Generic RT-nested-PCR for detection of flaviviruses using degenerated primers and internal control followed by sequencing for specific identification

被引:121
作者
Sánchez-Seco, MP
Rosario, D
Domingo, C
Hernández, L
Valdés, K
Guzmán, MG
Tenorio, A
机构
[1] Inst Salud Carlos III, Natl Ctr Microbiol, Serv Diagnost Microbiol, Lab Arboviruses & Imported Viral Dis, Madrid, Spain
[2] Inst Salud Carlos III, Natl Ctr Microbiol, Alert & Emergency Unit, Madrid, Spain
[3] Inst Trop Med Pedro Kouri, WHO Collaborating Ctr Viral Dis, Dept Virol, PAHO, Havana, Cuba
关键词
flavivirus; generic PCR; detection; degenerated primers;
D O I
10.1016/j.jviromet.2005.01.025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Flaviviruses are a widespread and numerous group of arboviruses that can cause serious illness in humans. The continuous and slow spread of certain flaviviruses, such as Dengue viruses, and the recent entry and spread of West Nile virus to the American continent, point to the need to control these infections. This control requires the use of suitable techniques for diagnostic and surveillance programmes. A generic RT-nested-PCR that is, theoretically, able to detect each member of the group has been designed. The identification of the detected virus is carried out by sequencing. The introduction of an internal control would reduce the number of false negative results and could be used to quantify the viral load in clinical samples where the method works well. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 109
页数:9
相关论文
共 38 条
[1]  
[Anonymous], 1999, STRENGTH IMPL GLOB S
[2]   Structures of immature flavivirus particles [J].
Zhang, Y ;
Corver, J ;
Chipman, PR ;
Zhang, W ;
Pletnev, SV ;
Sedlak, D ;
Baker, TS ;
Strauss, JH ;
Kuhn, RJ ;
Rossmann, MG .
EMBO JOURNAL, 2003, 22 (11) :2604-2613
[3]   Identification of a Kunjin/West Nile-like flavivirus in brains of patients with New York encephalitis [J].
Briese, T ;
Jia, XY ;
Huang, C ;
Grady, LJ ;
Lipkin, WI .
LANCET, 1999, 354 (9186) :1261-1262
[4]   NEW METHOD FOR THE EXTRACTION OF VIRAL-RNA AND DNA FROM CEREBROSPINAL-FLUID FOR USE IN THE POLYMERASE CHAIN-REACTION ASSAY [J].
CASAS, I ;
POWELL, L ;
KLAPPER, PE ;
CLEATOR, GM .
JOURNAL OF VIROLOGICAL METHODS, 1995, 53 (01) :25-36
[5]   AN INTEGRATED TARGET SEQUENCE AND SIGNAL AMPLIFICATION ASSAY, REVERSE TRANSCRIPTASE-PCR-ENZYME-LINKED IMMUNOSORBENT-ASSAY, TO DETECT AND CHARACTERIZE FLAVIVIRUSES [J].
CHANG, GJJ ;
TRENT, DW ;
VORNDAM, AV ;
VERGNE, E ;
KINNEY, RM ;
MITCHELL, CJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (02) :477-483
[6]   USE OF NS-3 CONSENSUS PRIMERS FOR THE POLYMERASE CHAIN-REACTION AMPLIFICATION AND SEQUENCING OF DENGUE VIRUSES AND OTHER FLAVIVIRUSES [J].
CHOW, VTK ;
SEAH, CLK ;
CHAN, YC .
ARCHIVES OF VIROLOGY, 1993, 133 (1-2) :157-170
[7]  
DOMINGO C, 2004, WHO DENGUE B, V28
[8]   Molecular diagnostics of viral hemorrhagic fevers [J].
Drosten, C ;
Kümmerer, BM ;
Schmitz, H ;
Günther, S .
ANTIVIRAL RESEARCH, 2003, 57 (1-2) :61-87
[9]   Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, Dengue virus, and Yellow fever virus by real-time reverse transcription-PCR [J].
Drosten, C ;
Göttig, S ;
Schilling, S ;
Asper, M ;
Panning, M ;
Schmitz, H ;
Günther, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (07) :2323-2330
[10]   Detection of flaviviruses by reverse transcriptase polymerase chain reaction with the universal primer set [J].
Fang, MY ;
Chen, HS ;
Chen, CH ;
Tian, XD ;
Jiang, LH ;
Peng, YF ;
Chen, WJ ;
Guo, HY .
MICROBIOLOGY AND IMMUNOLOGY, 1997, 41 (03) :209-213