Linking chronic wasting disease to scrapie by comparison of Spiroplasma mirum ribosomal DNA sequences

被引:50
作者
Bastian, FO
Dash, S
Garry, RF
机构
[1] Tulane Univ, Med Ctr, Dept Pathol & Lab Med, New Orleans, LA 70112 USA
[2] Tulane Univ, Hlth Sci Ctr, New Orleans, LA 70112 USA
关键词
prion; Creutzfeldt-Jakob disease; scrapie; chronic wasting disease; spiroplasma; ribosome; transmissible spongiform encephalopathy; polymerase chain reaction (PCR); southern blot;
D O I
10.1016/j.yexmp.2004.02.002
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
Transmissible spongiform encephalopathies (TSE) are fatal neurodegenerative diseases of man and animals and are transmitted by a filterable pathogen whose identity is currently unresolved. Our data indicates that Spiroplasma, a wall-less bacterium, is involved in the pathogenesis of TSE. We searched for Spiroplasma ribosomal gene sequences in 10 scrapie-infected sheep brains and 10 normal sheep brains, 7 cervid samples infected with chronic wasting disease (CWD), and 7 normal cervid brains. DNA was extracted from these tissue samples and amplified by polymerase chain reaction (PCR) using primers specific for Spiroplasma-specific 16S rDNA. Specificity of the amplicon was determined by Southern blotting and DNA sequence analyses. Spiroplasma 16S rDNA was found in 8 of 10 scrapie-infected sheep brains and 6 of 7 CWD-infected tissue samples. All normal animal brain samples were negative. Spiroplasma 16S rDNA was also found in two human Creutzfeldt-Jakob diseased (CJD) brains but not in two age-matched normal human brains. DNA sequence analyses of the amplified PCR products from human and animal TSE cases revealed greater than 99% nucleotide sequence homology with Spiroplasma mirum. The presence of Spiroplasma DNA in TSE-infected tissues supports our hypothesis that Spiroplasma may be involved in the pathogenesis of these diseases. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:49 / 56
页数:8
相关论文
共 36 条
[1]
Spiroplasma sp. 16S rDNA in Creutzfeldt-Jakob disease and scrapie as shown by PCR and DNA sequence analysis [J].
Bastian, FO ;
Foster, JW .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2001, 60 (06) :613-620
[2]
NEUROTROPIC RESPONSE OF SPIROPLASMA-MIRUM FOLLOWING PERIPHERAL INOCULATION IN THE RAT [J].
BASTIAN, FO ;
JENNINGS, RA ;
HOFF, CJ .
ANNALES DE L INSTITUT PASTEUR-MICROBIOLOGIE, 1987, 138 (06) :651-655
[3]
BASTIAN FO, 1981, LANCET, V1, P660
[4]
BASTIAN FO, 1984, AM J PATHOL, V114, P496
[5]
ANTISERUM TO SCRAPIE-ASSOCIATED FIBRIL PROTEIN CROSS-REACTS WITH SPIROPLASMA-MIRUM FIBRIL PROTEINS [J].
BASTIAN, FO ;
JENNINGS, RA ;
GARDNER, WA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (12) :2430-2431
[6]
BASTIAN FO, 1979, ARCH PATHOL LAB MED, V103, P665
[7]
BASTIAN FO, 1991, CREUTZFELDT JAKOB DI, P49
[8]
Creutzfeldt-Jakob disease in unusually young patients who consumed venison [J].
Belay, ED ;
Gambetti, P ;
Schonberger, LB ;
Parchi, P ;
Lyon, DR ;
Capellari, S ;
McQuiston, JH ;
Bradley, K ;
Dowdle, G ;
Crutcher, JM ;
Nichols, CR .
ARCHIVES OF NEUROLOGY, 2001, 58 (10) :1673-1678
[9]
Besnoit C., 1899, REV VET-TOULOUSE, V24, P265
[10]
DISTINCT PRP PROPERTIES SUGGEST THE MOLECULAR-BASIS OF STRAIN VARIATION IN TRANSMISSIBLE MINK ENCEPHALOPATHY [J].
BESSEN, RA ;
MARSH, RF .
JOURNAL OF VIROLOGY, 1994, 68 (12) :7859-7868