Research Article

Genetic surveillance in the Greater Mekong subregion and South Asia to support malaria control and elimination

Wellcome Sanger Institute, United Kingdom
Oxford University Clinical Research Unit, Viet Nam
Lao-Oxford-Mahosot Hospital-Wellcome Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Lao People's Democratic Republic
Institute of Research and Education Development (IRED), University of Health Sciences, Ministry of Health, Lao People's Democratic Republic
Centre for Tropical Medicine and Global Health, University of Oxford, United Kingdom
Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Thailand
Harvard TH Chan School of Public Health, Harvard University, United States
Institute of Malariology, Parasitology and Entomology (IMPE-QN), Viet Nam
Centre of Malariology, Parasitology, and Entomology, Lao People's Democratic Republic
National Institute of Malariology, Parasitology and Entomology (NIMPE), Viet Nam
National Center for Parasitology, Entomology, and Malaria Control, Cambodia
National Institute of Allergy and Infectious Diseases, National Institutes of Health, United States
Shoklo Malaria Research Unit, Thailand
Chittagong Medical College Hospital, Bangladesh
World Health Organization, Switzerland
Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Thailand
Institute of Malariology, Parasitology and Entomology (IMPEHCM), Viet Nam
Vysnova Partners Inc, Viet Nam
Kinshasa School of Public Health, University of Kinshasa, Democratic Republic of the Congo
Aix-Marseille Université, INSERM, IRD, SESSTIM, Aix Marseille Institute of Public Health, ISSPAM, France
Susan and Henry Samueli College of Health Sciences, University of California, Irvine, United States
Faculty of Tropical Medicine, Mahidol University, Thailand
The Royal Society of Thailand, Thailand
Myanmar-Oxford Clinical Research Unit, Myanmar
Department of Medical Research, Myanmar
Defence Services Medical Research Centre, Myanmar
Midnapore Medical College, India
Ispat General Hospital, India
Agartala Medical College, India
National Institute of Malaria Research, Indian Council of Medical Research, India
Ramu Upazila Health Complex, Bangladesh
Malaria Research Group and Dev Care Foundation, Bangladesh
Wellcome Trust Centre for Human Genetics, University of Oxford, United Kingdom
Worldwide Antimalarial Resistance Network (WWARN), Asia Regional Centre, Thailand
MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, United Kingdom

Aug 10, 2021

Open access
Copyright information

Abstract
Introduction
Materials and methods
Results
Discussion
Data availability
References
Article and author information
Metrics

Abstract

Background:

National Malaria Control Programmes (NMCPs) currently make limited use of parasite genetic data. We have developed GenRe-Mekong, a platform for genetic surveillance of malaria in the Greater Mekong Subregion (GMS) that enables NMCPs to implement large-scale surveillance projects by integrating simple sample collection procedures in routine public health procedures.

Methods:

Samples from symptomatic patients are processed by SpotMalaria, a high-throughput system that produces a comprehensive set of genotypes comprising several drug resistance markers, species markers and a genomic barcode. GenRe-Mekong delivers Genetic Report Cards, a compendium of genotypes and phenotype predictions used to map prevalence of resistance to multiple drugs.

Results:

GenRe-Mekong has worked with NMCPs and research projects in eight countries, processing 9623 samples from clinical cases. Monitoring resistance markers has been valuable for tracking the rapid spread of parasites resistant to the dihydroartemisinin-piperaquine combination therapy. In Vietnam and Laos, GenRe-Mekong data have provided novel knowledge about the spread of these resistant strains into previously unaffected provinces, informing decision-making by NMCPs.

Conclusions:

GenRe-Mekong provides detailed knowledge about drug resistance at a local level, and facilitates data sharing at a regional level, enabling cross-border resistance monitoring and providing the public health community with valuable insights. The project provides a rich open data resource to benefit the entire malaria community.

Funding:

The GenRe-Mekong project is funded by the Bill and Melinda Gates Foundation (OPP11188166, OPP1204268). Genotyping and sequencing were funded by the Wellcome Trust (098051, 206194, 203141, 090770, 204911, 106698/B/14/Z) and Medical Research Council (G0600718). A proportion of samples were collected with the support of the UK Department for International Development (201900, M006212), and Intramural Research Program of the National Institute of Allergy and Infectious Diseases.

Introduction

In low-income countries, particularly in sub-Saharan Africa, malaria continues to be a major cause of mortality, and intense efforts are underway to eliminate Plasmodium falciparum parasites, which cause the most severe form of the disease. However, P. falciparum has shown a remarkable ability to develop resistance to antimalarials, rendering therapies ineffective and frustrating control and elimination efforts. This problem is most acutely felt in the Greater Mekong Subregion (GMS), a region that has repeatedly been the origin of drug-resistant strains (Dondorp et al., 2009; Noedl et al., 2008; Plowe, 2009; Roper et al., 2004; Mita et al., 2011) and in neighboring countries including Bangladesh and India, where resistance could be imported. The GMS is a region of relatively low endemicity, with entomological inoculation rates 2–3 orders of magnitude lower than in Africa, where the vast majority of cases occur (Chaumeau et al., 2018; Hay et al., 2000). Infections are most common amongst individuals who work in or live near forests in remote rural parts of the region (Cui et al., 2012). Since infections are infrequent, a high proportion of individuals in this region are immunologically naïve, and develop symptoms that require treatment when infected. This results in high parasite exposure to drugs, which may be a major evolutionary driving force for the emergence of genetic factors that confer resistance to frontline therapies (Escalante et al., 2009). In the past, drug resistance alleles emerged in the GMS and subsequently spread to Africa multiple times, rolling back progress against the disease at the cost of many lives (Mita et al., 2009; Trape et al., 1998). Currently, global malaria control and elimination strategies depend on the efficacy of artemisinin combination therapies (ACTs) which are the frontline therapy of choice worldwide. Hence, in view of the emergence in the GMS of parasite strains resistant to artemisinin (Dondorp et al., 2009; Ashley et al., 2014; MalariaGEN Plasmodium falciparum Community Project, 2016) and its ACT partner drug piperaquine, (Amaratunga et al., 2016; van der Pluijm et al., 2019; Leang et al., 2015; Spring et al., 2015) the elimination of P. falciparum from this region has become a global health priority.

Elimination from the GMS presents significant challenges and, to ensure the most effective outcomes, NCMPs have to evaluate multiple changing factors: efficacy of frontline treatments, available alternatives, routes of spread, location of transmission hubs, importation of cases, and so on. In these assessments, NMCPs make extensive use of clinical and epidemiological data, such as those from routine clinical reporting and therapy efficacy studies. Parasite genetic data is less frequently available, and typically restricted to single genetic variants (Ménard et al., 2016), or small numbers of sites where quality sample collection protocols could be executed (Lim et al., 2013). However, routine mapping of a broad set resistance markers can keep NMCPs abreast of the spread of resistance strains, and help them predict changes in drug efficacy and assess alternative therapies, especially if dense geographical coverage allows mapping of resistance at province or district level. The increased affordability of high-throughput sequencing technologies now offers new opportunities for delivering such knowledge to public health, supporting the optimization of interventions where resources are limited (Nagar et al., 2019). Cost-effective implementation of genomic technologies, aimed at supporting public health decision-making, can make important contributions to malaria elimination (Desmond-Hellmann, 2016).

Here, we describe GenRe-Mekong, a genetic surveillance project conceived to provide public health experts in the GMS with timely and actionable knowledge, to support their decision-making in malaria elimination efforts. GenRe-Mekong analyzes small dried blood spots samples, which are easy to collect at public health facilities from patients with symptomatic malaria, and uses high-throughput technologies to extract large amounts of parasite genetic information from each sample. The results are captured in Genetic Report Cards (GRCs), datasets regularly delivered to NMCPs to keep them abreast of rapid epidemiological changes in the parasite population. The underlying technological platform is designed for low sample processing costs, promoting large-scale genetic epidemiology surveys with dense geographical coverage and large sample sizes.

To date, GenRe-Mekong has worked with NMCPs in Cambodia, Vietnam, Lao PDR (Laos), Thailand, and Bangladesh and has supported large-scale multisite research and elimination projects across the region (van der Pluijm et al., 2019; von Seidlein et al., 2019; Chang et al., 2019; Landier et al., 2018). The project has processed 9623 samples from eight countries, delivering data to the 12 studies that submitted samples. In its initial phase, GenRe-Mekong has focused on applications relevant to the urgent problem of drug resistance. To facilitate integration into NMCP decision-making workflows, our analysis pipelines translate genotypes into predictions of drug resistance phenotypes, and present these as maps which are easily interpreted by public health officials with no prior training in genetics. In Laos and Vietnam, where GenRe-Mekong is implemented in dozens of public health facilities in endemic provinces, results from GenRe-Mekong have been used by NMCPs in assessments of frontline therapy options and resource allocation to combat drug resistance.

GenRe-Mekong protects individual patient privacy, while encouraging aggregation and sharing of standardized data across national borders to answer regional questions about epidemiology, gene flow, and parasite evolution (Hamilton et al., 2019). Aggregated data from multiple studies within GenRe-Mekong have powered large-scale genetic and clinical studies of resistance to dihydroartemisinin-piperaquine (DHA-PPQ), revealing a regional cross-border spread of specific strains (van der Pluijm et al., 2019; Hamilton et al., 2019). To power such high-resolution genetic epidemiology analyses of population structure and gene flow, GenRe-Mekong conducts whole-genome sequencing of selected high-quality samples, contributing to the open-access MalariaGEN Parasite Observatory (http://www.malariagen.net/resource/26) (Pearson et al., 2019). In this article, we summarize some key results from GenRe-Mekong, highlighting how they are used by public health officers to improve interventions. The data used in this paper are openly available, together with detailed methods documentation and details of partner studies, at http://www.malariagen.net/resource/29.

Materials and methods

Additional detailed documentation on the methods used in this study is available from the article’s Resource Page, at https://www.malariagen.net/resource/29.

Sample collection

Request a detailed protocol

GenRe-Mekong samples were collected and contributed by independent studies with different goals, geographical coverage, and sampling strategies. Studies were managed by a local partner, such as a NMCP or a research organization, and often supported by a local technical partner. Most sampling sites were district or subdistrict health centres or provincial hospitals, selected by the local partner according to their public health or research needs. Each site was assigned a code, and its geographical coordinates recorded to support result mapping. GenRe-Mekong uses a common genetic surveillance study protocol covering the entire GMS, which can be locally adapted; this protocol was used for NMCP surveillance projects, after obtaining approval by a relevant local ethics review board and by the Oxford University Tropical Research Ethics Committee (OxTREC). Research studies included in their own protocol provisions for sample collection procedures, informed consent, patient privacy protection, and data sharing compatible with those in the GenRe-Mekong protocol, and obtained ethical approval from both a relevant local ethics review board, and their relevant institutional research ethics committee.

Samples were collected from patients of all ages diagnosed with P. falciparum malaria (including patients co-infected by other Plasmodium species) confirmed by positive rapid diagnostic test or blood smear microscopy. Participation in the study required written informed consent by patient, parent/guardian, or legally authorised representative (plus patient assent wherever required by national regulations), with the exception of Laos, where the Ministry of Health classified GenRe-Mekong as a surveillance activity for national benefit, requiring no additional informed consent. After obtaining consent, and before administering treatment, three 20 μL dried blood spots (DBS) on filter paper were obtained from each patient through finger-prick. GenRe-Mekong supplied study sites with kits containing all necessary materials, including strips of Whatman 31ET CHR filter paper, disposable lancet, 20 μl micropipette, cotton swab, alcohol pad, and plastic bag with silica gel for DBS storage. Scannable barcode stickers with unique identifiers were applied on the filter paper, the sample manifest where the collection date was recorded, and the site records. Samples were identified by means of these anonymous barcodes, and no patient-identifying information or clinical data were collected by GenRe-Mekong.

A number of participating studies also collected an optional anonymous questionnaire, to capture location of abode and work, occupation and travel history of the previous 2 months. These data are intended for in-depth epidemiological studies, such as analyses of the contribution of travel to gene flow (Chang et al., 2019). Data from these questionnaires were stored in a separate system, and linked to genetic data by means of the tracking barcodes. They were not used in the present work.

Sample preparation and genotyping

Request a detailed protocol

DBS samples were received and stored either at the Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam, or at the MORU/WWARN molecular laboratory, Bangkok, Thailand. Samples were registered and tracked in a secure bespoke online database, where location and date of collection were recorded. DNA was extracted from samples using high-throughput robotic equipment (Qiagen QIAsymphony) according to manufacturer’s instructions. Extracted DNA was plated and shipped to the MalariaGEN Laboratory at the Wellcome Sanger Institute (WSI), Hinxton, UK, for genotyping and whole genome sequencing. Parasite DNA was amplified by applying selective whole genome amplification (sWGA) as previously described (Oyola et al., 2016).

Genotyping was performed by the SpotMalaria platform, described in the separate document ‘SpotMalaria platform - Technical Notes and Methods’ available from the Resource Page, which includes the complete list of genotyped variants and the details of the genotyping procedures for these variants. Briefly, the first version of SpotMalaria used multiplexed mass spectrometry arrays on the Agena MassArray system for typing most SNPs, and capillary sequencing for the artemisinin resistance domains of the kelch13 gene. This was eventually replaced by an amplicon sequencing method, using Illumina sequencing of specific genome segments amplified by PCR reaction. The two implementations genotype a common set of variants, each iteration extending or improving on previous versions. Amplicon sequencing also offers greater portability, since it can be deployed on smaller sequencers in country-based laboratories.

Genetic Report Cards generation

Request a detailed protocol

For each sample, genotypes were called for each variant analysed by SpotMalaria, and further processed to determine commonly recognized haplotypes associated with drug resistance (e.g. in genes crt, dhfr, dhps). Genetic barcodes were constructed by concatenating 101 SNP alleles. The generated genotypes, combined with sample metadata, were returned in tabular form to those partners who had submitted the samples along with explanatory documentation for the interpretation of the reports.

The genotypes generated were used to classify samples by their predicted resistance to different drugs. The prediction rules were based on the available data and current knowledge of resistance markers and are detailed in the separate document ‘Mapping genetic markers to resistance status classification’ available from the Resource Page. For each drug, samples were classified as ‘sensitive’, ‘resistant’, ‘undetermined’, or ‘missing’– the latter identifying samples that failed to produce a valid genotype for the classification. Heterozygous samples, that is those containing genomes carrying both sensitive and resistant alleles, were classified as undetermined, due to lack of evidence for the drug resistance phenotype of such mixed infections.

In order to minimize the impact of call missingness, we also applied a set of imputation rules that predict missing alleles in the crt, dhfr, and dhps genes, based on statistically significant association with alleles at other positions. Associations were tested (using the threshold p < 0.05 by Fisher's exact test) using over 7000 samples in the MalariaGEN Pf Community Project Version 6 (Pearson et al., 2019). The rules for imputations were applied before phenotype prediction rules. They are detailed in the separate document ‘Imputation of genotypes for markers of drug resistance’ available from the Resource Page.

Data aggregation and mapping of drug resistance

Request a detailed protocol

To estimate the frequency of resistant parasites for a given drug, we selected samples at the desired level of geographical aggregation (e.g. province/state or district), based on sampling location. After removing samples with missing and undetermined phenotype predictions for the desired drug, we counted the individuals predicted to be resistant (n_r) and sensitive (n_s), giving a total aggregation sample size N=n_r+n_s. Resistant parasite frequency was then computed as f_r=n_r/N. Maps of resistance frequency were produced using Tableau Desktop 2020.1.8 (RRID:SCR_013994, http://www.tableau.com/). To indicate levels of resistance, markers were colored with a custom green-orange-red palette. Pie chart markers, used to represent allele proportions, were also derived from the same set of N aggregated samples.

Population structure analysis

Request a detailed protocol

Pairwise genetic distances between parasites were estimated by comparing genetic barcodes. To reduce error due to missingness, we first eliminated samples with more than 50% missing barcode genotypes; then we removed SNPs with missing calls in >20% of the remaining samples; and finally discarded samples with >25% missingness in the remaining SNPs. This produced a dataset of 87-SNP barcodes for 7490 samples from which genetic distances were estimated. For each sample s, we assigned a within-sample non-reference frequency g_s at each position carrying a valid genotype, as follows: g_s=0 if the sample carried the reference allele, g_s=one if it carried the alternative allele, g_s=0.5 if both alleles were present. The distance between two samples at that position was then estimated by: d = g₁(1 g2) + g₂(1 g1) where g₁ and g₂ are the g_s values for the two samples. The pairwise distance was estimated as the mean of d across all positions where d could be computed (i.e. where neither of the two samples had a missing call). Neighbour-joining trees (NJTs) were then produced using the nj implementation in the R package ape (RRID:SCR_017343) on R v4.0.2 (RRID:SCR_001905, http://www.r-project.org/) from square distance matrices.

Results

Collaborations, site selection, and sample collections

As of August 2019, GenRe-Mekong has partnered with NMCPs in five countries to conduct large-scale genetic surveillance (Vietnam, Laos), smaller-scale pilot projects (Cambodia, Thailand), and epidemiological surveys (Bangladesh). GenRe-Mekong also worked with large-scale research projects investigating drug efficacy and malaria risk, or piloting elimination interventions. A total of 9623 samples from eight countries have been processed in this period (Figure 1—figure supplement 1). The majority of samples (n=6905, 72%) were collected in GMS countries (Vietnam, Laos, Cambodia, Thailand, Myanmar), but GenRe-Mekong also supported projects submitting samples from Bangladesh, India, and DR Congo (Supplementary file 2). The vast majority of processed samples were collected prospectively, under partnership agreements with GenRe-Mekong (n=9002, 93.5%); two research projects submitted retrospective samples collected in the period 2012–2015 (n=621, 6.5%, Figure 1—figure supplement 1). Approximately 59% of samples (n=5716) were submitted by NMCP partnerships, whose contribution increased over time as surveillance projects ramped up (43.4% in 2016, vs. 94.6% in 2018, Figure 1—figure supplement 2). Details of the partnerships, the nature of the studies conducted and the number of processed samples are given in Table 1.

Table 1

Participating studies in GenRe-Mekong.

For each study, we list the NMCP and Research partners involved, the type of study, the geographical region covered and the number of collection sites. In the last two columns, we show the total number of samples submitted, and the number included in the final set of quality-filtered samples used in epidemiology analyses.

NMCP partner	Research / technical partner	Study type	Regions surveyed	Sites	Submitted samples	Filtered samples
Center for Malaria Parasitology and Entomology of Lao PDR (CMPE)	Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Vientiane	Genetic Surveillance	South Laos (five provinces)	51	1555	1387
Institute of Malariology, Parasitology, and Entomology Quy Nhon (IMPE-QN), Vietnam	Oxford University Clinical Research Unit (OUCRU), Ho Chi Minh City	Genetic Surveillance	Central Vietnam (seven provinces)	51	1632	1492
National Institute of Malariology, Parasitology, and Entomology (NIMPE), Vietnam	Vysnova Partners, Mahidol-Oxford Research Unit (MORU)	Epidemiological Study	South Vietnam (three provinces)	19	292	265
National Center for Parasitology, Entomology, and Malaria Control (CNM), Cambodia		Genetic Surveillance	Northeast Cambodia (two provinces)	19	182	174
Bangladesh National Malaria Control Programme	Mahidol-Oxford Research Unit (MORU)	Epidemiological Study	Bangladesh (Chittagong Division)	55	2055	1575
-	Mahidol-Oxford Research Unit (MORU)	Clinical Efficacy Study	Cambodia, Vietnam, Thailand, Lao PDR, Myanmar, Bangladesh, India, DR Congo	17	1875	1123
-	National Institutes of Health (NIH)	Clinical Efficacy Study	Cambodia	3	592	502
-	Oxford University Clinical Research Unit (OUCRU)	Epidemiological Study	South Vietnam	4	184	175
-	Mahidol-Oxford Research Unit (MORU)	Elimination Study	West Cambodia	1	69	32
-	Mahidol-Oxford Research Unit (MORU)	Epidemiological Study	Northeast Thailand	7	87	60
-	Shoklo Malaria Research Unit (SMRU)	Clinical Efficacy Study	Thailand (Tak province)	4	29	28
-	Shoklo Malaria Research Unit (SMRU)	Elimination Study	Myanmar (Kayin State)	51	1071	813
Total					9623	7626

Partnerships with NMCPs are often supported through collaborations with local malaria research groups, which provide support in implementing sample collections, and assist in the interpretation of results. To facilitate implementation in public health infrastructures, GenRe-Mekong provides template study protocols and associated documents; standardized kits of collection materials and documentation; and training for field and health centre staff. Study protocols are adapted to harmonize with local practices, and then approved by both a local ethical review board and the Oxford Tropical Research Ethics Committee (OxTREC). Informed consent forms and participant information sheets are translated to the local language(s), and public health facility staff are trained to execute sample collection procedures. Collection sites are mostly district-level or subdistrict-level health facilities, selected by NMCPs to cover the most informative endemic areas, often based on reported prevalence (Figure 1). Research studies and elimination projects included in their study protocol a sample collection procedure compatible with the standard GenRe-Mekong procedure, and sites were selected based on the study’s requirements.

Figure 1 with 2 supplements see all

Download asset Open asset

Map of GenRe-Mekong sample collection sites in Asia.

Sites markers are colored by country. One site in Kinshasa (DR Congo) not shown.

Sample processing and genotyping

GenRe-Mekong samples consist of dried blood spots (DBSs) on filter paper. DNA extracted from the samples was selectively amplified (Oyola et al., 2016) to increase the proportion of parasite DNA and reduce human DNA contamination before genotyping (see Materials and methods). The production of genetic report cards involves genotyping different types of variants: single nucleotide polymorphisms (SNPs), copy number variations and sequences of gene domains. These operations were performed by SpotMalaria, the genotyping platform underpinning GenRe-Mekong, whose implementation evolved during the course of the project; details of the methods used in different versions are provided in the Supplementary Materials. In the initial phase, SpotMalaria used a mixture of technologies: capillary sequencing of the kelch13 gene to detect SNPs associated with artemisinin resistance (Ashley et al., 2014; Ariey et al., 2014); and high-throughput mass spectrometry to genotype SNP variants. This was later replaced with an amplicon sequencing process, based on short-read deep sequencing of specific portions of the parasite genome, supporting a high degree of multiplexing (see Materials and methods). A total of 3473 samples (36%) were processed by the amplicon sequencing platform, which delivered a higher genotyping success rate than the earlier process (94% vs 82% mean success rate for genetic barcode positions).

The vast majority of samples were taken from malaria patients upon admission (92%, n=8866). The remainder were from recurrent clinical episodes, or collected as part of post-admission time series to study infection dynamics (n=757, 7.9%), and were excluded from epidemiological analyses in order to minimize biases and avoid duplicates. Genotypes at mitochondrial positions provided confirmation of the infecting parasite species: P. falciparum (Pf), P. vivax (Pv), P. knowlesi (Pk), P. malariae (Pm), and P. ovale (Po). All five species were detected in our dataset: non-Pf parasites were found in 8.8% of samples (n=745 out of 8486 samples for which species could be determined). A proportion of samples (n=414, 4.9%) only tested positive for non-Pf species, possibly due to misdiagnosis or extremely low Pf parasitaemia, and were excluded from epidemiological analyses. Pv was the most commonly detected non-Pf species (317 Pf/Pv mixed infections, and 405 Pv-only infections), followed by Pk (11 Pf/Pk and 6 Pk-only infections), while Pm and Po were detected in three and two samples, respectively.

Genetic barcodes

GenRe-Mekong produces a genetic barcode for each sample to enable analyses of relatedness, diversity, multiplicity of infection and population structure. Genetic barcodes are constructed by concatenating the alleles at 101 SNPs distributed across all nuclear chromosomes (see Materials and methods), chosen on the basis of their geographically widespread variability and their power to recapitulate genetic distance. Genetic barcodes can be used to detect loss of diversity due to demographic effects, (Daniels et al., 2015) or to compare parasites from the same patient to distinguish recrudescences from reinfections (Felger et al., 2020). They can also produce estimates of genetic distance, which may not be sufficiently accurate for detailed inferences, but are useful for visualizing macroscopic population-level features. For example, a neighbor-joining tree derived from these genetic distance estimates (Figure 2) clearly separates parasites from the Thai-Myanmar border region from those circulating along the Thai-Cambodian border, consistent with findings from WGS analyses (Miotto et al., 2015). Hence, while genetic barcodes produce lower resolution results than WGS data, they could be used for rapid low-cost detection of candidate imported parasites, to be further analysed using higher-definition approaches. We used genetic barcode results to discard 827 samples that failed to produce barcodes due to low Pf DNA content. This yielded a final set of 7626 Pf samples, corresponding to 90.2% of all Pf-containing samples taken upon admission, which provided the data used for epidemiological analyses.

Figure 2

Download asset Open asset

Neighbor-joining tree using barcode data to show genetic differentiation between parasites in the Thai-Myanmar and Thai-Cambodian border regions.

The tree was derived from a matrix distance matrix, computed by comparing the genetic barcodes of samples. The branch length separating each pair of parasites represents the amount of genetic differentiation between them: individuals separated by shorter branches are more similar to each other. Samples from provinces/states of Myanmar, Thailand, and Cambodia near to the borders were included. Each circular marker represents a sample, colored by the province/state of origin.

Survey of drug resistance mutations

GenRe-Mekong produces genotypes covering a broad range of known variants associated to drug resistance (Table 2) to support assessment of the spread and risk of drug resistance. The interpretation of these genetic markers in phenotypic terms requires extensive knowledge of relevant literature, which is often outside the domain of expertise of public health officers. To bridge this gap, we use genotypes to derive predicted phenotypes based on a set of rules derived from peer-reviewed publications (see Materials and methods and formal rules definitions available from the article’s Resource Page). These rules predict samples as resistant or sensitive to a particular drug or treatment, or undetermined. Since our procedures do not include the measurement of clinical or in vitro phenotypes, we are only able to predict a drug resistant phenotype based on known associations of certain markers with resistance to certain drugs. Although we report a large catalogue of variations which have been associated with resistance, we do not use all variations to predict resistance. Rather, our predictive rules are conservative and only use markers that have been strongly characterized and validated in published literature and shown to play a crucial role in clinical or in vitro resistance. These critical variants include single nucleotide polymorphisms (SNPs) in genes kelch13 (resistance to artemisinin), (Ariey et al., 2014) crt (chloroquine), dhfr (pyrimethamine), dhps (sulfadoxine), as well as an amplification breakpoint sequence in plasmepsin2/3 (marker of resistance to piperaquine) (Amato et al., 2017). In addition, we report several additional variants found in drug resistance backgrounds but not used to predict resistance, such as mutations in mdr1 (linked to resistance to multiple drugs), components of the predisposing ART-R background arps10, ferredoxin, mdr2 (Miotto et al., 2015), and the exo marker associated with resistance to piperaquine (Amato et al., 2017). Several samples had missing genotype calls which were required for phenotype prediction; therefore, we also devised a number of rules for imputation of missing genotypes based on information from linked alleles. These imputation rules (see Materials and methods) are based on an analysis of allele associations using data from over 7000 samples in the MalariaGEN Pf Community Project (Pearson et al., 2019) and are applied prior to phenotype prediction rules. Phenotypic predictions allow simple estimations of the proportions of resistant parasites at the population level, which can be readily tabulated and mapped for use in public health decision-making. By aggregating sample data at various geographic levels (site, district, province, region, country), GenRe-Mekong delivers to NMCPs maps that capture the current drug resistance landscape, and can be compared to detect changes over time. Most GenRe-Mekong maps use intuitive ‘traffic light’ color schemes, in which red signifies presence of resistance, and green its absence. Below, we illustrate some results at regional level for the GMS and nearby countries, which are also summarized in Table 3.

Table 2

Drug resistance-related SNPs genotyped by GenRe-Mekong (excludes kelch13).

Chromosome	Position	Gene Id	Gene Description	Mutation	Reference	Alternate
Pf3D7_04_v3	748239	PF3D7_0417200	dhfr (bifunctional dihydrofolate reductase-thymidylate synthase)	N51I	A	T
Pf3D7_04_v3	748262			C59R/Y	T	C
Pf3D7_04_v3	748263			C59R/Y	G	A
Pf3D7_04_v3	748410			S108N/T	G	AC
Pf3D7_04_v3	748577			I164L	A	T
Pf3D7_05_v3	958145	PF3D7_052300	mdr1 (multidrug resistance protein 1)	N86Y	A	T
Pf3D7_05_v3	958440			Y184F	A	T
Pf3D7_05_v3	961625			D1246Y	G	T
Pf3D7_07_v3	403623	PF3D7_0709000	crt (chloroquine resistance transporter)	N75D/E	T	A
Pf3D7_07_v3	403625			K76T	A	C
Pf3D7_07_v3	405362			N326S	A	G
Pf3D7_07_v3	405600			I356T	T	C
Pf3D7_08_v3	549681	PF3D7_0810800	dhps (dihydropteroate synthetase)	S436A/Y/F/G	T	GC
Pf3D7_08_v3	549682			S436A/Y/F/G	C	TAG
Pf3D7_08_v3	549685			A437G	G	C
Pf3D7_08_v3	549993			K540E/N	A	GT
Pf3D7_08_v3	549995			K540E/N	A	TG
Pf3D7_08_v3	550117			A581G	C	G
Pf3D7_08_v3	550212			A613S/T	G	TA
Pf3D7_13_v3	748395	PF3D7_1318100	fd (ferredoxin)	D193Y	C	A
Pf3D7_13_v3	2504560	PF3D7_1362500	exo (exonuclease)	E415G	A	G
Pf3D7_14_v3	-	PF3D7_1408000 and PF3D7_1408100	pm23 (plasmepsin 2 and plasmepsin 3)	Breakpoint	-	-
Pf3D7_14_v3	1956225	PF3D7_1447900	mdr2 (multidrug resistance protein 2)	T484I	G	A
Pf3D7_14_v3	2481070	PF3D7_1460900	arps10 (apicoplast ribosomal protein S10)	V127M	G	A
Pf3D7_14_v3	2481073	PF3D7_1460900	arps10 (apicoplast ribosomal protein S10)	D128Y/H	G	TC

Table 3

Frequencies of resistant parasites in provinces/states/divisions surveyed, for different antimalarials.

Country	Province, State, or Division	ART-R	PPQ-R	DHA-PPQ-R	CQ-R	PYR-R	SD-R	SP-R	SP-R (IPTp)
India	Odisha	0%	0%	0%	18%	57%	6%	1%	0%
	West Bengal	0%	0%	0%	47%	71%	14%	5%	0%
	Tripura	0%	0%	0%	85%	100%	99%	55%	0%
Bangladesh	Chittagong	0%	0%	0%	97%	100%	87%	46%	16%
Myanmar	Rakhine	0%	0%	0%	71%	100%	100%	51%	26%
	Bago	1%	0%	0%	88%	100%	100%	91%	74%
	Mandalay	29%	0%	0%	96%	98%	98%	29%	24%
	Kayin	54%	2%	0%	100%	100%	56%	73%	27%
Thailand	Tak	61%	-	0%	100%	100%	96%	100%	88%
	Sisakhet	100%	90%	90%	100%	100%	100%	100%	100%
	Ubon Ratchathani	80%	75%	56%	100%	100%	85%	100%	17%
Cambodia	Pailin	93%	97%	90%	100%	100%	100%	100%	56%
	Battambang	100%	100%	100%	100%	100%	88%	100%	29%
	Pursat	88%	98%	67%	100%	100%	92%	98%	44%
	Preah Vihear	61%	100%	11%	100%	100%	94%	98%	21%
	Steung Treng	93%	75%	70%	100%	100%	97%	100%	0%
	Ratanakiri	49%	79%	42%	99%	100%	76%	90%	5%
Laos	Champasak	66%	75%	56%	100%	100%	88%	94%	12%
	Attapeu	46%	43%	31%	100%	100%	82%	100%	18%
	Sekong	26%	6%	0%	100%	100%	91%	74%	5%
	Salavan	17%	2%	1%	89%	97%	28%	38%	1%
	Savannakhet	10%	1%	0%	87%	96%	21%	41%	2%
Vietnam	Binh Phuoc	92%	93%	83%	100%	100%	100%	100%	14%
	Dak Nong	94%	92%	88%	100%	100%	97%	96%	22%
	Dak Lak	96%	90%	86%	100%	100%	100%	99%	15%
	Gia Lai	84%	83%	76%	99%	100%	98%	95%	4%
	Khanh Hoa	22%	5%	2%	95%	100%	97%	74%	2%
	Ninh Thuan	13%	18%	0%	28%	100%	98%	75%	0%
	Quang Tri	16%	9%	0%	75%	76%	59%	26%	5%
Congo PDR	Kinshasa	0%	0%	0%	58%	98%	72%	88%	0%

The spread of artemisinin resistance (ART-R) is an urgent concern in the GMS. We estimated frequencies of predicted ART-R parasites based on the presence of nonsynonymous mutations in the kelch13 gene, as listed by the World Health Organization, 2018. The resulting map indicates that ART-R has reached very high levels in the lower Mekong region (Cambodia, northeastern Thailand, southern Laos, and Vietnam), nearing fixation in Cambodia and around its borders, with the exception of very few provinces of Laos and the Vietnam coast (Figure 3A). Predicted ART-R frequencies decline to the west of this region: no samples in this study were predicted to be ART-R in India and Bangladesh, thus showing no evidence of spread beyond the GMS, or of local emergence of resistant parasite populations. An analysis of the distribution of kelch13 ART-R alleles (Figure 3—figure supplement 1, Supplementary file 3) reveals a marked difference between the lower Mekong region, where the kelch13 C580Y mutation is the dominant allele, and the region comprising Myanmar and western Thailand, where a wide variety of non-synonymous kelch13 variants are found, and C580Y is not dominant. This reflects a recent increase of C580Y mutant prevalence in Cambodia and neighboring regions, resulting from the rapid spread of the KEL1/PLA1 strain of multidrug-resistant parasites (Hamilton et al., 2019; Amato et al., 2018). This hard selection sweep has replaced a variety of ART-R alleles previously present in that region, resulting from multiple soft sweeps (Miotto et al., 2015; Miotto et al., 2013); this process has not occurred along the Thai-Myanmar border, where allele diversity is still very pronounced. The spread of DHA-PPQ resistant (DHA-PPQ-R) strains in the lower Mekong region is confirmed when we map the frequency of plasmepsin2/3 amplifications conferring piperaquine resistance (PPQ-R, Figure 3—figure supplement 2), which occur where C580Y is most prevalent. Mapping the combined presence of C580Y and plasmepsin2/3 amplification shows that parasites carrying both markers are confined to a well-defined area of the lower Mekong region, and these resistant strains have not made their way into provinces of Laos and Vietnam where ART-R and PPQ-R alleles circulate separately (Figure 3B). Over time, GenRe-Mekong will continue to track across the region the spread of strains carrying drug resistance mutations.

Figure 3 with 5 supplements see all

Download asset Open asset

Map of the spread of (A) artemisinin resistance (ART-R) and (B) dihydroartemisinin-piperaquine resistance (DHA-PPQ-R) in Asian countries.

Marker text and color indicate the proportion of sample classified as resistant in each province/state/division surveyed. A total of 6762 samples were included in (A) and 3395 samples in (B), after excluding samples with undetermined phenotype prediction. The results are summarized in Table 3.

Figure 3—source data 1 Proportions of parasites predicted to be resistant to artemisinin and to the DHA-PPQ combination therapy in each province/state/division.: https://cdn.elifesciences.org/articles/62997/elife-62997-fig3-data1-v1.xlsx
Download elife-62997-fig3-data1-v1.xlsx

Resistant populations can revert to sensitive haplotypes after drugs are discontinued, as was the case for chloroquine-resistant parasites in East Africa (Laufer et al., 2006; Frosch et al., 2014). To help detect similar trends in the GMS, GenRe-Mekong reports on markers of resistance to previous frontline antimalarials that have been discontinued because of reduced efficacy. The resulting data show that, decades after the replacement of chloroquine as frontline therapy, the frequency of parasites predicted to be resistant (CQ-R) remains exceptionally high across the GMS (Figure 3—figure supplement 3). The reasons for such sustained levels of resistance are unclear; the continued use of chloroquine as frontline treatment for P. vivax malaria, and the low diversity associated with the extremely high prevalence of resistant haplotypes could be major contributing factors. Similarly, we found high levels of the dhfr and dhps markers associated with resistance to sulfadoxine-pyrimethamine (SP, Figure 3—figure supplements 4 and 5). It is unclear why resistance to SP is so widespread, several years after discontinuing this therapy in the GMS, although similar results have been seen in Malawi (Artimovich et al., 2015). Again, very low haplotype diversity may be an obstacle to reversion, and it is also possible that compensatory changes have minimized the fitness impact of resistant mutations over time, diminishing the pressure to revert. It is interesting that predicted resistance is lowest in India, where SP is still used with artesunate as the frontline ACT (Directorate of National Vector Borne Disease Control Programme DGoHS and Government of India, 2013).

Case study: Vietnam

In Vietnam, sample collections were carried out by two NMCP institutes (IMPE-QN and NIMPE), covering approximately 70 sites in seven provinces. Genetic report cards were delivered to public health officials over two malaria seasons (Figure 4), communicating new findings for malaria control. Prior to this surveillance activity, evidence of artemisinin resistance had been found in the provinces of Binh Phuoc, Gia Lai, Dak Nong, Khanh Hoa, and Ninh Thuan province (World Health Organization, 2017). GenRe-Mekong data confirmed the presence of parasites carrying ART-R markers in these provinces, and showed that the province of Dak Lak also has extremely high levels of predicted ART-R (Figure 4—figure supplement 1). Furthermore, our data showed that nearly all ART-R parasites collected near the border with were also predicted to be PPQ-R, in that they carried both the kelch13 C580Y mutation (Figure 4—figure supplement 2) and plasmepsin2/3 amplification (Hamilton et al., 2019; Amato et al., 2018). C580Y parasites were also found in the coastal provinces of Ninh Thuan, Khanh Hoa and Quang Tri, but they did not carry the PPQ-R marker; it is therefore likely the kelch13 mutations were introduced by an earlier sweep of ART-R parasites. Several parasites in Khang Hoa carried the kelch13 P553L mutation, previously associated with an ART-R founder population in Binh Phuoc province (Miotto et al., 2015; Takala-Harrison et al., 2015), supporting the hypothesis they belong to an earlier sweep (Figure 4—figure supplement 2).

Data from consecutive seasons offers a view of the dynamics of drug resistance spread. In the 2018/2019 season, there was a marked increase in the number of cases in the Krong Pa district of Gia Lai province (Figure 4). In 2017/2018, this district accounted for 15% of cases in the three central provinces that border with Cambodia (n=96 of 656); the following season, this increased to 64% (n=341 of 529, p<10⁻¹⁵). In the same timeframe, predicted DHA-PPQ-R parasites in Krong Pa rose from 65% (n=40 of 62) to 98% (n=298 of 305, p<10⁻¹⁴). These results suggest that an outbreak occurred in this district in 2018/2019, underpinned by strong selection of a genetic background able to survive the frontline ACT DHA-PPQ.

Figure 4 with 2 supplements see all

Download asset Open asset

Longitudinal sample counts and proportions of DHA-PPQ-R parasites in three provinces of Central Vietnam.

The same geographical area (Gia Lai, Dak Lak, and Dak Nong provinces) is shown for two malaria seasons: 2017/18 (12 months from May 2017, n=523) and 2018/2019 (the following 12 months, n=455). Districts are represented by markers whose size is proportional to the number of samples, and whose color indicates the frequency of samples carrying both the *kelch13* C580Y mutation and the *plasmepsin2/3* amplification, and thus predicted to be DHA-PPQ-R. Marker labels show district name, resistant parasite frequency, and sample count.

Figure 4—source data 1 Proportions of samples predicted to be resistant to DHA-PPQ in districts of Vietnam, in the seasones 2017/18 and 2018/19.: https://cdn.elifesciences.org/articles/62997/elife-62997-fig4-data1-v1.xlsx
Download elife-62997-fig4-data1-v1.xlsx

Case study: Laos

The Lao NMCP implemented genetic surveillance in five provinces of southern Laos, at over 50 public health facilities. Artemisinin-resistant parasites were found in all five provinces, at frequencies higher in districts bordering Thailand and Cambodia (Figure 5A). The kelch13 C580Y mutation was found in four of the five provinces, and was the most common ART-R allele (Figure 5—figure supplement 1). However, parasites carrying both C580Y and the plasmepsin2–3 amplification were restricted to the two southernmost provinces (Champasak and Attapeu, referred to as ‘Lower Zone’, Figure 5B), and completely absent from Savannakhet and Salavan provinces (‘Upper Zone’) where C580Y parasites lack the PPQ-R amplification. In other words, it appears that DHA-PPQ-R parasites, possibly imported from Cambodia or Thailand, have migrated into the Lower Zone but not the Upper Zone, where a different population of ART-R parasites circulates.

Figure 5 with 2 supplements see all

Download asset Open asset

Proportions of ART-R and KEL1/PLA1 parasites in southern Laos districts.

Districts in five provinces of southern Laos are represented by markers whose color and label indicates the frequency of samples classified as ART-R (A) and as DHA-PPQ-R, i.e. possessing markers of resistance to both artemisinin and piperaquine (B). Only districts with more than 10 samples with valid genotypes are shown. In panel (B), a dashed line denotes a hypothetical demarcation line between a Lower Zone, where DHA-PPQ-R strains have spread, and an Upper Zone, where they are absent and ART-R parasites belong to different strains.

Figure 5—source data 1 Counts and proportions of samples predicted to be resistant to artemisinin and DHA-PPQ in districts of Laos.: https://cdn.elifesciences.org/articles/62997/elife-62997-fig5-data1-v1.xlsx
Download elife-62997-fig5-data1-v1.xlsx

Given the very recent aggressive spread of DHA-PPQ-R strains, it is likely that ART-R parasites in the Upper Zone are remnants of an earlier sweep which may also have spread from the south, as suggested by the higher frequency in Salavan province than in Savannakhet. To confirm the presence of distinct ART-R populations, we used genetic barcodes to construct a tree that recapitulates population structure in Laos (Figure 5—figure supplement 2), which clearly separates Upper Zone and Lower Zone parasites. In this tree, DHA-PPQ-R parasites form a large, tight cluster clearly separated from the kelch13 wild-type samples from the Upper Zone. The Upper Zone C580Y mutants cluster separately from both these groups, and appear more similar to some C580Y mutants from the Lower Zone which do not carry the PPQ-R amplification, corroborating the hypothesis that Upper Zone mutants migrated from the South. It is likely that the northward spread of DHA-PPQ-R strains has been contained by the use of artemether-lumefantrine in Laos, which diminishes the survival advantage of resistance to piperaquine. However, the spread of DHA-PPQ-R parasites across the Lower Zone, probably displacing previous ART-R strains, suggests that they are well-adapted and highly competitive even in the absence of pressure from piperaquine.

Release of genetic report card data

GenRe-Mekong’s primary data outputs are Genetic Report Cards, delivered as spreadsheets comprising sample metadata (time and place of collection), drug resistance genotypes and phenotype predictions, detected species and genetic barcodes. As soon as sample processing is complete, GRCs are returned to the stakeholders of the studies that contributed the samples, which typically include the NMCP and local scientific partners. Detailed analyses of GRC data may also be conducted by the GenRe-Mekong analysis team and local partners, and their results reported to the NMCP. On a regular basis, GRC data from all studies will be aggregated and released to public access, to benefit the research and public health community. The public releases are detailed by sample, and comprise all genetic data and their derivatives such as phenotype predictions. The first public release is currently available from the article’s Resource Page at https://www.malariagen.net/resource/29.

Discussion

GenRe-Mekong provides a genetic surveillance platform suitable for endemic regions of low- and middle-income countries, which delivers to NMCPs detailed knowledge about the genetic epidemiology of malaria parasites, to support decision-making. Pilot studies have been conducted in all GMS countries, with the Vietnam and Laos NMCPs having implemented GenRe-Mekong on a long-term basis. GenRe-Mekong has multiple features that facilitate NMCP engagement: a sample collection procedure that easily integrates with standard medical facility workflows; standardized protocols and training to support implementation; clear presentation of results, including translation to phenotype predictions, to provide intuitive understanding and rapid communication; and support by our regional analysis team and local partners to deliver and discuss findings. GenRe-Mekong has also worked closely with research projects, contributing to their analyses of the genotyping data and supporting publication of key findings. The genetic data produced were valuable for a wide range of research applications, such as clinical studies of drug efficacy (van der Pluijm et al., 2019), evaluation of elimination interventions (Landier et al., 2018), and epidemiological investigation of malaria importation (Chang et al., 2019).

Collaborations with public health organizations have rapidly translated into real impact for malaria control, especially where GenRe-Mekong has been implemented over multiple seasons. Genetic surveillance results were used by the Vietnam NMCP and Ministry of Health in reviews of national drug policy, leading to the replacement of DHA-PPQ with artesunate-pyronaridine as frontline therapy in four provinces. These included the province of Dak Lak, where an early report by GenRe-Mekong in 2018 was the first evidence of ART-R, confirmed by treatment failure data from in vivo therapy efficacy studies (TES) in 2019. In addition, our report of a DHA-PPQ-R outbreak in Gia Lai province has alerted authorities to the need to review the use of DHA-PPQ in that province. In Laos, authorities have been equally responsive, using GenRe-Mekong reports in their review of frontline therapy choices: the Ministry of Health opted against adopting the DHA-PPQ ACT based on our evidence of the expansion of resistant strains in the Lower Zone of southern Laos. The impact has not been limited to the national level: data shared by surveillance and research projects participating in GenRe-Mekong has powered regional large-scale epidemiological analyses in the GMS and beyond, revealing patterns of spread and evolution of multidrug-resistant malaria (van der Pluijm et al., 2019). By combining results from areas populated by multidrug resistant strains with those from countries where these strains could potentially spread, such as Bangladesh and India, GenRe-Mekong maps support risk assessment and preparedness. GenRe-Mekong will continue to encourage public data sharing to increase the value of genetic data generated, while respecting patient anonymity and giving recognition to those who contributed to the project.

A major advantage of genetic surveillance, compared to more costly clinical studies, is the potential for dense coverage across all endemic areas, which can identify important spatial heterogeneities across the territory. For example, DHA-PPQ was adopted as frontline therapy in Thailand based on the drug’s efficacy in the western provinces; genetic data about the rise in prevalence of DHA-PPQ-R strains in the northeast of the country would probably have led to a different recommendation, had that information been available. Similarly, our data suggests that a single efficacy study in Savannakhet province could have convinced authorities that DHA-PPQ was suitable for Laos, with potential disastrous effects in the southernmost provinces. The extensive coverage provided by GenRe-Mekong routine surveillance allowed a more balanced evaluation of resistant strains prevalence across all endemic provinces. In addition to dense coverage, genetic surveillance should also feature systematic and continued sampling over time, to support the detection of epidemiological changes, and also to allow prevalence comparisons between region, which is most meaningful when collection periods are matched.

The SpotMalaria genotyping platform is designed for extensibility, and has been expanded twice in the course of the project: to test for the newly discovered marker for the plasmepsin2/3 amplification (Amato et al., 2017) and to add new mutations in crt which are associated to higher levels of piperaquine resistance in KEL1/PLA1 parasite (Hamilton et al., 2019; Ross et al., 2018; Agrawal et al., 2017). Such improvements will continue as new markers are identified, and new techniques developed. However, there are newer drugs such as pyronaridine, and established drugs such as lumefantrine and amodiaquine, for which clinical drug resistance markers are yet to be identified. GenRe-Mekong will support the identification of new markers in practical ways, by performing WGS on selected surveillance samples, and contributing these data to public repositories to study epidemiological effects, such as reductions in diversity, increases in cases and founder populations, (Miotto et al., 2013) and to identify genomic regions under selection that may lead to discovering new markers. As the project develops, Genetic Report Cards will be expanded, to address new public health use cases, including those not directly related to drug resistance. For example, genetic barcodes and WGS data can be used to detect imported cases; to distinguish recrudescences from reinfections; and to measure connectedness between sites, and routes of spread (Chang et al., 2019).

GenRe-Mekong was conceived as a versatile and extensible platform that can be easily integrated in a wide range of endemic settings, at relatively low cost to allow extensive geographical coverage. These properties demand trade-offs, imposing certain limitations on the platform. First, we work with small-volume DBS samples, which makes sample collection easy to integrate in routine public health operations; however, low blood volumes mean low genotyping success rates from sub-microscopic infection, and thus GenRe-Mekong only processes samples from cases confirmed by microscopy or rapid diagnostic test (RDT). Second, we focus on genotypes that can be obtained from our high-throughput amplicon sequencing platform, allowing us to contain costs and manpower requirements. In some cases, we have to relax this restriction: for example, mdr1 copy numbers currently cannot be reliably estimated from amplicon sequencing, because of the requirement for selective DNA amplification. Because of the importance of this genotype, we currently use an additional qPCR assay, but it is desirable to find innovative solutions that keep laboratory processes streamlined. Third, while our genetic barcodes can support useful analyses of populations, we plan to improve their resolution by including amplicons containing multiple highly polymorphic SNPs, which may be more informative of identity by descent.

In the future, the integration of genetic surveillance data in public health decision-making processes will be a major focus for GenRe-Mekong, to be addressed in several ways. First, we will make available online platforms for selecting, visualizing and retrieving genetic epidemiology data, which will provide customized views of the data. Second, we will integrate with public health information systems, such as NMCPs’ dashboards, at both national and international level. This includes sharing GenRe-Mekong data through the World Health Organization’s data visualization platform, Malaria Threats Map (http://apps.who.int/malaria/maps/threats/). Third, we will provide training and support to expand in-country expertise, developing local capacity to evaluate drug resistance data and other outputs that GenRe-Mekong will deliver in the future. Finally, we will promote in-country implementations of the SpotMalaria amplicon sequencing platform that underpins the system, to enable faster turnaround times and long-term self-sufficiency. As the adoption cycle continues, we envisage that a growing global network of public health experts will leverage on genetic surveillance to maximize the impact of their interventions, and accelerate progress toward malaria elimination.

Data availability

The data used in this paper, including all genotypes, sample metadata and resulting phenotype predictions, are openly available together with detailed methods documentation and details of partner studies, from the article's Resource Page, at http://www.malariagen.net/resource/29.

The following data sets were generated

1. Jacob CG
2. Miotto O
(2021) MalariaGEN
ID 29. Genetic surveillance in the Greater Mekong Subregion and South Asia to support malaria control and elimination: about the data.

https://www.malariagen.net/resource/29

References

1. Agrawal S
2. Moser KA
3. Morton L
4. Cummings MP
5. Parihar A
6. Dwivedi A
7. Shetty AC
8. Drabek EF
9. Jacob CG
10. Henrich PP
11. Parobek CM
12. Jongsakul K
13. Huy R
14. Spring MD
15. Lanteri CA
16. Chaorattanakawee S
17. Lon C
18. Fukuda MM
19. Saunders DL
20. Fidock DA
21. Lin JT
22. Juliano JJ
23. Plowe CV
24. Silva JC
25. Takala-Harrison S
(2017) Association of a novel mutation in the Plasmodium falciparum chloroquine resistance transporter with decreased piperaquine sensitivity
The Journal of Infectious Diseases 216:468–476.

https://doi.org/10.1093/infdis/jix334
- PubMed
- Google Scholar
1. Amaratunga C
2. Lim P
3. Suon S
4. Sreng S
5. Mao S
6. Sopha C
7. Sam B
8. Dek D
9. Try V
10. Amato R
11. Blessborn D
12. Song L
13. Tullo GS
14. Fay MP
15. Anderson JM
16. Tarning J
17. Fairhurst RM
(2016) Dihydroartemisinin–piperaquine resistance in Plasmodium falciparum malaria in Cambodia: a multisite prospective cohort study
The Lancet Infectious Diseases 16:357–365.

https://doi.org/10.1016/S1473-3099(15)00487-9
- Google Scholar
1. Amato R
2. Lim P
3. Miotto O
4. Amaratunga C
5. Dek D
6. Pearson RD
7. Almagro-Garcia J
8. Neal AT
9. Sreng S
10. Suon S
11. Drury E
12. Jyothi D
13. Stalker J
14. Kwiatkowski DP
15. Fairhurst RM
(2017) Genetic markers associated with dihydroartemisinin-piperaquine failure in Plasmodium falciparum malaria in Cambodia: a genotype-phenotype association study
The Lancet Infectious Diseases 17:164–173.

https://doi.org/10.1016/S1473-3099(16)30409-1
- PubMed
- Google Scholar
1. Amato R
2. Pearson RD
3. Almagro-Garcia J
4. Amaratunga C
5. Lim P
6. Suon S
7. Sreng S
8. Drury E
9. Stalker J
10. Miotto O
11. Fairhurst RM
12. Kwiatkowski DP
(2018) Origins of the current outbreak of multidrug-resistant malaria in Southeast Asia: a retrospective genetic study
The Lancet Infectious Diseases 18:337–345.

https://doi.org/10.1016/S1473-3099(18)30068-9
- PubMed
- Google Scholar
1. Ariey F
2. Witkowski B
3. Amaratunga C
4. Beghain J
5. Langlois A-C
6. Khim N
7. Kim S
8. Duru V
9. Bouchier C
10. Ma L
11. Lim P
12. Leang R
13. Duong S
14. Sreng S
15. Suon S
16. Chuor CM
17. Bout DM
18. Ménard S
19. Rogers WO
20. Genton B
21. Fandeur T
22. Miotto O
23. Ringwald P
24. Le Bras J
25. Berry A
26. Barale J-C
27. Fairhurst RM
28. Benoit-Vical F
29. Mercereau-Puijalon O
30. Ménard D
(2014) A molecular marker of artemisinin-resistant Plasmodium falciparum malaria
Nature 505:50–55.

https://doi.org/10.1038/nature12876
- Google Scholar
(2015) Persistence of Sulfadoxine-Pyrimethamine resistance despite reduction of drug pressure in Malawi
Journal of Infectious Diseases 212:694–701.

https://doi.org/10.1093/infdis/jiv078
- Google Scholar
1. Ashley EA
2. Dhorda M
3. Fairhurst RM
4. Amaratunga C
5. Lim P
6. Suon S
7. Sreng S
8. Anderson JM
9. Mao S
10. Sam B
11. Sopha C
12. Chuor CM
13. Nguon C
14. Sovannaroth S
15. Pukrittayakamee S
16. Jittamala P
17. Chotivanich K
18. Chutasmit K
19. Suchatsoonthorn C
20. Runcharoen R
21. Hien TT
22. Thuy-Nhien NT
23. Thanh NV
24. Phu NH
25. Htut Y
26. Han K-T
27. Aye KH
28. Mokuolu OA
29. Olaosebikan RR
30. Folaranmi OO
31. Mayxay M
32. Khanthavong M
33. Hongvanthong B
34. Newton PN
35. Onyamboko MA
36. Fanello CI
37. Tshefu AK
38. Mishra N
39. Valecha N
40. Phyo AP
41. Nosten F
42. Yi P
43. Tripura R
44. Borrmann S
45. Bashraheil M
46. Peshu J
47. Faiz MA
48. Ghose A
49. Hossain MA
50. Samad R
51. Rahman MR
52. Hasan MM
53. Islam A
54. Miotto O
55. Amato R
56. MacInnis B
57. Stalker J
58. Kwiatkowski DP
59. Bozdech Z
60. Jeeyapant A
61. Cheah PY
62. Sakulthaew T
63. Chalk J
64. Intharabut B
65. Silamut K
66. Lee SJ
67. Vihokhern B
68. Kunasol C
69. Imwong M
70. Tarning J
71. Taylor WJ
72. Yeung S
73. Woodrow CJ
74. Flegg JA
75. Das D
76. Smith J
77. Venkatesan M
78. Plowe CV
79. Stepniewska K
80. Guerin PJ
81. Dondorp AM
82. Day NP
83. White NJ
(2014) Spread of artemisinin resistance in Plasmodium falciparum Malaria
New England Journal of Medicine 371:411–423.

https://doi.org/10.1056/NEJMoa1314981
- Google Scholar
1. Chang HH
2. Wesolowski A
3. Sinha I
4. Jacob CG
5. Mahmud A
6. Uddin D
7. Zaman SI
8. Hossain MA
9. Faiz MA
10. Ghose A
11. Sayeed AA
12. Rahman MR
13. Islam A
14. Karim MJ
15. Rezwan MK
16. Shamsuzzaman AKM
17. Jhora ST
18. Aktaruzzaman MM
19. Drury E
20. Gonçalves S
21. Kekre M
22. Dhorda M
23. Vongpromek R
24. Miotto O
25. Engø-Monsen K
26. Kwiatkowski D
27. Maude RJ
28. Buckee C
(2019) Mapping imported malaria in Bangladesh using parasite genetic and human mobility data
eLife 8:e43481.

https://doi.org/10.7554/eLife.43481
- PubMed
- Google Scholar
(2018) Entomological determinants of malaria transmission in Kayin state, Eastern Myanmar: A 24-month longitudinal study in four villages
Wellcome Open Research 3:109.

https://doi.org/10.12688/wellcomeopenres.14761.1
- Google Scholar
1. Cui L
2. Yan G
3. Sattabongkot J
4. Cao Y
5. Chen B
6. Chen X
7. Fan Q
8. Fang Q
9. Jongwutiwes S
10. Parker D
11. Sirichaisinthop J
12. Kyaw MP
13. Su XZ
14. Yang H
15. Yang Z
16. Wang B
17. Xu J
18. Zheng B
19. Zhong D
20. Zhou G
(2012) Malaria in the greater mekong subregion: heterogeneity and complexity
Acta Tropica 121:227–239.

https://doi.org/10.1016/j.actatropica.2011.02.016
- PubMed
- Google Scholar
1. Daniels RF
2. Schaffner SF
3. Wenger EA
4. Proctor JL
5. Chang H-H
6. Wong W
7. Baro N
8. Ndiaye D
9. Fall FB
10. Ndiop M
11. Ba M
12. Milner DA
13. Taylor TE
14. Neafsey DE
15. Volkman SK
16. Eckhoff PA
17. Hartl DL
18. Wirth DF
(2015) Modeling malaria genomics reveals transmission decline and rebound in Senegal
PNAS 112:7067–7072.

https://doi.org/10.1073/pnas.1505691112
- Google Scholar
1. Desmond-Hellmann S
(2016) Progress lies in precision
Science 353:731.

https://doi.org/10.1126/science.aai7598
- Google Scholar
Report
1. Directorate of National Vector Borne Disease Control Programme DGoHS
2. Government of India
(2013)
National Drug Policy on Malaria

Ministry of Health and Family Welfare.
- Google Scholar
1. Dondorp AM
2. Nosten F
3. Yi P
4. Das D
5. Phyo AP
6. Tarning J
7. Lwin KM
8. Ariey F
9. Hanpithakpong W
10. Lee SJ
11. Ringwald P
12. Silamut K
13. Imwong M
14. Chotivanich K
15. Lim P
16. Herdman T
17. An SS
18. Yeung S
19. Singhasivanon P
20. Day NPJ
21. Lindegardh N
22. Socheat D
23. White NJ
(2009) Artemisinin resistance in Plasmodium falciparum Malaria
New England Journal of Medicine 361:455–467.

https://doi.org/10.1128/microbiolspec.EI10-0013-2016
- Google Scholar
(2009) The dynamics of mutations associated with anti-malarial drug resistance in Plasmodium falciparum
Trends in Parasitology 25:557–563.

https://doi.org/10.1016/j.pt.2009.09.008
- Google Scholar
1. Felger I
2. Snounou G
3. Hastings I
4. Moehrle JJ
5. Beck HP
(2020) PCR correction strategies for malaria drug trials: updates and clarifications
The Lancet Infectious Diseases 20:e20–e25.

https://doi.org/10.1016/S1473-3099(19)30426-8
- PubMed
- Google Scholar
(2014) Return of widespread Chloroquine-Sensitive Plasmodium falciparum to Malawi
The Journal of Infectious Diseases 210:1110–1114.

https://doi.org/10.1093/infdis/jiu216
- Google Scholar
1. Hamilton WL
2. Amato R
3. van der Pluijm RW
4. Jacob CG
5. Quang HH
6. Thuy-Nhien NT
7. Hien TT
8. Hongvanthong B
9. Chindavongsa K
10. Mayxay M
11. Huy R
12. Leang R
13. Huch C
14. Dysoley L
15. Amaratunga C
16. Suon S
17. Fairhurst RM
18. Tripura R
19. Peto TJ
20. Sovann Y
21. Jittamala P
22. Hanboonkunupakarn B
23. Pukrittayakamee S
24. Chau NH
25. Imwong M
26. Dhorda M
27. Vongpromek R
28. Chan XHS
29. Maude RJ
30. Pearson RD
31. Nguyen T
32. Rockett K
33. Drury E
34. Gonçalves S
35. White NJ
36. Day NP
37. Kwiatkowski DP
38. Dondorp AM
39. Miotto O
(2019) Evolution and expansion of multidrug-resistant malaria in Southeast Asia: a genomic epidemiology study
The Lancet Infectious Diseases 19:943–951.

https://doi.org/10.1016/S1473-3099(19)30392-5
- PubMed
- Google Scholar
1. Hay SI
2. Rogers DJ
3. Toomer JF
4. Snow RW
(2000) Annual Plasmodium falciparum entomological inoculation rates (EIR) across Africa: literature survey, internet access and review
Transactions of the Royal Society of Tropical Medicine and Hygiene 94:113–127.

https://doi.org/10.1016/S0035-9203(00)90246-3
- Google Scholar
1. Landier J
2. Parker DM
3. Thu AM
4. Lwin KM
5. Delmas G
6. Nosten FH
7. Andolina C
8. Aguas R
9. Ang SM
10. Aung EP
11. Baw NB
12. Be SA
13. B'Let S
14. Bluh H
15. Bonnington CA
16. Chaumeau V
17. Chirakiratinant M
18. Cho WC
19. Christensen P
20. Corbel V
21. Day NPJ
22. Dah SH
23. Delmas G
24. Dhorda M
25. Dondorp AM
26. Gaudart J
27. Gornsawun G
28. Haohankhunnatham W
29. Hla SK
30. Hsel SN
31. Htoo GN
32. Htoo SN
33. Imwong M
34. John S
35. Kajeechiwa L
36. Kereecharoen L
37. Kittiphanakun P
38. Kittitawee K
39. Konghahong K
40. Khin SD
41. Kyaw SW
42. Landier J
43. Ling C
44. Lwin KM
45. Lwin KSW
46. Ma NK
47. Marie A
48. Maung C
49. Marta E
50. Minh MC
51. Miotto O
52. Moo PK
53. Moo KL
54. Moo M
55. Na NN
56. Nay M
57. Nosten FH
58. Nosten S
59. Nyo SN
60. Oh EKS
61. Oo PT
62. Oo TP
63. Parker DM
64. Paw ES
65. Phumiya C
66. Phyo AP
67. Pilaseng K
68. Proux S
69. Rakthinthong S
70. Ritwongsakul W
71. Salathibuphha K
72. Santirad A
73. Sawasdichai S
74. von Seidlein L
75. Shee PW
76. Shee PB
77. Tangseefa D
78. Thu AM
79. Thwin MM
80. Tun SW
81. Wanachaloemlep C
82. White LJ
83. White NJ
84. Wiladphaingern J
85. Win SN
86. Yee NL
87. Yuwapan D
(2018) Effect of generalised access to early diagnosis and treatment and targeted mass drug administration on Plasmodium falciparum malaria in Eastern Myanmar: an observational study of a regional elimination programme
The Lancet 391:1916–1926.

https://doi.org/10.1016/S0140-6736(18)30792-X
- Google Scholar
(2006) Return of chloroquine antimalarial efficacy in Malawi
New England Journal of Medicine 355:1959–1966.

https://doi.org/10.1056/NEJMoa062032
- PubMed
- Google Scholar
1. Leang R
2. Taylor WRJ
3. Bouth DM
4. Song L
5. Tarning J
6. Char MC
7. Kim S
8. Witkowski B
9. Duru V
10. Domergue A
11. Khim N
12. Ringwald P
13. Menard D
(2015) Evidence of Plasmodium falciparum malaria multidrug resistance to artemisinin and piperaquine in western Cambodia: dihydroartemisinin-piperaquine Open-Label multicenter clinical assessment
Antimicrobial Agents and Chemotherapy 59:4719–4726.

https://doi.org/10.1128/AAC.00835-15
- Google Scholar
1. Lim P
2. Dek D
3. Try V
4. Eastman RT
5. Chy S
6. Sreng S
7. Suon S
8. Mao S
9. Sopha C
10. Sam B
11. Ashley EA
12. Miotto O
13. Dondorp AM
14. White NJ
15. Su X
16. Char MC
17. Anderson JM
18. Amaratunga C
19. Menard D
20. Fairhurst RM
(2013) Ex vivo Susceptibility of Plasmodium falciparum to Antimalarial Drugs in Western, Northern, and Eastern Cambodia, 2011-2012: Association with Molecular Markers
Antimicrobial Agents and Chemotherapy 57:5277–5283.

https://doi.org/10.1128/AAC.00687-13
- Google Scholar
1. MalariaGEN Plasmodium falciparum Community Project
(2016) Genomic epidemiology of artemisinin resistant malaria
eLife 5:e08714.

https://doi.org/10.7554/eLife.08714
- Google Scholar
1. Ménard D
2. Khim N
3. Beghain J
4. Adegnika AA
5. Shafiul-Alam M
6. Amodu O
7. Rahim-Awab G
8. Barnadas C
9. Berry A
10. Boum Y
11. Bustos MD
12. Cao J
13. Chen J-H
14. Collet L
15. Cui L
16. Thakur G-D
17. Dieye A
18. Djallé D
19. Dorkenoo MA
20. Eboumbou-Moukoko CE
21. Espino CJ
22. Fandeur T
23. Ferreira-da-Cruz M-F
24. Fola AA
25. Fuehrer H-P
26. Hassan AM
27. Herrera S
28. Hongvanthong B
29. Houzé S
30. Ibrahim ML
31. Jahirul-Karim M
32. Jiang L
33. Kano S
34. Ali-Khan W
35. Khanthavong M
36. Kremsner PG
37. Lacerda M
38. Leang R
39. Leelawong M
40. Li M
41. Lin K
42. Mazarati J-B
43. Ménard S
44. Morlais I
45. Muhindo-Mavoko H
46. Musset L
47. Na-Bangchang K
48. Nambozi M
49. Niaré K
50. Noedl H
51. Ouédraogo J-B
52. Pillai DR
53. Pradines B
54. Quang-Phuc B
55. Ramharter M
56. Randrianarivelojosia M
57. Sattabongkot J
58. Sheikh-Omar A
59. Silué KD
60. Sirima SB
61. Sutherland C
62. Syafruddin D
63. Tahar R
64. Tang L-H
65. Touré OA
66. Tshibangu-wa-Tshibangu P
67. Vigan-Womas I
68. Warsame M
69. Wini L
70. Zakeri S
71. Kim S
72. Eam R
73. Berne L
74. Khean C
75. Chy S
76. Ken M
77. Loch K
78. Canier L
79. Duru V
80. Legrand E
81. Barale J-C
82. Stokes B
83. Straimer J
84. Witkowski B
85. Fidock DA
86. Rogier C
87. Ringwald P
88. Ariey F
89. Mercereau-Puijalon O
(2016) A worldwide map of Plasmodium falciparum K13-Propeller Polymorphisms
New England Journal of Medicine 374:2453–2464.

https://doi.org/10.1056/NEJMoa1513137
- Google Scholar
1. Miotto O
2. Almagro-Garcia J
3. Manske M
4. MacInnis B
5. Campino S
6. Rockett KA
7. Amaratunga C
8. Lim P
9. Suon S
10. Sreng S
11. Anderson JM
12. Duong S
13. Nguon C
14. Chuor CM
15. Saunders D
16. Se Y
17. Lon C
18. Fukuda MM
19. Amenga-Etego L
20. Hodgson AVO
21. Asoala V
22. Imwong M
23. Takala-Harrison S
24. Nosten F
25. Su X
26. Ringwald P
27. Ariey F
28. Dolecek C
29. Hien TT
30. Boni MF
31. Thai CQ
32. Amambua-Ngwa A
33. Conway DJ
34. Djimdé AA
35. Doumbo OK
36. Zongo I
37. Ouedraogo J-B
38. Alcock D
39. Drury E
40. Auburn S
41. Koch O
42. Sanders M
43. Hubbart C
44. Maslen G
45. Ruano-Rubio V
46. Jyothi D
47. Miles A
48. O'Brien J
49. Gamble C
50. Oyola SO
51. Rayner JC
52. Newbold CI
53. Berriman M
54. Spencer CCA
55. McVean G
56. Day NP
57. White NJ
58. Bethell D
59. Dondorp AM
60. Plowe CV
61. Fairhurst RM
62. Kwiatkowski DP
(2013) Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia
Nature Genetics 45:648–655.

https://doi.org/10.1038/ng.2624
- Google Scholar
1. Miotto O
2. Amato R
3. Ashley EA
4. MacInnis B
5. Almagro-Garcia J
6. Amaratunga C
7. Lim P
8. Mead D
9. Oyola SO
10. Dhorda M
11. Imwong M
12. Woodrow C
13. Manske M
14. Stalker J
15. Drury E
16. Campino S
17. Amenga-Etego L
18. Thanh T-NN
19. Tran HT
20. Ringwald P
21. Bethell D
22. Nosten F
23. Phyo AP
24. Pukrittayakamee S
25. Chotivanich K
26. Chuor CM
27. Nguon C
28. Suon S
29. Sreng S
30. Newton PN
31. Mayxay M
32. Khanthavong M
33. Hongvanthong B
34. Htut Y
35. Han KT
36. Kyaw MP
37. Faiz MA
38. Fanello CI
39. Onyamboko M
40. Mokuolu OA
41. Jacob CG
42. Takala-Harrison S
43. Plowe CV
44. Day NP
45. Dondorp AM
46. Spencer CCA
47. McVean G
48. Fairhurst RM
49. White NJ
50. Kwiatkowski DP
(2015) Genetic architecture of artemisinin-resistant Plasmodium falciparum
Nature Genetics 47:226–234.

https://doi.org/10.1038/ng.3189
- Google Scholar
1. Mita T
2. Tanabe K
3. Kita K
(2009) Spread and evolution of Plasmodium falciparum drug resistance
Parasitology International 58:201–209.

https://doi.org/10.1016/j.parint.2009.04.004
- Google Scholar
1. Mita T
2. Venkatesan M
3. Ohashi J
4. Culleton R
5. Takahashi N
6. Tsukahara T
7. Ndounga M
8. Dysoley L
9. Endo H
10. Hombhanje F
11. Ferreira MU
12. Plowe CV
13. Tanabe K
(2011) Limited geographical origin and global spread of sulfadoxine-resistant dhps alleles in Plasmodium falciparum populations
The Journal of Infectious Diseases 204:1980–1988.

https://doi.org/10.1093/infdis/jir664
- PubMed
- Google Scholar
(2019) Population pharmacogenomics for precision public health in Colombia
Frontiers in Genetics 10:241.

https://doi.org/10.3389/fgene.2019.00241
- PubMed
- Google Scholar
1. Noedl H
2. Se Y
3. Schaecher K
4. Smith BL
5. Socheat D
6. Fukuda MM
(2008) Evidence of Artemisinin-Resistant malaria in western Cambodia
New England Journal of Medicine 359:2619–2620.

https://doi.org/10.1056/NEJMc0805011
- Google Scholar
1. Oyola SO
2. Ariani CV
3. Hamilton WL
4. Kekre M
5. Amenga-Etego LN
6. Ghansah A
7. Rutledge GG
8. Redmond S
9. Manske M
10. Jyothi D
11. Jacob CG
12. Otto TD
13. Rockett K
14. Newbold CI
15. Berriman M
16. Kwiatkowski DP
(2016) Whole genome sequencing of Plasmodium falciparum from dried blood spots using selective whole genome amplification
Malaria Journal 15:597.

https://doi.org/10.1186/s12936-016-1641-7
- Google Scholar
Preprint
(2019) An open dataset of Plasmodium falciparum genome variation in 7,000 worldwide samples
bioRxiv.

https://doi.org/10.1101/824730
- Google Scholar
1. Plowe CV
(2009) The evolution of drug-resistant malaria
Transactions of the Royal Society of Tropical Medicine and Hygiene 103:S11–S14.

https://doi.org/10.1016/j.trstmh.2008.11.002
- Google Scholar
1. Roper C
2. Pearce R
3. Nair S
4. Sharp B
5. Nosten F
6. Anderson T
(2004) Intercontinental spread of pyrimethamine-resistant malaria
Science 305:1124.

https://doi.org/10.1126/science.1098876
- PubMed
- Google Scholar
1. Ross LS
2. Dhingra SK
3. Mok S
4. Yeo T
5. Wicht KJ
6. Kümpornsin K
7. Takala-Harrison S
8. Witkowski B
9. Fairhurst RM
10. Ariey F
11. Menard D
12. Fidock DA
(2018) Emerging southeast asian PfCRT mutations confer Plasmodium falciparum resistance to the first-line antimalarial piperaquine
Nature Communications 9:3314.

https://doi.org/10.1038/s41467-018-05652-0
- PubMed
- Google Scholar
1. Spring MD
2. Lin JT
3. Manning JE
4. Vanachayangkul P
5. Somethy S
6. Bun R
7. Se Y
8. Chann S
9. Ittiverakul M
10. Sia-ngam P
11. Kuntawunginn W
12. Arsanok M
13. Buathong N
14. Chaorattanakawee S
15. Gosi P
16. Ta-aksorn W
17. Chanarat N
18. Sundrakes S
19. Kong N
20. Heng TK
21. Nou S
22. Teja-isavadharm P
23. Pichyangkul S
24. Phann ST
25. Balasubramanian S
26. Juliano JJ
27. Meshnick SR
28. Chour CM
29. Prom S
30. Lanteri CA
31. Lon C
32. Saunders DL
(2015) Dihydroartemisinin-piperaquine failure associated with a triple mutant including kelch13 C580Y in Cambodia: an observational cohort study
The Lancet Infectious Diseases 15:683–691.

https://doi.org/10.1016/S1473-3099(15)70049-6
- Google Scholar
1. Takala-Harrison S
2. Jacob CG
3. Arze C
4. Cummings MP
5. Silva JC
6. Dondorp AM
7. Fukuda MM
8. Hien TT
9. Mayxay M
10. Noedl H
11. Nosten F
12. Kyaw MP
13. Nhien NT
14. Imwong M
15. Bethell D
16. Se Y
17. Lon C
18. Tyner SD
19. Saunders DL
20. Ariey F
21. Mercereau-Puijalon O
22. Menard D
23. Newton PN
24. Khanthavong M
25. Hongvanthong B
26. Starzengruber P
27. Fuehrer HP
28. Swoboda P
29. Khan WA
30. Phyo AP
31. Nyunt MM
32. Nyunt MH
33. Brown TS
34. Adams M
35. Pepin CS
36. Bailey J
37. Tan JC
38. Ferdig MT
39. Clark TG
40. Miotto O
41. MacInnis B
42. Kwiatkowski DP
43. White NJ
44. Ringwald P
45. Plowe CV
(2015) Independent emergence of artemisinin resistance mutations among Plasmodium falciparum in Southeast Asia
The Journal of Infectious Diseases 211:670–679.

https://doi.org/10.1093/infdis/jiu491
- PubMed
- Google Scholar
1. Trape J-F
2. Pison G
3. Preziosi M-P
4. Enel C
5. du Loû AD
6. Delaunay V
7. Samb B
8. Lagarde E
9. Molez J-F
10. Simondon F
(1998) Impact of chloroquine resistance on malaria mortality
Comptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie 321:689–697.

https://doi.org/10.1016/S0764-4469(98)80009-7
- Google Scholar
1. van der Pluijm RW
2. Imwong M
3. Chau NH
4. Hoa NT
5. Thuy-Nhien NT
6. Thanh NV
7. Jittamala P
8. Hanboonkunupakarn B
9. Chutasmit K
10. Saelow C
11. Runjarern R
12. Kaewmok W
13. Tripura R
14. Peto TJ
15. Yok S
16. Suon S
17. Sreng S
18. Mao S
19. Oun S
20. Yen S
21. Amaratunga C
22. Lek D
23. Huy R
24. Dhorda M
25. Chotivanich K
26. Ashley EA
27. Mukaka M
28. Waithira N
29. Cheah PY
30. Maude RJ
31. Amato R
32. Pearson RD
33. Gonçalves S
34. Jacob CG
35. Hamilton WL
36. Fairhurst RM
37. Tarning J
38. Winterberg M
39. Kwiatkowski DP
40. Pukrittayakamee S
41. Hien TT
42. Day NP
43. Miotto O
44. White NJ
45. Dondorp AM
(2019) Determinants of dihydroartemisinin-piperaquine treatment failure in Plasmodium falciparum malaria in Cambodia, Thailand, and Vietnam: a prospective clinical, pharmacological, and genetic study
The Lancet Infectious Diseases 19:952–961.

https://doi.org/10.1016/S1473-3099(19)30391-3
- PubMed
- Google Scholar
1. von Seidlein L
2. Peto TJ
3. Landier J
4. Nguyen T-N
5. Tripura R
6. Phommasone K
7. Pongvongsa T
8. Lwin KM
9. Keereecharoen L
10. Kajeechiwa L
11. Thwin MM
12. Parker DM
13. Wiladphaingern J
14. Nosten S
15. Proux S
16. Corbel V
17. Tuong-Vy N
18. Phuc-Nhi TL
19. Son DH
20. Huong-Thu PN
21. Tuyen NTK
22. Tien NT
23. Dong LT
24. Hue DV
25. Quang HH
26. Nguon C
27. Davoeung C
28. Rekol H
29. Adhikari B
30. Henriques G
31. Phongmany P
32. Suangkanarat P
33. Jeeyapant A
34. Vihokhern B
35. van der Pluijm RW
36. Lubell Y
37. White LJ
38. Aguas R
39. Promnarate C
40. Sirithiranont P
41. Malleret B
42. Rénia L
43. Onsjö C
44. Chan XH
45. Chalk J
46. Miotto O
47. Patumrat K
48. Chotivanich K
49. Hanboonkunupakarn B
50. Jittmala P
51. Kaehler N
52. Cheah PY
53. Pell C
54. Dhorda M
55. Imwong M
56. Snounou G
57. Mukaka M
58. Peerawaranun P
59. Lee SJ
60. Simpson JA
61. Pukrittayakamee S
62. Singhasivanon P
63. Grobusch MP
64. Cobelens F
65. Smithuis F
66. Newton PN
67. Thwaites GE
68. Day NPJ
69. Mayxay M
70. Hien TT
71. Nosten FH
72. Dondorp AM
73. White NJ
(2019) The impact of targeted malaria elimination with mass drug administrations on falciparum malaria in Southeast Asia: A cluster randomised trial
PLOS Medicine 16:e1002745.

https://doi.org/10.1371/journal.pmed.1002745
- Google Scholar
Book
1. World Health Organization
(2017)
Update on Artemisinin Resistance

Geneva: World Health Organization.
- Google Scholar
Report
1. World Health Organization
(2018)
Status Report on Artemisinin Resistance and ACT Efficacy

Geneva: World Health Organization.
- Google Scholar

Article and author information

Author details

Christopher G Jacob

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Resources, Data curation, Software, Formal analysis, Validation, Investigation, Methodology, Writing - original draft, Writing - review and editing

Competing interests
No competing interests declared
Nguyen Thuy-Nhien

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam

Contribution
Supervision, Investigation, Project administration

Competing interests
No competing interests declared
Mayfong Mayxay
1. Lao-Oxford-Mahosot Hospital-Wellcome Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic
2. Institute of Research and Education Development (IRED), University of Health Sciences, Ministry of Health, Vientiane, Lao People's Democratic Republic
3. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
Contribution
Conceptualization, Resources, Data curation, Software, Formal analysis, Supervision, Funding acquisition, Investigation, Visualization, Methodology, Writing - original draft, Writing - review and editing

Competing interests
No competing interests declared
Richard J Maude
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
3. Harvard TH Chan School of Public Health, Harvard University, Boston, United States
Contribution
Supervision, Investigation, Methodology, Project administration

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-5355-0562
Huynh Hong Quang

Institute of Malariology, Parasitology and Entomology (IMPE-QN), Quy Nhon, Viet Nam

Contribution
Supervision, Investigation, Methodology, Project administration

Competing interests
No competing interests declared
Bouasy Hongvanthong

Centre of Malariology, Parasitology, and Entomology, Vientiane, Lao People's Democratic Republic

Contribution
Investigation, Project administration

Competing interests
No competing interests declared
Viengxay Vanisaveth

Centre of Malariology, Parasitology, and Entomology, Vientiane, Lao People's Democratic Republic

Contribution
Investigation, Project administration

Competing interests
No competing interests declared
Thang Ngo Duc

National Institute of Malariology, Parasitology and Entomology (NIMPE), Hanoi, Viet Nam

Contribution
Investigation, Project administration

Competing interests
No competing interests declared
Huy Rekol

National Center for Parasitology, Entomology, and Malaria Control, Phnom Penh, Cambodia

Contribution
Investigation, Project administration

Competing interests
No competing interests declared
Rob van der Pluijm
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Supervision, Investigation, Project administration

Competing interests
No competing interests declared
Lorenz von Seidlein
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Rick Fairhurst

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, United States

Present address
AstraZeneca, Gaithersburg, United States

Contribution
Supervision, Investigation

Competing interests
No competing interests declared
François Nosten
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Shoklo Malaria Research Unit, Mae Sot, Thailand
Contribution
Supervision, Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-7951-0745
Md Amir Hossain

Chittagong Medical College Hospital, Chittagong, Bangladesh

Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Naomi Park

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Investigation, Methodology

Competing interests
No competing interests declared
Scott Goodwin

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Methodology

Competing interests
No competing interests declared
Pascal Ringwald

World Health Organization, Geneva, Switzerland

Contribution
Investigation, Methodology

Competing interests
No competing interests declared
Keobouphaphone Chindavongsa

Centre of Malariology, Parasitology, and Entomology, Vientiane, Lao People's Democratic Republic

Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Paul Newton
1. Lao-Oxford-Mahosot Hospital-Wellcome Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic
2. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
3. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Elizabeth Ashley
1. Lao-Oxford-Mahosot Hospital-Wellcome Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic
2. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Sonexay Phalivong

Lao-Oxford-Mahosot Hospital-Wellcome Research Unit (LOMWRU), Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic

Contribution
Supervision, Investigation, Project administration

Competing interests
No competing interests declared
Rapeephan Maude
1. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
2. Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
Contribution
Investigation

Competing interests
No competing interests declared
Rithea Leang

National Center for Parasitology, Entomology, and Malaria Control, Phnom Penh, Cambodia

Contribution
Investigation, Project administration

Competing interests
No competing interests declared
Cheah Huch

National Center for Parasitology, Entomology, and Malaria Control, Phnom Penh, Cambodia

Contribution
Investigation

Competing interests
No competing interests declared
Le Thanh Dong

Institute of Malariology, Parasitology and Entomology (IMPEHCM), Ho Chi Minh City, Viet Nam

Contribution
Investigation

Competing interests
No competing interests declared
Kim-Tuyen Nguyen

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam

Contribution
Investigation

Competing interests
No competing interests declared
Tran Minh Nhat

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam

Contribution
Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-9500-8341
Tran Tinh Hien

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam

Contribution
Investigation

Competing interests
No competing interests declared
Hoa Nguyen

Vysnova Partners Inc, Hanoi, Viet Nam

Contribution
Investigation

Competing interests
is an employee of Vysnova Partners Inc
Nicole Zdrojewski

Vysnova Partners Inc, Hanoi, Viet Nam

Contribution
Supervision, Investigation

Competing interests
is an employee of Vysnova Partners Inc
Sara Canavati

Vysnova Partners Inc, Hanoi, Viet Nam

Contribution
Investigation

Competing interests
is an employee of Vysnova Partners Inc
Abdullah Abu Sayeed

Chittagong Medical College Hospital, Chittagong, Bangladesh

Contribution
Investigation

Competing interests
No competing interests declared
Didar Uddin

Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand

Contribution
Investigation

Competing interests
No competing interests declared
Caroline Buckee

Harvard TH Chan School of Public Health, Harvard University, Boston, United States

Contribution
Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-8386-5899
Caterina I Fanello
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Marie Onyamboko

Kinshasa School of Public Health, University of Kinshasa, Kinshasa, Democratic Republic of the Congo

Contribution
Investigation

Competing interests
No competing interests declared
Thomas Peto
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Investigation

Competing interests
No competing interests declared
Rupam Tripura
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Investigation

Competing interests
No competing interests declared
Chanaki Amaratunga

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, United States
Present address
1. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
2. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
Contribution
Investigation

Competing interests
No competing interests declared
Aung Myint Thu
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Shoklo Malaria Research Unit, Mae Sot, Thailand
Contribution
Investigation

Competing interests
No competing interests declared
Gilles Delmas
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Shoklo Malaria Research Unit, Mae Sot, Thailand
Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Jordi Landier
1. Shoklo Malaria Research Unit, Mae Sot, Thailand
2. Aix-Marseille Université, INSERM, IRD, SESSTIM, Aix Marseille Institute of Public Health, ISSPAM, Marseille, France
Contribution
Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0001-8619-9775
Daniel M Parker
1. Shoklo Malaria Research Unit, Mae Sot, Thailand
2. Susan and Henry Samueli College of Health Sciences, University of California, Irvine, Irvine, United States
Contribution
Data curation, Investigation

Competing interests
No competing interests declared
Nguyen Hoang Chau

Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam

Contribution
Investigation

Competing interests
No competing interests declared
Dysoley Lek

National Center for Parasitology, Entomology, and Malaria Control, Phnom Penh, Cambodia

Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Seila Suon

National Center for Parasitology, Entomology, and Malaria Control, Phnom Penh, Cambodia

Contribution
Investigation

Competing interests
No competing interests declared
James Callery
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-3218-2166
Podjanee Jittamala

Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

Contribution
Investigation

Competing interests
No competing interests declared
Borimas Hanboonkunupakarn

Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

Contribution
Investigation

Competing interests
No competing interests declared
Sasithon Pukrittayakamee
1. Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
2. The Royal Society of Thailand, Bangkok, Thailand
Contribution
Investigation

Competing interests
No competing interests declared
Aung Pyae Phyo
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Myanmar-Oxford Clinical Research Unit, Yangon, Myanmar
Contribution
Investigation

Competing interests
No competing interests declared
Frank Smithuis
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Myanmar-Oxford Clinical Research Unit, Yangon, Myanmar
Contribution
Supervision, Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-4704-9915
Khin Lin

Department of Medical Research, Pyin Oo Lwin, Myanmar

Contribution
Investigation

Competing interests
No competing interests declared
Myo Thant

Defence Services Medical Research Centre, Yangon, Myanmar

Contribution
Investigation

Competing interests
No competing interests declared
Tin Maung Hlaing

Defence Services Medical Research Centre, Yangon, Myanmar

Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Parthasarathi Satpathi

Midnapore Medical College, Midnapur, India

Contribution
Supervision, Investigation

Competing interests
No competing interests declared
Sanghamitra Satpathi

Ispat General Hospital, Rourkela, India

Contribution
Investigation

Competing interests
No competing interests declared
Prativa K Behera

Ispat General Hospital, Rourkela, India

Contribution
Investigation

Competing interests
No competing interests declared
Amar Tripura

Agartala Medical College, Agartala, India

Contribution
Investigation

Competing interests
No competing interests declared
Subrata Baidya

Agartala Medical College, Agartala, India

Contribution
Investigation

Competing interests
No competing interests declared
Neena Valecha

National Institute of Malaria Research, Indian Council of Medical Research, New Delhi, India

Contribution
Investigation

Competing interests
No competing interests declared
Anupkumar R Anvikar

National Institute of Malaria Research, Indian Council of Medical Research, New Delhi, India

Contribution
Investigation

Competing interests
No competing interests declared
Akhter Ul Islam

Ramu Upazila Health Complex, Cox's Bazar, Bangladesh

Contribution
Investigation

Competing interests
No competing interests declared
Abul Faiz

Malaria Research Group and Dev Care Foundation, Dhaka, Bangladesh

Contribution
Investigation

Competing interests
No competing interests declared
Chanon Kunasol

Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand

Contribution
Investigation

Competing interests
No competing interests declared
Eleanor Drury

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Investigation

Competing interests
No competing interests declared
Mihir Kekre

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Investigation

Competing interests
No competing interests declared
Mozam Ali

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Investigation

Competing interests
No competing interests declared
Katie Love

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Investigation

Competing interests
No competing interests declared
Shavanthi Rajatileka

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Supervision, Investigation, Methodology, Project administration

Competing interests
No competing interests declared
Anna E Jeffreys

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

Contribution
Supervision, Investigation, Methodology, Project administration

Competing interests
No competing interests declared
Kate Rowlands

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

Contribution
Investigation

Competing interests
No competing interests declared
Christina S Hubbart

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

Contribution
Investigation

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0001-9576-9581
Mehul Dhorda
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
3. Worldwide Antimalarial Resistance Network (WWARN), Asia Regional Centre, Bangkok, Thailand
Contribution
Supervision, Investigation, Methodology, Project administration

Competing interests
No competing interests declared
Ranitha Vongpromek
1. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
2. Worldwide Antimalarial Resistance Network (WWARN), Asia Regional Centre, Bangkok, Thailand
Contribution
Data curation, Supervision, Validation, Investigation, Methodology, Project administration

Competing interests
No competing interests declared
Namfon Kotanan

Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

Contribution
Data curation, Validation, Investigation, Methodology

Competing interests
No competing interests declared
Phrutsamon Wongnak

Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand

Contribution
Data curation, Formal analysis, Investigation, Methodology

Competing interests
No competing interests declared
Jacob Almagro Garcia

MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom

Contribution
Data curation, Software, Formal analysis, Investigation, Methodology

Competing interests
No competing interests declared
Richard D Pearson
1. Wellcome Sanger Institute, Hinxton, United Kingdom
2. MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom
Contribution
Data curation, Software, Formal analysis, Methodology

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-7386-3566
Cristina V Ariani

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Data curation, Formal analysis

Competing interests
No competing interests declared
Thanat Chookajorn

Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

Contribution
Data curation, Supervision, Project administration

Competing interests
No competing interests declared
Cinzia Malangone

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Software, Supervision, Project administration

Competing interests
No competing interests declared
T Nguyen

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Software

Competing interests
No competing interests declared
Jim Stalker

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Software, Supervision

Competing interests
No competing interests declared
Ben Jeffery

MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom

Contribution
Software, Supervision, Visualization

Competing interests
No competing interests declared
Jonathan Keatley

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Software, Supervision, Visualization

Competing interests
No competing interests declared
Kimberly J Johnson
1. Wellcome Sanger Institute, Hinxton, United Kingdom
2. MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom
Contribution
Software, Visualization, Project administration

Competing interests
No competing interests declared
Dawn Muddyman

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Software, Project administration

Competing interests
No competing interests declared
Xin Hui S Chan
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Investigation, Project administration

Competing interests
No competing interests declared
John Sillitoe

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Resources, Supervision, Investigation, Project administration

Competing interests
No competing interests declared
Roberto Amato

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Resources, Software, Supervision, Validation, Investigation, Project administration

Competing interests
No competing interests declared
Victoria Simpson
1. Wellcome Sanger Institute, Hinxton, United Kingdom
2. MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom
Contribution
Conceptualization, Resources, Software, Supervision, Validation, Investigation, Project administration

Competing interests
No competing interests declared
Sonia Gonçalves

Wellcome Sanger Institute, Hinxton, United Kingdom

Contribution
Conceptualization, Software, Supervision, Validation, Investigation, Methodology, Project administration

Competing interests
No competing interests declared
Kirk Rockett
1. Wellcome Sanger Institute, Hinxton, United Kingdom
2. Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
Contribution
Conceptualization, Formal analysis, Supervision, Validation, Investigation, Methodology, Project administration

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0002-6369-9299
Nicholas P Day
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Resources, Formal analysis, Supervision, Validation, Investigation, Methodology, Project administration

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0003-2309-1171
Arjen M Dondorp
1. Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
Contribution
Resources, Formal analysis, Supervision, Investigation, Methodology, Project administration

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0001-5190-2395
Dominic P Kwiatkowski
1. Wellcome Sanger Institute, Hinxton, United Kingdom
2. MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom
Contribution
Conceptualization, Resources, Supervision, Funding acquisition, Investigation, Project administration, Writing - review and editing

Competing interests
No competing interests declared
Olivo Miotto
1. Wellcome Sanger Institute, Hinxton, United Kingdom
2. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand
3. MRC Centre for Genomics and Global Health, Big Data Institute, Oxford University, Oxford, United Kingdom
Contribution
Conceptualization, Resources, Data curation, Software, Formal analysis, Supervision, Funding acquisition, Investigation, Visualization, Methodology, Writing - original draft, Project administration, Writing - review and editing

For correspondence
olivo@tropmedres.ac

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0001-8060-6771

Funding

Bill and Melinda Gates Foundation (OPP11188166)

Dominic P Kwiatkowski
Olivo Miotto

Bill and Melinda Gates Foundation (OPP1204268)

Olivo Miotto

Wellcome Trust (098051)

Dominic P Kwiatkowski

Wellcome Trust (206194)

Dominic P Kwiatkowski

Wellcome Trust (203141)

Dominic P Kwiatkowski

Wellcome Trust (090770)

Dominic P Kwiatkowski

Wellcome Trust (204911)

Dominic P Kwiatkowski

Wellcome Trust (106698/B/14/Z)

Dominic P Kwiatkowski

Medical Research Council (G0600718)

Dominic P Kwiatkowski

Department for International Development, UK Government (201900)

Arjen M Dondorp

Department for International Development, UK Government (M006212)

Arjen M Dondorp

The funders had no role in study design, data collection, data analysis, data interpretation, or report writing. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication

Acknowledgements

We are grateful all patients and health workers who participated in sample collections. This study used data from the MalariaGEN Pf3k Project and Plasmodium falciparum Community Project. We thank the staff of Wellcome Sanger Institute Sample Logistics, Sequencing, and Informatics facilities for their contribution; in particular, we are grateful to the Wellcome Sanger Institute DNA Pipelines Informatics team for supporting the development of the methods used in this work. We thank the many collaborators who contributed to the GenRe-Mekong Project, and especially: Pannapat Masingboon, Narisa Thongmee, Zoë Doran, Salwaluk Panapipat, Ipsita Sinha, Rapeephan Maude, Vilasinee Yuwaree, Tran Minh Nhat, Hoang Hai Phuc, Ro Mah Huan, Nguyen Minh Nhat, Tran Van Don. PR is a staff member of the World Health Organization; PR alone is responsible for the views expressed in this publication and they do not necessarily represent the decisions, policy or views of the World Health Organization. This work was supported, in whole or in part, by the Bill and Melinda Gates Foundation [OPP11188166, OPP1204268]. Under the grant conditions of the Foundation, a Creative Commons Attribution 4.0 Generic License has already been assigned to the Author Accepted Manuscript version that might arise from this submission.

Ethics

Human subjects: For each country where the surveillance project was implemented in collaboration with public health authorities, we submitted a common GenRe-Mekong protocol, and obtained approval by a relevant local ethics review board and by the Oxford University Tropical Research Ethics Committee (OxTREC). In all countries we obtain informed consent from each malaria patient providing a sample, except for Laos, where the Ministry of Health has classified the project as routine surveillance for the benefit of the country, and removed the requirement for consent. Collaborating research studies included in their own protocol provisions for sample collection procedures and informed consent, compatible with those in the GenRe-Mekong protocol, and obtained ethical approval from both a relevant local ethics review board, and their relevant institutional research ethics committee.

Copyright

This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

Metrics

3,165

views
396

downloads
60

citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Mendeley

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

Christopher G Jacob
Nguyen Thuy-Nhien
Mayfong Mayxay
Richard J Maude
Huynh Hong Quang
Bouasy Hongvanthong
Viengxay Vanisaveth
Thang Ngo Duc
Huy Rekol
Rob van der Pluijm
Lorenz von Seidlein
Rick Fairhurst
François Nosten
Md Amir Hossain
Naomi Park
Scott Goodwin
Pascal Ringwald
Keobouphaphone Chindavongsa
Paul Newton
Elizabeth Ashley
Sonexay Phalivong
Rapeephan Maude
Rithea Leang
Cheah Huch
Le Thanh Dong
Kim-Tuyen Nguyen
Tran Minh Nhat
Tran Tinh Hien
Hoa Nguyen
Nicole Zdrojewski
Sara Canavati
Abdullah Abu Sayeed
Didar Uddin
Caroline Buckee
Caterina I Fanello
Marie Onyamboko
Thomas Peto
Rupam Tripura
Chanaki Amaratunga
Aung Myint Thu
Gilles Delmas
Jordi Landier
Daniel M Parker
Nguyen Hoang Chau
Dysoley Lek
Seila Suon
James Callery
Podjanee Jittamala
Borimas Hanboonkunupakarn
Sasithon Pukrittayakamee
Aung Pyae Phyo
Frank Smithuis
Khin Lin
Myo Thant
Tin Maung Hlaing
Parthasarathi Satpathi
Sanghamitra Satpathi
Prativa K Behera
Amar Tripura
Subrata Baidya
Neena Valecha
Anupkumar R Anvikar
Akhter Ul Islam
Abul Faiz
Chanon Kunasol
Eleanor Drury
Mihir Kekre
Mozam Ali
Katie Love
Shavanthi Rajatileka
Anna E Jeffreys
Kate Rowlands
Christina S Hubbart
Mehul Dhorda
Ranitha Vongpromek
Namfon Kotanan
Phrutsamon Wongnak
Jacob Almagro Garcia
Richard D Pearson
Cristina V Ariani
Thanat Chookajorn
Cinzia Malangone
T Nguyen
Jim Stalker
Ben Jeffery
Jonathan Keatley
Kimberly J Johnson
Dawn Muddyman
Xin Hui S Chan
John Sillitoe
Roberto Amato
Victoria Simpson
Sonia Gonçalves
Kirk Rockett
Nicholas P Day
Arjen M Dondorp
Dominic P Kwiatkowski
Olivo Miotto

(2021)

Genetic surveillance in the Greater Mekong subregion and South Asia to support malaria control and elimination

eLife 10:e62997.

https://doi.org/10.7554/eLife.62997

Share this article

Cite this article

Participating studies in GenRe-Mekong.

Map of GenRe-Mekong sample collection sites in Asia.

Neighbor-joining tree using barcode data to show genetic differentiation between parasites in the Thai-Myanmar and Thai-Cambodian border regions.

Drug resistance-related SNPs genotyped by GenRe-Mekong (excludes kelch13).

Frequencies of resistant parasites in provinces/states/divisions surveyed, for different antimalarials.

Map of the spread of (A) artemisinin resistance (ART-R) and (B) dihydroartemisinin-piperaquine resistance (DHA-PPQ-R) in Asian countries.

Figure 3—source data 1

Longitudinal sample counts and proportions of DHA-PPQ-R parasites in three provinces of Central Vietnam.

Figure 4—source data 1

Proportions of ART-R and KEL1/PLA1 parasites in southern Laos districts.

Figure 5—source data 1

Author details

Christopher G Jacob

Contribution

Competing interests

Nguyen Thuy-Nhien

Contribution

Competing interests

Mayfong Mayxay

Contribution

Competing interests

Richard J Maude

Contribution

Competing interests

Huynh Hong Quang

Contribution

Competing interests

Bouasy Hongvanthong

Contribution

Competing interests

Viengxay Vanisaveth

Contribution

Competing interests

Thang Ngo Duc

Contribution

Competing interests

Huy Rekol

Contribution

Competing interests

Rob van der Pluijm

Contribution

Competing interests

Lorenz von Seidlein

Contribution

Competing interests

Rick Fairhurst

Present address

Contribution

Competing interests

François Nosten

Contribution

Competing interests

Md Amir Hossain

Contribution

Competing interests

Naomi Park

Contribution

Competing interests

Scott Goodwin

Contribution

Competing interests

Pascal Ringwald

Contribution

Competing interests

Keobouphaphone Chindavongsa

Contribution

Competing interests

Paul Newton

Contribution

Competing interests

Elizabeth Ashley

Contribution

Competing interests

Sonexay Phalivong

Contribution

Competing interests

Rapeephan Maude

Contribution