Comparison of the COBAS TAQMAN™ HIV-1HPS with VERSANT HIV-1 RNA 3.0 assay (bDNA) for plasma RNA quantitation indifferent HIV-1 subtypes

被引:10
作者
Gomes, Perpetua
Palma, Ana Carolina
Cabanas, Joaquim
Abecasis, Ana
Carvalho, Ana Patricia
Ziermann, Rainer
Diogo, Isabel
Gonçcalves, Fatima
Lobo, Ceu Sousa
Camacho, Ricardo
机构
[1] Hosp Egas Moniz, Virol Lab, Serv ImunoHemoterapia, P-1349019 Lisbon, Portugal
[2] Inst Super Ciencias Saude Egas Moniz, Caparica, Portugal
[3] Bayer HealthCare, Div Diagnost, Berkeley, CA USA
[4] Katholieke Univ Leuven, Rega Inst Med Res, Lab Clin & Epidemiol Virol, Louvain, Belgium
关键词
HIV-1; TAQMAN; bDNA; subtypes;
D O I
10.1016/j.jviromet.2006.03.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantitation of HIV-1 RNA levels in plasma has an undisputed prognostic value and is extremely important for evaluating response to antiretroviral therapy. The purpose of this study was to evaluate the performance of the real-time PCR COBAS TaqMan 48 analyser, comparing it to the existing VERSANT 3.0 (bDNA) for HIV-1 RNA quantitation in plasma of individuals infected with different HIV-1 subtypes (104 blood samples). A positive linear correlation between the two tests (r(2) = 0.88) was found. Quantitation by the COBAS TaqMan assay was approximately 0.32 log(10) higher than by bDNA. The relationship between the two assays was similar within all subtypes with a Deming regression of < 1 and < 0 for the Bland-Altman plots. Overall, no significant differences were found in plasma viral load quantitation in different HIV-1 subtypes between both assays; therefore these assays are suitable for viral load quantitation of highly genetically diverse HIV-1 plasma samples. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:223 / 228
页数:6
相关论文
共 40 条
[1]   Subtype-specific problems with quantification of plasma HIV-1 RNA [J].
Alaeus, A ;
Lidman, K ;
Sonnerborg, A ;
Albert, J .
AIDS, 1997, 11 (07) :859-865
[2]   Comparative evaluation of the QUANTIPLEX HIV-1 RNA 2.0 and 3.0 (bDNA) assays and the AMPLICOR HIV-1 MONITOR v1.5 test for the quantitation of human immunodeficiency virus type 1 RNA in plasma [J].
Anastassopoulou, CG ;
Toulomi, G ;
Katsoulidou, A ;
Hatzitheodorou, H ;
Pappa, M ;
Paraskevis, D ;
Lazanas, M ;
Gargalianos, P ;
Hatzakis, A .
JOURNAL OF VIROLOGICAL METHODS, 2001, 91 (01) :67-74
[3]   Evaluation of the clinical sensitivities of three viral load assays with plasma samples from a pediatric population predominantly infected with human immunodeficiency virus type 1 subtype G and BG recombinant forms [J].
Antunes, R ;
Figueiredo, S ;
Bártolo, I ;
Pinheiro, M ;
Rosado, L ;
Soares, I ;
Lourenço, H ;
Taveira, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (07) :3361-3367
[4]  
ARMITAGE P, 2002, STAT METHODS MED
[5]   STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT [J].
BLAND, JM ;
ALTMAN, DG .
LANCET, 1986, 1 (8476) :307-310
[6]   Identification of a novel HIV-1 circulating AIDG intersubtype recombinant form (CRF1 9_cpx) in Cuba [J].
Casado, G ;
Thomson, MM ;
Sierra, M ;
Nájera, R .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2005, 40 (05) :532-537
[7]   Multiple sequence alignment with the Clustal series of programs [J].
Chenna, R ;
Sugawara, H ;
Koike, T ;
Lopez, R ;
Gibson, TJ ;
Higgins, DG ;
Thompson, JD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3497-3500
[8]   A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml [J].
Collins, ML ;
Irvine, B ;
Tyner, D ;
Fine, E ;
Zayati, C ;
Chang, CA ;
Horn, T ;
Ahle, D ;
Detmer, J ;
Shen, LP ;
Kolberg, J ;
Bushnell, S ;
Urdea, MS ;
Ho, DD .
NUCLEIC ACIDS RESEARCH, 1997, 25 (15) :2979-2984
[9]  
Coste J, 1996, J MED VIROL, V50, P293, DOI 10.1002/(SICI)1096-9071(199612)50:4&lt
[10]  
293::AID-JMV3&gt