Chronic wasting disease

William Leiss of the University of Ottawa, in Ontario, Canada, and colleagues there and elsewhere in Canada and the USA, explain how CWD is a fatal neurodegenerative disease of various species of animals in the cervid family of mammals. This family includes deer, elk, reindeer, caribou, and moose. The team points out that CWD is endemic in both wild (free-ranging) and captive (farmed) populations of these species which further complicates disease control. The disease is most prevalent among deer species, affecting in particular mule deer, but also black-tailed deer and white-tailed deer.

Chronic wasting disease is closely related to so-called "mad cow disease," bovine spongiform encephalopathy (BSE), the equivalent disease in sheep known as scrapie and the human disease variant Creutzfeldt-Jakob disease (variant CJD). These various diseases are caused by the misfolding of proteins or protein fragments, known as prions, which self-replicate, or propagate, in tissue, specifically brain tissue, and lead to cell death and the ultimate demise of the affected organ.

The team points out that disease surveillance in North America has provided some qualitative assessments of the overall risk of CWD in Canada and the USA. Animals in almost half of all US states and two Canadian provinces are afflicted. The first case outside North America was identified in South Korea in 1997 and while the European Union has strict rules and surveillance in place, an afflicted farmed reindeer was identified in 2016 by the Norwegian Institute for Nature Research and subsequently two wild individuals. The problem is thus likely to become an intercontinental one unless more research is done to understand the disease and find ways to control it.

A new risk control strategy has been proposed for CWD in North America in which controlled forest fires are lit in areas where vegetation and soil are heavily contaminated with the pathogenic prions shed by animal waste and carcasses.