首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Development of a Polymerase Chain Reaction (PCR) method based on amplification of mitochondrial DNA to detect Plasmodium falciparum and Plasmodium vivax.
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Development of a Polymerase Chain Reaction (PCR) method based on amplification of mitochondrial DNA to detect Plasmodium falciparum and Plasmodium vivax.

机译:开发一种基于线粒体DNA扩增的聚合酶链反应(PCR)方法,以检测恶性疟原虫和间日疟原虫。

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摘要

In this study we standardized a new technical approach in which the target mitochondrial DNA sequence (mtDNA) is amplified using a simple but sensitive PCR method as a tool to detect Plasmodium falciparum and Plasmodium vivax. Specific primers were designed to hybridize with cytochrome c oxidase genes of P. falciparum (cox III) and P. vivax (cox I). Amplification products were obtained for all positive samples, presenting homology only for species-specific mtDNA. Sensitivity and specificity were 100%. The applicability of the method was tested in a cross-sectional study, in which 88 blood samples from individuals naturally exposed to malaria in the Brazilian Amazon region were analyzed. Based on the results, the sensitivity and specificity were 100% and 88.3%, respectively. This simple and sensitive PCR method can be useful in specific situations and in different settings of malaria management, in endemic as well as non-endemic areas (travelers), and in clinical or epidemiological studies, with applications in malaria control programs.
机译:在这项研究中,我们标准化了一种新技术方法,其中使用简单但灵敏的PCR方法作为检测恶性疟原虫和间日疟原虫的工具,扩增靶线粒体DNA序列(mtDNA)。设计特异性引物以与恶性疟原虫(cox III)和间日疟原虫(cox I)的细胞色素c氧化酶基因杂交。获得了所有阳性样品的扩增产物,仅对物种特异性的mtDNA具有同源性。敏感性和特异性为100%。在一项横断面研究中测试了该方法的适用性,在该研究中分析了来自巴西亚马逊地区自然暴露于疟疾的个人的88份血液样本。根据结果​​,敏感性和特异性分别为100%和88.3%。这种简单而灵敏的PCR方法可在特定情况下以及在疟疾管理的不同环境中,地方性和非地方性地区(旅行者)以及临床或流行病学研究中应用,并应用于疟疾控制程序中。

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