Impact of HIV-1 genetic diversity on plasma HIV-1 RNA quantification -: Usefulness of the Agence Nationale de Recherches sur le SIDA second-generation long terminal repeat-based real-time reverse transcriptase polymerase chain reaction test

被引:120
作者
Rouet, Francois [1 ]
Chaix, Marie-Laure
Nerrienet, Eric
Ngo-Giang-Huong, Nicole
Plantier, Dean-Christophe
Burgard, Marianne
Peeters, Martine
Damond, Florence
Ekouevi, Didier Koumavi
Msellati, Philippe
Ferradini, Laurent
Rukobo, Sandra
Marechal, Valerie
Schvachsa, Nilda
Wakrim, Lahcen
Rafalimanana, Christian
Rakotoambinina, Benjamin
Viard, Jean-Paul
Seigneurin, Jean-Marie
Rouzioux, Christine
机构
[1] Ctr Muraz, Virol Lab, Bobo Dioulasso, Burkina Faso
[2] Univ Paris 05, CHU Necker Enfants Malad, Virol Lab, Paris, France
[3] Inst Pasteur, HIV Hepatitis Lab, Phnom Penh, Cambodia
[4] Ctr Pasteur Cameroun, Virol Lab, Yaounde, Cameroon
[5] Inst Rech Dev, URI 174, Chiang Mai, Thailand
[6] CHU C Nicole, Virol Lab, Rouen, France
[7] Inst Rech Dev, UMR145, Lab Retrovirus, Montpellier, France
[8] Hop Bichat Claude Bernard, Virol Lab, F-75877 Paris, France
[9] Programme PACCI, Abidjan, Cote Ivoire
[10] Inst Rech Dev, UMR 145, Bobo Dioulasso, Burkina Faso
[11] Epi Ctr, Paris, France
[12] ZVITAMBO Project, Harare, Zimbabwe
[13] Inst Pasteur, Bangui, Cent Afr Republ
[14] Univ Buenos Aires, Fac Med, Ctr Nacl Reference SIDA, Buenos Aires, DF, Argentina
[15] Inst Pasteur, Casablanca, Morocco
[16] Hop Joseph Ravoahangy Andrianavalona, CHUA, Bacteriol Lab, Antananarivo, Madagascar
[17] CHU Necker Enfants Malad, Serv Malad Infect, Paris, France
[18] CHU Michallon, Virol Lab, Grenoble, France
关键词
HIV-1; diversity; HIV-1 RNA viral load; real-time polymerase chain reaction;
D O I
10.1097/QAI.0b013e3180640cf5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The high genetic diversity of HIV-1 has a major impact on the quantification of plasma HIV-1 RNA, representing an increasingly difficult challenge. A total of 898 plasma specimens positive for HIV-1 RNA by commercial assays (Amplicor v1.5; Roche Diagnostic Systems, Alameda, CA or Versant v3.0; Bayer Diagnostics, Emeryville, CA) were tested using the Agence Nationale de Recherches sur le SIDA second-generation (G2) real-time reverse transcriptase polymerase chain reaction (RT-PCR) test: 518 samples containing HIV-1 of known subtype, including 88 from 2 subtype panels and 430 harboring B (n = 266) and non-B (n = 164) group M HIV-1 subtypes from patients followed up in 2002 through 2005 at Necker Hospital (Paris, France), and 380 samples from 10 different countries (Argentina, Cambodia, Cameroon, Central African Republic, France, Ivory Coast, Madagascar, Morocco, Thailand, and Zimbabwe). HFV-1 RNA values obtained by G2 real-time PCR were highly correlated with those obtained by the Amplicor v1.5 for B and non-B subtypes (R-2 = 0.892 and 0.892, respectively) and for samples from diverse countries (R-2 = 0.867 and 0.893 for real-time PCR vs. Amplicor v1.5 and real-time PCR vs. Versant v3.0, respectively). Approximately 30% of specimens harboring non-B subtypes were underquantified by at least -0.51 log(10) in Amplicor v1.5 versus 5% underquantified in G2 real-time PCR. Discrepant results were also obtained with subtype B samples (14% underquantified by Amplicor v1.5 vs. 7% by G2 real-time PCR). Similar percentages were observed when comparing results obtained with the G2 real-time PCR assay with those obtained using the Versant assay. Addressing HIV-1 diversity, continual monitoring of HIV-1 RNA assays, together with molecular epidemiology studies, is required to improve the accuracy of all HIV RNA assays.
引用
收藏
页码:380 / 388
页数:9
相关论文
共 50 条
[1]   Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder [J].
Afonina, I ;
Zivarts, M ;
Kutyavin, I ;
Lukhtanov, E ;
Gamper, H ;
Meyer, RB .
NUCLEIC ACIDS RESEARCH, 1997, 25 (13) :2657-2660
[2]   Comparison of LCx with other current viral load assays for detecting and quantifying human immunodeficiency virus type 1 RNA in patients infected with the circulating recombinant form A/G (CRF02) [J].
Amendola, A ;
Bordi, L ;
Angeletti, C ;
Girardi, E ;
Ippolito, G ;
Capobianchi, MR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (02) :811-815
[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]   Can routine clinical markers be used longitudinally to monitor antiretroviral therapy success in resource-limited settings? [J].
Bagchi, Shashwatee ;
Kempf, Mirjam C. ;
Westfall, Andrew O. ;
Maherya, Anastasiya ;
Willig, James ;
Saag, Michael S. .
CLINICAL INFECTIOUS DISEASES, 2007, 44 (01) :135-138
[5]   Diagnostic virologic accuracy of CD4 cell count increase for response after initiating highly active antiretroviral therapy [J].
Bisson, Gregory P. ;
Gross, Robert ;
Strom, Jordan B. ;
Rollins, Caitlin ;
Bellamy, Scarlett ;
Weinstein, Rachel ;
Friedmand, Harvey ;
Dickinson, Diana ;
Frank, Ian ;
Strom, Brian L. ;
Gaolathe, Tendani ;
Ndwapi, Ndwapi .
AIDS, 2006, 20 (12) :1613-1619
[6]   COMPARING METHODS OF MEASUREMENT - WHY PLOTTING DIFFERENCE AGAINST STANDARD METHOD IS MISLEADING [J].
BLAND, JM ;
ALTMAN, DG .
LANCET, 1995, 346 (8982) :1085-1087
[7]  
Bürgisser P, 2000, J ACQ IMMUN DEF SYND, V23, P138
[8]   Quantitative real-time RT-PCR - a perspective [J].
Bustin, SA ;
Benes, V ;
Nolan, T ;
Pfaffl, MW .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2005, 34 (03) :597-601
[9]   HIV viral load monitoring in resource-limited regions: Optional or necessary? [J].
Calmy, Alexandra ;
Ford, Nathan ;
Hirschel, Bernard ;
Reynolds, Steven J. ;
Lynen, Lut ;
Goemaere, Eric ;
de la Vega, Felipe Garcia ;
Perrin, Luc ;
Rodriguez, William .
CLINICAL INFECTIOUS DISEASES, 2007, 44 (01) :128-134
[10]   Multiplex real-time quantitative RT-PCR assay for hepatitis B virus, hepatitis C virus, and human immunodeficiency virus type 1 [J].
Candotti, D ;
Temple, J ;
Owusu-Ofori, S ;
Allain, JP .
JOURNAL OF VIROLOGICAL METHODS, 2004, 118 (01) :39-47