Ngasala Billy, Opoku Kofi B, Amagai Kano, Assefa Ashenafi, Loya Mwajabu, Nyange Mwanaidi, Muller Meredith, Said Hamza, Basham Christopher, Rogier Eric, Juliano Jonathan J, Parr Jonathan B, Lin Jessica T
Department of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Institute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina.
Am J Trop Med Hyg. 2025 Jan 21;112(4):765-770. doi: 10.4269/ajtmh.24-0209. Print 2025 Apr 2.
Malaria rapid diagnostic tests (mRDTs) that detect histidine-rich protein 2 (HRP2) remain the mainstay of falciparum malaria diagnosis in Sub-Saharan Africa. Understanding their test characteristics when used for surveillance in asymptomatic populations is important. We explored the rate of false-positive and false-negative mRDT results among asymptomatic persons >5 years old screened for malaria at schools and clinics in the rural Bagamoyo District using 18S ribosomal RNA real-time polymerase chain reaction (qPCR) as the reference test. Among 5,966 persons screened using mRDTs, microscopy, and qPCR tests from 2018 to 2021, 14% (832) were mRDT-positive. Twelve percent of these (98/832) were negative by both microscopy and qPCR, with children overrepresented among those with false-positive mRDTs. Among those who were mRDT-negative, 22% (1,136/5,134) tested qPCR-positive, predominantly because of low-density parasitemia (92% had <100 p/µL by qPCR). Among mRDT-negative samples with >100 p/µL, we looked for evidence of hrp2 or histidine-rich protein 3 (hrp3) deletion using two methods, multiplexed qPCR and multiplex bead-based immunoassay. When sufficient parasite material existed for a reliable deletion assessment, 12/34 (35%) had evidence of hrp2/3 deletion by qPCR (nine hrp2-/3+ and three hrp2-/3-), and 20/52 (38%) had evidence of deletion by immunoassay. Only three isolates showed evidence of hrp2 deletion by both assays. In an area of low to moderate transmission in Tanzania, false-positive mRDTs are relatively common (12% of positive tests), and false-negative mRDTs are even more common (22% of negative tests), but hrp2/3 deletion causing false-negative mRDTs remains rare (<1% of negative tests).
检测富含组氨酸蛋白2(HRP2)的疟疾快速诊断检测(mRDTs)仍是撒哈拉以南非洲地区恶性疟原虫疟疾诊断的主要手段。了解其在无症状人群监测中的检测特性很重要。我们以18S核糖体RNA实时聚合酶链反应(qPCR)作为参考检测方法,对巴加莫约农村地区学校和诊所中5岁以上无症状疟疾筛查人群的mRDT假阳性和假阴性结果发生率进行了探究。在2018年至2021年期间,对5966人进行了mRDTs、显微镜检查和qPCR检测,其中14%(832人)mRDT检测呈阳性。其中12%(98/832)的人显微镜检查和qPCR检测均为阴性,mRDT假阳性人群中儿童比例过高。在mRDT检测为阴性的人群中,22%(1136/5134)qPCR检测呈阳性,主要原因是低密度寄生虫血症(92%的人qPCR检测结果<100个寄生虫/微升)。在qPCR检测>100个寄生虫/微升的mRDT阴性样本中,我们使用多重qPCR和基于多重微珠的免疫测定两种方法寻找hrp2或富含组氨酸蛋白3(hrp3)缺失的证据。当有足够的寄生虫材料进行可靠的缺失评估时,34例中有12例(35%)通过qPCR检测有hrp2/3缺失证据(9例hrp2 - /3 +,3例hrp2 - /3 -),52例中有20例(38%)通过免疫测定有缺失证据。只有3株分离株两种检测方法均显示有hrp2缺失证据。在坦桑尼亚低至中度传播地区,mRDT假阳性相对常见(阳性检测的12%),mRDT假阴性更为常见(阴性检测的22%),但由hrp2/3缺失导致的mRDT假阴性仍然很少见(阴性检测的<1%)。