Genetic diversity of Plasmodium falciparum among school-aged children from the Man region, western Côte d’Ivoire
© Mara et al.; licensee BioMed Central Ltd. 2013
Received: 5 August 2013
Accepted: 12 November 2013
Published: 15 November 2013
The genetic diversity of Plasmodium falciparum allows the molecular discrimination of otherwise microscopically identical parasites and the identification of individual clones in multiple infections. The study reported here investigated the P. falciparum multiplicity of infection (MOI) and genetic diversity among school-aged children in the Man region, western Côte d’Ivoire.
Blood samples from 292 children aged seven to 15 years were collected in four nearby villages located at altitudes ranging from 340 to 883 m above sea level. Giemsa-stained thick and thin blood films were prepared and examined under a microscope for P. falciparum prevalence and parasitaemia. MOI and genetic diversity of the parasite populations were investigated using msp2 typing by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).
Plasmodium falciparum prevalence and parasitaemia were both found to be significantly lower in the highest altitude village. Genotyping of the isolates revealed 25 potentially new msp2 alleles. MOI varied significantly across villages but did not correlate with altitude nor children’s age, and only to a limited extent with parasitaemia. An analysis of molecular variance (AMOVA) indicated that a small, but close to statistical significance (p = 0.07), fraction of variance occurs specifically between villages of low and high altitudes.
Higher altitude was associated with lower prevalence of P. falciparum but not with reduced MOI, suggesting that, in this setting, MOI is not a good proxy for transmission. The evidence for partially parted parasite populations suggests the existence of local geographical barriers that should be taken into account when deploying anti-malarial interventions.
KeywordsPlasmodium falciparum msp2 Genetic diversity PCR-RFLP Côte d’Ivoire
The widespread genetic diversity of Plasmodium falciparum populations plays an important role on several aspects of parasite biology, and consequently on the efficacy of anti-plasmodial interventions. For example, polymorphic elements and genetic plasticity contribute to modulate malaria morbidity and mortality and play a key role in P. falciparum immune evasion and the parasite’s adaptation to evolving environmental conditions such as drug pressure [1, 2]. This highly polymorphic nature can also be harnessed to study the structure and dynamics of parasite populations (see, for example, references [3, 4]) and molecular investigations in epidemiological studies and clinical trials, allowing discrimination between re-infection and recrudesce . This is typically achieved by typing one or more of three highly polymorphic genes: msp1 (merozoite surface protein 1), msp2 (merozoite surface protein 2), and glurp (glutamate-rich protein), which encode antigenic proteins of poorly characterized functions .
Studies pertaining to the genetic diversity of P. falciparum have been essentially comparing either very distant locations (e.g. intercontinental or spread within one or several countries, see [7–11]), or a small number of epidemiologically very distinct locations [12–15] and reported observations on the complex interplay between transmission intensity, the multiplicity of infection (MOI) with Plasmodium and the genetic structure of local parasite populations. High transmission settings have been frequently, but not always, associated with greater genetic diversity and MOI [16, 17].
The study protocol was approved by the institutional research commission of the Swiss Tropical and Public Health Institute (Basel, Switzerland) and the Centre Suisse de Recherches Scientifiques en Côte d’Ivoire (Abidjan, Côte d’Ivoire). Ethical clearance was obtained from the Ministry of Health in Côte d’Ivoire. Regional health and education authorities, village leaders (chief, school director and teachers) and parents of school-going children were informed about the purpose and procedures of the study. Written informed consent was obtained from parents/legal guardians, whereas children assented orally. Participation was voluntary and children could withdraw anytime without further obligations.
Study sites and population
The study sites are located in the Man region in western Côte d’Ivoire, where P. falciparum is hyperendemic . It is a humid forest area with a dense river network that drains the entire region . The northern part of the study area is mountainous whereas the southern part is a plain.
Between October 2001 and February 2002, 57 villages of this area were investigated to study the spatial distribution of infections with Plasmodium spp. [20, 21], Schistosoma mansoni[18, 25], and hookworm  among school-aged children. For the present study, a subset of four villages was selected, namely (i) Bogouiné II (geographical coordinates: 7 09.000 N latitude, 7 45.000 W longitude, 340 m above sea level); (ii) Bloleu (6 52.250 N, 8 16.333 W, 346 m); (iii) Mélapleu (7 32.800 N, 7 39.000 W, 529 m); and (iv) Sandougou-soba (7 35.833 N, 7 28.916 E, 883 m). The villages are located in a close range, at 120 km maximal distance, but in contrasting geographical settings with a maximal altitude difference of approximately 540 m. Mélapleu and Sandougou-soba are located northwest of Man, in the mountainous area, whereas Bogouiné II and Bloleu are located south of Man in a plain (Figure 1).
As described in detail elsewhere , all primary school children attending grades 3-5 were invited to participate. The study population in the four selected villages consisted of 292 school-going children, aged between seven and 15 years. Anti-malarial treatments were given to children with malaria-related symptoms (e.g. headache) and axillary temperature ≥37.5°C. Children found with helminth eggs in their stool were given anthelminthic drugs (i.e. praziquantel, 40 mg/kg against S. mansoni; albendazole, 400 mg against soil-transmitted helminths) [18, 19].
Sampling and molecular analysis
Finger-prick whole blood samples were obtained from each child. Thick and thin blood films were prepared on microscope slides and air-dried. Additionally, approximately 200 μl of blood was collected into microtainer tubes. Samples were transferred to a laboratory in the town of Man. Slides were stained with 10% Giemsa and forwarded to a laboratory in Abidjan, where they were examined under a microscope by experienced laboratory technicians for Plasmodium species identification and parasitaemia, assuming a count of 8,000 leukocytes per μl of blood [20, 21]. Microtainers were stored at −20°C pending molecular analyses.
Blood samples were thawed on ice and used for Plasmodium DNA extraction, msp2 nested polymerase chain reaction (PCR) amplification and analysis by restriction fragment length polymorphism (RFLP), as described elsewhere [26–28]. Briefly, 10 μl of whole blood were washed twice in cold sodium phosphate buffer (5 mM, pH 8.0), boiled for 10 min in 50 μl of sterile ddH2O and centrifuged at 14,000 g for 10 min. Next, 5 μl of the supernatant were used for the P. falciparum msp2 nested PCR reactions. The presence of PCR amplification products was determined using ethidium bromide stained 1% agarose gel photographed under UV illumination. PCR amplification products were digested with HinfI restriction enzymes. Restriction digest products were resolved on a 10% acrylamide gel subsequently stained with ethidium bromide and photographed under UV illumination.
The size of restriction fragments was determined using the ImageJ software  together with the MolWT macro (supplied by PHASE GmbH; Luebeck, Germany). Allelic determination was performed as recommended previously and using 10 bp bins for the 3D7 variable fragment .
The data were entered into Microsoft Excel 2007 and analysed using Prism version 6.0c or GenAlEx version 6.5 [30, 31]. The number of effective alleles was calculated as [1/Σpi2], the Shannon’s information index as [−1*Σ(pi*Ln(pi)], the haploid genetic diversity as [1-Σpi2], and the theoretical probability of two clones to share the same genotype as [Σpi2], where n is the sample size and pi the frequency of allele i.
Plasmodium falciparum prevalence and parasitaemia
Overall, 292 blood samples from four selected villages were analysed by PCR for the presence of P. falciparum parasites. A total of 241 samples were found positive, resulting in a prevalence of 82.5%, which is slightly higher than the prevalence originally determined by microscopy, at 78.8% (see Additional file 1). For all subsequent analyses, the 27 samples found positive by PCR but negative by microscopy, were assigned a parasitaemia of four parasites/μl of blood. The prevalence in Bogouiné II, Bloleu and Mélapleu were 87.0%, 89.7% and 88.5%. A significantly lower prevalence was found in Sandougou-soba (57.4%), the village at the highest altitude (p < 0.01, χ2-test).
Plasmodium falciparum prevalence and parasitaemia at the study sites
Altitude (m above sea level)
Sampling date (dd.mm.yyyy)
P. falciparum- infected (%)b
Parasitaemia (95% CI)c
msp2 genotyping and multiplicity of infection
msp2 allele type
P. falciparum infection
Mean MOI (SD)b
Details of potentially new msp2 alleles
Hinf I fragment sizesa
Overall, 694 distinct P. falciparum infections were recorded from the 241 PCR-positive samples analysed. MOI, that is the number of clonal infection per individual, ranges from 1 to 8, with a mean of 2.88 (Table 2). The mean MOI were found to be significantly different across the study sites with values ranging from 2.32 to 3.42 (Table 2). This difference occurs between the geographically related villages and does not seem to correlate with the site-specific P. falciparum prevalence or mean parasitaemia. For instance, the highest parasitaemia GM (425.0) was observed in Bogouiné II, where the lowest mean MOI was found (2.32).
Relationship between MOI and age or parasitaemia
Plasmodium falciparum genetic diversity
Plasmodium falciparum prevalence and parasitaemia, contrary to MOI, appear to be linked to some extent with the geographical location of the study sites. To further explore the specificity of the investigated sites, the site-specific P. falciparum genetic diversities were assessed.
Plasmodium falciparum genetic diversity at the study sites
Nevertheless, the haploid diversity indices were found to be very similar, with values close to 1 in all villages. Similarly, the Shanon’s information indices are relatively high, approaching or exceeding 3.5, in all populations. These two indices are indicative of a similarly high degree of diversity and evenness across study locations, suggesting that the local parasite populations investigated are genetically similar and display the same degree of diversity.
Two-setting nested analysis of molecular variance (AMOVA)
% of total variation
ϕ RT 0.001
Among populations within settings
ϕ PR −0.001
Among all populations
ϕ PT 0.000
A detailed molecular profiling and genetic diversity analysis of P. falciparum in four villages of a hyperendemic area of western Côte d’Ivoire is presented. The study sites were chosen for their relative closeness and contrasted geographical settings, with two villages located in a plain area and two in mountainous area. The P. falciparum prevalence, as determined by PCR, was found to be close to that previously reported by microscopy and above 85% in all villages except Sandougou-soba, the most elevated village, where it was measured to be 57.4% and where the parasitaemia GM was also found to be significantly lower. Importantly, the average age of participating children, a potential confounding factor for estimating P. falciparum prevalence and parasitaemia, is comparable from one village to another (Table 1), suggesting that geographical factors might be underlying these differences in the local parasitological pictures. This is in line with several previous studies reporting reduced malaria prevalence at higher altitude, with African highlands, at elevation of 1,500 m above sea level and higher, being generally malaria free but subject to epidemics [34–36]. Lower temperatures at high altitude reduce the development rates of both mosquitoes and Plasmodium parasites, preventing optimal transmission. At intermediate altitude, the fact that hilly environments are less susceptible to stagnant water bodies, which are potential mosquito breeding sites, might also play a role in locally reduced transmission . It is, however, not clear whether these, or other factors, are responsible for the lower malaria prevalence and parasitaemia levels observed in Sandougou-soba.
The genetic diversity of the P. falciparum populations was characterized using msp2 typing, whose higher discriminatory power, as compared to other polymorphic genes, is particularly relevant in hyperendemic areas . The overall theoretical probability to have two clones sharing the same genotype in this study is of 3.4%, which is below the maximal value of 5% recommended by others , and warrants the use of msp2 as a single marker for genotyping in this context. The genotyping methodology employed in the current study is based on electrophoresis in polyacrylamide gels coupled with computer-assisted fragment sizing using free software. This approach is well adapted to resource-limited settings and was found to be only marginally less precise than more costly methods based on capillary electrophoresis [17, 38].
A total of 85 distinct msp2 alleles were found in the current study and revealed 25 alleles not yet reported elsewhere, expending on a previous study of msp2 genetic diversity in Côte d’Ivoire . Two newly identified FC27 alleles, Cot13 and Cot14, display deletion in the 137 bp fragment, while an insertion is apparent in Cot31, possibly due the amplification of a 9 bp unit . Some of the potentially new 3D7-type allele display an unusual fragment of approximately 45 bp (Cot18, Cot27 and Cot28), which might be similar to the 51 bp fragment previously observed in Tanzania . Altogether, the limit in precision for fragment size determination does not exclude that some of these potentially new alleles are similar to the ones already described in the literature (e.g. Cot27 appears relatively similar to Ifa6; Cot31 to Ifa34) and sequencing would be required to univocally characterize these msp2 alleles. Altogether, Wos3 is the most prevalent allele, similarly to what has been observed in south-central Côte d’Ivoire, and two of the newly described alleles in this earlier study were also observed here (Cot5 and Cot6) at low frequencies .
Apparent MOI is often used as surrogate for transmission, with higher multiplicity of infections observed in those areas where transmission is particularly high . Consequently, correlations between MOI and parasitaemia or age have been reported [11, 17, 32, 41–43]. In these studies, higher MOI are associated with higher parasitaemia and with younger age, possibly due to lower semi-immunity . The complex interplay between MOI, parasitaemia, age and transmission is not fully understood and other studies failed to report correlations between these parameters, suggesting setting-specific relationships [9, 45–47]. In the present investigation, significant differences in MOI averages across the four villages were observed, but with no apparent link with P. falciparum prevalence, parasitaemia, village altitude or sampling date (Table 1), the last being a potential confounding factor. A low multiplicity was found in Sandougou-soba, where the lowest prevalence and average parasitaemia were observed, but an equally low multiplicity was also apparent in Bogouiné II, where these parameters were comparatively higher. The factors involved that might explain local differences in MOI are currently not understood. When considering the four villages together, no clear relation was found between age and MOI and only a limited relation with parasitaemia. It appears that in the context of this study, no clear link can be made between MOI and P. falciparum prevalence or parasitaemia and, by extension, transmission or with altitude. This is contrasting with a previous study in Kenya, where highland infections display a significantly lower average MOI as compared with lowland areas . The reasons for this difference are unknown and the intrinsic limitations of the current MOI measurements, which are by definition underestimating the real multiplicity of infection, due to clone fluctuation, parasite sequestration in deep vasculature, failure to distinguish different clones or true multiple infections by similar clones, might play a role. Nevertheless, these limitations would be expected to operate equally in all villages and therefore to bias absolute values but not relative comparison.
The msp2 typing data were also used to evaluate the genetic diversity present in each of the study sites. It can be expected that lower transmission, observed at higher altitude, might result in lower genetic diversity. This hypothesis is supported by the lower number of effective alleles found at higher altitudes. This value can be biased by the sample size, so the most relevant comparison occurs between Bloleu (low altitude) and Mélapleu (high altitude), where an equal number of distinct alleles were observed out of a similar number of infections but with a marked difference in the number of effective alleles, that is 33.2 and 27.4, respectively. A similar trend can be observed, but to a much lower extent, when considering other measures of diversity, such as Shannon’s information index and the haploid genetic diversity, which is nearing its maximum value of one in all villages, similar to values previously observed in sub-Saharan Africa . A low but close to significance degree of genetic variance is apparent between villages of plain and mountainous areas, suggesting the existence of a partially effective partition between the parasite populations of these locations. This is contrasting with a similar study conducted in Uganda, where no difference in strain distribution was observed when comparing villages located in an area of the same scale as the one considered here . The current analysis is intrinsically limited by the fact that only one locus was investigated. It is conceivable that the typing of additional loci, including microsatellites, might have revealed stronger genetic differences. Moreover, the fact that msp2 is under immune selection might partially mask the true genetic diversity of the populations investigated here. It would also be important to evaluate the temporal evolution of the genetic structures, as time has been identified as a diversity factor almost as important than geographical location in various transmission settings [15, 48].
The current study revealed marked differences in P. falciparum epidemiological and genetic factors within a context of hyperendemicity. Significant differences in prevalence and parasitaemia as well as signs of population partitions could be observed within a distance of approximately 120 km. The local topography in the Man region might partially govern these differences, suggesting the existence of geographical barriers susceptible to locally isolated parasite populations in Côte d’Ivoire. It would be interesting to measure the current genetic diversity in the four study villages in order to evaluate the evolution of the diversity over the past decade. The malERA consortium has highlighted the need for better tools and maps to guide malaria elimination , and the identification of natural or human-related barriers defining distinct or partially distinct populations will contribute to address this need. The identification of partially isolated parasite populations might be relevant to guide local malaria elimination intervention when a geographically limited area is targeted.
We thank the local health and education authorities, the parents/guardians and the participating children from whom the samples were obtained. We are grateful to M Traoré for the re-examination of a subset of the Giemsa-stained thick and thin blood films from the original study. We acknowledge the scientific support of I Felger as well as the technical support of T Voss with the PCR-RFLP analyses. We are also thankful to H-P Beck for critical reading of the manuscript.
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