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首页> 外文期刊>Journal of Clinical Microbiology >Simple DNA Extraction Method for Dried Blood Spots and Comparison of Two PCR Assays for Diagnosis of Vertical Human Immunodeficiency Virus Type 1 Transmission in Rwanda
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Simple DNA Extraction Method for Dried Blood Spots and Comparison of Two PCR Assays for Diagnosis of Vertical Human Immunodeficiency Virus Type 1 Transmission in Rwanda

机译:简单的干血斑DNA提取方法和两种PCR诊断卢旺达人垂直免疫缺陷病毒1型传播的比较

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Dried blood spots (DBS) on filter paper facilitate the collection, transport, and storage of blood samples for laboratory use. A rapid and simple DNA extraction procedure from DBS was developed and evaluated for the diagnosis of human immunodeficiency virus type 1 (HIV-1) infection in children by an in-house nested-PCR assay on three genome regions and by the Amplicor HIV-1 DNA prototype assay version 1.5 (Roche Molecular Systems). A total of 150 samples from children born to HIV-1-infected mothers were collected in Kigali, Rwanda, in parallel as DBS and as peripheral blood mononuclear cell (PBMC) pellets. The results obtained on DBS by the two PCR assays were compared to the results of nested PCR on PBMCs. Of 150 PBMC samples, 10 were positive, 117 were negative, and 23 were indeterminate for HIV-1 infection. In DNA extracted from filter papers and amplified by using the in-house nested PCR, 9 of these 10 positive samples (90%) were found to be positive, and 1 was found to be indeterminate (only the pol region could be amplified). All of the negative samples and all of the 23 indeterminate samples tested negative for HIV-1 infection. When we used the Amplicor DNA test on DBS, all of the 10 PBMC-positive samples were found to be positive and all of the 23 indeterminate samples were found to be negative. Of the PBMC-negative samples, 115 were found to be negative and 2 were found to be indeterminate. We conclude that this simple rapid DNA extraction method on DBS in combination with both detection methods gave a reliable molecular diagnosis of HIV-1 infection in children born to HIV-infected mothers.
机译:滤纸上的干血斑(DBS)有助于收集,运输和存储供实验室使用的血样。开发了一种从DBS进行的快速简单的DNA提取程序,并通过对三个基因组区域的内部巢式PCR测定法和Amplicor HIV-1进行了评估,以诊断儿童的人类1型免疫缺陷病毒(HIV-1)感染DNA原型测定版本1.5(Roche Molecular Systems)。在卢旺达的基加利,从DB-1和外周血单核细胞(PBMC)沉淀物中平行收集了150份来自感染HIV-1的母亲所生孩子的样品。将通过两次PCR分析在DBS上获得的结果与在PBMC上嵌套PCR的结果进行比较。在150份PBMC样本中,有10份阳性,117份阴性和23份不确定的HIV-1感染。在从滤纸中提取的DNA并通过内部巢式PCR扩增的DNA中,这10份阳性样品中有9份(90%)被鉴定为阳性,其中1份是不确定的(仅 pol 区域可以放大)。所有阴性样品和所有23个不确定样品的HIV-1感染测试均为阴性。当我们在DBS上使用Amplicor DNA测试时,发现所有10个PBMC阳性样品均为阳性,而所有23个不确定的样品均为阴性。在PBMC阴性样本中,发现115例阴性,另2例不确定。我们得出的结论是,结合DBS的这种简单的快速DNA提取方法和两种检测方法,可以对感染HIV的母亲所生的孩子进行HIV-1感染的可靠分子诊断。

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