Competitive Reporter Monitored Amplification (CMA) - Quantification of Molecular Targets by Real Time Monitoring of Competitive Reporter Hybridization

被引:12
|
作者
Ullrich, Thomas [1 ]
Ermantraut, Eugen [1 ]
Schulz, Torsten [1 ]
Steinmetzer, Katrin [1 ]
机构
[1] Alere Technol GmbH, Jena, Germany
来源
PLOS ONE | 2012年 / 7卷 / 04期
关键词
RT-PCR; SENSITIVE DETECTION; CLINICAL MICROBIOLOGY; REVERSE-TRANSCRIPTION; INTERNAL CONTROL; ARMORED RNA; DEVICE; HIV-1; ARRAY; ASSAY;
D O I
10.1371/journal.pone.0035438
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
Background: State of the art molecular diagnostic tests are based on the sensitive detection and quantification of nucleic acids. However, currently established diagnostic tests are characterized by elaborate and expensive technical solutions hindering the development of simple, affordable and compact point-of-care molecular tests. Methodology and Principal Findings: The described competitive reporter monitored amplification allows the simultaneous amplification and quantification of multiple nucleic acid targets by polymerase chain reaction. Target quantification is accomplished by real-time detection of amplified nucleic acids utilizing a capture probe array and specific reporter probes. The reporter probes are fluorescently labeled oligonucleotides that are complementary to the respective capture probes on the array and to the respective sites of the target nucleic acids in solution. Capture probes and amplified target compete for reporter probes. Increasing amplicon concentration leads to decreased fluorescence signal at the respective capture probe position on the array which is measured after each cycle of amplification. In order to observe reporter probe hybridization in real-time without any additional washing steps, we have developed a mechanical fluorescence background displacement technique. Conclusions and Significance: The system presented in this paper enables simultaneous detection and quantification of multiple targets. Moreover, the presented fluorescence background displacement technique provides a generic solution for real time monitoring of binding events of fluorescently labelled ligands to surface immobilized probes. With the model assay for the detection of human immunodeficiency virus type 1 and 2 (HIV 1/2), we have been able to observe the amplification kinetics of five targets simultaneously and accommodate two additional hybridization controls with a simple instrument set-up. The ability to accommodate multiple controls and targets into a single assay and to perform the assay on simple and robust instrumentation is a prerequisite for the development of novel molecular point of care tests.
引用
收藏
页数:13
相关论文
共 3 条
  • [1] Rapid and simple detection ofBacillus cereusin milk by real-time competitive annealing mediated isothermal amplification
    Bao, Haiyan
    Li, Wei
    Yue, Xiqing
    Wu, Junrui
    Qiao, Yu
    Peng, Qing
    Shi, Bo
    Du, Yuguang
    Chen, Xu
    Wu, Rina
    ANALYST, 2020, 145 (20) : 6677 - 6682
  • [2] Real-time and visual detection of viable Salmonella in milk by a competitive annealing mediated isothermal amplification (CAMP) combined with propidium monoazide (PMA)
    Chen, Xu
    Li, Wei
    Ma, Yue
    ANALYTICAL METHODS, 2022, 14 (38) : 3773 - 3779
  • [3] Real-time in vivo monitoring of circadian E-box enhancer activity: A robust and sensitive zebrafish reporter line for developmental, chemical and neural biology of the circadian clock
    Weger, Meltem
    Weger, Benjamin D.
    Diotel, Nicolas
    Rastegar, Sepand
    Hirota, Tsuyoshi
    Kay, Steve A.
    Straehle, Uwe
    Dickmeis, Thomas
    DEVELOPMENTAL BIOLOGY, 2013, 380 (02) : 259 - 273