Abstract

Host behavior can interact with environmental context to influence outcomes of pathogen exposure and the impact of disease on species and populations. Determining whether the thermal behaviors of individual species influence susceptibility to disease can help enhance our ability to explain and predict how and when disease outbreaks are likely to occur. The widespread disease chytridiomycosis (caused by the fungal pathogen Batrachochytrium dendrobatidis, Bd) often has species-specific impacts on amphibian communities; some host species are asymptomatic, whereas others experience mass mortalities and population extirpation. We determined whether the average natural thermal regimes experienced by sympatric frog species in nature, in and of themselves, can account for differences in vulnerability to disease. We did this by growing Bd under temperatures mimicking those experienced by frogs in the wild. At low and high elevations, the rainforest frogs Litoria nannotis, L. rheocola, and L. serrata maintained mean thermal regimes within the optimal range for pathogen growth (15–25°C). Thermal regimes for L. serrata, which has recovered from Bd-related declines, resulted in slower pathogen growth than the cooler and less variable thermal regimes for the other two species, which have experienced more long-lasting declines. For L. rheocola and L. serrata, pathogen growth was faster in thermal regimes corresponding to high elevations than in those corresponding to low elevations, where temperatures were warmer. For L. nannotis, which prefers moist and thermally stable microenvironments, pathogen growth was fastest for low-elevation thermal regimes. All of the thermal regimes we tested resulted in pathogen growth rates equivalent to, or significantly faster than, rates expected from constant-temperature experiments. The effects of host body temperature on Bd can explain many of the broad ecological patterns of population declines in our focal species, via direct effects on pathogen fitness. Understanding the functional response of pathogens to conditions experienced by the host is important for determining the ecological drivers of disease outbreaks.

Highlights

  • Epidemic disease can drive rapid population declines that can lead to extinction in some species, despite the persistence of other sympatric and susceptible species

  • Ecology and Evolution published by John Wiley & Sons Ltd

  • The average thermal regimes of L. serrata and L. rheocola differed strongly between high- and low-elevation sites, while those of L. nannotis, which spends much of its time in the water, were more similar (Fig. 1)

Read more

Summary

Introduction

Epidemic disease can drive rapid population declines that can lead to extinction in some species, despite the persistence of other sympatric and susceptible species. Disease emergence can be triggered by changes in the ecology of the host and/or pathogen through stressors such as climate change and habitat disturbance, and epidemics can spread rapidly through populations (Harvell et al 2002; Kiesecker 2011). The population-level processes that control the outcomes of epidemics can be summarized by epidemiological models that describe fractions of the population as follows: Susceptible to infection (S), Exposed to infection (E), Infective to other individuals (I), or Recovered (R, i.e., immune) (Hethcote 1976; Liu et al 1987; deCastro and Bolker 2005).

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call