Literature DB >> 29738078

Tick-borne disease risk in a forest food web.

Richard S Ostfeld1, Taal Levi2, Felicia Keesing3, Kelly Oggenfuss1, Charles D Canham1.   

Abstract

Changes to the community ecology of hosts for zoonotic pathogens, particularly rodents, are likely to influence the emergence and prevalence of zoonotic diseases worldwide. However, the complex interactions between abiotic factors, pathogens, vectors, hosts, and both food resources and predators of hosts are difficult to disentangle. Here we (1) use 19 yr of data from six large field plots in southeastern New York to compare the effects of hypothesized drivers of interannual variation in Lyme disease risk, including the abundance of acorns, rodents, and deer, as well as a series of climate variables; and (2) employ landscape epidemiology to explore how variation in predator community structure and forest cover influences spatial variation in the infection prevalence of ticks for the Lyme disease bacterium, Borrelia burgdorferi, and two other important tick-borne pathogens, Anaplasma phagocytophilum and Babesia microti. Acorn-driven increases in the abundance of mice were correlated with a lagged increase in the abundance of questing nymph-stage Ixodes scapularis ticks infected with Lyme disease bacteria. Abundance of white-tailed deer 2 yr prior also correlated with increased density of infected nymphal ticks, although the effect was weak. Density of rodents in the current year was a strong negative predictor of nymph density, apparently because high current abundance of these hosts can remove nymphs from the host-seeking population. Warm, dry spring or winter weather was associated with reduced density of infected nymphs. At the landscape scale, the presence of functionally diverse predator communities or of bobcats, the only obligate carnivore, was associated with reduced infection prevalence of I. scapularis nymphs with all three zoonotic pathogens. In the case of Lyme disease, infection prevalence increased where coyotes were present but smaller predators were displaced or otherwise absent. For all pathogens, infection prevalence was lowest when forest cover within a 1 km radius was high. Taken together, our results suggest that a food web perspective including bottom-up and top-down forcing is needed to understand drivers of tick-borne disease risk, a result that may also apply to other rodent-borne zoonoses. Prevention of exposure based on ecological indicators of heightened risk should help protect public health.
© 2018 by the Ecological Society of America.

Entities:  

Keywords:  Lyme disease; blacklegged tick; bottom-up control; predator; tick-borne disease; top-down control; white-footed mouse; zoonoses

Mesh:

Year:  2018        PMID: 29738078     DOI: 10.1002/ecy.2386

Source DB:  PubMed          Journal:  Ecology        ISSN: 0012-9658            Impact factor:   5.499


  38 in total

1.  How the Distance Between Drag-Cloth Checks Affects the Estimate of Adult and Nymphal Ixodes scapularis (Acari: Ixodidae) Density.

Authors:  Ben Borgmann-Winter; David Allen
Journal:  J Med Entomol       Date:  2020-02-27       Impact factor: 2.278

2.  Lymelight: forecasting Lyme disease risk using web search data.

Authors:  Adam Sadilek; Yulin Hswen; John S Brownstein; Evgeniy Gabrilovich; Shailesh Bavadekar; Tomer Shekel
Journal:  NPJ Digit Med       Date:  2020-02-04

3.  The Density of the Lyme Disease Vector, Ixodes scapularis (Blacklegged Tick), Differs Between the Champlain Valley and Green Mountains, Vermont.

Authors:  David Allen; Benjamin Borgmann-Winter; Laura Bashor; Jeremy Ward
Journal:  Northeast Nat (Steuben)       Date:  2019-07-24       Impact factor: 0.583

4.  The problem of scale in the prediction and management of pathogen spillover.

Authors:  Daniel J Becker; Alex D Washburne; Christina L Faust; Erin A Mordecai; Raina K Plowright
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-08-12       Impact factor: 6.237

5.  Host infection and community composition predict vector burden.

Authors:  Jordan Salomon; Alexandra Lawrence; Arielle Crews; Samantha Sambado; Andrea Swei
Journal:  Oecologia       Date:  2021-02-12       Impact factor: 3.225

6.  Three reasons why expanded use of natural enemy solutions may offer sustainable control of human infections.

Authors:  I J Jones; S H Sokolow; G A De Leo
Journal:  People Nat (Hoboken)       Date:  2021-10-07

Review 7.  Dilution effects in disease ecology.

Authors:  Felicia Keesing; Richard S Ostfeld
Journal:  Ecol Lett       Date:  2021-09-04       Impact factor: 11.274

8.  LYMESIM 2.0: An Updated Simulation of Blacklegged Tick (Acari: Ixodidae) Population Dynamics and Enzootic Transmission of Borrelia burgdorferi (Spirochaetales: Spirochaetaceae).

Authors:  Holly Gaff; Rebecca J Eisen; Lars Eisen; Robyn Nadolny; Jenna Bjork; Andrew J Monaghan
Journal:  J Med Entomol       Date:  2020-05-04       Impact factor: 2.435

9.  Citizen science informs human-tick exposure in the Northeastern United States.

Authors:  W Tanner Porter; Peter J Motyka; Julie Wachara; Zachary A Barrand; Zahraa Hmood; Marya McLaughlin; Kelsey Pemberton; Nathan C Nieto
Journal:  Int J Health Geogr       Date:  2019-05-07       Impact factor: 3.918

10.  Active Forest Management Reduces Blacklegged Tick and Tick-Borne Pathogen Exposure Risk.

Authors:  Christine E Conte; Jessica E Leahy; Allison M Gardner
Journal:  Ecohealth       Date:  2021-06-22       Impact factor: 3.184

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