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      A review of sarcoptic mange in North American wildlife

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          Abstract

          The “itch mite” or “mange mite”, Sarcoptes scabiei, causes scabies in humans and sarcoptic mange in domestic and free-ranging animals. This mite has a wide host range due to its ability to adapt to new hosts and has been spread across the globe presumably through human expansion. While disease caused by S. scabiei has been very well-studied in humans and domestic animals, there are still numerous gaps in our understanding of this pathogen in free-ranging wildlife. The literature on sarcoptic mange in North American wildlife is particularly limited, which may be due to the relatively limited number of clinically-affected species and lack of severe population impacts seen in other continents. This review article provides a summary of the current knowledge of mange in wildlife, with a focus on the most common clinically-affected species in North America including red foxes ( Vulpes vulpes), gray wolves ( Canis lupus), coyotes ( Canis latrans), and American black bears ( Ursus americanus).

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          Highlights

          • Sarcoptic mange is an important wildlife disease across the globe.

          • There is a lack of field surveys on mange in North American wildlife.

          • This review summarizes the natural history of Sarcoptes scabiei.

          • There are few reports on methods to control mange in wildlife.

          • The known host range in North American wildlife is also addressed.

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          Most cited references184

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          Disease Reveals the Predator: Sarcoptic Mange, Red Fox Predation, and Prey Populations

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            Problems in diagnosing scabies, a global disease in human and animal populations.

            Scabies is a worldwide disease and a major public health problem in many developing countries, related primarily to poverty and overcrowding. In remote Aboriginal communities in northern Australia, prevalences of up to 50% among children have been described, despite the availability of effective chemotherapy. Sarcoptic mange is also an important veterinary disease engendering significant morbidity and mortality in wild, domestic, and farmed animals. Scabies is caused by the ectoparasitic mite Sarcoptes scabiei burrowing into the host epidermis. Clinical symptoms include intensely itchy lesions that often are a precursor to secondary bacterial pyoderma, septicemia, and, in humans, poststreptococcal glomerulonephritis. Although diagnosed scabies cases can be successfully treated, the rash of the primary infestation takes 4 to 6 weeks to develop, and thus, transmission to others often occurs prior to therapy. In humans, the symptoms of scabies infestations can mimic other dermatological skin diseases, and traditional tests to diagnose scabies are less than 50% accurate. To aid early identification of disease and thus treatment, a simple, cheap, sensitive, and specific test for routine diagnosis of active scabies is essential. Recent developments leading to the expression and purification of S. scabiei recombinant antigens have identified a number of molecules with diagnostic potential, and current studies include the investigation and assessment of the accuracy of these recombinant proteins in identifying antibodies in individuals with active scabies and in differentiating those with past exposure. Early identification of disease will enable selective treatment of those affected, reduce transmission and the requirement for mass treatment, limit the potential for escalating mite resistance, and provide another means of controlling scabies in populations in areas of endemicity.
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              Flexible spatial organization of urban foxes, Vulpes vulpes, before and during an outbreak of sarcoptic mange.

              The social and spatial organization of urban fox groups prior to and during an outbreak of sarcoptic mange was compared with predictions derived from the resource dispersion hypothesis (RDH). We investigated the availability of three key resources. Neither daytime rest sites nor breeding sites appeared to be limited in availability. The availability of food deliberately supplied by local householders was examined by questionnaire surveys. The daily and weekly amount of food supplied was greatly in excess of the minimum requirements of a pair of foxes, but was consistent between territories. The availability of this food source increased markedly as a result of more people feeding the foxes. In agreement with the RDH, group size prior to the outbreak of mange increased from 2.25 animals (N=4) to 6.57 animals (N=7). Before the outbreak of mange, two territories were divided. Increased scavenge availability on smaller territories may have promoted these changes. Excluding these spatial changes, territories were very stable between years. After the outbreak of mange, group size declined as a direct result of mange-induced mortality. Surviving animals increased their ranges only after neighbouring groups had died out. Ranges did not increase in size in response to a decline in food availability. Nor were the increases in range size associated with the relinquishment of parts of the existing territory. These postmange changes are contrary to the RDH. Three factors may have promoted these changes: the elimination of interstitial space, the forced dispersal of young or future division of the territory. Copyright 2000 The Association for the Study of Animal Behaviour.
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                Author and article information

                Contributors
                Journal
                Int J Parasitol Parasites Wildl
                Int J Parasitol Parasites Wildl
                International Journal for Parasitology: Parasites and Wildlife
                Elsevier
                2213-2244
                13 June 2019
                August 2019
                13 June 2019
                : 9
                : 285-297
                Affiliations
                [a ]Southeastern Cooperative Wildlife Disease Study, 589 D.W. Brooks Drive, Wildlife Health Building, College of Veterinary Medicine, University of Georgia, Athens, GA, 30602, USA
                [b ]Department of Veterinary and Biomedical Sciences, 115 Henning Building, Pennsylvania State University, University Park, PA, 16802, USA
                [c ]College of Veterinary Medicine, 501 D.W. Brooks Drive, University of Georgia, Athens, GA, 30602, USA
                [d ]Warnell School of Forestry and Natural Resources, 180 E Green Street, University of Georgia, Athens, GA, 30602, USA
                Author notes
                []Corresponding author. kevindn@ 123456uga.edu
                [∗∗ ]Corresponding author. 589 D.W. Brooks Drive, Wildlife Health Building, Athens, GA, 30602, USA. myabsley@ 123456uga.edu
                Article
                S2213-2244(19)30090-2
                10.1016/j.ijppaw.2019.06.003
                6599944
                31304085
                16bb26cf-502f-4bd5-9d30-f32f0faffa84
                © 2019 Published by Elsevier Ltd on behalf of Australian Society for Parasitology.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 16 April 2019
                : 5 June 2019
                : 6 June 2019
                Categories
                Article

                mange,sarcoptes scabiei,wildlife,north america
                mange, sarcoptes scabiei, wildlife, north america

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