Quantitation of polyomavirus DNA by a competitive nested polymerase chain reaction

被引:12
作者
Fedele, CG
Avellón, A
Ciardi, M
Delia, S
Tenorio, A
机构
[1] Inst Salud Carlos III, Ctr Nacl Microbiol, Diagnost Microbiol Serv, E-28220 Madrid, Spain
[2] Univ Roma La Sapienza, Dept Infect & Trop Dis, Rome, Italy
关键词
competitive PCR; quantitative PCR; polyomavirus;
D O I
10.1016/S0166-0934(00)00172-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new method to quantitate small amounts of DNA in clinical specimens is described. The method, a nested competitive polymerase chain reaction (ncPCR), is able to quantitate between 10 and 10(6) copies per tube of polyomavirus DNA and shows good reproducibility when clinical samples are analysed. Throughout the whole procedure, an internal standard (IS) competes for the primers with the target DNA. The internal standard, a heterologous sequence containing the four primer recognition sites, was constructed using a modification of the 'MIMIC' approach that is useful for obtaining competitor sequences for any viral, bacterial or eukaryotic target. The ncPCR method for polyomavirus was applied to cerebrospinal fluids (CSF) from AIDS patients with progressive multifocal leukoencephalopathy (PML) and urine specimens from bone marrow transplant patients affected by haemorrhagic cystitis. The results obtained suggest that the ncPCR method is a sensitive and useful method for quantitating genomic load in clinical samples. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:51 / 61
页数:11
相关论文
共 36 条
[21]   QUANTIFICATION OF HEPATITIS-C VIRUS-RNA BY COMPETITIVE AMPLIFICATION OF RNA FROM DENATURED SERUM AND HYBRIDIZATION ON MICROTITER PLATES [J].
RAVAGGI, A ;
ZONARO, A ;
MAZZA, C ;
ALBERTINI, A ;
CARIANI, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (02) :265-269
[22]   Use of quantitative competitive PCR to measure Epstein-Barr virus genome load in the peripheral blood of pediatric transplant patients with lymphoproliferative disorders [J].
Rowe, DT ;
Qu, L ;
Reyes, J ;
Jabbour, N ;
Yunis, E ;
Putnam, P ;
Todo, S ;
Green, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (06) :1612-1615
[23]  
SABROOCK J, 1989, MOL CLONING LAB MANU
[24]   A WORKBENCH FOR MULTIPLE ALIGNMENT CONSTRUCTION AND ANALYSIS [J].
SCHULER, GD ;
ALTSCHUL, SF ;
LIPMAN, DJ .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1991, 9 (03) :180-190
[25]  
SIEBERT PD, 1993, BIOTECHNIQUES, V14, P244
[26]   Prognostic value of JC virus load in cerebrospinal fluid of patients with progressive multifocal leukoencephalopathy [J].
Taoufik, Y ;
Gasnault, J ;
Karaterki, A ;
Ferey, MP ;
Marchadier, E ;
Goujard, C ;
Lannuzel, A ;
Delfraissy, JF ;
Dussaix, E .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (06) :1816-1820
[27]   COMPETITIVE POLYMERASE CHAIN-REACTION USING AN INTERNAL STANDARD - APPLICATION TO THE QUANTITATION OF VIRAL-DNA [J].
TELENTI, A ;
IMBODEN, P ;
GERMANN, D .
JOURNAL OF VIROLOGICAL METHODS, 1992, 39 (03) :259-268
[28]   Development of a reverse transcriptase PCR-enzyme-linked immunosorbent assay for quantification of human immunodeficiency virus type 1 RNA in plasma: Comparison with commercial quantitative assays [J].
Trabaud, MA ;
Audoly, G ;
Leriche, K ;
Cotte, L ;
Ritter, J ;
Sepetjan, M ;
Trepo, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (05) :1251-1254
[29]  
Uberla K, 1991, PCR Methods Appl, V1, P136
[30]   JCV-DNA and BKV-DNA in the CNS tissue and CSF of AIDS patients and normal subjects. Study of 41 cases and review of the literature [J].
Vago, L ;
Cinque, P ;
Sala, E ;
Nebuloni, M ;
Caldarelli, R ;
Racca, S ;
Ferrante, P ;
Trabattoni, G ;
Costanzi, G .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 1996, 12 (02) :139-146