Analysis of false-negative rapid diagnostic tests for symptomatic malaria in the Democratic Republic of the Congo

• Published in: Scientific reports Vol. 11; no. 1; pp. 6495 - 12
• Main Authors: Parr, Jonathan B., Kieto, Eddy, Phanzu, Fernandine, Mansiangi, Paul, Mwandagalirwa, Kashamuka, Mvuama, Nono, Landela, Ange, Atibu, Joseph, Efundu, Solange Umesumbu, Olenga, Jean W., Thwai, Kyaw Lay, Morgan, Camille E., Denton, Madeline, Poffley, Alison, Juliano, Jonathan J., Mungala, Pomie, Likwela, Joris L., Sompwe, Eric M., Rogier, Eric, Tshefu, Antoinette K., N’Siala, Adrien, Kalonji, Albert
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 22.03.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/326/417/2550; 692/308/174; 692/699/255/1629; Antigens; Diagnostic tests; Erythrocytes; Genomes; Genotyping; Histidine; Humanities and Social Sciences; Malaria; Microscopy; multidisciplinary; Parasites; Plasmodium falciparum; Science; Science (multidisciplinary); Vector-borne diseases; Whole genome sequencing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-85913-z

The majority of Plasmodium falciparum malaria diagnoses in Africa are made using rapid diagnostic tests (RDTs) that detect histidine-rich protein 2. Increasing reports of false-negative RDT results due to parasites with deletions of the pfhrp2 and/or pfhrp3 genes ( pfhrp2/3 ) raise concern about existing malaria diagnostic strategies. We previously identified pfhrp2 -negative parasites among asymptomatic children in the Democratic Republic of the Congo (DRC), but their impact on diagnosis of symptomatic malaria is unknown. We performed a cross-sectional study of false-negative RDTs in symptomatic subjects in 2017. Parasites were characterized by microscopy; RDT; pfhrp2/3 genotyping and species-specific PCR assays; a bead-based immunoassay for Plasmodium antigens; and/or whole-genome sequencing. Among 3627 symptomatic subjects, 427 (11.8%) had RDT-/microscopy + results. Parasites from eight (0.2%) samples were initially classified as putative pfhrp2/3 deletions by PCR, but antigen testing and whole-genome sequencing confirmed the presence of intact genes. 56.8% of subjects had PCR-confirmed malaria. Non-falciparum co-infection with P. falciparum was common (13.2%). Agreement between PCR and HRP2-based RDTs was satisfactory (Cohen’s kappa = 0.66) and superior to microscopy (0.33). Symptomatic malaria due to pfhrp2/3 -deleted P. falciparum was not observed. Ongoing HRP2-based RDT use is appropriate for the detection of falciparum malaria in the DRC.