Pathogen dynamics under both bottom-up host resistance and top-down hyperparasite attack

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Parratt , S R & Laine , A-L 2018 , ' Pathogen dynamics under both bottom-up host resistance and top-down hyperparasite attack ' , Journal of Applied Ecology , vol. 55 , no. 6 , pp. 2976-2985 . https://doi.org/10.1111/1365-2664.13185

Title: Pathogen dynamics under both bottom-up host resistance and top-down hyperparasite attack
Author: Parratt, Steven R.; Laine, Anna-Liisa
Other contributor: University of Helsinki, Plant Biology
University of Helsinki, Ecology and Evolutionary Biology







Date: 2018-11
Language: eng
Number of pages: 10
Belongs to series: Journal of Applied Ecology
ISSN: 0021-8901
DOI: https://doi.org/10.1111/1365-2664.13185
URI: http://hdl.handle.net/10138/309762
Abstract: 1. The relative importance of bottom-up versus top-down control of population dynamics has been the focus of much debate. In infectious disease biology, research is typically focused on the bottom-up process of host resistance, wherein the direction of control flows from the lower to the higher trophic level to impact on pathogen population size and epidemiology. However, the importance of top-down control by a pathogen's natural enemies has been mostly overlooked. 2. Here, we explore the effects of, and interaction between, host genotype (i.e., genetic susceptibility to pathogen infection) and infection by a hyperparasitic fungus, Ampelomyces spp., on the establishment and early epidemic growth and transmission of a powdery mildew plant pathogen (Podosphaera plantaginis). We used a semi-natural field experiment to contrast the impacts of hyperparasite infection, host-plant resistance and spatial structure to reveal the key factors that determine pathogen spread. We then used a laboratory-based inoculation approach to test whether the field experiment results hold across multiple pathogen-host genetic combinations and to explore hyperparasite effects on the pathogen's later life-history stages. 3. We found that hyperparasite infection had a negligible effect on within-host infection development and between-host spread of the pathogen during the onset of epidemics. In contrast, host-plant resistance was the major determinant of whether plants became infected, and host genotype and proximity to an infection source determined infection severity. 4. Our laboratory study showed that, while the interaction between host and pathogen genotypes was the key determinant of infection outcome, hyperparasitism did, on average, reduce the severity of infection. Moreover, hyperparasite infection negatively influenced the production of the pathogen's overwintering structures. 5. Synthesis and applications. Our results suggest that bottom-up host resistance affects pathogen spread, but top-down control of powdery mildew pathogens is likely more effective against later life-history stages. Further, while hyperparasitism in this system can reduce early pathogen growth under stable laboratory conditions, this effect is not detectable in a semi-natural environment. Considering the effects of hyperparasites at multiple points in pathogen's life history will be important when considering hyperparasite-derived biocontrol measures in other natural and agricultural systems.
Subject: Ampelomyces spp.
bottom-up
disease biology
hyperparasite
plant pathogen
Plantago lanceolata
Podosphaera plantaginis
top-down
INFECTIOUS-DISEASE DYNAMICS
WILD PLANT-PATHOGEN
BIOLOGICAL-CONTROL
CHESTNUT BLIGHT
POWDERY MILDEW
CRYPHONECTRIA-PARASITICA
ENVIRONMENT INTERACTIONS
AMPELOMYCES-QUISQUALIS
POPULATION-DYNAMICS
LOCAL ADAPTATION
1181 Ecology, evolutionary biology
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