Abstract Biodiversity has been linked to reduced disease transmission through the dilution effect process. Traditional ecological measures of biological diversity, such as species richness, are most commonly used to test for the dilution effect. However, such metrics of species diversity do not consider the evolutionary relationship between species, which has important implications for host immune processes and disease transmission. Phylogenetic diversity incorporates the evolutionary relationships of a wildlife community. Host reservoir competency is partly determined by their capacity to mount effective immune responses, which may be phylogenetically determined. As a result, phylogenetic diversity may be a better metric to evaluate the relationship between host diversity and disease transmission, given that closely related species may have more similar pathogen competencies than distantly related ones. Few studies have examined the relationship between phylogenetic diversity and disease transmission, particularly in vector‐borne transmission systems. This study seeks to quantify phylogenetic diversity in the western United States Lyme disease system, where the causal agentBorrelia burgdorferiis vectored by the western black‐legged tick,Ixodes pacificus.We empirically measured mammalian diversity and tick data over seven years. We collected data on ticks, host community, and infection prevalence withBorrelia burgdorferiand constructed generalized linear mixed‐effect models to evaluate the utility of phylogenetic diversity in predicting the prevalence of a tick‐borne pathogen. We found that phylogenetic diversity metrics improved our disease prediction models. Predictions of the overall density and infection prevalence of ticks were improved by the addition of phylogenetic metrics, whereas the density of infected nymphs was solely predicted by a phylogenetic metric over traditional species diversity or richness. Our study found that phylogenetic diversity improves statistical predictions of the Lyme disease pathogen and entomological risk in the western United States and may be informative in other contexts and systems as well.
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Functional vertebrate group diversity differentially impacts vector‐borne pathogen transmission and genetic diversity
Abstract Anthropogenic land use change has led to considerable biodiversity loss, affecting ecosystem functions with unresolved consequences for zoonotic disease transmission. Functional diversity is understudied but potentially important for understanding the role of biodiversity because many zoonotic disease systems are maintained by species with different roles in disease transmission. Here, we explore how functional groups and pathogen genetic diversity influence transmission and human disease risk within the Lyme disease system. Our field and molecular ecology study examined ticks and vertebrates across a fragmented landscape and evaluated several metrics of disease risk. For predicting vector and infected vector density, rodent host richness had a positive effect and was most important, but vector infection prevalence was best predicted by rodent and predator richness together, reflecting how indirect effects may alter tick–host interactions and disease risk. These results indicate that examining species richness generally may obscure important interactions driven by richness within functional groups. Pathogen genotype richness was best predicted by overall vertebrate richness, providing support for the multiple niche polymorphism hypothesis. Our study offers an important perspective on the relationship between biodiversity and disease risk, suggesting that richness within functional groups may offer more nuanced insight into pathogen transmission dynamics than overall biodiversity.
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- Award ID(s):
- 1750037
- PAR ID:
- 10668854
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Ecosphere
- Volume:
- 16
- Issue:
- 6
- ISSN:
- 2150-8925
- Page Range / eLocation ID:
- 70292
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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