Performance of the applied biosystems ViroSeq human immunodeficiency virus type 1 (HIV-I) genotyping system for sequence-based analysis of HIV-1 in pediatric plasma samples
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作者:
Cunningham, S
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Cunningham, S
Ank, B
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Ank, B
Lewis, D
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Lewis, D
Lu, W
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Lu, W
Wantman, M
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Wantman, M
Dileanis, J
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Dileanis, J
Jackson, JB
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Jackson, JB
Palumbo, P
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Palumbo, P
Krogstad, P
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Krogstad, P
Eshleman, SH
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机构:Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
Eshleman, SH
机构:
[1] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
[2] Univ Calif Los Angeles, Dept Pediat, Los Angeles, CA 90024 USA
[3] Appl Biosyst, Foster City, CA USA
[4] Univ Med & Dent New Jersey, Dept Pediat, Newark, NJ 07103 USA
[5] Harvard Univ, Sch Publ Hlth, Stat Data Anal Ctr, Boston, MA 02115 USA
The ViroSeq HIV-1 Genotyping System is a commercially available, integrated sequence-based system for analysis of human immunodeficiency virus type I (HIV-1) drug resistance. We evaluated the performance of this system by analyzing HIV-1 in pediatric plasma samples. Plasma samples front children 4 months to 17 years of age were obtained from a clinical trial protocol (PACTG 377), Children in PACTG 377 were randomized to four treatment arms, including different combinations of antiretroviral drugs. HIV-1 genotyping was performed using samples collected prior to antiretroviral therapy (baseline) and at the time of virologic failure. Performance of the genotyping system was compared in three university laboratories. A total of 196 samples were analyzed, including 135 baseline and 61 failure samples. Plasma volumes ranged from 0.05 to 0.5 ml, and viral loads ranged from 1,081 to 3,183,991 copies/ml. PCR products suitable for sequencing were obtained for 192 of the 196 samples. Complete sequences for protease and reverse transcriptase were obtained for all of these 192 samples. For 180 samples, data were obtained from both DNA strands for the entire region analyzed. There was no evidence of sample cross-contamination based on phylogenetic analysis of HIV-1 sequences, Performance of the genotyping system was similar in three laboratories. This genotyping: system performs well for analysis of HIV-1 in pediatric plasma samples, including those with low volume and low viral load. The availability of this system should facilitate studies of HIV-1 drug resistance.