Detection of hepatitis C virus by single-step hairpin primer RT-PCR

被引:9
作者
Takei, Fumie [1 ]
Tani, Hideki [2 ]
Matsuura, Yoshiharu [2 ]
Nakatani, Kazuhiko [1 ]
机构
[1] Osaka Univ, Inst Sci & Ind Res, Ibaraki, Osaka 5670047, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
关键词
Fluorescent molecule; PCR; Hairpin primer; HCV; Detection method; POLYMERASE-CHAIN-REACTION; REAL-TIME PCR; NUCLEIC-ACID HYBRIDIZATION; DYE CONCENTRATION; DNA; AMPLIFICATION; MICROBIOLOGY; TEMPERATURE; DIAGNOSIS; PRODUCTS;
D O I
10.1016/j.bmcl.2013.10.021
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We developed a novel single-step virus detection system using the fluorescent molecule with a hairpin primer on the reverse transcription (RT)-polymerase chain reaction (PCR). Primers that are specific to Hepatitis C virus (HCV) having a hairpin tag at the 5 '-end were used for RT and PCR. The HCV-RNA template was reverse transcribed by reverse transcriptase with the hairpin primer (HP), and the resulting cDNA was amplified directly by HP-PCR (RT-HP-PCR). Using the RT-HP-PCR, we succeeded in demonstrating the detection of HCV-RNA in single-step. The RT-HP-PCR selectively detected HCV-RNA extracted from patients' sera containing contaminant materials. The method could be applicable to the quantitative detection of HCV. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:394 / 396
页数:3
相关论文
共 27 条
[1]   Real-time polymerase chain reaction in transfusion medicine:: Applications for detection of bacterial contamination in blood products [J].
Dreier, Jens ;
Stoermer, Melanie ;
Kleesiek, Knut .
TRANSFUSION MEDICINE REVIEWS, 2007, 21 (03) :237-254
[2]   RECENT ADVANCES IN THE POLYMERASE CHAIN-REACTION [J].
ERLICH, HA ;
GELFAND, D ;
SNINSKY, JJ .
SCIENCE, 1991, 252 (5013) :1643-1651
[3]   Real-time PCR in clinical microbiology: Applications for a routine laboratory testing [J].
Espy, MJ ;
Uhl, JR ;
Sloan, LM ;
Buckwalter, SP ;
Jones, MF ;
Vetter, EA ;
Yao, JDC ;
Wengenack, NL ;
Rosenblatt, JE ;
Cockerill, FR ;
Smith, TF .
CLINICAL MICROBIOLOGY REVIEWS, 2006, 19 (01) :165-+
[4]   Diagnosis of canine visceral leishmaniasis: Biotechnological advances [J].
Gomes, Y. M. ;
Cavalcanti, M. Paiva ;
Lira, R. A. ;
Abath, F. G. C. ;
Alves, L. C. .
VETERINARY JOURNAL, 2008, 175 (01) :45-52
[5]   Comparison of multiple DNA dyes for real-time PCR: effects of dye concentration and sequence composition on DNA amplification and melting temperature [J].
Gudnason, Haukur ;
Dufva, Martin ;
Bang, D. D. ;
Wolff, Anders .
NUCLEIC ACIDS RESEARCH, 2007, 35 (19)
[6]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994
[7]  
Kubista Mikael, 2006, Molecular Aspects of Medicine, V27, P95, DOI 10.1016/j.mam.2005.12.007
[8]   Seven-color, homogeneous detection of six PCR products [J].
Lee, LG ;
Livak, KJ ;
Mullah, B ;
Graham, RJ ;
Vinayak, RS ;
Woudenberg, TM .
BIOTECHNIQUES, 1999, 27 (02) :342-349
[9]  
Livak K. J., 1999, GENET ANAL, V14, P143
[10]  
LIVAK KJ, 1995, PCR METH APPL, V4, P357