ODBA and activity according to predictors of earthworm (food) availability and cooling potential. In spring, maximal ODBA expenditure at intermediate rainfall and temperature values suggested that badgers traded foraging success against thermoregulatory losses, where lower-condition badgers maintained higher spring ODBA irrespective of temperature while badgers in better body condition reduced ODBA at colder temperatures. Conversely, in summer, lower-condition badgers modulated ODBA according to temperature, likely in response to super-abundant food supply. Between 35% (spring, summer) and 57% (autumn) of residual total daily ODBA variance related to inter-individual differences unexplained by seasonal predictors, suggesting within-season tactical activity typologies. We propose that this heterogeneity among individual energy-expenditure profiles may contribute to population resilience under rapid environmental change.

Herpesviruses are ubiquitous pathogens infecting most animals. Although host immunity continually coevolves to combat virulence, viral variants with enhanced transmissibility or virulence occasionally emerge, resulting in disease burdens in host populations. Mustelid gammaherpesvirus 1 (MusGHV-1) is the only herpesvirus species identified thus far in European badgers, Meles meles. No MusGHV-1 associated pathomorbidity has been reported, but reactivation of MusGHV-1 in genital tracts is linked to impaired female reproductive success. An analysis of a short sequence from the highly conserved DNA polymerase (DNApol) gene previously identified two variants in a single host population. Here we compared genetic variance in blood samples from 66 known individuals of this same free-ranging badger population using a partial sequence comprising 2874 nucleotides of the DNApol gene, among which we identified 15 nucleotide differences resulting in 5 amino acid differences. Prevalence was 86% (59/66) for the common and 17% (11/66) for the novel variant, with 6% (4/66) of badgers presenting with coinfection. MusGHV-1 variants were distributed unevenly across the population, with individuals infected with the novel genotype clustered in 3 of 25 contiguous social groups. Individuals infected with the novel variant had significantly higher MusGHV-1 viral loads in their blood (p = 0.002) after adjusting for age (juveniles > adults, p < 0.001) and season (summer > spring and autumn, p = 0.005; mixed-effect linear regression), likely indicating higher virulence of the novel variant. Further genome-wide analyses of MusGHV-1 host resistance genes and host phenotypic variations are required to clarify the drivers and sequelae of this new MusGHV-1 variant.