Subtype-specific problems with qualitative Amplicor HIV-1 DNA PCR test

被引:16
作者
Bogh, M
Machuca, R
Gerstoft, J
Pedersen, C
Obel, N
Kvinesdal, B
Nielsen, H
Nielsen, C
机构
[1] Statens Serum Inst, Retrovirus Lab, Dept Virol, DK-2300 Copenhagen S, Denmark
[2] Rigshosp, DK-2100 Copenhagen, Denmark
[3] Odense Univ Hosp, DK-5000 Odense, Denmark
[4] Marselisborg Hosp, Aarhus, Denmark
[5] Hvidovre Hosp, Copenhagen, Denmark
[6] Aalborg Hosp, Aalborg, Denmark
关键词
HIV-1; Amplicor HIV-l test; qualitative HIV-1PCR; subtypes;
D O I
10.1016/S1386-6532(00)00147-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: commercial HIV-1 qualitative DNA PCR tests have the potential to detect virus in patients in whom antibody tests may be ineffective, such as patients with primary HIV infection and infants born to HIV seropositive mothers. However, the genetic diversity of HIV-1 raises concern about the ability of the PCR tests to detect all current subtypes. Objectives: to asses the sensitivity of the Amplicor HIV-1 test on 126 whole-blood samples representing seven different subtypes and to investigate the sensitivity when the standard assay was modified by including the primer pair SK145 and SKCC1B. Results: of the 126 HIV-1 infected persons, 113 were tested positive and 13 were DNA PCR negative. On the basis of these results, the standard Amplicor HIV-1 test had a sensitivity of 90% in our cohort. In addition, 9% of the positive samples showed a low reactivity but above the cut-off of the assay. The standard assay yielded sensitivities of 100%, for subtype B (n = 16), D (n = 9) and G (n = 1), but only 83% for subtype A (n = 41), 98% for subtype C (n = 43), 79% for subtype E (n = 14) and 0% for subtype F (n = 2). All samples with low reactivity were non-B subtype. Eight of the DNA PCR negative samples, four subtype A, one C and three E were amplified with the modified Amplicor HIV-1 test with addition of SK145/SKCC1B primers. Using this modified protocol, six samples out of eight became positive. However, two samples (one A and one C) remained DNA PCR negative. Conclusion: this study confirms that the Amplicor HIV-1 test does not detect all subtypes with equivalent sensitivity and 10% of the samples, tested negative. Thus, it is preferable to add the SK145/SKCC1B primers to the standard test, where infection with non-B subtype is suspected. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 153
页数:5
相关论文
共 12 条
[1]   HIV TYPE-1 SEQUENCE SUBTYPE-G TRANSMISSION FROM MOTHER-TO-INFANT - FAILURE OF VARIANT SEQUENCE SPECIES TO AMPLIFY IN THE ROCHE AMPLICOR TEST [J].
ARNOLD, C ;
BARLOW, KL ;
KAYE, S ;
LOVEDAY, C ;
BALFE, P ;
CLEWLEY, JP .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1995, 11 (08) :999-1001
[2]   RAPID SCREENING FOR EARLY DETECTION OF MOTHER-TO-CHILD TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
CASSOL, S ;
BUTCHER, A ;
KINARD, S ;
SPADORO, J ;
SY, T ;
LAPOINTE, N ;
READ, S ;
GOMEZ, P ;
FAUVEL, M ;
MAJOR, C ;
OSHAUGHNESSY, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (11) :2641-2645
[3]   Evaluation and comparison of the Amplicor HIV-1 PCR kit with an 'in-house' nested PCR [J].
Fransen, K ;
vanKerckhoven, I ;
Piot, P ;
vanderGroen, G .
CLINICAL AND DIAGNOSTIC VIROLOGY, 1995, 4 (04) :311-319
[4]   The emerging genetic diversity of HIV - The importance of global surveillance for diagnostics, research, and prevention [J].
Hu, DJ ;
Dondero, TJ ;
Rayfield, MA ;
George, JR ;
Schochetman, G ;
Jaffe, HW ;
Luo, CC ;
Kalish, ML ;
Weniger, BG ;
Pau, CP ;
Schable, CA ;
Curran, JW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (03) :210-216
[5]   COMPARISON OF A RAPID NONISOTOPIC POLYMERASE CHAIN-REACTION ASSAY WITH 4 COMMONLY USED METHODS FOR THE EARLY DIAGNOSIS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION IN NEONATES AND CHILDREN [J].
KOVACS, A ;
XU, J ;
RASHEED, S ;
LI, XL ;
KOGAN, T ;
LEE, M ;
LIU, C ;
CHAN, L .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1995, 14 (11) :948-954
[6]   GENETIC DIVERSITY AND HIV DETECTION BY POLYMERASE CHAIN-REACTION [J].
LOUSSERTAJAKA, I ;
DESCAMPS, D ;
SIMON, F ;
BRUNVEZINET, F ;
EKWALANGA, M ;
SARAGOSTI, S .
LANCET, 1995, 346 (8979) :912-913
[7]  
MACHUCA R, 2000, UNPUB HIV 1 SUBTYPES
[8]  
Myers G, 1995, HUMAN RETROVIRUSES A, P35
[9]   Detection of genetically diverse human immunodeficiency virus type 1 group M and O isolates by PCR [J].
Respess, RA ;
Butcher, A ;
Wang, H ;
Chaowanachan, T ;
Young, N ;
Shaffer, N ;
Mastro, TD ;
Biryahwaho, B ;
Downing, R ;
Tanuri, A ;
Schechter, M ;
Pascu, R ;
Zekeng, L ;
Kaptue, L ;
Gurtler, L ;
Eberle, J ;
Ellenberger, D ;
Fridlund, C ;
Rayfield, M ;
Kwok, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (05) :1284-1286
[10]   Primary subtype C HIV-1 infection in Harare, Zimbabwe [J].
Tien, PC ;
Chiu, T ;
Latif, A ;
Ray, S ;
Batra, M ;
Contag, CH ;
Zejena, L ;
Mbizvo, M ;
Delwart, EL ;
Mullins, JI ;
Katzenstein, DA .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1999, 20 (02) :147-153