Volume 14, Number 7—July 2008
Anthropogenic Influence on Prevalence of 2 Amphibian Pathogens
Highlight and copy the desired format.
|EID||St-Amour V, Wong WM, Garner TW, Lesbarrères D. Anthropogenic Influence on Prevalence of 2 Amphibian Pathogens. Emerg Infect Dis. 2008;14(7):1175-1176. https://dx.doi.org/10.3201/eid1407.070602|
|AMA||St-Amour V, Wong WM, Garner TW, et al. Anthropogenic Influence on Prevalence of 2 Amphibian Pathogens. Emerging Infectious Diseases. 2008;14(7):1175-1176. doi:10.3201/eid1407.070602.|
|APA||St-Amour, V., Wong, W. M., Garner, T. W., & Lesbarrères, D. (2008). Anthropogenic Influence on Prevalence of 2 Amphibian Pathogens. Emerging Infectious Diseases, 14(7), 1175-1176. https://dx.doi.org/10.3201/eid1407.070602.|
To the Editor: Although the relationship between the emergence of zoonotic diseases and human influenced landscapes is accepted (1–3), the relationship between human-influenced landscapes and wildlife disease is less so. Evidence does support correlations between human activities and environmental conditions affecting wildlife disease emergence (2,3). These studies assume relationships between component(s) of human habitat modification and the virulence of disease, and derive estimates of virulence from counts of the visibly diseased or those that have seroconverted (3). This explains only part of the host and pathogen dynamic; it seems reasonable to extend the relationship to include prevalence of infection. Data supporting this extension are lacking. Here we present data from a study examining the correlations between human influences on habitat and prevalence of 2 amphibian pathogens (Batrachochytrium dendrobatidis and ranavirus FV3) in populations of Rana clamitans in central and northeastern Ontario, Canada.
We sampled an average of 25 animals (standard deviation ± 6.16) from 11 populations during summer 2005. We washed equipment in bleach and air-dried equipment between visits and sites. All animals were kept individually to avoid cross-contamination, euthanized with MS22, and assessed for infection using molecular diagnostics. We tested for ranavirus infection of livers by amplifying the major capsid protein using standard PCR (4). We tested for infection with B. dendrobatidis by using a quantitative real-time PCR (5). Prevalence for each pathogen was estimated as the proportion of animals testing positive at a pond.
Site coordinates were determined by using global positioning satellite (GPS), and 4 quantitative measures of human habitat modification were also assessed. GPS coordinates were used to map sites and to measure distance to the nearest road, industrial activity (agriculture, mine, paper mill), and human habitation; all measurements were in meters. We further assigned a qualitative measure of human influence on each breeding pond by assigning ponds to each of the following categories: 1) human presence without human habitat modification or extensive disturbance; 2) recreational activities (fishing, boating); 3) property development (housing or commercial buildings); 4) agricultural activity; and 5) industrial activity. Each of the 5 categories was assigned a 0/1 score; scores for each pond were summed 1–5 (by definition no site scored 0 due to sampling strategy) to derive the final measure of human influence. We modeled the relationship between prevalence and human habitat modification or influence using general linear models (GLM) with prevalence as the dependent variable and with all human influence variables log-transformed to meet assumptions of normality. A type III model structure was used to account for the influence of all explanatory variables in each analysis.
Eight ponds exhibited signs of FV3 infection (range 0%–63% prevalence); 6 ponds contained frogs infected with the amphibian chytrid (range 0%–36% prevalence). GLM did not show any relationship between the prevalence of chytrid infection and all of our explanatory variables (Table). In contrast, 3 of our explanatory variables had a significant influence of ranavirus prevalence. Distance to industrial activity (p<0.05), to human habitation (p<0.05), and degree of human influence (p<0.01) all had a significant effect on the dependent variable (Table).
The disparity between results for the 2 pathogens generates several possible hypotheses. First, proximity to human activities may correlate with the probability of pathogen introduction through introduced species (6), fomites, or other sources of infectious particles, with the likelihood of introduction higher for ranavirus. Certainly, both pathogens are presumed to be vectored in association with human activities (7,8), but B. dendrobatidis exhibits a greater host and geographic range and thus should exhibit greater prevalence if humans were mediating introduction across the range of our study. Second, human activities such as construction and industry, may directly or indirectly influence the basic reproductive number, R0, of ranavirus to a greater extent than for that of B. dendrobatidis. Although ranavirus does exhibit optimal environmental ranges for replication and infection, the virulence of B. dendrobatidis can be directly influenced by the environment (2). Furthermore, infection by B. dendrobatidis occurs through a free-living stage; ranavirus is more likely transmitted through direct contact, which suggests that B. dendrobatidis would be more sensitive to environmental factors. Last, human activities may influence host ability to mediate immune responses that have the capability to prevent infection. Evidence exists that amphibian host responses to ranavirus are predominantly acquired (9); those for B. dendrobatidis may be more innate and less prone to environmental manipulation (10). Although the observed correlation should be further tested and the disturbance index should be refined, we believe our observed pattern may reflect the influence of human activities and habitat modification in the dispersal of infectious diseases. With increasing evidence pointing towards the role of emerging infectious diseases in the decline of amphibian populations, management plans should therefore account for the indirect effects related to human activities.
We thank Albrecht Schulte-Hostedde and Eric Gauthier for use of their molecular equipment for ranaviral analysis. Earlier versions of this manuscript also benefited from comments given by Scott Kaufman, Bruce Pauli, and 2 anonymous reviewers.
This research was funded by NSERC and Laurentian University Research Fund and has been approved by the Laurentian Animal Care Committee (Protocols no. 2005-05-01 and 2005-05-02).
- Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, Global trends in emerging infectious diseases. Nature. In press.
- Bosch J, Carrascal LM, Durán L, Walker S, Fisher MC. Climate change and outbreaks of amphibian chytridiomycosis in a montane area of Central Spain; is there a link? Proc Biol Sci. 2007;274:253–60.
- Bradley CA, Altizer S. Urbanization and the ecology of wildlife diseases. Trends Ecol Evol. 2007;22:95–102.
- St.-Amour V, Lesbarrères D. Genetic evidence of Ranavirus in toe clips: an alternative to lethal sampling methods. Conserv Genet. 2007;8:1247–50.
- Garner TWJ, Perkins M, Govindarajulu P, Seglie D, Walker SJ, Cunningham AA, The emerging amphibian pathogen Batrachochytrium dendrobatidis globally infects introduced populations of the North American bullfrog, Rana catesbeiana. Biol Lett. 2006;2:455–9.
- Garner TWJ, Walker S, Bosch J, Hyatt A, Cunningham A, Fisher MC. Chytrid fungus in Europe. Emerg Infect Dis. 2005;11:1639–41.
- Jancovich JK, Davidson EW, Parameswaran N, Mao J, Chinchar G, Collins JP, Evidence for emergence of an amphibian iridoviral disease because of human-enhanced spread. Mol Ecol. 2005;14:213–24.
- Fisher MC, Garner TWJ. The relationship between the introduction of Batrachochytrium dendrobatidis, the international trade in amphibians and introduced amphibian species. Fungal Biol Rev. 2007;21:2–9.
- Robert J, Morales H, Buck W, Cohen N, Marr S, Gantress J. Adaptive immunity and histopathology in frog virus 3-infected Xenopus. Virology. 2005;332:667–75.
- Woodhams DC, Ardipradja K, Alford RA, Marantelli G, Reinert LK, Rollins-Smith LA. Resistance to chytridiomycosis varies among amphibian species and is correlated with skin peptide defenses. Anim Conserv. 2007;10:409–17.
- Table. General linear models for the relationships of amphibian emerging infectious disease prevalence and anthropogenic variables
Please use the form below to submit correspondence to the authors or contact them at the following address:
David Lesbarrères, Biology Department, Laurentian University, Ramsey Lake Rd, Sudbury, Ontario P3B 3C8, Canada;
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: July 12, 2010
- Page last updated: July 12, 2010
- Page last reviewed: July 12, 2010
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)