Literature DB >> 19697235

Surveillance for transmissible spongiform encephalopathy in scavengers of white-tailed deer carcasses in the chronic wasting disease area of Wisconsin.

Christopher S Jennelle1, Michael D Samuel, Cherrie A Nolden, Delwyn P Keane, Daniel J Barr, Chad Johnson, Joshua P Vanderloo, Judd M Aiken, Amir N Hamir, Edward A Hoover.   

Abstract

Chronic wasting disease (CWD), a class of neurodegenerative transmissible spongiform encephalopathies (TSE) occurring in cervids, is found in a number of states and provinces across North America. Misfolded prions, the infectious agents of CWD, are deposited in the environment via carcass remains and excreta, and pose a threat of cross-species transmission. In this study tissues were tested from 812 representative mammalian scavengers, collected in the CWD-affected area of Wisconsin, for TSE infection using the IDEXX HerdChek enzyme-linked immunosorbent assay (ELISA). Only four of the collected mammals tested positive using the ELISA, but these were negative when tested by Western blot. While our sample sizes permitted high probabilities of detecting TSE assuming 1% population prevalence in several common scavengers (93%, 87%, and 87% for raccoons, opossums, and coyotes, respectively), insufficient sample sizes for other species precluded similar conclusions. One cannot rule out successful cross-species TSE transmission to scavengers, but the results suggest that such transmission is not frequent in the CWD-affected area of Wisconsin. The need for further surveillance of scavenger species, especially those known to be susceptible to TSE (e.g., cat, American mink, raccoon), is highlighted in both a field and laboratory setting.

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Year:  2009        PMID: 19697235     DOI: 10.1080/15287390903084249

Source DB:  PubMed          Journal:  J Toxicol Environ Health A        ISSN: 0098-4108


  10 in total

1.  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
Journal:  J Vet Diagn Invest       Date:  2019-01-29       Impact factor: 1.279

2.  Quantitative assessment of prion infectivity in tissues and body fluids by real-time quaking-induced conversion.

Authors:  Davin M Henderson; Kristen A Davenport; Nicholas J Haley; Nathaniel D Denkers; Candace K Mathiason; Edward A Hoover
Journal:  J Gen Virol       Date:  2014-10-10       Impact factor: 3.891

Review 3.  Occurrence, transmission, and zoonotic potential of chronic wasting disease.

Authors:  Samuel E Saunders; Shannon L Bartelt-Hunt; Jason C Bartz
Journal:  Emerg Infect Dis       Date:  2012-03       Impact factor: 6.883

4.  Genetic predictions of prion disease susceptibility in carnivore species based on variability of the prion gene coding region.

Authors:  Paula Stewart; Lauren Campbell; Susan Skogtvedt; Karen A Griffin; Jon M Arnemo; Morten Tryland; Simon Girling; Michael W Miller; Michael A Tranulis; Wilfred Goldmann
Journal:  PLoS One       Date:  2012-12-07       Impact factor: 3.240

5.  Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein.

Authors:  Malin K Sandberg; Huda Al-Doujaily; Christina J Sigurdson; Markus Glatzel; Catherine O'Malley; Caroline Powell; Emmanuel A Asante; Jacqueline M Linehan; Sebastian Brandner; Jonathan D F Wadsworth; John Collinge
Journal:  J Gen Virol       Date:  2010-07-07       Impact factor: 3.891

Review 6.  Evolution of Diagnostic Tests for Chronic Wasting Disease, a Naturally Occurring Prion Disease of Cervids.

Authors:  Nicholas J Haley; Jürgen A Richt
Journal:  Pathogens       Date:  2017-08-05

7.  Shedding and stability of CWD prion seeding activity in cervid feces.

Authors:  Joanne M Tennant; Manci Li; Davin M Henderson; Margaret L Tyer; Nathaniel D Denkers; Nicholas J Haley; Candace K Mathiason; Edward A Hoover
Journal:  PLoS One       Date:  2020-03-03       Impact factor: 3.240

8.  Mother to offspring transmission of chronic wasting disease in reeves' muntjac deer.

Authors:  Amy V Nalls; Erin McNulty; Jenny Powers; Davis M Seelig; Clare Hoover; Nicholas J Haley; Jeanette Hayes-Klug; Kelly Anderson; Paula Stewart; Wilfred Goldmann; Edward A Hoover; Candace K Mathiason
Journal:  PLoS One       Date:  2013-08-14       Impact factor: 3.240

9.  Dietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.

Authors:  Zoreh Davanipour; Eugene Sobel; Argyrios Ziogas; Carey Smoak; Thomas Bohr; Keith Doram; Boleslaw Liwnicz
Journal:  Br J Med Med Res       Date:  2014-04-21

10.  CWD prions remain infectious after passage through the digestive system of coyotes (Canis latrans).

Authors:  Tracy A Nichols; Justin W Fischer; Terry R Spraker; Qingzhong Kong; Kurt C VerCauteren
Journal:  Prion       Date:  2015       Impact factor: 3.931

  10 in total

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