Comparative performance of three viral load assays on human immunodeficiency virus type 1 (HIV-1) isolates representing group M (subtypes A to G) and group O: LCx HIV RNA Quantitative, AMPLICOR HIV-1 MONITOR version 1.5, and Quantiplex HIV-1 RNA version 3.0

被引:46
作者
Swanson, P
Soriano, V
Devare, SG
Hackett, J
机构
[1] Abbott Labs, AIDS Res & Retrovirus Discovery, Abbott Pk, IL 60064 USA
[2] Inst Salud Carlos III, Infect Dis Serv, Madrid, Spain
关键词
D O I
10.1128/JCM.39.3.862-870.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The performance of the LCx HIV RNA Quantitative (LCx HIV), AMPLICOR HIV-1 MONITOR version 1.5 (MONITOR v1.5), and Quantiplex HIV-1 RNA version 3.0 (bDNA v3.0) viral load assays aas evaluated with 39 viral isolates (3 A, 7 B, 6 C, 4 D, 8 E, 4 F, 1 G, 4 mosaic, and 2 group O). Quantitation across the assay dynamic ranges was assessed using serial fivefold dilutions of the viruses. In addition, sequences of gag-encoded p24 (gag p24),pol-encoded integrase, and env-encoded gp41 were analyzed to assign group and subtype and to assess nucleotide mismatches at primer and probe binding sites. For group M isolates, quantification was highly correlated among all three assays. In contrast, only the LCx HN assay reliably quantified group O isolates. The bDNA v3.0 assay detected hut consistently underquantified group O viruses, whereas the MONITOR v1.5 test failed to detect group O viruses. Analysis of target regions revealed fewer primer or probe mismatches in the LCx HIV assay than in the MONITOR v1.5 test. Consistent with the high level of nucleotide conservation is the ability of the LCx HIV assay to quantify efficiently human immunodeficiency virus type 1 group M and the genetically diverse group O.
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页码:862 / 870
页数:9
相关论文
共 50 条
[1]   Most HIV-1 genetic subtypes have entered Sweden [J].
Alaeus, A ;
Leitner, T ;
Lidman, K ;
Albert, J .
AIDS, 1997, 11 (02) :199-202
[2]   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
[3]   AT LEAST 5 HIV-1 SEQUENCE SUBTYPES (SUBTYPE-A, SUBTYPE-B, SUBTYPE-C, SUBTYPE-D, SUBTYPE-A/E) OCCUR IN ENGLAND [J].
ARNOLD, C ;
BARLOW, KL ;
PARRY, JV ;
CLEWLEY, JP .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1995, 11 (03) :427-429
[4]   Increasing diversity of HIV-1(M) serotypes in French blood donors over a 10-year period (1985-1995) [J].
Barin, F ;
Courouce, AM ;
Pillonel, J ;
Buzelay, L ;
Baudelot, J ;
Botte, C ;
Chamaret, S ;
Durand, F ;
Elghouzzi, MH ;
Lemaire, JM ;
Maisonneuve, P ;
Maniez, M ;
Moncharmont, P ;
Noel, L ;
North, ML ;
Piquet, Y ;
Rouzioux, C ;
Smilovici, W ;
Tirtaine, C .
AIDS, 1997, 11 (12) :1503-1508
[5]   Serologic and phylogenetic characterization of HIV-1 subtypes in Uganda [J].
Brennan, CA ;
Lund, JK ;
Golden, A ;
Yamaguchi, J ;
Vallari, AS ;
Phillips, JF ;
Kataaha, PK ;
Jackson, JB ;
Devare, SG .
AIDS, 1997, 11 (15) :1823-1832
[6]   The enigma of local recurrence [J].
Brennan, MF .
ANNALS OF SURGICAL ONCOLOGY, 1997, 4 (01) :1-12
[7]   DETECTION OF DIVERSE HIV-1 GENETIC SUBTYPES IN THE USA [J].
BRODINE, SK ;
MASCOLA, JR ;
WEISS, PJ ;
ITO, SI ;
PORTER, KR ;
ARTENSTEIN, AW ;
GARLAND, FC ;
MCCUTCHAN, FE ;
BURKE, DS .
LANCET, 1995, 346 (8984) :1198-1199
[8]   The effects of internal primer-template mismatches on RT-PCR: HIV-1 model studies [J].
Christopherson, C ;
Sninsky, J ;
Kwok, S .
NUCLEIC ACIDS RESEARCH, 1997, 25 (03) :654-658
[9]   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
[10]  
Coste J, 1996, J MED VIROL, V50, P293, DOI 10.1002/(SICI)1096-9071(199612)50:4&lt