Literature DB >> 15362835

Epidemiology of chronic wasting disease in captive white-tailed and mule deer.

Michael W Miller1, Margaret A Wild.   

Abstract

The natural occurrence of chronic wasting disease (CWD) in a 1993 cohort of captive white-tailed deer (Odocoileus virginianus) afforded the opportunity to describe epidemic dynamics in this species and to compare dynamics with those seen in contemporary cohorts of captive mule deer (O. hemionus) also infected with CWD. The overall incidence of clinical CWD in white-tailed deer was 82% (nine of 11) among individuals that survived >15 mo. Affected white-tailed deer died or were killed because of terminal CWD at age 49-76 mo (x = 59.6 mo, SE = 3.9 mo). Epidemic dynamics of CWD in captive white-tailed deer were similar to dynamics in mule deer cohorts. Incidence of clinical CWD was 57% (4/7) among hand-raised (HR) and 67% (4/6) among dam-raised (DR) mule deer; affected HR mule deer succumbed at 64-86 mo of age (x = 72 mo; SE = 5 mo), and affected DR mule deer died at age 31-58 mo (x = 41.3 mo; SE = 6.1 mo). Sustained horizontal transmission of CWD most plausibly explained epidemic dynamics, but the original source of exposures could not be determined. Apparent differences in mean age at CWD-caused death among these cohorts may be attributable to differences in the timing or intensity of exposure to CWD, and these factors appear to be more likely to influence epidemic dynamics than species differences. It follows that CWD epidemic dynamics in sympatric, free-ranging white-tailed and mule deer sharing habitats in western North American ranges also may be similar.

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Year:  2004        PMID: 15362835     DOI: 10.7589/0090-3558-40.2.320

Source DB:  PubMed          Journal:  J Wildl Dis        ISSN: 0090-3558            Impact factor:   1.535


  16 in total

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2.  Deterministic and stochastic analysis of an eco-epidemiological model.

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Journal:  J Biol Phys       Date:  2017-10-07       Impact factor: 1.365

3.  Pathogenesis of chronic wasting disease in cervidized transgenic mice.

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Authors:  Anthony E Kincaid; Kathryn F Hudson; Matthew W Richey; Jason C Bartz
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5.  Raccoons accumulate PrPSc after intracranial inoculation of the agents of chronic wasting disease or transmissible mink encephalopathy but not atypical scrapie.

Authors:  S Jo Moore; Jodi D Smith; Jürgen A Richt; Justin J Greenlee
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6.  Minor oral lesions facilitate transmission of chronic wasting disease.

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7.  The nasal cavity is a route for prion infection in hamsters.

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9.  Homogenization, sex, and differential motility predict spread of chronic wasting disease in mule deer in southern Utah.

Authors:  Martha J Garlick; James A Powell; Mevin B Hooten; Leslie R MacFarlane
Journal:  J Math Biol       Date:  2013-07-12       Impact factor: 2.259

10.  Infectious prions in pre-clinical deer and transmission of chronic wasting disease solely by environmental exposure.

Authors:  Candace K Mathiason; Sheila A Hays; Jenny Powers; Jeanette Hayes-Klug; Julia Langenberg; Sallie J Dahmes; David A Osborn; Karl V Miller; Robert J Warren; Gary L Mason; Edward A Hoover
Journal:  PLoS One       Date:  2009-06-16       Impact factor: 3.240

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