Markers of sulfadoxine–pyrimethamine resistance in Eastern Democratic Republic of Congo; implications for malaria chemoprevention
Sulfadoxine–pyrimethamine (SP) is a cornerstone of malaria chemoprophylaxis and is considered for programmes in the Democratic Republic of Congo (DRC). However, SP efficacy is threatened by drug resistance, that is conferred by mutations in the dhfr and dhps genes. The World Health Organization has specified that intermittent preventive treatment for infants (IPTi) with SP should be implemented only if the prevalence of the dhps K540E mutation is under 50%. There are limited current data on the prevalence of resistance-conferring mutations available from Eastern DRC. The current study aimed to address this knowledge gap.
Dried blood-spot samples were collected from clinically suspected malaria patients [outpatient department (OPD)] and pregnant women attending antenatal care (ANC) in four sites in North and South Kivu, DRC. Quantitative PCR (qPCR) was performed on samples from individuals with positive and with negative rapid diagnostic test (RDT) results. Dhps K450E and A581G and dhfr I164L were assessed by nested PCR followed by allele-specific primer extension and detection by multiplex bead-based assays.
Across populations, Plasmodium falciparum parasite prevalence was 47.9% (1160/2421) by RDT and 71.7 (1763/2421) by qPCR. Median parasite density measured by qPCR in RDT-negative qPCR-positive samples was very low with a median of 2.3 parasites/µL (IQR 0.5–25.2). Resistance genotyping was successfully performed in RDT-positive samples and RDT-negative/qPCR-positive samples with success rates of 86.2% (937/1086) and 55.5% (361/651), respectively. The presence of dhps K540E was high across sites (50.3–87.9%), with strong evidence for differences between sites (p < 0.001). Dhps A581G mutants were less prevalent (12.7–47.2%). The dhfr I164L mutation was found in one sample.
The prevalence of the SP resistance marker dhps K540E exceeds 50% in all four study sites in North and South Kivu, DRC. K540E mutations regularly co-occurred with mutations in dhps A581G but not with the dhfr I164L mutation. The current results do not support implementation of IPTi with SP in the study area.
KeywordsMalaria DRC Sulfadoxine–pyrimethamine (SP) Chemoprophylaxis dhps dhfr K540E A581G I164L IPTi
allele specific primer extension
dried blood spots
Democratic Republic of Congo
histidine-rich protein 2
Integrated Community Case Management
intermittent preventive therapy for infants
intermittent preventive treatment of malaria in pregnancy
malaria HRP2-test rapid diagnostic test
Médecins sans Frontières
Médecins sans Frontières–Operational Centre Amsterdam
quantitative polymerase chain reaction
seasonal malaria chemoprophylaxis
World Health Organization
Despite a decline in cases and deaths over the past 20 years, malaria forms a major health problem in Africa. In the Democratic Republic of Congo (DRC) cases of malaria are rising, and the death toll is increasing . In 2017 in DRC there was an estimated number of 25 million (15.7–36.8) cases of malaria and an estimated 46,800 (36,200–57,300) deaths. The majority of malaria cases in DRC are caused by Plasmodium falciparum, although Plasmodium ovale , Plasmodium malariae, and Plasmodium vivax are present among symptomatic cases . Médecins sans Frontières (MSF) has been working in DRC since 1991. The Operational Centre Amsterdam of MSF (MSF–OCA) has several projects in Eastern DRC, most notably in North and South Kivu. Both provinces are the scene of chronic and at times intense conflict, leading to frequent internal displacement, outbreaks of disease, sexual violence, malnutrition, and a collapse of healthcare services. MSF supports several large hospitals and health centres and has adopted a strategy of Integrated Community Case Management (ICCM). Within the ICCM programme, community members are trained to diagnose and treat malaria, diarrhoea and pneumonia in children under 5 years of age. MSF and the Ministry of Health distribute insecticide-treated bed nets in the community as well as targeted distribution to pregnant women, severe malaria patients and other specific groups. Additional interventions are implemented where supportive evidence warrants it, aiming to reduce the burden of malaria. These interventions include chemoprevention strategies that are delivered without the need for testing. Sulfadoxine–pyrimethamine (SP) is a cornerstone of malaria chemoprophylaxis across the African continent. Intermittent preventive treatment of malaria in pregnancy (IPTp) and intermittent preventive therapy for infants (IPTi) use SP alone, while seasonal malaria chemoprophylaxis (SMC) combines SP with amodiaquine. The efficacy of SP for these interventions is influenced by drug resistance levels in parasite populations  and the drug resistance levels are influenced by the use of SP in target populations [5, 6].
The genetic basis of SP resistance is well understood, and consequently molecular surveillance of resistance mutations underpins current policy on SP use in Africa. SP resistance occurs via the accumulation of mutations in the dihydrofolate reductase (dhfr) gene and in the dihydropteroate synthase (dhps) gene and these progressively reduce susceptibility to pyrimethamine and sulfadoxine, respectively. Infections harbouring triple mutant dhfr, i.e., a combination of N51I, C59R and S108N mutations, are common throughout Africa. When this triple mutation in dhfr is combined with double-mutant dhps (A437G and K540E) the risk of SP treatment failure is up to 75% [7, 8]. A ‘sextuple mutant’ genotype in which these five key mutations in dhfr and dhps gene are accompanied by dhps A581G is increasingly reported .
There are indications that the range and prevalence of the sextuple genotype is increasing . This study aimed to update molecular surveillance data from North and South Kivu with more substantial sample sizes and examine the geographic heterogeneity in prevalence of 540E and 581G in order to determine if IPTi could be a preventive strategy used in MSF mission sites within these provinces of Eastern DRC.
Study area, subjects and sample collection
From August to September 2017, samples were collected in the context of MSF projects in two provinces: North Kivu and South Kivu. Each province provided samples from two study sites. The aim was to obtain a minimum of 250 samples with confirmed P. falciparum infection per study site from either pregnant women attending ANC or individuals attending the clinic with suspected malaria.
The sample size was based on the assumption of 50% prevalence of dhps K540E and the ability to estimate this expected proportion with 5% precision for each site. The study received ethical approval from the London School of Hygiene & Tropical Medicine (#11976), the Ethics Review Board of MSF (#1708) and the Commission Institutionnelle d’Ethique of the Catholic University of Bukavu (UCB/ClE/NC/005B/2017). Informed consent was obtained from all participants or their carers prior to participation. Young adolescents received information appropriate for their age before they were asked for consent.
Study participants were passively recruited at MSF clinics from pregnant women presenting for ANC and from patients presenting with signs/symptoms of malaria (axillary temperature ≥ 37.5 °C or history of fever). Malaria HRP2-test rapid diagnostic tests (RDTs) (SD BIOLINE Malaria Ag P.f, 05FK50; Gyeonggi-do, Republic of Korea) were performed to detect presence of P. falciparum antigen. Two blood spots were collected on filter papers (Whatman® 903 Protein Saver Card; Maidstone, UK), air-dried, stored individually in zip-lock bags with desiccant at room temperature, and kept away from humidity, excessive heat and light. All dried blood spots (DBS) samples, whether RDT positive or negative, were shipped at ambient temperature to Radboud University Medical Centre, The Netherlands, for further processing.
5′ GATTCTTTTTCAGATGGAGG 3′
5′ TTCCTCATGTAATTCATCTGA 3′
5′ AACCTAAACGTGCTGTTCAA 3′
5′ AATTGTGTGATTTGTCCACAA 3′
5′ TGATGGAACAAGTCTGC 3′
5′ ACTTTGTTTATTTCCATTCA 3′
5′ TGTGCATGTTGTAAGGTTGA 3′
5′ GATACTCATTTTCATTTATTTCTGGA 3′
5′ ATTAAACAACTCTTAACTACACAAGGAAATCCACATACAATGGATA 3′
5′ CTTTCTTAATACATTACAACATACGAAATCCACATACAATGGATG 3′
5′ CATAAATCTTCTCATTCTAACAAATTGATATTGGATTAGGATTTGC 3′
5′ CAAACAAACATTCAAATATCAATCTTGATATTGGATTAGGATTTGG 3′
5′ CATAAATCTTCTCATTCTAACAAAGAAATTAAATTACTATAAATGTTTTATTA 3′
5′ CAAACAAACATTCAAATATCAATCGAAATTAAATTACTATAAATGTTTTATTT 3′
dhps K450E and A581G and dhfr I164L were assessed by nested PCR followed by allele specific primer extension (ASPE) and detection on a Luminex instrument (MAGPIX®; Luminex Corp) with xPONENT® 4.2 software. Briefly, amplified DNA was incubated with ExoSAPit for 30 min at 37 °C, followed by 15 min at 80 °C. Samples were then assembled with the ASPE master mix [250 nM each of ASPE probes and 200 µM Biotin-14-dCTP (Invitrogen, UK)] using primers from Table 1 and incubated 30 cycles (30 s 90 °C, 1 min 53.5 °C, 2 min 72 °C). Utilizing different TAGs on different ASPE primers, multiple magnetic bead sets could be hybridized to the ASPE reactions. For each reaction, 1 μL of each bead set was used. After two washes with Tm buffer (0.2 M NaCl, 0.1 M Tris, 0.08% TritonX-100, pH 8), Tm buffer + 0.1% BSA + 2.5 μg/mL Streptavidin-R-phycoerythrin (SAPE) was added to each sample. Samples were analysed at 37 °C on the Luminex analyser according to manufacturer’s instructions.
Statistical analyses were performed in STATA version 15.0 (StataCorp; College Station, TX, USA). Data were typically presented per site and separately for sample donors recruited at clinics with suspected malaria (suspected clinical cases) or pregnant women attending antenatal care (ANC participants). Age was categorized in 5 categories (< 2 years, 2–4 years, 5–9 years, 10–14 years, ≥ 15 years). Parasite density estimates were compared between RDT-positive and -negative individuals by non-parametric Wilcoxon rank-sum test; median values with 25th and 75th percentile (IQR) were presented. Parasite prevalence estimates were given for suspected clinical cases and ANC participants separately, adjusting 95% CI for the cluster-design of data collection using the survey (svy) command in STATA. Genotyping results were presented per site and separately for suspected clinical cases and ANC participants.
Characteristics of study participants
Suspected clinical malaria
Age, % (n)
< 2 years
≥ 15 years
Parasite prevalence RDT, % (n/N)
Parasite prevalence qPCR, % (n/N)
The prevalence of mutations in Dhps 540 and Dhps 581 in the different study sites
Dhps 540, % (n)
Dhps 581, % (n)
The dhfr gene was successfully amplified in 94.9% (333/351) of randomly selected samples (Baraka: n = 78; Kimbi: n = 91; Walikale: n = 96; Mweso: n = 68). Among these samples, the dhfr I164L mutation was found in only one sample (0.3%, 1/333). The sample was collected from an RDT-confirmed clinical malaria case from Walikale and was wild type for dhps K540E and A581G.
High numbers of malaria cases continue to pose an intense burden to DRC and to the individuals affected. Due to conflict and unrest in the country, there is limited current information available on parasite resistance to anti-malarial drugs. This knowledge gap hinders the informed use of anti-malarial interventions. The current study aimed to provide estimates of molecular markers conferring SP resistance in four settings in an area of chronic conflict in Eastern DRC.
Parasite prevalence among suspected malaria cases was uniformly high in the study settings. When sensitive qPCR was used to detect P. falciparum parasites, parasite prevalence was 70–80% among suspected malaria cases and 32–65% among women attending ANC visits. These findings confirm the high malaria burden in this part of DRC . The higher prevalence of parasites by qPCR compared to RDT corroborates an increasing body of literature on low-density infections that are present in all age groups and across all endemicities in Africa and elsewhere [19, 20]. Parasite densities among RDT-negative qPCR-positive individuals were very low on average, below the threshold density typically detected by microscopy or RDT . Whilst this suggests adequate performance of RDTs in the study settings in symptomatic cases, deletions in histidine-rich protein (HRP2), as described in DRC by Parr et al.  will be examined in the current dataset in future studies. It is currently unclear whether parasite densities below the threshold for detection by RDT contribute to acute clinical disease in semi-immune individuals, although low-density infections have been associated with haemolysis, inflammation, co-infection with invasive bacterial disease, cognitive impairment , and ongoing transmission of parasites to mosquitoes . At present, it may be assumed that RDT-negative individuals presenting with suspected malaria had fever due to causes other than P. falciparum infection .
A high level of the dhps K540E mutation was observed in this region and this is consistent with studies that reviewed and mapped all publicly available data on 540E in Africa [9, 25, 26]. At all sites, the prevalence of dhps K540E mutant exceeds 50%, the threshold level defined by WHO to determine whether or not to introduce IPTi . The highest prevalence of 540E was in the eastern sites (Mweso and Baraka), closest to the border with southwest Uganda and western Rwanda, a region previously identified as a hotspot with a high level of SP resistance [25, 26]. This is consistent with the east–west gradient in the spatial distribution of the dhps mutations across DRC observed by Aydemir et al.  and summarized in Fig. 1. Okell et al. showed that resistance patterns are similar for sites up to 300 km apart  and Mweso is < 300 km from resistant hotspots in southwest Uganda [29, 30].
This study is consistent with a sequential build-up of resistance markers for SP. The A581G mutation almost exclusively occurred in the presence of K540E mutations . The prevalence of I164L mutation on the dhfr gene was still very low, detected in only one of 333 samples. Future monitoring is needed to examine if the prevalence of this mutation is increasing and will have implications for SP efficacy. A relevant limitation of the current study is that samples were collected on one time-point only and solely collected at clinical facilities in suspected malaria cases and women attending ANC (routine screening of all pregnant women, including asymptomatically infected individuals). Some of the suspected malaria cases with measured fever and qPCR-or RDT-detected infections may have had fever due to causes other than malaria  and may have inappropriately received the diagnosis of clinical malaria. Whilst this misclassification is of no concern for the current objectives, estimating the prevalence of resistance markers among health facility attendees, it complicates a direct comparison of resistance in clinical versus asymptomatic infections.
The findings in this study are disappointing from a programmatic perspective. The study was initiated with the hope that IPTi could be introduced in the region to reduce morbidity and mortality. However, with resistance markers well above the threshold of 50% (for K540E) this cannot be supported. Although WHO still recommends IPTp with SP in areas with high level of resistance to SP, based on studies in Tanzania and Malawi , the current findings of high prevalence of SP resistance among the target population suggest that the efficacy of IPTp in this setting should continue to be monitored  and alternative drugs such as dihydroartemisinin–piperaquine, mefloquine or doxycycline may be worth considering [34, 35, 36].
The current findings highlight significant challenges for the use of SP for chemoprevention in this region in DRC. It is therefore of utmost importance that other interventions, including vector control and prompt access to diagnosis and treatment, are implemented to the highest attainable standards to reduce exposure and prevent severe disease.
In the study areas of intense malaria transmission in North and South Kivu, the prevalence of the SP resistance marker dhps K540E was above 50% in all study sites. K540E mutations regularly coincided with mutations in dhps A581G but not with the dhfr I164L mutation. The current results do not support implementation of IPTi. Given the high morbidity and mortality from malaria in DRC, alternative approaches are needed for prevention and early treatment of malaria.
Thanks to all laboratory technicians who collected the samples for their dedicated work: Gabriel Mulangano (Mweso), Gédéon Mulanda Monga (Kimbi), Justin Bazibuhe Bahati (Walikale), Pascal Kahindo Kabengwa (Baraka).
MvL designed and lead the work and drafted the manuscript. RvdM performed all lab analysis and drafted the manuscript. ML instructed all field lab staff and supervised collection of samples. She passed away in 2019 before submission of this manuscript. AO contributed to local design of the study, obtained ethical approval in DRC and supervised field staff in North Kivu. EB contributed to local design of the study, obtained ethical approval in DRC and supervised field staff In South Kivu. CB contributed to local design of the study, obtained ethical approval in DRC and supervised field staff in South Kivu. DC facilitated the design of the study to make it locally appropriate. LO contributed to the design of the study. EP was responsible for the field lab design of the study. LG was responsible for supervision of laboratory assays for resistance genotyping. KL was responsible for supervision of laboratory assays for DNA extraction and parasite quantification. VB Rao contributed to the design the study and wrote the study protocol. TB designed and supervised the study, the analysis and the writing of the manuscript. CR designed and supervised the study, the lab-analysis and the writing of the manuscript. All authors read and approved the final manuscript.
The funding for this study came from MSF-OCA.
Ethics approval and consent to participate
The study received ethical approval from the London School of Hygiene & Tropical Medicine (#11976), the Ethics Review Board of Médecins Sans Frontières (#1708) and the Commission Institutionnelle d’Ethique of the Catholic University of Bukavu (UCB/ClE/NC/005B/2017).
Consent for publication
The authors declare that they have no competing interests.
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