Schneider Renate, Lamien-Meda Aline, Auer Herbert, Wiedermann-Schmidt Ursula, Chiodini Peter L, Walochnik Julia
Institute for Specific Prophylaxis and Tropical Medicine, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Austria.
UK NEQAS Parasitology, Public Health England, London, UK.
Bio Protoc. 2022 Apr 5;12(7):e4381. doi: 10.21769/BioProtoc.4381.
Malaria is the most important parasitic disease worldwide, and accurate diagnosis and treatment without delay are essential for reducing morbidity and mortality, especially in malaria. Real-time PCR is highly sensitive and highly specific, therefore an excellent diagnostic tool for laboratory detection and species-specific diagnosis of malaria, especially in non-endemic regions where experience in microscopic malaria diagnostics is limited. In contrast to many other real-time PCR protocols, our new fluorescence resonance energy transfer-based real-time PCR (FRET-qPCR) allows the quantitative and species-specific detection of all human spp. in one run. Species identification is based on single nucleotide polymorphisms (SNPs) within the MalFL probe, detectable by melting curve analysis. A significant advantage of our FRET-qPCR is the short turn-around time of less than two hours, including DNA extraction, which qualifies it for routine diagnostics. Rapid and reliable species-specific malaria diagnosis is important, because treatment is species-dependent. Apart from first-line diagnosis, the quantitative results of our new FRET-qPCR can be helpful in therapy control, to detect early treatment failure. Graphic abstract.
疟疾是全球最重要的寄生虫病,准确诊断并及时治疗对于降低发病率和死亡率至关重要,尤其是在疟疾流行地区。实时荧光定量聚合酶链反应(Real-time PCR)具有高度敏感性和特异性,因此是疟疾实验室检测和种特异性诊断的优秀工具,特别是在疟疾显微镜诊断经验有限的非流行地区。与许多其他实时荧光定量聚合酶链反应方案不同,我们新的基于荧光共振能量转移的实时荧光定量聚合酶链反应(FRET-qPCR)能够在一次检测中对所有人类疟原虫进行定量和种特异性检测。种属鉴定基于MalFL探针内的单核苷酸多态性(SNP),可通过熔解曲线分析检测。我们的FRET-qPCR的一个显著优点是周转时间短,不到两小时,包括DNA提取,这使其适用于常规诊断。快速可靠的种特异性疟疾诊断很重要,因为治疗取决于疟原虫种类。除一线诊断外,我们新的FRET-qPCR的定量结果有助于治疗监测,以检测早期治疗失败。图形摘要。