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首页> 外文期刊>Journal of Clinical Microbiology >Prospective Value of PCR Amplification and Sequencing for Diagnosis and Typing of Old World Leishmania Infections in an Area of Nonendemicity
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Prospective Value of PCR Amplification and Sequencing for Diagnosis and Typing of Old World Leishmania Infections in an Area of Nonendemicity

机译:PCR扩增和测序对非传染性地区旧世界利什曼原虫感染的诊断和分型的前瞻性价值

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摘要

We assessed the prospective value of PCR amplification of a repetitive sequence from Leishmania nuclear DNA and sequencing for the diagnosis and typing of Old World Leishmania infection in an area of nonendemicity. During this 42-month study, 29 of 168 consecutive samples were examined and classified as positive for Leishmania by direct examination and/or in vitro culture. This molecular approach showed excellent sensitivity (97%) and specificity (100%) compared to direct examination (86 and 100%, respectively) and in vitro culture (72 and 100%, respectively). Isoenzymatic and molecular typing allowed similar identification for 12 samples. Besides, PCR and subsequent sequencing of DNA products permitted the species identification of 14 samples for which parasite culture remained negative or did not allow isoenzymatic characterization, indicating the complementarity of parasitological and molecular tools.
机译:我们评估了利什曼原虫核DNA的重复序列的PCR扩增和测序对非传染性地区旧世界利什曼原虫感染的诊断和分型的潜在价值。在这项为期42个月的研究中,对168个连续样本中的29个进行了检查,并通过直接检查和/或体外培养将其归类为“利什曼原虫”阳性。与直接检查(分别为86%和100%)和体外培养(分别为72%和100%)相比,这种分子方法显示出极好的灵敏度(97%)和特异性(100%)。同功酶和分子分型可以对12个样品进行相似的鉴定。此外,PCR和随后的DNA产物测序可以鉴定14个样品的物种,这些样品的寄生虫培养仍为阴性或无法进行同工酶鉴定,表明寄生虫学和分子工具的互补性。

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