Literature DB >> 23236066

Susceptibility of domestic cats to chronic wasting disease.

Candace K Mathiason1, Amy V Nalls, Davis M Seelig, Susan L Kraft, Kevin Carnes, Kelly R Anderson, Jeanette Hayes-Klug, Edward A Hoover.   

Abstract

Domestic and nondomestic cats have been shown to be susceptible to feline spongiform encephalopathy (FSE), almost certainly caused by consumption of bovine spongiform encephalopathy (BSE)-contaminated meat. Because domestic and free-ranging nondomestic felids scavenge cervid carcasses, including those in areas affected by chronic wasting disease (CWD), we evaluated the susceptibility of the domestic cat (Felis catus) to CWD infection experimentally. Cohorts of 5 cats each were inoculated intracerebrally (i.c.) or orally (p.o.) with CWD-infected deer brain. At 40 and 42 months postinoculation, two i.c.-inoculated cats developed signs consistent with prion disease, including a stilted gait, weight loss, anorexia, polydipsia, patterned motor behaviors, head and tail tremors, and ataxia, and the cats progressed to terminal disease within 5 months. Brains from these two cats were pooled and inoculated into cohorts of cats by the i.c., p.o., and intraperitoneal and subcutaneous (i.p./s.c.) routes. Upon subpassage, feline CWD was transmitted to all i.c.-inoculated cats with a decreased incubation period of 23 to 27 months. Feline-adapted CWD (Fel(CWD)) was demonstrated in the brains of all of the affected cats by Western blotting and immunohistochemical analysis. Magnetic resonance imaging revealed abnormalities in clinically ill cats, which included multifocal T2 fluid attenuated inversion recovery (FLAIR) signal hyperintensities, ventricular size increases, prominent sulci, and white matter tract cavitation. Currently, 3 of 4 i.p./s.c.- and 2 of 4 p.o. secondary passage-inoculated cats have developed abnormal behavior patterns consistent with the early stage of feline CWD. These results demonstrate that CWD can be transmitted and adapted to the domestic cat, thus raising the issue of potential cervid-to-feline transmission in nature.

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Year:  2012        PMID: 23236066      PMCID: PMC3571486          DOI: 10.1128/JVI.02592-12

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  68 in total

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3.  Salivary prions in sheep and deer.

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4.  Oral transmission and early lymphoid tropism of chronic wasting disease PrPres in mule deer fawns (Odocoileus hemionus).

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5.  Evidence for distinct chronic wasting disease (CWD) strains in experimental CWD in ferrets.

Authors:  Matthew R Perrott; Christina J Sigurdson; Gary L Mason; Edward A Hoover
Journal:  J Gen Virol       Date:  2011-09-14       Impact factor: 3.891

Review 6.  Creutzfeldt-Jakob disease.

Authors:  Beata Sikorska; Richard Knight; James W Ironside; Paweł P Liberski
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7.  Early detection of neuropathophysiology using diffusion-weighted magnetic resonance imaging in asymptomatic cats with feline immunodeficiency viral infection.

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Review 8.  Occurrence, transmission, and zoonotic potential of chronic wasting disease.

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Journal:  Emerg Infect Dis       Date:  2012-03       Impact factor: 6.883

Review 9.  An overview of human prion diseases.

Authors:  Muhammad Imran; Saqib Mahmood
Journal:  Virol J       Date:  2011-12-24       Impact factor: 4.099

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  25 in total

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Review 2.  Molecular Mechanisms of Chronic Wasting Disease Prion Propagation.

Authors:  Julie A Moreno; Glenn C Telling
Journal:  Cold Spring Harb Perspect Med       Date:  2018-06-01       Impact factor: 6.915

3.  Experimental Transmission of the Chronic Wasting Disease Agent to Swine after Oral or Intracranial Inoculation.

Authors:  S Jo Moore; M Heather West Greenlee; Naveen Kondru; Sireesha Manne; Jodi D Smith; Robert A Kunkle; Anumantha Kanthasamy; Justin J Greenlee
Journal:  J Virol       Date:  2017-09-12       Impact factor: 5.103

4.  Lesion profiling and subcellular prion localization of cervid chronic wasting disease in domestic cats.

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Journal:  Vet Pathol       Date:  2014-02-27       Impact factor: 2.221

5.  Assessing transmissible spongiform encephalopathy species barriers with an in vitro prion protein conversion assay.

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6.  Use of a 2-aminothiazole to Treat Chronic Wasting Disease in Transgenic Mice.

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7.  Insights into Chronic Wasting Disease and Bovine Spongiform Encephalopathy Species Barriers by Use of Real-Time Conversion.

Authors:  Kristen A Davenport; Davin M Henderson; Jifeng Bian; Glenn C Telling; Candace K Mathiason; Edward A Hoover
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8.  Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers.

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Review 9.  Cross-species transmission of CWD prions.

Authors:  Timothy D Kurt; Christina J Sigurdson
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10.  Procedures for identifying infectious prions after passage through the digestive system of an avian species.

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