首页> 外文期刊>The Journal of communicable diseases >Evaluation of quantitative buffy coat (QBC) assay and polymerase chain reaction (PCR) for diagnosis of malaria.
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Evaluation of quantitative buffy coat (QBC) assay and polymerase chain reaction (PCR) for diagnosis of malaria.

机译:评价定量血沉棕黄层(QBC)分析和聚合酶链反应(PCR)诊断疟疾。

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A prospective study was undertaken to compare the Polymerase Chain Reaction (PCR) and Quantitative Buffy Coat (QBC) assay with conventional Giemsa technique for diagnosis of malaria. A total of 104 samples were taken for the purpose. They comprised of fever cases suggestive of malaria (n=74) and control group, fever cases other than malaria (n=30). Peripheral blood smears were prepared by Giemsa staining and QBC assay was performed as per standard protocol. From the stored blood samples, parasite DNA was extracted and PCR was performed using P. falciparum and P. vivax specific sets of primers. The QBC assay was 100% in agreement with the Giemsa stain. Specificity of the PCR detection of P. falciparum parasites was 100%. However, sensitivity for detection of P. falciparum and P. vivax by PCR was 64.28% and 82.35% respectively. In mixed cases of malaria (n=2), PCR results were in 100% agreement with that of Giemsa. The lower sensitivity of PCR for P. falciparum could probably be due to inaccessibility of target DNA, presence of PCR inhibitors in samples and parasite strain variations.
机译:进行了一项前瞻性研究,以比较聚合酶链反应(PCR)和定量Buffy大衣(QBC)测定法与传统Giemsa技术在疟疾诊断中的作用。总共采集了104个样本。他们包括提示疟疾的发热病例(n = 74)和对照组,除疟疾以外的发热病例(n = 30)。通过吉姆萨(Giemsa)染色制备外周血涂片,并根据标准方案进行QBC测定。从储存的血液样本中提取寄生虫DNA,并使用恶性疟原虫和间日疟原虫特异性引物对进行PCR。 QBC测定与吉姆萨染色法一致,为100%。 PCR检测恶性疟原虫寄生虫的特异性为100%。然而,PCR检测恶性疟原虫和间日疟原虫的灵敏度分别为64.28%和82.35%。在疟疾混合病例(n = 2)中,PCR结果与Giemsa的结果100%一致。 PCR对恶性疟原虫的敏感性较低可能是由于靶DNA难以接近,样品中存在PCR抑制剂以及寄生虫菌株变异。

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