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采用静脉血和干血斑,通过手动和自动DNA提取方法对1.5版Amplicor HIV-1 DNA检测进行HIV-1 DNA PCR检测的比较评估。

Comparative evaluation of Amplicor HIV-1 DNA test, version 1.5, by manual and automated DNA extraction methods using venous blood and dried blood spots for HIV-1 DNA PCR testing.

作者信息

Nsojo Anthony, Aboud Said, Lyamuya Eligius

机构信息

Department of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania.

出版信息

Tanzan J Health Res. 2010 Oct;12(4):229-35. doi: 10.4314/thrb.v12i4.58621.

Abstract

Human immunodeficiency virus (HIV) DNA polymerase chain reaction (PCR) test using venous blood sample has been used for many years in low resource settings for early infant diagnosis of HIV infection in children less than 18 months. The aim of this study was to evaluate and compare the performance characteristics of Amplicor HIV-1 DNA assay version 1.5 following processing of venous blood and dried blood spot (DBS) samples by Roche manual DNA extraction and automated Roche MagNA Pure LC instrument (MP) for HIV-1 DNA PCR testing in Dar es Salaam, Tanzania, in order to scale up early infant diagnosis of HIV infection in routine practice. Venous blood samples from children under 18 months born to HIV-infected mothers between January and April 2008 were collected. Venous blood was used to prepare cell pellet and DBS samples. DNA extractions by manual procedure and MP were performed each on cell pellet, venous blood and DBS samples and tested by Amplicor HIV-1 DNA assay. Of 325 samples included, 60 (18.5%) were confirmed HIV-infected by manual extraction performed on cell pellets. Sensitivity of the assay following MP processing of venous blood was 95% (95% CI; 86.1-99.0%) and 98.3% (95% CI; 91.1 to 99.9%) for the manual extraction and processing by MP performed on DBS samples. Specificity of the assay with all DNA extraction methods was 99.6% (95% CI; 97.9 to 100%). Performance of the assay with Roche manual extraction and processing by MP on DBS samples compared well with Roche manual extraction performed on cell pellet samples. The choice of DNA extraction method needs to be individualized based on the level of laboratory facility, volume of testing and cost benefit analysis before it is adopted for use.

摘要

多年来,在资源匮乏地区,利用静脉血样本进行人类免疫缺陷病毒(HIV)DNA聚合酶链反应(PCR)检测,用于18个月以下儿童HIV感染的早期婴儿诊断。本研究的目的是评估并比较罗氏手动DNA提取法和罗氏MagNA Pure LC自动化仪器(MP)处理静脉血和干血斑(DBS)样本后,Amplicor HIV-1 DNA检测试剂盒1.5版在坦桑尼亚达累斯萨拉姆用于HIV-1 DNA PCR检测的性能特征,以便在常规实践中扩大HIV感染早期婴儿诊断的规模。收集了2008年1月至4月期间感染HIV的母亲所生的18个月以下儿童的静脉血样本。用静脉血制备细胞沉淀和DBS样本。对细胞沉淀、静脉血和DBS样本分别采用手动方法和MP进行DNA提取,并通过Amplicor HIV-1 DNA检测试剂盒进行检测。在纳入的325份样本中,通过对细胞沉淀进行手动提取,有60份(18.5%)被确诊为HIV感染。对静脉血进行MP处理后该检测方法的灵敏度,对于手动提取和对DBS样本进行MP处理分别为95%(95%可信区间;86.1 - 99.0%)和98.3%(95%可信区间;91.1至99.9%)。所有DNA提取方法的检测特异性为99.6%(95%可信区间;97.9至100%)。罗氏手动提取并通过MP对DBS样本进行处理的检测性能,与对细胞沉淀样本进行罗氏手动提取的性能相当。在采用DNA提取方法之前,需要根据实验室设施水平、检测量和成本效益分析进行个体化选择。

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