Volume 14, Number 1—January 2008
International Polar Year
Dogs as Sources and Sentinels of Parasites in Humans and Wildlife, Northern Canada
A minimum of 11 genera of parasites, including 7 known or suspected to cause zoonoses, were detected in dogs in 2 northern Canadian communities. Dogs in remote settlements receive minimal veterinary care and may serve as sources and sentinels for parasites in persons and wildlife, and as parasite bridges between wildlife and humans.
Throughout their long history of domestication, dogs have been sources of zoonotic parasites and have served as a link for parasite exchange among livestock, wildlife, and humans (1). Globally, dogs remain an important source of emerging disease in humans (e.g., eosinophilic enteritis caused by Ancylostoma caninum), a bridge for reemerging infections (Echinococcus multilocularis), and a source of parasites for immunocompromised persons (1).
Human disease and parasite infections in dogs in northern Canada have been recognized for some time (2–5). Historically, attention was focused on rabies virus, parvovirus, and canine distemper virus. However, dogs were also recognized as sources of zoonotic parasites such as Echinococcus spp. and as a possible bridge for rabies between wildlife and humans (4,5). Today, in many northern communities, veterinary services are absent or restricted, and disease surveillance programs and routine preventive health measures such as vaccination and parasite control are rare. These conditions have limited our understanding of disease interactions at the dog-human-wildlife interface and our ability to detect and respond to emerging diseases.
Northern environments and socioeconomic systems are changing rapidly and altering interactions among humans, animals, and their pathogens (6,7). In this study, we examined parasite diversity among dogs in 2 northern Canadian communities and evaluated the role of dogs as sentinels and sources of zoonotic infections in this changing landscape.
Canine preventative healthcare clinics were available in Fort Chipewyan, Alberta, and Fort Resolution, Northwest Territories, in August 2006. Dogs were presented by their owners voluntarily and a detailed history, blood, and fresh fecal samples were obtained. Feces were stored at 4°C until examined within 6–12 days by quantitative sugar flotation and light microscopy (8). Fecal samples positive for Giardia spp. were genotyped (9). Serum samples were tested for antibodies against Toxoplasma gondii and Neospora caninum by using modified direct agglutination and immunofluorescence assays, respectively, at the US Department of Agriculture (Beltsville, MD, USA). Dilutions >1:25 were considered positive. Associations between parasitism and host (sex, age, community) and husbandry factors (housing, food type, community) were examined for adult dogs by χ2 analysis and Fisher exact test by using analytical software (Statistix, Tallahassee, FL, USA).
The study population consisted of a variety of breeds and cross-breeds, including Siberian husky, Laborador retriever, German shepherd, terriers, and other types. Most dogs were housed outdoors and many were fed fish and game (raw, frozen, fresh, cooked, or dry). Of dogs eating wild game, they ate moose (95.8%), muskrat (53.5%), caribou (54.9%), bison (45.1%), rabbit (28.2%), beaver (25.4%), elk (15.5%), and deer (14.1%) (Figures 1, 2).
A minimum of 11 parasite genera were detected and 47% of dogs had >1 gastrointestinal parasite (Tables 1, 2). Taeniid eggs were either from Echinococcus spp. or Taenia spp. Dogs housed outdoors were more likely to have housing-associated parasites such as Toxocara spp., Toxascaris spp., Cystoisospora spp., and Uncinaria spp. (p<0.0001). Dogs who ate wild game were more likely to have game-associated parasites such as Sarcocystis spp., Taenia spp., and Echinococcus spp. (p<0.05). No statistically significant associations were found between food or housing, and T. gondii or N. caninum infections and previous veterinary care or deworming had no effect on parasite prevalence.
In the Northwest Territories, harvesting country foods is a key cultural activity and is important for sustenance; 75% of persons eat harvested meat and fish (10). Dogs fed fish and game can serve as indicators of parasites in these human food sources. Diet-associated zoonotic parasites detected in dogs included Diphyllobothrium spp., cestodes acquired by eating undercooked or inadequately frozen fish (found in humans throughout northern Canada); Alaria spp., trematodes acquired by eating frogs or paratenic hosts; and T. gondii, tissue protozoans acquired by eating oocysts from felid feces or tissue cysts in intermediate hosts (a worldwide human pathogen). In aboriginal persons in northern Canada, seroconversion for T. gondii during pregnancy has been associated with diets that include caribou (11). High seroprevalence in dogs indicates that T. gondii is common in the study area; however, the source of exposure was not identified. Given potential consequences for infection of parasite-negative pregnant women, further research is warranted on the association of human toxoplasmosis with a diet of country foods in northern regions.
Toxocara spp. are nematodes that cause visceral and ocular migrans in humans, particularly children. Although Toxocara spp. are considered limited to more southern regions (3), their presence in puppies and adults in Fort Resolution suggests that completion of their life cycle at northern latitudes is possible. Continuing warming trends may lead to increased occurrence of this parasite in the north. Giardia sp. Assemblage A is a protozoan that causes gastrointestinal disease in humans. Isolation of this zoonotic strain was unexpected because dogs are typically infected with Assemblage D, and Assemblage A suggests transmission from humans to dogs (9,12). This finding highlights a need to further investigate the apparent emergence of Assemblage A in domestic and wild animals in remote northern regions and transmission patterns among dogs, wildlife, and humans (S.J. Kutz, unpub. data). Echinococcus spp. are cestodes that cause hydatid (E. granulosus) or alveolar cysts (E. multilocularis) in the lungs and livers of humans. Although a reduction in dog teams in northern Canada has resulted in decreased prevalence of E. granulosus spp., the distribution, epidemiology, and role of the more pathogenic E. multilocularis spp. are not well understood in this region. Uncinaria spp. and Toxascaris spp. are also occasionally reported as zoonoses; however, evidence for these findings remains equivocal.
Dogs can also be sources of disease in parasite-naïve wildlife populations. They were the source for devastating distemper outbreaks in lions in the Serengeti (13), and lice of presumed dog origin are causing serious disease in Alaskan wolf populations (K.B. Beckmen, pers. comm.). Neospora caninum detected in this study may be a new parasite in this ecosystem with potentially serious consequences for wildlife. The remaining parasites are presumed present in local wildlife and can have a negative effect on the health of dogs and wildlife. More detailed, quantitative investigation is required to evaluate the role of dogs as potential sources of new, or amplifiers of existing, pathogens for wildlife.
Our results highlight important health issues associated with the interface between dogs, wildlife, and humans in remote northern communities. Disease associated with parasites in this study is often subclinical but can have serious effects on health and productivity of humans, dogs, and wildlife (e.g., Giardia spp.) (14). Although these parasites are relatively easy to control, there was no evidence that sporadic veterinary presence in Fort Chipewyan reduced parasitism. This finding emphasizes the need for a new approach to domestic animal healthcare in the north. Inaccessibility of communities, uncertain and changing roles of dogs, and current regulations in the veterinary profession restricting remote delivery of services hinder development of effective disease detection and preventative medicine programs. Innovative new methods for delivery of animal healthcare services are required. These methods should include long-term commitment to an integrated health approach, focusing on education, engagement, and development and support of local capacity for delivery of basic animal health services. Ongoing communication and partnerships between animal and human health professionals will enhance the effectiveness of such initiatives.
Dr Salb is currently pursuing a PhD in epidemiology in the Department of Medical Sciences and Faculty of Veterinary Medicine at the University of Calgary. Her research interests include wildlife disease surveillance, anthrax in wood bison, and disease management of the wildlife/agriculture interface.
We thank Judit Smits and the participants of the 2006 Ecosystem Health Rotation; the communities of Fort Chipewyan and Fort Resolution, especially Robert Grandjambe, Dana Wylie, Natalie Bourke, Moe O’Dean, Fred Mandeville, Patrick Simon; Meghan Logie; Klauss Neilssen; the Fort Chipewyan Nursing Station; the staff of the Calgary Zoo Animal Health Centre and Calgary Zoo Centre for Conservation Research; the Western Drug Distribution Centre; Bayer Animal Health; Idexx Laboratories; and Pfizer Animal Health for their assistance. We also thank Lyyden Polley and Brent Wagner for helpful comments on an earlier version of this article.
This study was supported in part by Natural Sciences and Engineering Research Council of Canada PromoScience, University of Calgary, the Calgary Zoo, Western College of Veterinary Medicine (Saskatoon, Saskatchewan), Ontario Veterinary College (Guelph, Ontario), Faculté de Médicine Vétérinaire (St. Hyacinthe, Quebec), and Atlantic Veterinary College (Charlottetown, Prince Edward Island).
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Table of Contents – Volume 14, Number 1—January 2008
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Susan J. Kutz, Faculty of Veterinary Medicine, University of Calgary, 3330 Hospital Dr NW, Calgary, Alberta T2N 4N1, Canada;