Mapping Plasmodium falciparum sequence variants associated with antimalarial drug resistance across the Democratic Republic of Congo using ‘MOSAIC’ a high throughput methodology

Geographical differences in antimalarial drug efficacy are known to exist in the Democratic Republic of Congo (DRC), and so accurate mapping of resistance is required to inform and optimise the sub-national tailoring of treatment and chemoprevention. Therapeutic efficacy studies (TES) are the gold standard for monitoring clinical and parasitological response to treatment but to perform them with adequate coverage and regularity is costly. A further limitation of efficacy studies is that resistance to one drug in a combination treatment is masked by the antiparasitic effects of its partner. Genetic surveillance for the sequence determinants of parasite resistance is therefore a useful addition to efficacy studies, enabling an affordable expansion of coverage and actionable warnings of resistance before it becomes apparent in the clinic. We used a sampling framework based upon national sentinel surveillance sites, sampling between 100–200 patients from a single clinic location in 16 of the 26 provinces in DRC. We employed a high-throughput low-cost genotyping methodology pipeline to characterize molecular determinants of resistance and generate maps of the distribution of artemisinin and partner drug resistance across the Country. There were few observations of Pfk13 validated or candidate markers of artemisinin resistance in any part of the DRC but genotype profiles for resistance to partner drugs were regionally distinct. In Eastern provinces bordering the Great Lakes Region, we found high prevalence of Pfcrt and Pfmdr1 markers linked to 4-aminoquinoline resistance; and associated with a significant risk of ASAQ treatment failure. By contrast, parasite populations in the North and South of DRC predominantly carried Pfmdr1 and Pfcrt haplotypes which are associated with risk of ALU treatment failure. We extended the coverage of national drug resistance surveillance by TES, by using supplementary sampling and then used high throughput genotyping to describe drug resistance profiles of parasites sampled in 16 of the 26 Provinces. We demonstrate the operational utility of this approach to inform subnational tailoring of malaria treatment and chemoprevention to administrative level 1.

Authors

Institutions

Publication Details

Journal
Malaria Journal
Published
2026-10-15
DOI
https://doi.org/10.1186/s12936-026-06115-4
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mapping Plasmodium falciparum sequence variants associated with antimalarial drug resistance across the Democratic Republic of Congo using ‘MOSAIC’ a high throughput methodology

Ana Chopo-Pizarro, Marius Ahm Stauning, Valerie Akoua Bedia, Andria Mousa et al.
Malaria Journal
Malaria Research and Control
article

Mapping Plasmodium falciparum sequence variants associated with antimalarial drug resistance across the Democratic Republic of Congo using ‘MOSAIC’ a high throughput methodology

Ana Chopo-Pizarro, Marius Ahm Stauning, Valerie Akoua Bedia, Andria Mousa, Emma Filtenborg Hocke, Madalena Raposo, Max Benjamin Sauerland, Corine Ngufor, Colin J. Sutherland, Georges Mvumbi Lelo, Gauthier Mesia Kahunu, Rosario Martinez-Vega, Helle Smedegaard Hansson, William Yavo, Khalid B. Beshir, Lucas Naam-Kayagre Amenga-Etego, Doudou Malekita Yobi, Cally Roper, R Matthew Chico, Michael Alifrangis, Lise Kuseke, Innocent Mbulli Ali, Roland D. Gosling, Hervé Ignace Eby Menan, Mona-Liza Ebiere Sakyi, Wilfred Fon Mbacham, Azizath Mousilliou, Sissel Manscher Iversen, Louise Wellmann, Hypolite Muhindo
article en

Abstract

Geographical differences in antimalarial drug efficacy are known to exist in the Democratic Republic of Congo (DRC), and so accurate mapping of resistance is required to inform and optimise the sub-national tailoring of treatment and chemoprevention. Therapeutic efficacy studies (TES) are the gold standard for monitoring clinical and parasitological response to treatment but to perform them with adequate coverage and regularity is costly. A further limitation of efficacy studies is that resistance to one drug in a combination treatment is masked by the antiparasitic effects of its partner. Genetic surveillance for the sequence determinants of parasite resistance is therefore a useful addition to efficacy studies, enabling an affordable expansion of coverage and actionable warnings of resistance before it becomes apparent in the clinic. We used a sampling framework based upon national sentinel surveillance sites, sampling between 100–200 patients from a single clinic location in 16 of the 26 provinces in DRC. We employed a high-throughput low-cost genotyping methodology pipeline to characterize molecular determinants of resistance and generate maps of the distribution of artemisinin and partner drug resistance across the Country. There were few observations of Pfk13 validated or candidate markers of artemisinin resistance in any part of the DRC but genotype profiles for resistance to partner drugs were regionally distinct. In Eastern provinces bordering the Great Lakes Region, we found high prevalence of Pfcrt and Pfmdr1 markers linked to 4-aminoquinoline resistance; and associated with a significant risk of ASAQ treatment failure. By contrast, parasite populations in the North and South of DRC predominantly carried Pfmdr1 and Pfcrt haplotypes which are associated with risk of ALU treatment failure. We extended the coverage of national drug resistance surveillance by TES, by using supplementary sampling and then used high throughput genotyping to describe drug resistance profiles of parasites sampled in 16 of the 26 Provinces. We demonstrate the operational utility of this approach to inform subnational tailoring of malaria treatment and chemoprevention to administrative level 1.

Malaria Journal
University of Copenhagen (DK), Université de Yaoundé I (CM), University of Ghana (GH), Université Nangui Abrogoua (CI), Université de Dschang (CM), Copenhagen University Hospital (DK), Rigshospitalet (DK), University of Kinshasa (CD), London School of Hygiene & Tropical Medicine (GB), Ministère de la Santé (TN), LEO Foundation (DK), Université Félix Houphouët-Boigny (CI)
Unitaid
Good health and well-being
Openalex Percentile: Top 11%
Malaria Research and Control
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.