首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Performance of the Applied Biosystems ViroSeq Human Immunodeficiency Virus Type 1 (HIV-1) Genotyping System for Sequence-Based Analysis of HIV-1 in Pediatric Plasma Samples
【2h】

Performance of the Applied Biosystems ViroSeq Human Immunodeficiency Virus Type 1 (HIV-1) Genotyping System for Sequence-Based Analysis of HIV-1 in Pediatric Plasma Samples

机译:应用生物系统ViroSeq 1型人类免疫缺陷病毒(HIV-1)基因分型系统对小儿血浆样品中HIV-1进行基于序列分析的性能

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The ViroSeq HIV-1 Genotyping System is a commercially available, integrated sequence-based system for analysis of human immunodeficiency virus type 1 (HIV-1) drug resistance. We evaluated the performance of this system by analyzing HIV-1 in pediatric plasma samples. Plasma samples from 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 1,084 to 3,484,991 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.
机译:ViroSeq HIV-1基因分型系统是一种可商购的,基于序列的集成系统,用于分析人类1型免疫缺陷病毒(HIV-1)的耐药性。我们通过分析儿科血浆样本中的HIV-1评估了该系统的性能。从临床试验方案(PACTG 377)中获得4个月至17岁儿童的血浆样品。 PACTG 377中的儿童被随机分配到四个治疗组,包括不同组合的抗逆转录病毒药物。使用抗逆转录病毒治疗之前(基线)和病毒学衰竭时收集的样本进行HIV-1基因分型。在三个大学实验室中比较了基因分型系统的性能。共分析了196个样本,包括135个基线和61个失败样本。血浆体积范围为0.05到0.5 ml,病毒载量范围为1,084到3,484,991拷贝/ ml。从196个样品中的192个中获得了适合测序的PCR产物。对于所有这192个样品,均获得了蛋白酶和逆转录酶的完整序列。对于180个样品,从两条DNA链获得了整个分析区域的数据。根据HIV-1序列的系统发育分析,没有证据表明样品存在交叉污染。在三个实验室中,基因分型系统的性能相似。该基因分型系统在分析儿童血浆样本中的HIV-1方面表现良好,包括低容量和低病毒载量的样本。该系统的可用性应有助于研究HIV-1耐药性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号