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American Bison - Buffalo Field Campaign

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Alaska (Zarnke 1993) and from bison at Elk Island National<br />

Park (EINP) in Alberta (Cool 1999; Gates et al. 2001b). In YNP,<br />

positive antibody titres were detected in 31% of tested animals<br />

(Taylor et al. 1997). There are unpublished data regarding sero-<br />

reactivity from bison transported to Montana from WCNP in<br />

South Dakota (K. Kunkel, personal communication). The Jackson<br />

bison herd, with a known history of commingling with cattle,<br />

has demonstrated low-level titres, but no evidence of BVD<br />

antigen or clinical disease has been found (T. Roffe, personal<br />

communication). Clinical BVD was reported in the EINP plains<br />

bison herd in 1996, prompting a serological survey of plains<br />

bison and wood bison herds (Cool 1999; Gates et al. 2001b).<br />

Forty-seven percent of 561 plains bison from EINP tested sero-<br />

positive for BVD; one tested positive for the virus antigen. At<br />

least six plains bison deaths in EINP were attributed to the BVD<br />

virus (Cool 1999). Tissues from the suspected cases of BVD<br />

infected plains bison were submitted to the Animal Disease<br />

Research Institute, Lethbridge, Alberta, Canada, and type 1<br />

BVD virus was isolated (Tessaro and Deregt 1999). None of 352<br />

wood bison in the Park tested sero-positive for BVD at the time.<br />

Both plains and wood bison populations at EINP are vaccinated<br />

for BVD during annual roundups. However, calves used in<br />

translocations are not vaccinated to allow future screening of<br />

recipient populations for BVD. In Poland, Sosnowski (1977)<br />

reported BVD in a captive European bison. BVD is common in<br />

cattle in North America and poses no known risk to humans.<br />

5.1.8 Johne’s disease<br />

Johne’s disease (JD) is caused by the etiologic agent<br />

Mycobacterium avium subsp. paratuberculosis, a hardy<br />

bacterium related to the agents of leprosy and tuberculosis.<br />

It occurs worldwide affecting a variety of domestic and wild<br />

ruminants including bison, cattle, and sheep (Buergelt et<br />

al. 2000; Williams 2001). Infections often lead to chronic<br />

granulomatous enteritis with clinical signs of diarrhoea, weight<br />

loss, decreased milk production, and mortality. JD is common<br />

in cattle. Recent studies have shown that more than 20% of<br />

dairy herds in the U.S. have JD (Chi et al. 2002; Ott et al. 1999)<br />

causing an estimated economic loss of more than US$200<br />

million annually. JD typically enters a herd when infected,<br />

asymptomatic animals are introduced. Unpasteurised raw<br />

milk or colostrum may be a source of infection for artificially<br />

raised calves. Animals are most susceptible to infection during<br />

their first year of life. Neonates most often become infected<br />

by swallowing small amounts of contaminated manure from<br />

the ground or from their mother’s udder. Animals exposed to a<br />

very small dose of bacteria at a young age, and older animals,<br />

are not likely to develop clinical disease until they are much<br />

older. After several years, infected animals may become patent<br />

and shed mycobacteria in their faeces. Typically, pre-patent<br />

animals do not show symptoms of disease; consequently, most<br />

32 <strong>American</strong> <strong>Bison</strong>: Status Survey and Conservation Guidelines 2010<br />

infections go unnoticed and undiagnosed. There is no treatment<br />

for animals infected with JD and prevention is the best control<br />

measure. Humans are not considered susceptible, but M. a.<br />

paratuberculosis has been isolated in patients with chronic<br />

enteritis (Crohn’s disease) (Chiodini 1989). JD is not considered<br />

to be a disease problem when bison are on open rangelands<br />

and managed at low density. However, restrictions may apply<br />

to inter-jurisdictional movement of animals from known infected<br />

herds. Hence, maintaining low risk status for bison herds<br />

used as a source for conservation projects is an important<br />

consideration.<br />

In 1998, the U.S. Animal Health Association approved the<br />

Voluntary Johne’s Disease Herd Status Program for cattle<br />

(VJDHSP). The VJDHSP provides testing guidelines for States<br />

to use to identify livestock herds as low risk for JD infection.<br />

With numerous tests over several years, herds progress to<br />

higher status levels. The higher the status level, the more<br />

likely it is that a herd is not infected with JD. In April 2002,<br />

USDA-APHIS-Veterinary Service incorporated portions of<br />

this programme into national programme standards: Uniform<br />

Program Standards for the Voluntary Bovine Johne’s Disease<br />

Control Program (VBJDCP). VBJDCP-test-negative herds serve<br />

as a source of low JD risk stock. Testing for JD in conservation<br />

herds has been sporadic and opportunistic. Diagnostic tools<br />

are being developed and improved. There are no reports of JD<br />

in conservation bison herds in the literature, however, some<br />

commercial operations have discovered JD, and in many cases<br />

are managing to prevent its spread and reduce its impact on<br />

the industry.<br />

5.1.9 Malignant catarrhal fever (sheep associated)<br />

Malignant catarrhal fever (MCF) is a serious, often fatal disease<br />

affecting many species of the Order Artiodactyla. It is caused<br />

by viruses of the genus Rhadinovirus. At least 10 MCF viruses<br />

have been recognised worldwide and five viruses have been<br />

linked to disease. The viruses most significant to livestock are<br />

those carried by sheep, goats or wildebeest (Connochaetes<br />

spp.). Although ovine herpes virus type 2 (sheep associated<br />

MCF) does not cause disease in its natural host, domestic<br />

sheep, it does cause MCF in bison. Serological testing indicated<br />

that it is common in domestic goats (61%) and sheep (53%)<br />

in the U.S. (Li et al. 1996). MCF is an important disease in the<br />

commercial bison industry as it is one of the most infectious<br />

diseases of bison, especially at high densities (Heuschele and<br />

Reid 2001). It causes highly lethal infections in bison, with<br />

the reported incidence of mortality in a herd of up to 100%<br />

(Schultheiss et al. 2001). Infections proceed rapidly to clinical<br />

disease. MCF is expressed in two forms, acute and chronic,<br />

but regardless, death ensues in most cases. In the acute form,<br />

bison usually die within 7–10 days of infection or within 48 hr<br />

of becoming symptomatic. Alternatively, death may ensue as

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