首页> 外文期刊>Malaria Journal >Detection of Plasmodium knowlesi, Plasmodium falciparum and Plasmodium vivax using loop-mediated isothermal amplification (LAMP) in a co-endemic area in Malaysia
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Detection of Plasmodium knowlesi, Plasmodium falciparum and Plasmodium vivax using loop-mediated isothermal amplification (LAMP) in a co-endemic area in Malaysia

机译:使用环介导的等温扩增(LAMP)在马来西亚的共同流行地区检测诺氏疟原虫,恶性疟原虫和间日疟原虫

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Background Plasmodium knowlesi is the most common cause of malaria in Malaysia. However, microscopic diagnosis is inaccurate and rapid diagnostic tests (RDTs) are insufficiently sensitive. PCR is sensitive and specific but not feasible at a district level. Loop-mediated isothermal amplification (LAMP) shows potential with only basic requirements. A commercially available LAMP assay, the Eiken Loopamp? MALARIA Pan Detection kit, is sensitive for Plasmodium falciparum and Plasmodium vivax , but has not previously been evaluated for P. knowlesi . This study aims to determine the sensitivity of this LAMP assay for detecting P. knowlesi infection. MethodsStudy participants included 73 uncomplicated malaria patients with PCR species confirmation: 50 P. knowlesi , 20 P. falciparum and 3 P. vivax . Nineteen malaria-negative, non-endemic area controls were also included. The sensitivity of the Eiken Loopamp? MALARIA Pan Detection kit (Pan LAMP) for detecting each Plasmodium species was evaluated. Sensitivity and specificity of the Eiken Loopamp? MALARIA Pf Detection kit ( Pf LAMP) for P. falciparum were also determined. The limit of detection for each LAMP assay was evaluated, with results compared to PCR. All P. knowlesi patients were also tested by CareStart? (Pf/VOM) and OptiMAL-IT? (Pan/Pf) RDTs. ResultsThe sensitivity of the Pan LAMP assay was 100% for P. knowlesi (95% CI 92.9–100), P. falciparum (95% CI 83.2–100), and P. vivax (95% CI 29.2–100). The Pf LAMP was 100% sensitive and specific for P. falciparum detection, with all P. knowlesi samples having a negative reaction. LAMP sensitivity was superior to both RDTs, with only 10 and 28% of P. knowlesi samples testing positive to CareStart? and OptiMAL-IT?, respectively. Limit of detection using the Pan LAMP for both P. knowlesi and P. vivax was 2?parasites/μL, comparable to PCR. For P. falciparum both the Pan LAMP and Pf LAMP demonstrated a limit of detection of 20?parasites/μL. ConclusionsThe Eiken Loopamp? MALARIA Pan Detection kit is sensitive for detection of P. knowlesi in low parasitaemia clinical infections, as well as P. falciparum and P. vivax. However, a P. knowlesi -specific field assay in a simpler format would assist correct species identification and initiation of optimal treatment for all malaria patients.
机译:背景知识疟原虫是马来西亚疟疾的最常见原因。但是,显微镜诊断不准确,快速诊断测试(RDT)不够灵敏。 PCR具有敏感性和特异性,但在地区范围内不可行。回路介导的等温扩增(LAMP)仅根据基本要求即可显示潜力。市售的LAMP测定法Eiken Loopamp? MALARIA Pan检测试剂盒对恶性疟原虫和间日疟原虫敏感,但以前尚未对诺氏疟原虫进行过评估。这项研究旨在确定这种LAMP测定法检测诺氏杆菌感染的敏感性。方法研究参与者包括73例经PCR确诊的单纯性疟疾患者:50个诺氏疟原虫,20个恶性疟原虫和3个间日疟原虫。还包括19个疟疾阴性,非流行地区的对照。 Eiken Loopamp的灵敏度?评估了用于检测每种疟原虫物种的MALARIA Pan检测试剂盒(Pan LAMP)。 Eiken Loopamp的灵敏度和特异性?还确定了恶性疟原虫的疟疾Pf检测试剂盒(Pf LAMP)。评估了每种LAMP测定的检出限,并将结果与​​PCR进行了比较。所有的诺氏疟原虫患者也都通过CareStart进行了测试? (Pf / VOM)和OptiMAL-IT? (Pan / Pf)RDT。结果Pan LAMP测定对诺氏疟原虫(95%CI 92.9–100),恶性疟原虫(95%CI 83.2–100)和间日疟原虫(95%CI 29.2–100)的敏感性为100%。 Pf LAMP对恶性疟原虫检测具有100%的敏感性和特异性,所有诺氏疟原虫样品均具有阴性反应。 LAMP灵敏度优于两个RDT,仅10%和28%的诺氏疟原虫样品对CareStart?检测呈阳性。和OptiMAL-IT?对于P. Knowlesi和间日疟原虫,使用Pan LAMP的检出限为2?寄生虫/μL,与PCR相当。对于恶性疟原虫,Pan LAMP和Pf LAMP的检出限均为20?寄生虫/μL。结论Eiken Loopamp? MALARIA Pan检测试剂盒可用于检测低寄生虫血症临床感染中的诺氏疟原虫以及恶性疟原虫和间日疟原虫。然而,以更简单的形式进行的诺氏疟原虫特异性田间测定将有助于正确识别物种,并为所有疟疾患者提供最佳治疗方法。

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