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首页> 外文期刊>Journal of Clinical Microbiology >Detection and Quantification of Plasmodium falciparumin Blood Samples Using Quantitative Nucleic Acid Sequence-Based Amplification
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Detection and Quantification of Plasmodium falciparumin Blood Samples Using Quantitative Nucleic Acid Sequence-Based Amplification

机译:使用基于核酸序列的定量扩增检测和定量恶性疟原虫血样

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摘要

A quantitative nucleic acid sequence-based amplification (QT-NASBA) assay for the detection of Plasmodium parasites has been developed. Primers and probes were selected on the basis of the sequence of the small-subunit rRNA gene. Quantification was achieved by coamplification of the RNA in the sample with one modified in vitro RNA as a competitor in a single-tube NASBA reaction. Parasite densities ranging from 10 to 108 Plasmodium falciparum parasites per ml could be demonstrated and quantified in whole blood. This is approximately 1,000 times more sensitive than conventional microscopy analysis of thick blood smears. Comparison of the parasite densities obtained by microscopy and QT-NASBA with 120 blood samples from Kenyan patients with clinical malaria revealed that for 112 of 120 (93%) of the samples results were within a 1-log difference. QT-NASBA may be especially useful for the detection of low parasite levels in patients with early-stage malaria and for the monitoring of the efficacy of drug treatment.
机译:已经开发了用于检测疟原虫寄生虫的基于定量核酸序列的扩增(QT-NASBA)分析方法。根据小亚基rRNA基因的序列选择引物和探针。通过将样品中的RNA与一种修饰的体外RNA作为单管NASBA反应中的竞争剂进行共扩增来实现定量。可以证明并量化全血中每毫升10至10 8 恶性疟原虫的寄生虫密度。这比常规显微镜对浓血涂片的敏感性高约1,000倍。通过显微镜和QT-NASBA对来自肯尼亚临床疟疾患者的120份血液样本进行的寄生虫密度比较表明,在120份样本中,有112份(93%)的结果相差1个对数。 QT-NASBA对于检测早期疟疾患者的低寄生虫水平以及监测药物治疗效果可能特别有用。

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