全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
PLOS ONE  2012 

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

DOI: 10.1371/journal.pone.0035438

Full-Text   Cite this paper   Add to My Lib

Abstract:

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.

References

[1]  Mackay IM (2004) Real-time PCR in the microbiology laboratory. Clin Microbiol Infect 10: 190–212.
[2]  Finan JE, Zhao RY (2007) From molecular diagnostics to personalized testing. Pharmacogenomics 8: 85–99.
[3]  Hadd AG, Andruss BF, Ye F, Walker Peach CR (2005) Adoption of array technologies into the clinical laboratory. Expert Rev Mol Diagn 5: 409–420.
[4]  Ling MM, Ricks C, Lea P (2007) Multiplexing molecular diagnostics and immunoassays using emerging microarray technologies. Expert Rev Mol Diagn 7: 87–98.
[5]  Espy MJ, Uhl JR, Sloan L, Buckwalter SP, Jones MF, et al. (2006) Real-time PCR in clinical microbiology: applications for routine laboratory testing. Clin Microbiol Rev 19: 165–256.
[6]  Christopherson C, Lu SD, Kwok S (1998) Laboratory markers of antiviral activity. Antivir Ther 3: 247–250.
[7]  Kashanchi F, Melpolder JC, Epstein JS, Sadaie MR (1997) Rapid and sensitive detection of cell-associated HIV-1 in latently infected cell lines and in patient cells using sodium-n-butyrate induction and RT-PCR. J Med Virol 52: 179–189.
[8]  Stals A, Werbrouck H, Baert L, Botteldoorn N, Herman L, et al. (2009) Laboratory efforts to eliminate contamination problems in the real-time RT-PCR detection of noroviruses. J Microbiol Methods 77: 72–76.
[9]  ValentineThon E (2002) Quality control in nucleic acid testing-where do we stand? J Clin Virol 25: Suppl 313–21.
[10]  Benjamin RJ (2001) Nucleic acid testing: update and applications. Semin Hematol 38: 11–16.
[11]  Curtis KA, Rudolph DL, Owen SM (2008) Rapid detection of HIV-1 by reverse-transcription, loop-mediated isothermal amplification (RT-LAMP). J Virol Methods 151: 264–270.
[12]  Lamhoujeb S, Charest H, Fliss I, Ngazoa S, Jean J (2009) Real-time molecular beacon NASBA for rapid and sensitive detection of norovirus GII in clinical samples. Can J Microbiol 55: 1375–1380.
[13]  Collins RA, Ko LS, Fung KY, Chan KY, Xing J, et al. (2003) Rapid and sensitive detection of avian influenza virus subtype H7 using NASBA. Biochem Biophys Res Commun 300: 507–515.
[14]  Hofmann WP, Dries V, Herrmann E, Gartner B, Zeuzem S, et al. (2005) Comparison of transcription mediated amplification (TMA) and reverse transcription polymerase chain reaction (RT-PCR) for detection of hepatitis C virus RNA in liver tissue. J Clin Virol 32: 289–293.
[15]  Saha K, Tian B, Bucy RP (2001) Quantitation of HIV-1 by real-time PCR with a unique fluorogenic probe. J Virol Methods 93: 33–42.
[16]  Avettand Fenoel V, Chaix ML, Blanche S, Burgard M, Floch C, et al. (2009) LTR real-time PCR for HIV-1 DNA quantitation in blood cells for early diagnosis in infants born to seropositive mothers treated in HAART area (ANRS CO 01). J Med Virol 81: 217–223.
[17]  Pau CP, Wells SK, Rudolph DL, Owen S, Granade TC (2010) A rapid real-time PCR assay for the detection of HIV-1 proviral DNA using double-stranded primer. J Virol Methods 164: 55–62.
[18]  Anthony RM, Brown TJ, French GL (2001) DNA array technology and diagnostic microbiology. Expert Rev Mol Diagn 1: 30–38.
[19]  Miller MB, Tang YW (2009) Basic concepts of microarrays and potential applications in clinical microbiology. Clin Microbiol Rev 22: 611–633.
[20]  Liu H, Wang H, Shi Z, Wang H, Yang C (2006) TaqMan probe array for quantitative detection of DNA targets. Nucl Acids Res 34: e4.
[21]  Anderson RC, Su X, Bogdan GJ, Fenton J (2000) A miniature integrated device for automated multistep genetic assays. Nucleic Acids Res 28: E60.
[22]  Liu RH, Lodes MJ, Nguyen T, Siuda T, Slota M, et al. (2006) Validation of a fully integrated microfluidic array device for influenza A subtype identification and sequencing. Anal Chem 78: 4184–4193.
[23]  Liu RH, Nguyen T, Schwarzkopf K, Fuji HS, Petrova A, et al. (2006) Fully integrated miniature device for automated gene expression DNA microarray processing. Anal Chem 78: 1980–1986.
[24]  Bienvenue JM, Legendre LA, Ferrance JP, Landers JP (2010) An integrated microfluidic device for DNA purification and PCR amplification of STR fragments. Forensic Sci Int Genet 4: 178–186.
[25]  Soderlund H (1990) DNA hybridization: comparison of liquid and solid phase formats. Ann Biol Clin (Paris) 48: 489–491.
[26]  Applied Biosystems (2006) Real Time RT- PCR: Understanding CT. Application Note: Applied Biosystems. pp. 1–2.
[27]  Claas EJC, Melchers WJG, van den Brule AJC (2007) The Role of Real- Time PCR in Routine Microbial Diagnostics. Real-time PCR in Microbiology. Norfolk: Caister Academic Press. pp. 231–267.
[28]  Stranska R, Schuurman R, de Vos M, van Loon AM (2004) Routine use of a highly automated and internally controlled real-time PCR assay for the diagnosis of herpes simplex and varicella-zoster virus infections. J Clin Virol 30: 39–44.
[29]  Neuzil P, Zhang C, Pipper J, Oh S, Zhuo L (2006) Ultra fast miniaturized real-time PCR: 40 cycles in less than six minutes. Nucleic acids research 34: e77.
[30]  Mrotzek G, Haryanti , Koesharyani I, Tretyakov AN, Sugama K, et al. (2010) Fast short-fragment PCR for rapid and sensitive detection of shrimp viruses. Journal of virological methods 168: 262–266.
[31]  Han SH, Lee DB, Lee DW, Kim EH, Yoon BS (2008) Ultra-rapid real-time PCR for the detection of Paenibacillus larvae, the causative agent of American Foulbrood (AFB). J Invertebr Pathol 99: 8–13.
[32]  Zhao W, Ali MM, Brook MA, Li Y (2008) Rolling circle amplification: applications in nanotechnology and biodetection with functional nucleic acids. Angew Chem Int Ed Engl 47: 6330–6337.
[33]  Tang J, Zhou L, Gao W, Cao X, Wang Y (2009) Visual DNA microarrays for simultaneous detection of human immunodeficiency virus type-1 and Treponema pallidum coupled with multiplex asymmetric polymerase chain reaction. Diagn Microbiol Infect Dis 65: 372–378.
[34]  Cirino N, Tavakoli NP, Madison Antenucci S, Egan C (2007) Multiplex rtPCR in Microbology. Real-Time PCR in Microbiology. Norfolk: Caister Academic Press. pp. 183–185.
[35]  Ferns RB, Garson JA (2006) Development and evaluation of a real-time RT-PCR assay for quantification of cell-free human immunodeficiency virus type 2 using a Brome Mosaic Virus internal control. J Virol Methods 135: 102–108.
[36]  Muska A, Peck E, Palmer S (2007) Standard and Controls: Concepts for preparation and Use in Real-time PCR Applications. Real-time PCR in Microbiology. Norfolk: Caister Academic Press. pp. 101–131.
[37]  Brightwell G, Pearce M, Leslie D (1998) Development of internal controls for PCR detection of Bacillus anthracis. Mol Cell Probes 12: 367–377.
[38]  Stevenson J, Hymas W, Hillyard D (2008) The use of Armored RNA as a multi-purpose internal control for RT-PCR. J Virol Methods 150: 73–76.
[39]  Pasloske BL, Walkerpeach CR, Obermoeller RD, Winkler M, DuBois DB (1998) Armored RNA technology for production of ribonuclease-resistant viral RNA controls and standards. J Clin Microbiol 36: 3590–3594.
[40]  Rebrikov DV, Trofimov D (2006) Real-time PCR: approaches to data analysis. Prikl Biokhim Mikrobiol 42: 520–528.
[41]  Larionov A, Krause A, Miller W (2005) A standard curve based method for relative real time PCR data processing. BMC Bioinformatics 6: 62.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133