Cellular contaminants of adeno-associated virus vector stocks can enhance transduction

被引:22
作者
Tenenbaum, L
Hamdane, M
Pouzet, M
Avalosse, B
Stathopoulos, A
Jurysta, F
Rosenbaum, C
Hanemann, CO
Levivier, M
Velu, T
机构
[1] Free Univ Brussels, IRIBHN, B-1070 Brussels, Belgium
[2] Free Univ Brussels, Erasme Hosp, Dept Neurosurg, B-1070 Brussels, Belgium
[3] Free Univ Brussels, Inst Jules Bordet, Mol Biol Lab, B-1070 Brussels, Belgium
[4] Univ Dusseldorf, Dept Neurol, D-4000 Dusseldorf, Germany
基金
新加坡国家研究基金会;
关键词
adeno-associated virus; gfp; contaminants; titration; brain;
D O I
10.1038/sj.gt.3300904
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transduction efficiency of different types of recombinant (r)AAV-2 based vectors preparations markedly differed, with apparently no correlation with the replicative titers. Using HeLa cells as target for transduction, 10(5) and 30 infectious units were necessary to observe one transductant using respectively cesium-chloride-purified rAAV and crude lysates of producer cells obtained by sonication. The purified vectors were however able to transduce HEK-193 cells efficiently, but transgene expression was detected with some delay compared with crude lysates. The unexpected high transduction efficiency of sonicated crude lysates was due to virally mediated gene transfer, since similar sonicated crude lysates, but with no AAV rep and cap genes, did not lead to detection of transgene products after incubation with HeLa cells. Furthermore, sonicated cellular extracts of 293 or 293/T cells given in trans stimulate transduction of HeLa cells by purified rAAV. In contrast neither extracts from the adenovirus E1-transformed 911 cell line, nor from other cell lines not harboring any adenovirus gene, had enhancing effect on rAAV-mediated transduction. These data suggest that 293 sonicated extracts contain factors which stimulate rAAV-mediated transduction of cells that are normally poorly transduced and offer a system to identify such factors and to characterize further the steps limiting the transfer of gene by AAV vectors.
引用
收藏
页码:1045 / 1053
页数:9
相关论文
共 44 条
[1]   Transfer of contaminants in adeno-associated virus vector stocks can mimic transduction and lead to artifactual results [J].
Alexander, IE ;
Russell, DW ;
Miller, AD .
HUMAN GENE THERAPY, 1997, 8 (16) :1911-1920
[2]   Effects of gamma irradiation on the transduction of dividing and nondividing cells in brain and muscle of rats by adeno-associated virus vectors [J].
Alexander, IE ;
Russell, DW ;
Spence, AM ;
Miller, AD .
HUMAN GENE THERAPY, 1996, 7 (07) :841-850
[3]   Method for concentrating and purifying recombinant autonomous parvovirus vectors designed for tumour-cell-targeted gene therapy [J].
Avalosse, B ;
Dupont, F ;
Spegelaere, P ;
Mine, N ;
Burny, A .
JOURNAL OF VIROLOGICAL METHODS, 1996, 62 (02) :179-183
[4]   Selective and rapid uptake of adeno-associated virus type 2 in brain [J].
Bartlett, JS ;
Samulski, RJ ;
McCown, TJ .
HUMAN GENE THERAPY, 1998, 9 (08) :1181-1186
[5]   EXPRESSION FROM THE ADENO-ASSOCIATED VIRUS-P5 AND VIRUS-P19 PROMOTERS IS NEGATIVELY REGULATED IN TRANS BY THE REP PROTEIN [J].
BEATON, A ;
PALUMBO, P ;
BERNS, KI .
JOURNAL OF VIROLOGY, 1989, 63 (10) :4450-4454
[6]   High-efficiency transfer of the T cell co-stimulatory molecule B7-2 to lymphoid cells using high-titer recombinant adeno-associated virus vectors [J].
Chiorini, JA ;
Wendtner, CM ;
Urcelay, E ;
Safer, B ;
Hallek, M ;
Kotin, RM .
HUMAN GENE THERAPY, 1995, 6 (12) :1531-1541
[7]   CELL-LINES FOR THE PRODUCTION OF RECOMBINANT ADENOASSOCIATED VIRUS [J].
CLARK, KR ;
VOULGAROPOULOU, F ;
FRALEY, DM ;
JOHNSON, PR .
HUMAN GENE THERAPY, 1995, 6 (10) :1329-1341
[8]  
Clark KR, 1996, GENE THER, V3, P1124
[9]  
FALLAUX F, 1995, HUM GENE THER, V7, P215
[10]   Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors [J].
Ferrari, FK ;
Samulski, T ;
Shenk, T ;
Samulski, RJ .
JOURNAL OF VIROLOGY, 1996, 70 (05) :3227-3234