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Malaria infection diagnosis: comparison between traditional methods and a new freeze-dried PCR multiplex test

机译:疟疾感染诊断:传统方法与新型冻干PCR多重检测的比较

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摘要

Malaria is the most diffused parasitic disease that affects humans.A rapid and accurate diagnosis is a prerequisite for an effective treatment. The development of a new ready-to-use test for the screening and the typing of malaria solve the temperature storage requests of common molecular tests and PCR reagents. The performances of STAT-NAT Malaria Screening and STAT-NAT Malaria Typing kits were tested on samples obtained from patients suspected to be infected by malaria’s parasites, Immigrants (I) and International Travellers (IT), and were compared with the gold standard method (microscopy). Samples of peripheral blood of 35 patients (25 IT and 10 I) obtained from San Matteo Hospital in Pavia were analysed.The microscopy identified 18 of them as positive samples: 11 samples were positive for Plasmodium falciparum (5 IT, 6 I), 3 for Plasmodium vivax (3 IT), 2 for Plasmodium ovale (1I, 1 IT) and 2 for Plasmodium malariae (2 I). No co-infections were found. STAT-NAT Malaria kits confirmed the results of 18 positive samples as well as of 17 negative samples (100% sensitivity). In a case STAT-NAT Malaria Typing kit identified the presence of Plasmodium ovale in a sample instead of Plasmodium vivax, as previously diagnosed with the microscopic analysis.The epidemiological analysis and a new microscopic diagnosis confirmed the infection as caused by Plasmodium ovale species (100% specificity). We conclude that the association of the freeze-dried STAT-NAT Malaria tests could be determinant for the correct detection and typing of malaria, mainly where the temperature controlled storage could be problematic.
机译:疟疾是影响人类的最广泛的寄生虫病,快速准确的诊断是有效治疗的先决条件。新的即用型疟疾筛查和分型检测方法的开发解决了普通分子检测和PCR试剂对温度存储的要求。 STAT-NAT疟疾筛查和STAT-NAT疟疾分型试剂盒的性能进行了测试,样品取自怀疑被疟原虫,移民(I)和国际旅行者(IT)感染的患者,并与黄金标准方法进行了比较(显微镜)。分析了从Pavia的San Matteo医院获得的35例患者的外周血样本(25 IT和10 I),显微镜检查发现其中18例为阳性样本:11例恶性疟原虫为阳性(5 IT,6 I),3间日疟原虫(3 IT),椭圆形疟原虫2(1I,1 IT)和疟原虫2(2 I)2。未发现共感染。 STAT-NAT疟疾试剂盒确认了18份阳性样品和17份阴性样品的结果(灵敏度为100%)。在一个STAT-NAT疟疾分型试剂盒中,如先前通过显微镜分析所诊断的那样,发现样品中存在卵形疟原虫而不是间日疟原虫。流行病学分析和新的显微镜诊断证实了感染是由卵形疟原虫物种引起的(100特异性百分比)。我们得出的结论是,冷冻干燥的STAT-NAT疟疾检测的关联可能是正确检测和确定疟疾类型的决定因素,主要是在温度控制存储可能存在问题的地方。

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