Rapid determination of adenoviral vector titers by quantitative real-time PCR

被引:56
作者
Ma, L
Bluyssen, HAR
De Raeymaeker, M
Laurysens, V
van der Beek, N
Pavliska, H
van Zonneveld, AJ
Tomme, P
van Es, HHG
机构
[1] Galapagos Genom BV, NL-2301 CA Leiden, Netherlands
[2] KU Leuven, Ctr Transgene Technol & Gene Therapy, Crucell Belgium, B-3000 Louvain, Belgium
[3] Galapagos Genom NV, B-2800 Mechelen, Belgium
关键词
adenovirus vectors; functional genomics; real-time quantitative PCR; vector titer;
D O I
10.1016/S0166-0934(01)00257-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Replication defective adenoviruses have been used as vectors in a variety of settings including gene transfer, gene manipulation, and functionality studies. A quantitative real-time PCR-based assay is described for rapid determination of physical titers of recombinant adenovirus vectors. This method is based on amplification of a 77 bp fragment located near the left end of the adenovirus type 5 genome. Evaluation of this method demonstrated that it is simple, sensitive and reproducible, and has a dynamic range of quantitation over 5 logs. This assay is applicable to purified adenovirus as well as vectors prepared by simple cell lysis procedure, requiring only a small amount of starting material. The simplicity and short turn-around time of this assay should facilitate rapid titer determination for a large collection of adenoviral vectors. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:181 / 188
页数:8
相关论文
共 17 条
  • [1] A high-throughput hybridization method for titer determination of viruses and gene therapy vectors
    Atkinson, EM
    Debelak, DJ
    Hart, LA
    Reynolds, TC
    [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (11) : 2821 - 2823
  • [2] An improved anion-exchange HPLC method for the detection and purification of adenoviral particles
    Blanche, F
    Cameron, B
    Barbot, A
    Ferrero, L
    Guillemin, T
    Guyot, S
    Somarriba, S
    Bisch, D
    [J]. GENE THERAPY, 2000, 7 (12) : 1055 - 1062
  • [3] Highly purified recombinant adeno-associated virus vectors are biologically active and free of detectable helper and wild-type viruses
    Clark, KR
    Liu, XL
    McGrath, JP
    Johnson, PR
    [J]. HUMAN GENE THERAPY, 1999, 10 (06) : 1031 - 1039
  • [4] New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses
    Fallaux, FJ
    Bout, A
    Van der Velde, I
    Van den Wollenberg, DJM
    Hehir, KM
    Keegan, J
    Auger, C
    Cramer, SJ
    Van Ormondt, H
    Van der Eb, AJ
    Valerio, D
    Hoeben, RC
    [J]. HUMAN GENE THERAPY, 1998, 9 (13) : 1909 - 1917
  • [5] A rapid and quantitative assay to estimate gene transfer into retrovirally transduced hematopoietic stem progenitor cells using a 96-well format PCR and fluorescent detection system universal for MMLV-based proviruses
    Gerard, CJ
    Arboleda, MJ
    Solar, G
    Mule, JJ
    Kerr, WG
    [J]. HUMAN GENE THERAPY, 1996, 7 (03) : 343 - 354
  • [6] CHARACTERISTICS OF A HUMAN CELL LINE TRANSFORMED BY DNA FROM HUMAN ADENOVIRUS TYPE-5
    GRAHAM, FL
    SMILEY, J
    RUSSELL, WC
    NAIRN, R
    [J]. JOURNAL OF GENERAL VIROLOGY, 1977, 36 (JUL) : 59 - 72
  • [7] Real time quantitative PCR
    Heid, CA
    Stevens, J
    Livak, KJ
    Williams, PM
    [J]. GENOME RESEARCH, 1996, 6 (10): : 986 - 994
  • [8] Hitt M M, 1997, Adv Pharmacol, V40, P137, DOI 10.1016/S1054-3589(08)60140-4
  • [9] DETECTION OF SPECIFIC POLYMERASE CHAIN-REACTION PRODUCT BY UTILIZING THE 5'-]3' EXONUCLEASE ACTIVITY OF THERMUS-AQUATICUS DNA-POLYMERASE
    HOLLAND, PM
    ABRAMSON, RD
    WATSON, R
    GELFAND, DH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) : 7276 - 7280
  • [10] Evaluation of the concentration and bioactivity of adenovirus vectors for gene therapy
    Mittereder, N
    March, KL
    Trapnell, BC
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (11) : 7498 - 7509