Abstract
BackgroundHistidine-rich protein-2 (HRP2)-based rapid diagnostic tests (RDTs) are the only RDTs recommended for malaria diagnosis in Uganda. However, the emergence of Plasmodium falciparum histidine rich protein 2 and 3 (pfhrp2 and pfhrp3) gene deletions threatens their usefulness as malaria diagnostic and surveillance tools. The pfhrp2 and pfhrp3 gene deletions surveillance was conducted in P. falciparum parasite populations in Uganda.MethodsThree-hundred (n = 300) P. falciparum isolates collected from cross-sectional malaria surveys in symptomatic individuals in 48 districts of eastern and western Uganda were analysed for the presence of pfhrp2 and pfhrp3 genes. Presence of parasite DNA was confirmed by PCR amplification of the 18s rRNA gene, msp1 and msp2 single copy genes. Presence or absence of deletions was confirmed by amplification of exon1 and exon2 of pfhrp2 and pfhrp3 using gene specific PCR.ResultsOverall, pfhrp2 and pfhrp3 gene deletions were detected in 29/300 (9.7%, 95% CI 6.6–13.6%) parasite isolates. The pfhrp2 gene was deleted in 10/300 (3.3%, 95% CI 1.6–6.0%) isolates, pfhrp3 in 9/300 (3.0%, 95% CI 1.4–5.6%) while both pfhrp2 and pfhrp3 were deleted in 10/300 (3.3%, 95% CI 1.6–6.0%) parasite isolates. Proportion of pfhrp2/3 deletions was higher in the eastern 14.7% (95% CI 9.7–20.0%) compared to the western region 3.1% (95% CI 0.8–7.7%), p = 0.001. Geographical location was associated with gene deletions aOR 6.25 (2.02–23.55), p = 0.003.ConclusionsThis is the first large-scale survey reporting the presence of pfhrp2/3 gene deletions in P. falciparum isolates in Uganda. Roll out of RDTs for malaria diagnosis should take into consideration the existence of pfhrp2/3 gene deletions particularly in areas where they were detected. Periodic pfhrp2/3 surveys are recommended to inform future decisions for deployment of alternative RDTs.
Highlights
Histidine-rich protein-2 (HRP2)-based rapid diagnostic tests (RDTs) are the only RDTs recommended for malaria diagnosis in Uganda
The pfhrp2 and pfhrp3 genes were deleted in 9.7% (29/300) of the P. falciparum isolates
The pfhrp2 and pfhrp3 genes were present and detected in 62.0% (186/300) of the P. falciparum isolates
Summary
Histidine-rich protein-2 (HRP2)-based rapid diagnostic tests (RDTs) are the only RDTs recommended for malaria diagnosis in Uganda. The emergence of Plasmodium falciparum histidine rich protein 2 and 3 (pfhrp and pfhrp3) gene deletions threatens their usefulness as malaria diagnostic and surveillance tools. The pfhrp and pfhrp gene deletions surveillance was conducted in P. falciparum parasite populations in Uganda. In 2018, the World Health Organization (WHO) estimated there were 228 million cases and 405,000 deaths globally due to malaria. Bosco et al Malar J (2020) 19:300 continues to contribute a disproportionately high share of the global burden (93% of malaria cases and 94% of malaria deaths) in 2018 alone [1]. Most malaria cases in the region are caused by Plasmodium falciparum. Plasmodium falciparum is the most predominant parasite in Uganda, accounting for > 95% of malaria infections [3, 5]
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