AMPHOTERICIN-B DELAYS BOTH SCRAPIE AGENT REPLICATION AND PRP-RES ACCUMULATION EARLY IN INFECTION

被引:50
作者
MCKENZIE, D
KACZKOWSKI, J
MARSH, R
AIKEN, J
机构
关键词
D O I
10.1128/JVI.68.11.7534-7536.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Amphotericin B delays the onset of clinical symptoms in hamsters infected with scrapie agent strain 263K. Here we show that accumulation of a scrapie-specific isoform of the prion protein (PrP-res) and agent replication were delayed early in amphotericin B-treated animals. By 8 weeks postinfection, only untreated animals exhibited clinical symptoms of scrapie infection whereas PrP-res levels and titers were similar in treated and untreated animals. This suggests that although PrP-res accumulation and agent replication are linked, they are not the sole factors required for the onset of clinical disease.
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页码:7534 / 7536
页数:3
相关论文
共 19 条
[1]   IDENTIFICATION OF 2 BIOLOGICALLY DISTINCT STRAINS OF TRANSMISSIBLE MINK ENCEPHALOPATHY IN HAMSTERS [J].
BESSEN, RA ;
MARSH, RF .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :329-334
[2]   BIOCHEMICAL AND PHYSICAL-PROPERTIES OF THE PRION PROTEIN FROM 2 STRAINS OF THE TRANSMISSIBLE MINK ENCEPHALOPATHY AGENT [J].
BESSEN, RA ;
MARSH, RF .
JOURNAL OF VIROLOGY, 1992, 66 (04) :2096-2101
[3]   ISOLATION AND STRUCTURAL STUDIES OF THE INTACT SCRAPIE AGENT PROTEIN [J].
BOLTON, DC ;
BENDHEIM, PE ;
MARMORSTEIN, AD ;
POTEMPSKA, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 258 (02) :579-590
[4]   IDENTIFICATION OF A PROTEIN THAT PURIFIES WITH THE SCRAPIE PRION [J].
BOLTON, DC ;
MCKINLEY, MP ;
PRUSINER, SB .
SCIENCE, 1982, 218 (4579) :1309-1311
[5]  
Bruce M E, 1991, Curr Top Microbiol Immunol, V172, P125
[6]   PRECISE TARGETING OF THE PATHOLOGY OF THE SIALOGLYCOPROTEIN, PRP, AND VACUOLAR DEGENERATION IN MOUSE SCRAPIE [J].
BRUCE, ME ;
MCBRIDE, PA ;
FARQUHAR, CF .
NEUROSCIENCE LETTERS, 1989, 102 (01) :1-6
[7]   REPLICATION OF THE SCRAPIE AGENT IN HAMSTERS INFECTED INTRACEREBRALLY CONFIRMS THE PATHOGENESIS OF AN AMYLOID-INDUCING VIROSIS [J].
CZUB, M ;
BRAIG, HR ;
DIRINGER, H .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :1753-1756
[8]   PRO-]LEU CHANGE AT POSITION-102 OF PRION PROTEIN IS THE MOST COMMON BUT NOT THE SOLE MUTATION RELATED TO GERSTMANN-STRAUSSLER SYNDROME [J].
DOHURA, K ;
TATEISHI, J ;
SASAKI, H ;
KITAMOTO, T ;
SAKAKI, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) :974-979
[9]   MUTATIONS IN FAMILIAL CREUTZFELDT-JAKOB DISEASE AND GERSTMANN-STRAUSSLER-SCHEINKERS SYNDROME [J].
GOLDGABER, D ;
GOLDFARB, LG ;
BROWN, P ;
ASHER, DM ;
BROWN, WT ;
LIN, S ;
TEENER, JW ;
FEINSTONE, SM ;
RUBENSTEIN, R ;
KASCSAK, RJ ;
BOELLAARD, JW ;
GAJDUSEK, DC .
EXPERIMENTAL NEUROLOGY, 1989, 106 (02) :204-206
[10]   LINKAGE OF THE SCRAPIE-ASSOCIATED FIBRIL PROTEIN (PRP) GENE AND SINC USING CONGENIC MICE AND RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS [J].
HUNTER, N ;
HOPE, J ;
MCCONNELL, I ;
DICKINSON, AG .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :2711-2716