Contrasting Transmission Dynamics of Co-endemic Plasmodium vivax and P. falciparum: Implications for Malaria Control and Elimination

Background Outside of Africa, P. falciparum and P. vivax usually coexist. In such co-endemic regions, successful malaria control programs have a greater impact on reducing falciparum malaria, resulting in P. vivax becoming the predominant species of infection. Adding to the challenges of elimination, the dormant liver stage complicates efforts to monitor the impact of ongoing interventions against P. vivax. We investigated molecular approaches to inform the respective transmission dynamics of P. falciparum and P. vivax and how these could help to prioritize public health interventions. Methodology/ Principal Findings Genotype data generated at 8 and 9 microsatellite loci were analysed in 168 P. falciparum and 166 P. vivax isolates, respectively, from four co-endemic sites in Indonesia (Bangka, Kalimantan, Sumba and West Timor). Measures of diversity, linkage disequilibrium (LD) and population structure were used to gauge the transmission dynamics of each species in each setting. Marked differences were observed in the diversity and population structure of P. vivax versus P. falciparum. In Bangka, Kalimantan and Timor, P. falciparum diversity was low, and LD patterns were consistent with unstable, epidemic transmission, amenable to targeted intervention. In contrast, P. vivax diversity was higher and transmission appeared more stable. Population differentiation was lower in P. vivax versus P. falciparum, suggesting that the hypnozoite reservoir might play an important role in sustaining local transmission and facilitating the spread of P. vivax infections in different endemic settings. P. vivax polyclonality varied with local endemicity, demonstrating potential utility in informing on transmission intensity in this species. Conclusions/ Significance Molecular approaches can provide important information on malaria transmission that is not readily available from traditional epidemiological measures. Elucidation of the transmission dynamics circulating in a given setting will have a major role in prioritising malaria control strategies, particularly against the relatively neglected non-falciparum species.


Introduction
Plasmodium vivax is a major global health burden, with an estimated 2.85 billion people living at risk of infection [1]. Rising levels of multidrug resistance and severe disease [2][3][4][5][6][7], and the demonstrated transmission amongst Duffy blood group-negative individuals [8][9][10][11][12], demand concerted efforts to control and eliminate the parasite. However, relative to the other major human malaria pathogen, P. falciparum, interventions against P. vivax have been less effective [13]. Critical to the success of control and elimination programs is the acquisition of data on the intensity and dynamics of local malaria transmission. Measures of transmission intensity have been used to inform public health interventions for P. falciparum [14], however the dormant hypnozoite stage of P. vivax result in its dynamics being far more challenging to interpret. Outside of Africa, P. vivax usually co-exists with P. falciparum. In these co-endemic regions, potential differences in the respective transmission of the two species further complicate decision-making on the prioritization of intervention activities.
Previous studies have demonstrated the utility of genotyping parasite population samples to inform on P. vivax and P. falciparum diversity, population structure and underlying transmission patterns . These molecular approaches complement the more traditional measures of transmission intensity. As well as providing an independent gauge of intensity, parasite genotyping can inform on other features of transmission such as outbreak dynamics, infection spread within and across borders, and reservoirs of infection [36]. However few studies have demonstrated the utility of genotyping to compare the transmission dynamics of co-endemic P. vivax and P. falciparum isolates [18,19,28]. A combination of the widely contrasting malaria epidemiology and the physical geography of the Indonesian archipelago rendered this an ideal setting within which to further address the comparative patterns of transmission in P. vivax and P. falciparum populations in multiple co-endemic sites.
Malaria remains a major public health burden in Indonesia, with over 400 thousand confirmed cases in 2012 representing just a fraction of the actual suspected burden [37]. Malaria caused by P. vivax infection is a particular concern in Indonesia owing to the occurrence of high-grade chloroquine-resistant infections [38,39]. In 2009, the Ministry of Health instigated a malaria control and elimination strategy to be rolled out island by island with the aim of achieving nation-wide malaria elimination by 2030. One of the greatest challenges in achieving this target is the extensive heterogeneity in malaria epidemiology across an archipelago comprising more than 6,000 inhabited islands. The country is characterised by marked variation in the incidence of malaria, distribution of Anopheles vectors, prevalence of anti-malarial drug resistance, and ethnic, cultural and socio-economic diversity [40]. Malaria caused by P. knowlesi is also an emerging problem in Indonesia. However, until recently, the burden of P. knowlesi malaria has not been comprehensively investigated in Indonesia, with only two published studies confirming the presence of this species [41,42]. Hence interventions need to be tailored to the epidemiological setting in question. Furthermore, the highly mobile population increases the risk of re-introduction of malaria to areas with no malaria transmission.
As a prerequisite to developing a comprehensive national surveillance for malaria transmission, we used simple genotyping methods to characterize the genetic diversity and structure of P. vivax and P. falciparum isolates collected between 2011 and 2013 at four Indonesian sites with differing endemicity. The resultant insights into the local P. vivax versus P. falciparum transmission dynamics are reviewed and interpreted in the context of the country's malaria elimination goals. The broader implications for prioritization of intervention strategies in other regions of the globe where the prevalence of non-falciparum malaria is rising are also discussed.

Study Sites and Sample Collection
The study was conducted in two sites on Bangka island (Bangka-Belitung, Sumatra), one site in Ketapang Province in West Kalimantan, two sites in Sumba (East Nusa Tenggara) and one site in West Timor (East Nusa Tenggara) (Fig 1). Details on the study sites are provided in S1 Table. Bangka, Sumba and West Timor are defined as moderate stable endemic or 'hypomesoendemic', and the Kalimantan site as unstable endemic [14]. Whilst Bangka and Ketapang have been assigned goals of elimination by 2015, the goals for Sumba and West Timor are to reach pre-elimination by 2020, with national malaria elimination by 2030. In all four study sites, dihydroartemisinin-piperaquine is used as the primary treatment for both P. vivax and P. falciparum malaria as recommended by the Ministry of Health since 2008. As well as malaria incidence, the study sites exhibit several socio-economic and ecological differences reflective of the heterogeneity generally found across the Indonesian archipelago. Whilst Bangka is the largest producer of tin in Indonesia, in Ketapang the main industries are palm oil and rubber production and logging. In East Nusa Tenggara the main economy is subsistence agriculture, with Sumba being one of the poorest islands in Indonesia. The available information on vector species demonstrates heterogeneity across the study sites [43]. Details on the bionomics of each species can be found on the Malaria Atlas Project website [44]. Briefly, in West and Central Bangka, the dominant malaria vectors appear to be Anopheles leucosphyrus, An. latens and An. sundaicus sensu lato. All three species/species complexes can transmit both P. vivax and P. The colour scales reflect the model-based geostatistical point estimates of the annual mean P. falciparum parasite rate in the 2-10 year age group (PfPR 2-10 ) (top) [45] and P. vivax parasite rate in the 1-99 year age range (PvPR 1-99 ) (bottom) [46] within the stable spatial limits of transmission in 2010. The approximate locations of the study sites described here are indicated with black stars. falciparum and tend to bite in the evening/night. Both endophilic and exophilic feeding behaviour has been demonstrated in An. sundaicus. s.l. and An. leucosphyrus. Whilst An. sundaicus. s.l. display varying degrees of indoor and outdoor resting, An. leucosphyrus and An. latens do not tend to rest indoors in the day. In Ketapang Province, An. balabacensis, An. leucosphyrus and An. latens are prevalent. An. barbirostris s.l. is also observed but likely to play little if any role in malaria transmission. An. balabacensis can transmit both P. vivax and P. falciparum, is largely exophagic, feeding in the evening/night. In East Nusa Tenaggarra, An. sundaicus s.l., An. balabacensis and An. flavirostis are prevalent. An. flavirostis is primarily zoophilic, displaying both endophagic and exophagic feeding in the evening/night. The vectorial capacity of this species in Indonesia remains unclear.
In Kalimantan, Bangka and Sumba, parasite DNA was collected by both active and passive detection of malaria-infected individuals, whilst in West Timor only active case detection was undertaken ( Table 1). Passive case detection involved symptomatic patients presenting to outpatient health clinics in West Bangka, a hospital in South West Sumba, and West Kalimantan. At these locations, local policy stipulates that all malaria treatment should be based on microscopic screening of thick blood films. Active case detection was performed either through community surveys or through screening of individuals with fever.
Following informed consent of the patient or their guardian, individuals with P. falciparum or P. vivax parasitaemia detected by blood film examination were asked to donate a venous (~1-2 ml) or capillary (~250 ul) blood sample collected into an EDTA-coated Vacutainer or

DNA Extraction and Species Confirmation
DNA extraction was undertaken using the QIAamp blood mini kit (Qiagen) according to the manufacturer's protocol. Plasmodium spp. was confirmed by PCR using the method described by Snounou et al. [47] and Boonma et al. [48].
Genotyping P. falciparum genotyping was undertaken at nine previously described short tandem repeat (STR) markers including ARAII, PfPK2, poly-alpha, TA1, TA42, TA60,TA81, TA87 and TA109, using the primers and PCR conditions described by Anderson and colleagues [49]. P. vivax genotyping was undertaken at nine previously described STR markers including Pv3.27, msp1F3, MS1, MS5, MS8, MS10, MS12, MS16 and MS20 [50,51]. These markers are included in a consensus panel selected by partners within the Asia Pacific Malaria Elimination Network (www.apmen.org). The Pv3.27, MS16 and msp1F3 loci were amplified using methods described elsewhere [15]. The protocol for the remaining loci and the details of the primer sequences and chromosomal locations for each marker have been provided previously [15,20].
The labelled PCR products were sized by denaturing capillary electrophoresis on an ABI 3100 Genetic Analyzer with GeneScan LIZ-600 (Applied Biosystems) internal size standards. Genotype calling was facilitated with GeneMapper Version 4.0. To reduce potential artefacts, an arbitrary fluorescent intensity threshold of 50 rfu was applied for peak detection. All electropherogram traces were additionally inspected manually. For each isolate, at each locus, the predominant allele and any additional alleles with minimum 33% height of the predominant allele were scored [49].

Population Genetic Analysis
An infection was defined as polyclonal if more than one allele was observed at one or more loci. The Multiplicity of infection (MOI) for a given sample was defined as the maximum number of alleles observed at any of the loci investigated. With the exception of measures of polyclonality and MOI, only the predominant allele at each locus in each isolate was used for analysis [49]. The expected heterozygosity (H E ) was measured as an index of population diversity using the formula , where n is the number of isolates analyzed and pi is the frequency of the ith allele in the population. The pairwise F ST metric was used to gauge the genetic distance between populations. Calculations were undertaken using Arlequin software (version 3.5) [52]. Standardized measures (F' ST ) were additionally calculated to adjust for high marker diversity [53]. Population structure was further assessed using STRUCTURE software version 2.3.3 [54]. Twenty replicates, with 100,000 burn-in and 100,000 post burn-in iterations were run for each of K (populations) from 1-10 using the model parameters of admixture with correlated allele frequencies. The most probable K was derived by applying the delta K method [55]. STRUCTURE results were displayed using bar plots prepared with distruct software version 1.1 [56]. Multi-locus haplotypes were reconstructed from the predominant allele at each locus in isolates with no missing data. Multi-locus linkage disequilibrium (LD) was measured by the standardised index of association (I A S ) using the web-based LIAN 3.5 software [57]. The significance of the I A S estimates was assessed using 10,000 random permutations of the data. For each population, LD was assessed in 1) all samples, 2) samples with a maximum of one multi-allelic locus, and 3) with each unique haplotype represented just once. The genetic relatedness between sample pairs was assessed by measuring the proportion of alleles shared between multi-locus haplotype pairs (ps). Using (1-ps) as a measure of genetic distance [58], an unrooted neighbourjoining tree [59] was generated with the ape package in R [60]. Mantel's r-test was used to assess the correlation between genetic and temporal distance using the ade4 package in R [61].

Statistical Tests
Statistical comparisons of patient gender ratio and infection polyclonality between sites and species were undertaken using Pearson's Chi-square test. The significance of difference between sites and species in patient age, parasite density and expected heterozygosity were assessed using the Mann-Whitney U test. Statistical comparison of the MOI between sites and species was undertaken using the Kruskal-Wallis test and Mann-Whitney U test, respectively. All tests were performed using R software, with a significance threshold of 0.05.

Ethical Approval
Ethical approval for this study was obtained from the Eijkman Institute Research Ethics Commission (EIREC) number 45/2011. Written informed consent was obtained from all adults or a parent or guardian for participants less than 18 years of age.

Patient Sampling
Between October 2011 and July 2013, a total of 334 blood samples were collected from malaria-infected individuals across the 4 sites (Table 1). With the exception of Kalimantan, where caution is advised in data interpretation, a minimum of 30 isolates were available for each species in each site. In Bangka and Sumba, malaria-positive individuals detected by both active (ACD) and passive case detection (PCD) contributed a moderate proportion of all samples. Comparison between these sample subsets did not however identify significant differences in sample diversity for either P. falciparum or P. vivax (S2 Table). Studies in other endemic regions have found similar results [62][63][64][65][66]. Therefore, ACD and PCD infections were pooled for subsequent analyses. In Bangka and Kalimantan, the majority of patients were young adults. No significant difference was observed in the median age between P. vivax (25 years, range: 1-50) and P. falciparum patients (26 years, range: 1-72) (P = 0.223). In Bangka, the median age of PCD patients with P. vivax (27 years, range: 3-50) was 2 years older than the ACD patients (25 years, range: 1-45) (P = 0.021). In the same population, a 5 year difference was observed in the median age of the P. falciparum PCD (25 years, range: 5-72) versus ACD (30 years, range: 3-50) patients but the difference was not significant (P = 0.389). In Sumba and West Timor, the patient demographic was younger, with a significant difference in age between P. vivax (median 6 years, range: 0-54) and P. falciparum cases (median 13 years, range: 1-67) (P = 3.08 x 10 -5 ). In Sumba, the median age of PCD patients with P. vivax (30 years, range: 5-54) was 25 years older than the ACD patients (5 years, range: 0-30) (P = 3.7 x 10 -4 ), although caution is advised in interpretation owing to the modest sample size of the former group (n = 9). The median age of P. falciparum PCD patients (15 years, range: 1-54) was also higher than the ACD patients (9 years, range: 3-65) but the difference was not significant (P = 0.060).
Relative to the two western provinces (78% males), the representation of male patients was less skewed in Sumba and West Timor (55% males) (P = 1.78 x 10 -5 ). In Bangka, the proportion of males was significantly higher amongst PCD versus ACD groups in both P. vivax (92% vs 65%, P = 0.005) and P. falciparum (89% vs 59%, P = 0.021). In Sumba, no significant difference was observed in gender proportions between PCD and ACD groups in either species (both P >0.05).
No significant difference was observed in the median parasite density (parasites ul -1 blood) between P. falciparum (3,099 ul -1 , range: 32-755,400) and P. vivax (2,110 ul -1 , range: 48-529,600) (P = 0.057). In both species, parasite density was significantly lower in ACD versus PCD patients. In P. vivax, the median parasite density was 1,126 ul -1 (range: 48-87,770) in ACD versus 6,551 ul -1 (range: 73-529,600) in PCD (P = 1.25 x 10 -5 ). In P. falciparum, the median parasite density was 1,412 ul -1 (range: 32-446,439) in ACD versus 21,160 ul -1 (range: 198-755,400) in PCD (P = 7.28 x 10 -11 ). In P. vivax, no significant difference was observed between the sites in the parasite density in the PCD (P = 0.097) or ACD (P = 0.261) patients. In P. falciparum, no significant difference was observed between the sites in the parasite density in the PCD (P = 0.084) patients. A significant difference was observed amongst the P. falciparum ACD patients (P = 8.01 x 10 -5 ), largely reflecting the low parasite density in West Timor (median = 480 ul -1 ). The various differences observed in parasite density justified the implementation of the 33% predominant peak height threshold for calling additional alleles to reduce potential bias in characterising polyclonal infections.
The distribution of allele frequencies at each marker is illustrated in S1 Fig, and measures of diversity in each population are presented in S5 Table. With the exception of the TA109 locus, where the predominant allele accounted for 96.2% of all alleles, all loci exhibited a minimum of one allele with minor allele frequency 5%. Owing to the low level of polymorphism, the TA109 locus was excluded from further analysis. After exclusion of the TA109 locus, the only observations of monomorphic loci within populations were at the TA42 and TA60 loci in Kalimantan, and the TA1 locus in West Timor (S5 Table). These loci were therefore excluded from the analysis of LD in the given populations.

Within-host and Population Diversity
A summary of polyclonality, MOI and population diversity is presented in Table 2. Variation was observed in the proportion of polyclonal P. falciparum infections (0-20%) and mean MOI (1-1.23) across sites, although none of the differences reached statistical significance. In contrast, the variation in the polyclonality of P. vivax infections (23-79%) was highly significant (P = 0.0002), as was the variation in mean MOI (1.23-1.90); P = 0.0002. Across the sites, higher proportions of polyclonal infections (P = 1.042 x 10 -12 ) and higher mean MOI (P = 4.39 x 10 -13 ) were observed in P. vivax versus P. falciparum. In P. falciparum, 41.7% (10/24) of polyclonal infections were multi-allelic at just one of the nine loci. A similar proportion of the polyclonal P. vivax infections, 38% (33/87) were multi-allelic at just one locus. In both P. falciparum and P. vivax 95% or more polyclonal infections could be identified with the seven most diverse markers. P. falciparum population diversity varied between sites (H E = 0.397-0.715), with the highest diversity observed in Sumba. The differences between Sumba and each of Bangka (P = 0.031) and Kalimantan (P = 0.024) reached significance. Less variation was observed between the sites for P. vivax infections (H E = 0.806-0.856) (all P > 0.05). The diversity in P. vivax was consistently higher than in sympatric P. falciparum populations, reaching significance in Bangka, Kalimantan and West Timor (all P 0.001) but not Sumba (P > 0.05).

Population Structure and Differentiation
With the exception of Sumba and West Timor (F ST = 0.087; P <1 x10 -5 ), the differentiation between the P. falciparum populations was high (F ST range: 0.238-0.415; all P <1 x10 -5 ) ( Table 3). Differentiation was lower in P. vivax (F ST range: -0.003-0.066), with significance in all comparisons (all P <1 x10 -5 ) with the exception of Kalimantan, possibly reflecting the limited sample size. STRUCTURE analysis demonstrated clear sub-structure in the P. falciparum population (Fig 2). The delta K method demonstrated K = 2 as having the greatest likelihood (S2 Fig). At K = 2, the large majority of isolates from Bangka and Kalimantan, and approximately one third from West Timor demonstrated predominant ancestry to the K1 cluster, whilst all isolates from Sumba and the remaining two thirds from West Timor demonstrated predominant ancestry to the K2 cluster. At higher estimates of K, greater distinction was observed between the two eastern (Sumba and West Timor) populations, and increasing sub-structure was observed within West Timor. In P. vivax, the delta K method identified K = 5 as the most likely number of sub-populations (S2 Fig). However, the large majority of isolates from all 4 populations demonstrated mixed ancestry to the various clusters (Fig 3).

Relatedness
Neighbour-joining analysis demonstrated moderately distinct separation between the western and eastern P. falciparum isolates (Fig 4). Clusters of isolates with 4 or more identical or nearidentical multi-locus haplotypes were observed in Bangka and West Timor, whilst the Sumba isolates were generally less related to one another.
Fewer identical isolates were observed in P. vivax relative to P. falciparum. The isolates from West Timor largely clustered together, and four identical isolates were observed in this population. Two of the identical isolates were collected on the same day, and the other two were both collected four days later. Within these sampling dates, other more distinct isolates were also collected. Nonetheless, a significant correlation was observed between the distance in sampling date and the proportion of alleles shared between the P. vivax infections in West Timor (Mantel r-test, r = 0.12, P = 0.02). Relative to P. falciparum, little distinction was observed between the P. vivax infections from the other three sites. With the exception of the P. vivax population in West Timor, no significant correlation was observed between the distance in sampling date and the proportion of alleles shared between infections for P. falciparum or P. vivax.   Contrasting Transmission of Co-endemic P. vivax and P. falciparum

Linkage Disequilibrium
In P. falciparum, LD ranged from an I A S of 0.018 to 0.239 (all P 0.05) ( Table 4). However, after removing duplicate haplotypes, the I A S levels dropped more than two-fold in each of Bangka, Kalimantan, and West Timor. In P. vivax, significant LD was observed in Bangka, Sumba and West Timor (I A S = 0.017-0.188; all P < = 0.003), but not Kalimantan (I A S = -0.003; P > 0.05). Identical isolates were less frequent than in P. falciparum, and the I A S scores from the unique multi-locus data sets retained equivalent significance to the unfiltered data sets.

Discussion
The heterogeneous epidemiology of malaria in Indonesia provided an opportunity to investigate the comparative transmission dynamics of co-endemic P. vivax and P. falciparum isolates in multiple settings. Using molecular approaches, we demonstrated striking contrasts in diversity and population structure, indicative of varying transmission patterns within and between the two species in different endemicities. A range of patterns were observed in P. falciparum diversity and structure across the sites. In all populations, polyclonal infection rates (0-20%) were comparable to rates observed in low endemic settings in Southeast Asia [17,23], South America [16,26] and post-intervention sites elsewhere [19,30], suggestive of low transmission and infrequent superinfection. Greater variation was observed in the population diversity (H E = 0.397-0.715). The highest level of diversity was observed in Sumba, reflecting the higher prevalence in this population relative to the other three sites. Whilst the population diversity in Sumba was comparable to levels observed in hyper-holoendemic regions common to Africa [16,27,30], Bangka, Kalimantan and West Timor were more similar to hypo-mesoendemic and unstable endemic regions of South America [16,26] and Southeast Asia [17,23,29]. Relative to Sumba, the latter three populations also exhibited higher levels of LD.  Owing to pooling of P. falciparum samples collected from two regencies (West and Central Bangka), as well as population sub-structure, one possible explanation for the significant LD observed in Bangka was admixture. However, STRUCTURE analysis demonstrated that the majority of isolates in Bangka exhibited predominant ancestry to a single population. In contrast, although sampled from a single administrative district, STRUCTURE analysis indicated that the West Timor population comprised isolates from at least two sub-populations. Thus, admixture may have contributed to the LD observed in West Timor. As demonstrated by the greater than two-fold decline in the index of association (I A S ) after accounting for identical multi-locus haplotypes, epidemic expansions also appear to have contributed to the LD observed in West Timor, as well as in Bangka, and Kalimantan. In accordance with epidemic dynamics, clusters of isolates with identical multi-locus haplotypes were prevalent in these populations. Whilst it is possible that the modest number of loci reduced the ability to discriminate between different 'strains', the high diversity observed in Sumba suggests that the resolving capacity was adequate.
In concert, the observed trends in diversity and LD demonstrated a pattern of low, epidemic P. falciparum transmission in Bangka, Kalimantan and West Timor. These trends are consistent with Ministry of Health data on malaria incidence in these regions, where P. falciparum endemicity is characterised as unstable endemic to hypo-mesoendemic. Relative to Sumba, patients from Bangka, Kalimantan and West Timor were older (largely teenagers and young adults), with a higher proportion of males in Bangka and Kalimantan. These demographics might in part reflect at-risk populations such as particular occupational groups, and might explain some of the epidemic transmission dynamics. In contrast to the other populations, the high diversity and linkage equilibrium in Sumba indicated that local P. falciparum transmission remained disconcertingly high and stable in this region. In accordance, the endemicity in Sumba lay at the higher end of the hypo-mesoendemic spectrum, and the P. falciparum patient demographic largely reflected children, with limited gender bias.
As discussed with the specific examples from our data in Indonesia, the heterogeneity in the dynamics of P. falciparum transmission across populations has important implications for elimination. Although Sumba and West Timor are grouped in the same target category for elimination by the national malaria elimination program (elimination by 2020), our data demonstrates that they would likely benefit from different intervention activities. The P. falciparum dynamics in Sumba demonstrate the need for total coverage intervention activities such as broad-ranging distribution of long lasting insecticide-treated bed nets. In contrast, more targeted approaches such as reactive case detection and treatment or indoor residual spraying targeted to households in transmission hot-spots or at-risk populations would be more costeffective in West Timor [14]. We note that present MOH policies in these regions, based upon passively reported confirmed malaria cases, are consistent with the results of our genetic analysis. With greater sample size, further investigation of both the parasite and patient dynamics should enable identification of at-risk populations for target intervention in West Timor, Bangka and Kalimantan.
Differentiation between the P. falciparum populations was generally high, comparable to levels observed in Malaysian Borneo, where declining transmission and limited migration led to a fragmented parasite population [17]. The declining transmission, distance and island setting should all have facilitated the isolation of the parasite populations assessed here. However, differentiation remained moderate between Sumba and West Timor, highlighting the challenge of parasite introductions into West Timor from the stable transmission setting of Sumba. Indeed, the demonstration of multiple distinct sub-populations by STRUCTURE analysis indicated that other populations such as neighbouring Timor-Leste may present additional reservoirs of infection to West Timor. Identifying the major reservoirs sustaining infection in such populations will be paramount to the success of Indonesia's elimination campaign. Other global populations will no doubt face similar challenges in the strive toward elimination.
Albeit less marked than in P. falciparum, variation was also observed between sites in P. vivax diversity and structure. Polyclonal infection rates ranged from 23 to 79%, in broad agreement with local API estimates, indicating potential utility in informing on transmission intensity. In the eastern provinces, where patient demographics largely reflected young children, within-host diversity was comparable to high transmission regions of the Pacific [24], Southeast Asia [20,28] and the Horn of Africa [20]. In the western provinces, patient demographics were skewed toward young adults, with a high proportion of males in Bangka. In these populations, within-host diversity was more comparable to post-intervention sites in the Pacific [19] and Malaysia [15]. Relative to the sympatric P. falciparum populations, within-host diversity was consistently higher in P. vivax, in accordance with other studies [18,19,28]. The available evidence suggests that the hypnozoite reservoir and the early, often pre-treatment, development of gametocytes in P. vivax likely explain these observations, and thus have implications for P. vivax control and elimination in other endemic populations.
In contrast to within-host diversity, as demonstrated in other studies across a range of endemic sites across the globe [18][19][20][21][22]24,25,33,50], P. vivax population diversity was high in all four sites (H E = 0.81-0.86), with no apparent correlation with endemicity. Furthermore, the P. vivax populations demonstrated consistently higher diversity than their sympatric P. falciparum populations. The factor(s) responsible for these trends remain unclear. A plausible explanation is that relapsing infections, by enhancing infection complexity, increase the probability that different clones are taken up in the mosquito blood meal, thus promoting the opportunity for new variants to be generated via recombination. However, in temperate regions such as Central China and South Korea, relapse rates are low (20%) and yet P. vivax population diversity remains comparably high [22,25]. Another non-mutually exclusive possibility is that imported infections sustain the diversity of local P. vivax populations [22,67].
The observation of significant LD in P. vivax populations with extensive within-host and population diversity presents a conundrum also encountered in other studies [18,20,21,28,34,67]. Possible explanations for this include a frequently clonal (non-recombining) mode of propagation and/or potential artefact such as selection at or near several of the markers used [28].
In contrast to the P. falciparum populations, the LD patterns in P. vivax did not demonstrate evidence of epidemic transmission in any of the populations investigated. In concert with the observed differences in within-host and population diversity, the differences in LD demonstrated that in several of the endemic settings investigated here, the P. vivax isolates exhibited more frequent and stable transmission than their P. falciparum counterparts. Hence different interventions may be optimal for the respective malaria species in certain settings; local intervention strategies will need to reconcile these differences to ensure adequate impact against all species of malaria. For example, in Bangka, it appears that ongoing interventions have effectively reduced the intensity of local P. falciparum transmission. The current dynamics are moderately unstable with frequent clonal outbreaks amenable to containment by targeted approaches such as reactive case detection and treatment, and indoor residual spraying of case and surrounding households where the predominant vector species behaviour is compatible, prioritizing cases with rapidly emerging outbreak strains. However, the available evidence indicates that targeted approaches would be less effective for the co-endemic P. vivax population. Likely owing to biological differences between the two species such as the hypnozoite stage or comparatively early development of gametocytes in P. vivax versus P. falciparum, the Bangka P. vivax population appeared to have been less impacted by ongoing interventions than the P. falciparum population, displaying more stable transmission with no evidence of clonal outbreaks. These patterns suggest that broad ranging interventions such as large-scale long lasting insecticide-treated bed net coverage are still needed against P. vivax. In addition, effective treatment of the dormant liver stage may be critical to the success of P. vivax intervention efforts.
In contrast to P. falciparum, genetic differentiation was generally low in P. vivax. This observation might reflect the enhanced 'mobility' of the parasite afforded by the asymptomatic hypnozoite reservoir, with important implications for the containment of infection, particularly with the rise of anti-malarial drug resistance in P. vivax infection [68]. Alternatively, as discussed by Koepfli and Orjuela-Sanchez, observed trends in P. vivax population diversity and differentiation may in part reflect older, historical events [24,28]. A better understanding of the mechanisms sustaining the diversity, and limiting the observed genetic differentiation between geographically isolated P. vivax populations will be critical to the successful elimination of this species.

Conclusions
Concerted efforts are required to target the major reservoirs of P. vivax infection if malaria elimination is to be successful in co-endemic regions. A better understanding of the local variation in how frequently parasites are transmitted, how focal these transmission events are in time and space, and the 'mobility', or potential for parasite spread, can facilitate more optimal malaria intervention strategies. Parasite genotyping can provide useful insights on these dynamics, providing a complementary surveillance tool to the more traditional epidemiological measures, particularly in regions where non-falciparum species circulate.
Supporting Information S1 Table. Site details. 1 2010 Census. 2 Annual parasite incidence (API) expressed as cases per 1000 population of the administrative region examined (year of investigation and percentage of the population at risk examined are provided in parentheses). Details on the API were provided by Dr Iqbal Elyazar, Malaria Atlas Project. (DOCX) S2 Table. Within-host and population diversity in P. falciparum and P. vivax in passive versus actively detected cases from Bangka and Sumba. (DOCX) S3