Abstract

Diseases often display complex and distinct associations with their environment due to differences in etiology, modes of transmission between hosts, and the shifting balance between pathogen virulence and host resistance. Statistical modeling has been underutilized in coral disease research to explore the spatial patterns that result from this triad of interactions. We tested the hypotheses that: 1) coral diseases show distinct associations with multiple environmental factors, 2) incorporating interactions (synergistic collinearities) among environmental variables is important when predicting coral disease spatial patterns, and 3) modeling overall coral disease prevalence (the prevalence of multiple diseases as a single proportion value) will increase predictive error relative to modeling the same diseases independently. Four coral diseases: Porites growth anomalies (PorGA), Porites tissue loss (PorTL), Porites trematodiasis (PorTrem), and Montipora white syndrome (MWS), and their interactions with 17 predictor variables were modeled using boosted regression trees (BRT) within a reef system in Hawaii. Each disease showed distinct associations with the predictors. Environmental predictors showing the strongest overall associations with the coral diseases were both biotic and abiotic. PorGA was optimally predicted by a negative association with turbidity, PorTL and MWS by declines in butterflyfish and juvenile parrotfish abundance respectively, and PorTrem by a modal relationship with Porites host cover. Incorporating interactions among predictor variables contributed to the predictive power of our models, particularly for PorTrem. Combining diseases (using overall disease prevalence as the model response), led to an average six-fold increase in cross-validation predictive deviance over modeling the diseases individually. We therefore recommend coral diseases to be modeled separately, unless known to have etiologies that respond in a similar manner to particular environmental conditions. Predictive statistical modeling can help to increase our understanding of coral disease ecology worldwide.

Highlights

  • The notion of a complex web of interactions between a disease and its environment has been postulated for centuries [1] and stems from the fact that diseases often have intricate etiologies [2] and different modes of pathogen transmission between hosts [3]

  • With the use of boosted regression tree (BRT) modeling, this study has shown that different coral diseases do show complex associations with a range of environmental variables and that these associations are distinct between diseases

  • Abiotic and Physical Associations with Disease Within our study the relative importance of disease associations with biotic, abiotic and physical parameters differed across coral disease states

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Summary

Introduction

The notion of a complex web of interactions between a disease and its environment has been postulated for centuries [1] and stems from the fact that diseases often have intricate etiologies [2] and different modes of pathogen transmission between hosts [3]. Pathogen virulence can respond positively or negatively to a range of variables, such as temperature, nutrient availability, or habitat quality [4,5,6]; changes in environmental conditions can promote physiological stress that impairs host immunity [7,8,9], and there may be differences in disease susceptibility between host genotypes [10,11] With this in mind, it is easy to envisage how complex associations between a disease, the host, and the environment can become established. Researchers and monitoring programs are still, on occasion, attempting to understand spatial patterns of overall coral disease prevalence (combining the prevalence of multiple diseases into a single proportion value as the response variable) with the environment This approach ignores the common-sense notion that diseases with different pathogens and hosts are unlikely to have common spatial/temporal patterns or environmental associations, and should be monitored and analyzed individually unless known to have a similar cause

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