A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions

被引:263
作者
Klöhn, PC [1 ]
Stoltze, L [1 ]
Flechsig, E [1 ]
Enari, M [1 ]
Weissmann, C [1 ]
机构
[1] UCL Natl Hosp Neurol & Neurosurg, Med Res Council Prion Unit, Dept Neurodegenerat Dis, Inst Neurol, London WC1N 3BG, England
关键词
D O I
10.1073/pnas.1834432100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prions are usually quantified by bioassays based on intracerebral inoculation of mice that are slow, imprecise, and costly. We have isolated neuroblastoma N2a sublines highly susceptible to mouse prions, as evidenced by accumulation of infectivity and the scrapie form of prion protein (PrP(Sc)), and developed quantitative in vitro assays for prion infectivity. In the scrapie cell (SC) assay, susceptible N2a cells are exposed to prion-containing samples for 3 days, grown to confluence, and split 1:10 three times, and the proportion of PrP(Sc)-containing cells is determined with automated counting equipment. In a log/log plot, the dose-response is linear over two logs of prion concentrations. The SC assay is about as sensitive as the mouse bioassay, 10 times faster, >2 orders of magnitude less expensive, and suitable for robotization. SC assays performed in a more time-consuming end point titration format extend the sensitivity and show that infectivity titers measured in tissue culture and in the mouse are similar.
引用
收藏
页码:11666 / 11671
页数:6
相关论文
共 25 条
[1]   Cell culture models of transmissible spongiform encephalopathies [J].
Béranger, F ;
Mangé, A ;
Solassol, J ;
Lehmann, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 289 (02) :311-316
[2]   Scrapie strains maintain biological phenotypes on propagation in a cell line in culture [J].
Birkett, CR ;
Hennion, RM ;
Bembridge, DA ;
Clarke, MC ;
Chree, A ;
Bruce, ME ;
Bostock, CJ .
EMBO JOURNAL, 2001, 20 (13) :3351-3358
[3]   Cultured cell sublines highly susceptible to prion infection [J].
Bosque, PJ ;
Prusiner, SB .
JOURNAL OF VIROLOGY, 2000, 74 (09) :4377-4386
[4]   MICE DEVOID OF PRP ARE RESISTANT TO SCRAPIE [J].
BUELER, H ;
AGUZZI, A ;
SAILER, A ;
GREINER, RA ;
AUTENRIED, P ;
AGUET, M ;
WEISSMANN, C .
CELL, 1993, 73 (07) :1339-1347
[5]   SCRAPIE-INFECTED MURINE NEURO-BLASTOMA CELLS PRODUCE PROTEASE-RESISTANT PRION PROTEINS [J].
BUTLER, DA ;
SCOTT, MRD ;
BOCKMAN, JM ;
BORCHELT, DR ;
TARABOULOS, A ;
HSIAO, KK ;
KINGSBURY, DT ;
PRUSINER, SB .
JOURNAL OF VIROLOGY, 1988, 62 (05) :1558-1564
[6]  
CHANDLER RL, 1961, LANCET, V1, P1378
[7]   Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody [J].
Enari, M ;
Flechsig, E ;
Weissmann, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9295-9299
[8]   Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie [J].
Fischer, M ;
Rulicke, T ;
Raeber, A ;
Sailer, A ;
Moser, M ;
Oesch, B ;
Brandner, S ;
Aguzzi, A ;
Weissmann, C .
EMBO JOURNAL, 1996, 15 (06) :1255-1264
[9]   PrP expression and replication by Schwann cells:: Implications in prion spreading [J].
Follet, J ;
Lemaire-Vieille, C ;
Blanquet-Grossard, F ;
Podevin-Dimster, V ;
Lehmann, S ;
Chauvin, JP ;
Decavel, JP ;
Varea, R ;
Grassi, J ;
Fontès, M ;
Cesbron, JY .
JOURNAL OF VIROLOGY, 2002, 76 (05) :2434-2439
[10]   Transfer of scrapie prion infectivity by cell contact in culture [J].
Kanu, N ;
Imokawa, Y ;
Drechsel, DN ;
Williamson, RA ;
Birkett, CR ;
Bostock, CJ ;
Brockes, JP .
CURRENT BIOLOGY, 2002, 12 (07) :523-530