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Biology subjects

Laggan, N. A.

Publications and source records attributed to Laggan, N. A..

3 recordsLinked to original sources

Loss of a belowground mutualist disrupts a fundamental biodiversity-disease relationship

Diverse ecological communities can reduce pathogen transmission; a phenomenon known as the dilution effect of biodiversity. This effect, in turn, depends on variation in host species' ability to spread disease (i.e., host competence) and which host species persist under biodiversity loss. Mutualistic symbionts can influence host competence and are sensitive to variation in host biodiversity; yet whether mutualists can modify dilution effects is unknown, partially because quantifying host competence during epidemics remains challenging. We experimentally tested whether mutualists could modify dilution effects by establishing gradients of host species richness, community competence, and access to the below-ground arbuscular mycorrhizal fungus (AMF), Rhizoglomus irregulare. Plant hosts were then exposed to the fungal root pathogen, Rhizoctonia solani, and disease spread was monitored over the course of an epidemic. Overall, host richness did not affect epidemic outcomes. Instead, AMF inoculation increased disease risk via species-specific increases in host competence. Moreover, communities containing highly competent host species experienced more disease, but only in the presence of mutualistic AMF. These results underscore the importance of plant community composition in mycorrhiza-mediated disease dynamics and suggest that predicting disease in our changing world might require a deeper understanding of host-symbiont and pathogen-symbiont interactions under global change.

ecology↗

Amplified transmission in host communities following disease-induced declines

Pathogen transmission is a fundamental component of infectious disease systems, governing the speed and extent of pathogen outbreaks. Predicting transmission within and among species is therefore critical for outbreak preparedness and the effective implementation of control strategies. Epidemics themselves can alter host populations in ways that fundamentally reshape transmission, but the long-term consequences remain poorly understood. Here, we quantify changes in transmission using a surrogate pathogen in bat communities before and after the emergence of white-nose syndrome, a fungal disease that has caused widespread population declines across North America. We find that transmission increased following disease-induced declines across all species in the community. We also observed an increase in environmental contacts and expanded habitat use by individuals, suggesting that surviving bats, on average, increased their activity and opportunities for interaction despite the substantial reductions in density and costs of infection. Together, these findings demonstrate that pathogen emergence can fundamentally alter host contact patterns and transmission dynamics, emphasizing the importance of considering behavioral and ecological changes imposed by epidemics when predicting pathogen spread in naive host populations.

ecology↗

Host abundance and heterogeneity in infectiousness determine extent of the environmental reservoir

Environmental pathogen reservoirs exist for many globally important diseases and can fuel epidemics, influence pathogen evolution, and increase the threat of host extinction. Species composition can be an important factor that shapes reservoir dynamics and ultimately determines the outcome of a disease outbreak. However, disease induced mortality can change species communities, indicating that species responsible for environmental reservoir maintenance may change over time. Here we examine reservoir dynamics of Pseudogymnoascus destructans, the fungal pathogen that causes white-nose syndrome in bats. We quantified changes in pathogen shedding, infection prevalence and intensity, host abundance, and the subsequent propagule pressure imposed by each species over time. We find that highly shedding species are important during pathogen invasion, but contribute less over time to environmental contamination as they also suffer the greatest declines. Less infected species remain more abundant, resulting in equivalent or higher propagule pressure. More broadly, we demonstrate that high infection intensity and subsequent mortality during disease progression can reduce the contributions of high shedding species to long-term pathogen maintenance.

ecology↗