Literature DB >> 6408182

Genetic control of scrapie and Creutzfeldt-Jakob disease in mice.

D T Kingsbury, K C Kasper, D P Stites, J D Watson, R N Hogan, S B Prusiner.   

Abstract

Genetic control of experimental scrapie and Creutzfeldt-Jakob disease (CJD) was studied in inbred strains of mice by measuring the times from intracerebral inoculation with the agents to the onset of neurological dysfunction. Every strain of mice examined was susceptible to infection; however, a wide range of incubation times was found for both scrapie and CJD. New Zealand (NZ) mice, which eventually develop an autoimmune disorder, were inoculated intracerebrally with 10(6) ID50 units of the scrapie agent in a Chandler isolate. NZW mice showed incubation periods of less than 95 days; this is the shortest period recorded for any murine host with scrapie. In NZB and NZB X W F1 mice, the incubation periods were approximately 130 days and were similar to those in BALB/c and C57BL mice. Male and female NZ mice exhibited scrapie incubation periods of the same length. Similar results were obtained when B10.Q and C57BL/6J mice were inoculated intracerebrally with 10(4) ID50 units of the CJD agent in a K.Fu. isolate. These observations define a genetic locus or loci controlling the length of scrapie and CJD incubation periods; alleles coding for longer incubation times appear to be autosomal dominant. When congenic mice with a C57BL/10J background differing only in their H-2 haplotypes were studied, the results showed that the D subregion of the H-2 complex played a central role in controlling the length of the CJD incubation period. The q allele at the D subregion resulted in shorter incubation times, whereas the d allele resulted in long incubation times. The p, s, b, and k alleles gave intermediate incubation times. We propose the symbol PID-1 for designating this genetic locus which is located within the D subregion of the major histocompatibility (H-2) complex on murine chromosome 17. In addition, observations on congenic mice provide evidence for the influence of sex on CJD incubation periods. In some strains of inbred mice, males showed significantly shorter incubation periods compared with those for females with experimental CJD. These studies with inbred mice have defined previously unrecognized genes that control the length of scrapie and CJD incubation periods.

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Year:  1983        PMID: 6408182

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  32 in total

Review 1.  The sclera, the prion, and the ophthalmologist.

Authors:  J S Mehta; W A Franks
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2.  Identification of multiple quantitative trait loci linked to prion disease incubation period in mice.

Authors:  S E Lloyd; O N Onwuazor; J A Beck; G Mallinson; M Farrall; P Targonski; J Collinge; E M Fisher
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-15       Impact factor: 11.205

Review 3.  Copper-dependent regulation of NMDA receptors by cellular prion protein: implications for neurodegenerative disorders.

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4.  Assignment of the human and mouse prion protein genes to homologous chromosomes.

Authors:  R S Sparkes; M Simon; V H Cohn; R E Fournier; J Lem; I Klisak; C Heinzmann; C Blatt; M Lucero; T Mohandas
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5.  Altered lymphocyte proliferation and innate immune function in scrapie 139A- and ME7-infected mice.

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6.  Immunological analysis of host and agent effects on Creutzfeldt-Jakob disease and scrapie prion proteins.

Authors:  J M Bockman; D T Kingsbury
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

7.  Murine resistance to street rabies virus: genetic analysis by testing second-backcross progeny and verification of allelic resistance genes in SJL/J and CBA/J mice.

Authors:  D L Lodmell; B Chesebro
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8.  Loss of Hsp70 exacerbates pathogenesis but not levels of fibrillar aggregates in a mouse model of Huntington's disease.

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9.  Shadoo (Sprn) and prion disease incubation time in mice.

Authors:  Sarah E Lloyd; Julia Grizenkova; Hirva Pota; John Collinge
Journal:  Mamm Genome       Date:  2009-06-10       Impact factor: 2.957

10.  A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse.

Authors:  Sarah E Lloyd; Emma G Maytham; Julia Grizenkova; Holger Hummerich; John Collinge
Journal:  Neurogenetics       Date:  2009-10-01       Impact factor: 2.660

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