Literature DB >> 17617870

Classical sheep transmissible spongiform encephalopathies: pathogenesis, pathological phenotypes and clinical disease.

M Jeffrey1, L González.   

Abstract

Scrapie is a prion disease or transmissible spongiform encephalopathy (TSE) of sheep, goats and moufflon. As with its human counterparts, pathology consists of vacuolation, gliosis and accumulations of abnormal forms of a host prion protein (PrPd) in the brain of affected individuals. Immunohistochemical methods can be used to identify both the intracellular truncation sites of PrPd in different cell types (PrPd epitope mapping) and the different morphological patterns of accumulation (PrPd profiling). Differences in the inferred truncation sites of PrPd are found for different strains of sheep TSEs and for different infected cell types within individual strains. Immunochemical methods of characterizing strains broadly correspond to PrPd mapping discriminatory results, but distinct PrPd profiles, which provide strain- and source-specific information on both the cell types which sustain infection (cellular tropisms) and the cellular processing of PrPd, have no immunoblotting counterparts. The cause of neurological dysfunction in human is commonly considered to be neuronal loss secondary to a direct or indirect effect of the accumulation of PrPd. However, in sheep scrapie there is no significant neuronal loss, and relationships between different magnitudes, topographical and cytological forms of PrPd accumulation and clinical signs are not evident. PrPd accumulation also occurs in lymphoid tissues, for which there is indirect evidence of a pathological effect, in the peripheral nervous system and in other tissues. It is generally assumed that neuroinvasion results from infection of the enteric nervous system neurones subsequent to amplification of infectivity in lymphoid tissues and later spread via sympathetic and parasympathetic pathways. The evidence for this is, however, circumstantial. Accumulation of PrPd and presence of infectivity in tissues other than the nervous and lymphoreticular systems gives insights on the ways of transmission of infection and on food safety.

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Year:  2007        PMID: 17617870     DOI: 10.1111/j.1365-2990.2007.00868.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  44 in total

1.  Calretinin-immunopositive cells and fibers in the cerebellar cortex of normal sheep.

Authors:  María-Isabel Alvarez; César Lacruz; Adolfo Toledano-Díaz; Eva Monleón; Marta Monzón; Juan-José Badiola; Adolfo Toledano
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

2.  Statins are ineffective at reducing neuroinflammation or prolonging survival in scrapie-infected mice.

Authors:  James A Carroll; Brent Race; Katie Phillips; James F Striebel; Bruce Chesebro
Journal:  J Gen Virol       Date:  2017-07-31       Impact factor: 3.891

3.  Endogenous proteolytic cleavage of disease-associated prion protein to produce C2 fragments is strongly cell- and tissue-dependent.

Authors:  Michel Dron; Mohammed Moudjou; Jérôme Chapuis; Muhammad Khalid Farooq Salamat; Julie Bernard; Sabrina Cronier; Christelle Langevin; Hubert Laude
Journal:  J Biol Chem       Date:  2010-02-12       Impact factor: 5.157

4.  Prion infection of mouse brain reveals multiple new upregulated genes involved in neuroinflammation or signal transduction.

Authors:  James A Carroll; James F Striebel; Brent Race; Katie Phillips; Bruce Chesebro
Journal:  J Virol       Date:  2014-12-10       Impact factor: 5.103

Review 5.  Prion strains: shining new light on old concepts.

Authors:  Alyssa J Block; Jason C Bartz
Journal:  Cell Tissue Res       Date:  2022-07-07       Impact factor: 5.249

6.  Ovine serum biomarkers of early and late phase scrapie.

Authors:  Isabelle Batxelli-Molina; Nicolas Salvetat; Olivier Andréoletti; Luc Guerrier; Guillaume Vicat; Franck Molina; Chantal Mourton-Gilles
Journal:  BMC Vet Res       Date:  2010-11-02       Impact factor: 2.741

Review 7.  Prion protein scrapie and the normal cellular prion protein.

Authors:  Caroline J Atkinson; Kai Zhang; Alan L Munn; Adrian Wiegmans; Ming Q Wei
Journal:  Prion       Date:  2016       Impact factor: 3.931

8.  Tau Protein Phosphorylated at Threonine-231 is Expressed Abundantly in the Cerebellum in Prion Encephalopathies.

Authors:  Vıctor Manuel Gómez-López; Amparo Viramontes-Pintos; Miguel Ángel Ontiveros-Torres; Linda Garcés-Ramírez; Fidel de la Cruz; Ignacio Villanueva-Fierro; Marely Bravo-Muñoz; Charles R Harrington; Sandra Martínez-Robles; Petra Yescas; Parménides Guadarrama-Ortíz; Mario Hernandes-Alejandro; Francisco Montiel-Sosa; Mar Pacheco-Herrero; José Luna-Muñoz
Journal:  J Alzheimers Dis       Date:  2021       Impact factor: 4.472

9.  BSE can propagate in sheep co-infected or pre-infected with scrapie.

Authors:  Angela Chong; James D Foster; Wilfred Goldmann; Lorenzo Gonzalez; Martin Jeffrey; Matthew J O'Connor; Keith Bishop; Ben C Maddison; E Fiona Houston; Kevin C Gough; Nora Hunter
Journal:  Sci Rep       Date:  2021-06-07       Impact factor: 4.379

10.  Caprine PRNP polymorphisms N146S and Q222K are associated with proteolytic cleavage of PrPC.

Authors:  Sally A Madsen-Bouterse; Paula Stewart; Helen Williamson; David A Schneider; Wilfred Goldmann
Journal:  Genet Sel Evol       Date:  2021-06-19       Impact factor: 4.297

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