The flea that feeds on prairie dogs and other mammals serves as the vector for transmission of Sylvatic plague to the new host, primarily through flea bites, or contact with contaminated fluids or tissue, through predation or scavenging. Humans can contract plague from wildlife through flea bites and handling animal carcasses.
Epidemiology and distribution
Yersinia pestis circulates in rodent and prairie dog reservoirs on all continents except Australia. Sylvatic plague affects over 50 species of rodents worldwide. It is vectored by a variety of flea species. Non-rodent animals susceptible to the disease include shrews, Lagomorphs, ferrets, badgers, skunks, weasels, coyotes, domestic dogs and cats, bobcats, mountain lions, camels, goats, sheep, pigs, deer, and primates including humans. Birds are not known to be susceptible. Sylvatic plague is normally enzootic, meaning it occurs at regular, predictable rates in populations and specific areas. At unpredictable times it becomes epizootic in unexpected places. It is during these epizootic outbreaks that transmission to humans is most common. Factors that predispose to epizootic cycles include dense populations of rodents, multiple species of rodents in a particular area, and multiple rodent species in diverse habitats. Prairie dog colonies reach nearly 100% mortality rates during outbreaks. Prairie dogs are a keystone species and play a vital role as the primary prey of black footed ferrets. Developing methods to control plague is of high concern for preserving ferrets and the conservation of Western prairie and grassland ecosystems.
Prairie dogs evolved over 3,000,000 years ago, and have been surviving sylvatic plague as a species for a long time. In the absence of understanding the natural prairie dog/plague cycles, dusting rodent dens with pesticides to kill fleas is currently the main method of controlling sylvatic plague in the wild, with some interest in using vaccines developing. An oral live vaccine for prairie dogs was developed by the U.S. Geological Survey, National Wildlife Health Center, from a recombinant raccoon poxvirus expressing plague antigens. It was originally developed by a Fort Detrick company in 2003 which showed it protected mice against lethal plague.