A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml

被引:257
作者
Collins, ML
Irvine, B
Tyner, D
Fine, E
Zayati, C
Chang, CA
Horn, T
Ahle, D
Detmer, J
Shen, LP
Kolberg, J
Bushnell, S
Urdea, MS
Ho, DD
机构
[1] CHIRON DIAGNOST,EMERYVILLE,CA 94608
[2] AARON DIAMOND AIDS RES CTR,NEW YORK,NY 10016
关键词
D O I
10.1093/nar/25.15.2979
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The branched DNA hybridization assay has been improved by the inclusion of the novel nucleotides, isoC and isoG, in the amplification sequences to prevent non-specific hybridization. The novel isoC, isoG-containing amplification sequences have no detectable interaction with any natural DNA sequence, The control of non-specific hybridization in turn permits increased signal amplification, Addition of a 14 site preamplifier was found to increase the signal/noise ratio 8-fold. A set of 74 oligonucleotide probes was designed to the consensus HIV POL sequence, The detection limit of this new HIV branched DNA amplifier assay was similar to 50 molecules/ml. The assay was used to measure viral load in 87 plasma samples of HIV- infected patients on triple drug therapy whose RNA titers were <500 molecules/ml. In all 11 patients viral load eventually declined to below the detection limit with the new assay.
引用
收藏
页码:2979 / 2984
页数:6
相关论文
共 42 条
[1]
EVALUATION OF BRANCHED DNA SIGNAL AMPLIFICATION FOR THE DETECTION OF HEPATITIS-C VIRUS-RNA [J].
ALTER, HJ ;
SANCHEZPESCADOR, R ;
URDEA, MS ;
WILBER, JC ;
LAGIER, RJ ;
DIBISCEGLIE, AM ;
SHIH, JW ;
NEUWALD, PD .
JOURNAL OF VIRAL HEPATITIS, 1995, 2 (03) :121-132
[2]
USEFULNESS OF HCV-RNA COUNTS BY THE METHOD OF HCV-BDNA PROBE IN INTERFERON RETREATMENT FOR PATIENTS WITH HCV-RNA POSITIVE CHRONIC HEPATITIS-C [J].
ARASE, Y ;
KUMADA, H ;
CHAYAMA, K ;
NAOYA, M ;
TSUBOTA, A ;
KOIDA, I ;
KOBAYASHI, M ;
SUZUKI, Y ;
IKEDA, K ;
SAITOH, S ;
KOBAYASHI, M .
INTERNATIONAL HEPATOLOGY COMMUNICATIONS, 1995, 4 (01) :19-25
[3]
DETECTION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROVIRUS IN MONONUCLEAR-CELLS BY INSITU POLYMERASE CHAIN-REACTION [J].
BAGASRA, O ;
HAUPTMAN, SP ;
LISCHNER, HW ;
SACHS, M ;
POMERANTZ, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (21) :1385-1391
[4]
BRONSTEIN I, 1989, CLIN CHEM, V35, P1441
[5]
VIROLOGICAL AND IMMUNOLOGICAL CHARACTERIZATION OF LONG-TERM SURVIVORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
CAO, YZ ;
QIN, LM ;
ZHANG, LQ ;
SAFRIT, J ;
HO, DD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (04) :201-208
[6]
IMPROVED METHODS FOR THE SYNTHESIS OF BRANCHED DNA (BDNA) FOR USE AS AMPLIFICATION MULTIMERS IN BIOASSAYS [J].
CHANG, CA ;
HORN, T ;
AHLE, D ;
URDEA, MS .
NUCLEOSIDES & NUCLEOTIDES, 1991, 10 (1-3) :389-392
[7]
PREPARATION AND CHARACTERIZATION OF RNA STANDARDS FOR USE IN QUANTITATIVE BRANCHED DNA HYBRIDIZATION ASSAYS [J].
COLLINS, ML ;
ZAYATI, C ;
DETMER, JJ ;
DALY, B ;
KOLBERG, JA ;
CHA, TA ;
IRVINE, BD ;
TUCKER, J ;
URDEA, MS .
ANALYTICAL BIOCHEMISTRY, 1995, 226 (01) :120-129
[8]
A SHORT-TERM STUDY OF THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF RITONAVIR, AN INHIBITOR OF HIV-1 PROTEASE [J].
DANNER, SA ;
CARR, A ;
LEONARD, JM ;
LEHMAN, LM ;
GUDIOL, F ;
GONZALES, J ;
RAVENTOS, A ;
RUBIO, R ;
BOUZA, E ;
PINTADO, V ;
AGUADO, AG ;
DELOMAS, JG ;
DELGADO, R ;
BORLEFFS, JCC ;
HSU, A ;
VALDES, JM ;
BOUCHER, CAB ;
COOPER, DA ;
GIMENO, C ;
CLOTET, B ;
TOR, J ;
FERRER, E ;
MARTINEZ, PL ;
MORENO, S ;
ZANCADA, G ;
ALCAMI, J ;
NORIEGA, AR ;
PULIDO, F ;
GLASSMAN, HN .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (23) :1528-1533
[9]
Accurate quantification of hepatitis C virus (HCV) RNA from all HCV genotypes by using branched-DNA technology [J].
Detmer, J ;
Lagier, R ;
Flynn, J ;
Zayati, C ;
Kolberg, J ;
Collins, M ;
Urdea, M ;
SanchezPescador, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :901-907
[10]
INVITRO SELECTION OF RNA MOLECULES THAT BIND SPECIFIC LIGANDS [J].
ELLINGTON, AD ;
SZOSTAK, JW .
NATURE, 1990, 346 (6287) :818-822