Background

Despite some progress over the last decade, malaria continues to be a significant global health burden with a vaccine deemed essential to effectively control the disease in high malaria transmission zones [1]. The RTS,S vaccine has been rolled out in three African countries [2] but is < 50% protective [3], suggesting further iterations are required. There are other candidates in the pipeline that show promise for incorporation into second-generation vaccines. One leading candidate antigen is Plasmodium falciparum Reticulocyte Binding homologue 5 (Rh5, PF3D7_0424100), which is currently advancing through clinical trials [4].

Rh5 is the smallest in the Reticulocyte Binding Protein homolog (Rh) family that includes Rh1, Rh2a, Rh2b and Rh4 [5, 6]. Furthermore, it is the only member of the Rh family without a transmembrane domain. Rh5 has been shown to be refractory to gene knockout experiments, suggesting it plays an essential role in the invasion of erythrocytes [5, 6] via interactions with the erythrocyte receptor basigin (BSG) [7]. Both monoclonal and polyclonal anti-Rh5 antibodies inhibit erythrocyte invasion of multiple parasite strains by blocking the Rh5-BSG interaction in vitro [8,9,10,11]. Rh5 vaccination field trials in non-human primates, Aotus monkeys, demonstrated protection from heterologous P. falciparum challenge [12], while non-exposed vaccinated human volunteers from a phase 1a clinical trial, generated anti-Rh5 antibodies that blocked merozoite invasion in vitro [4]. Furthermore, while individuals from malaria endemic regions, who are naturally exposed to P. falciparum infections develop anti-PfRH5 antibodies at a relatively low prevalence, the presence of these antibodies have been associated with protection from symptomatic malaria in Papua New Guinea, and Mali [13,14,15]. Based on these findings, Rh5 has been considered as a next generation blood-stage malaria vaccine candidate even though it has low immunogenicity in natural infections.

Rh5 does not function in isolation during erythrocyte invasion, but acts as part of a multi-protein complex with Rh5 interacting protein (Ripr, PF3D7_0323400) [16], cysteine rich protein antigen (CyRPA, PF3D7_0423800) (17) and P113 (PF3D7_1420700) [18]. The Rh5-CyRPA-Ripr complex binds better to the erythrocyte cell surface than Rh5 alone [19], and interaction of Rh5 with its erythrocyte surface protein receptor, basigin, triggers a transient increase in Ca2+ concentration and alters the erythrocyte cytoskeleton [20]. Rh5 undergoes proteolytic cleavage, resulting in fragments of approximately 18 kDa and 45 kDa. Rh5 binds directly to P113 (via the smaller Rh5 fragment, [18] and CyRPA [17], while Ripr is associated with Rh5 through its interaction with CyRPA [21]. Therefore, CyRPA forms the contact sites for Rh5 and Ripr. It has been suggested that CyRPA dissociates from the complex and it is excluded from the membrane during binding to basigin. The Rh5-CyRPA-Ripr complex can bind to BSG without interaction with p113. However, P113 anchors Rh5 onto the merozoite membrane, while CyRPA and Ripr do not bind to erythrocytes on their own [16,17,18, 21].

Similar to Rh5, the genes encoding CyRPA and Ripr cannot be knocked out, suggesting that they are essential for parasite growth [16, 18], and conditional deletion of either Ripr and CyRPA results in non-invasive merozoites [19]. Antibodies to all three proteins (Rh5, CyRPA and Ripr) of the complex can inhibit erythrocyte invasion by multiple P. falciparum strains [16, 17, 22]. Furthermore, antibodies to CyRPA have been reported to block its interaction with the Rh5/Ripr complex and the formation of the multi-protein complex, leading to invasion inhibition [17]. In African and Papua New Guinean populations, P113 antibodies have been associated with protection against clinical malaria [13, 23]. All members of the Rh5 protein complex can, therefore, be considered potential blood-stage vaccine targets.

Polymorphisms are a particular barrier for the development of blood-stage vaccines, as proteins that are exposed to the immune system during invasion are often very diverse, presumably the result of pressure from the immune system [24]. This problem of diversity has impeded the development of blood-stage vaccines in the past, with AMA1 being a prime example. Like the Rh5 complex, AMA1 is essential for invasion, but it is highly polymorphic, resulting in immune responses that are allele-specific, a fact that may have limited the efficacy of previous Phase IIb trials [25]. However, Rh5, Ripr and CyRPA have been shown to be highly conserved [5, 22, 26], although polymorphisms in these genes including p113 have not been intensively investigated. In addition, exploring genetic diversity in all members of the complex in the same infections would identify whether polymorphisms are associated, which would need to be taken into consideration during vaccine design. To explore these questions, we examined all the four Rh5 complex genes by capillary and whole genome sequencing of a cross-sectional sample of parasites from Kilifi.

Methods

Sampling, DNA amplification and capillary sequencing

For capillary sequencing (CS), parasite DNA was extracted from 162 blood samples from children below 11 years admitted and attended to at the Kilifi County Hospital in 2013 and 2014. The children had variable parasitaemia ranging from 160 to 705,600 parasites/µl, with a median of 7440 parasites/µl. This study was reviewed and approved by the Centre Scientific Committee and the Scientific Ethical Review Unit (SERU) of the Kenya Medical Research Institute, on SERU protocol number 3149. CyRPA (PF3D7_0423800), P113 (PF3D7_1420700), Ripr (PF3D7_0323400) and Rh5 (PF3D7_0424100) genes were examined. Genomic DNA was previously extracted from packed frozen erythrocytes using the QIAcube (Qiagen), according to the manufacturer’s instructions (QIAGEN, UK). All four genes were amplified using High Fidelity Taq polymerase (Roche) (primers used are shown in Additional file 1: Table S1). PCR products were visualized on 1% agarose gels prior to sequencing to confirm their expected band size (Additional file 2: Table S2). Purified amplicons were directly sequenced using the PCR primers and additional sequencing primers (Additional file 1: Table 1), BigDye terminator chemistry v3.1 (Applied Biosystems, UK) and an ABI 3730xl capillary sequencer (Applied Biosystems, UK). The raw sequences for each targeted gene were assembled, edited, and aligned using SeqMan and MegAlign software (Lasergene 12; DNASTAR). All singleton SNP sites were confirmed by independent reamplification and resequencing of the relevant samples. Positions of the sequences that showed mixed or superimposed nucleotides (peak within a peak) were marked with IUPAC ambiguity codes and consider as a mixed infection and excluded from the SNP and haplotype frequencies.

Sampling, DNA preparation and whole genome sequencing

For whole genome sequencing, parasite DNA was previously extracted from 68 blood samples obtained from children recruited into an artemisinin-based combination therapy (ACT) drug trial of dihydroartemisinin-piperaquine and artemether-lumefantrine conducted in Pingilikani dispensary, Kilifi from 2005 to 2007 [27]. Additionally, some samples were from patients admitted to the Kilifi County Hospital with severe malaria. All studies obtained clearance from the Kenya Medical Research Institute (KEMRI) Ethical Review Committee under protocol numbers SSC 945. Samples were cryopreserved in glycerolyte and later adapted to culture for about 2 months for chemosensitivity testing [28]. DNA was also extracted and contributed to MalariaGEN for whole genome sequencing (WGS) and genotyping on an Illumina Genome Analyzer to a read depth of approximately 98 × in genotyped sites, and reads of length 37–76 base pairs as described in Wendler et al. [29]. The genotype data generated from the sequence reads were obtained from the MalariaGEN P. falciparum Community Project [30]. The selected SNPs were from those identified in release 6.0.

Read mapping and coverage analysis

A VCF file containing 68 samples obtained from Kilifi, Kenya, were used as the input file in the downstream analysis. Using VCFtools (v. 0.1.13) a targeted analysis of four genes: Rh5, Ripr, CyRPA and P113 was filtered, by using a bed file containing the chromosome numbers and genomic positions, to generate one VCF file. Using PLINK [31], the VCF files were then examined to obtain a list of high quality SNPs, by excluding variants based on the following criteria: a) the SNPs with the ‘FAIL’ filter; b) non-coding SNPs; c) SNPs that have extremely low support (< 10 reads in one sample); and d) variants that did not pass the minor allele threshold of < 0.5% based on the number of reads obtained per variant.

Global malariaGEN data retrieval and analysis

To further validate the SNPs, we identified through CS and WGS, data from the MalariaGEN Plasmodium falciparum community project version 4.0 was used. This data was generated through an analysis of 3488 P. falciparum samples collected at 43 different locations in West Africa (WAF), Central Africa (CAF), East Africa (EAF), South Asia (SAS), West South East Asia (WSEA), East South East Asia (ESEA), Oceanic (OCE) and South America (SAM). A total 930,000 exonic SNPs and their frequencies were obtained. The method used to generate the data are described in Amato et al. [32]. The dplyr v1.0.0 package [33] in R v4.0.2 [34] was used to filter our four genes of interest based on their unique Gene IDs: CyRPA (PF3D7_0423800), P113 (PF3D7_1420700), Ripr (PF3D7_0323400) and Rh5 (PF3D7_0424100). The pool of SNPs identified were filtered to obtain their frequencies.

Population genetics statistical tests

The allele frequency distribution indices, Tajima’s D and Fu and Li’s D* and F*, were computed using DnaSP v5.10 software [35] for the capillary sequence data. Tajima’s D computed the differences between two estimators of theta, based on the number of segregating sites and the average number of nucleotide differences [36]. Fu and Li’s D* test statistic calculated the differences between the observed number of singletons (mutations appearing only once among the sequences), and the total number of mutations [37] Fu and Li’s F* test statistic considered the differences between the number of singletons and the average number of nucleotide differences between pairs of sequences [37]. For the p values DnaSP calculated the confidence limits of D (two-tailed test) and assumed that the statistic follows a beta distribution.

Linkage disequilibrium analysis

For each of the four genes obtained from the whole genome data, the minor and major allele frequencies of all the SNPs were computed using PLINK. Only SNPs with a > 5% minor allele frequency were included in the analysis. The extent of linkage disequilibrium (LD) between pairs of SNPs in Rh5, Ripr, CyRPA and P113 was determined within and between genes using R v3.6.0. The statistical significance of LD was tested, at the 5% level, using χ2 tests.

Rh5-CyRPA-Ripr complex protein structures

The cryo-electron microscopy structure of Rh5-CyRPA-Ripr (PDB ID: 6MPV) was downloaded from the Protein Data Bank (http://www.rcsb.org/). Wong et al. [21] reported only the structures for Rh5 (residues 175–243 and 298–504) and CyRPA (residues 31–122, 126–242, 254–319 and 323–362) as the Ripr model could not be built de novo owing to resolution of the electron density map. However, based on the alpha helix structures described we use this to obtain a partial structure for Ripr. Using the generated dataset in this study, the Rh5 and CyRPA polymorphic sites were mapped onto their protein structures in Pymol (The PyMOL Molecular Graphics System, Version 2.2.0, Schrödinger, LLC), to determine the location of the polymorphisms in the three-dimensional conformation of the complex and whether the polymorphic sites were found in the binding regions of each protein.

Results

Population genetics summary statistics

All genes had a negative summary statistic, although only P113 and Ripr reached significance with a negative value for either the Tajima’s D or Fu & Li D* & F* or both statistics (Tables 1 and 2). P113 yielded values of -2.2, -3.2 and -3.4, respectively for CS data, with comparable results observed using the whole genome data of -2, -3.2 and -3.4. A similar observation was made with Ripr with the capillary data giving only significant values of − 2.5, and − 2.5 for the Fu & Li D* and F*, respectively, while the whole genome data yielded results of -2.8 and -2.9, respectively.

Table 1 Capillary sequence population genetics summary statistics
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Table 2 Whole genome sequence population genetics summary statistics
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Genetic diversity in the Rh5 complex genes identified using capillary sequencing data

Capillary sequencing data was attempted from 162 samples taken from children admitted to Kilifi Hospital. Data on all four genes was not obtained by capillary sequencing for any single sample, but data was obtained for multiple pairs of genes from individual isolates: p113 & CyRPA, p113 & Ripr and Rh5 & CyRPA. Capillary sequence data for both p113 & Rh5 and CyRPA & Ripr gene pairs were obtained in less than 20 samples, while 46 samples yielded sequence data for P113 and CyRPA (Table 3). No synonymous SNPs were detected, while 32 non-synonymous (ns) SNPS were identified in total. CyRPA, p113, Rh5 and Ripr sequences contained 4, 10, 6 and 12 SNPs, respectively (Table 4). Most SNPs were found in multiple isolates (Additional file 3), although 3 SNPs in CyRPA and Ripr and 5 in p113 were singletons (found in only a single isolate). Indels were only found in p113, with variation in repeat regions at codon 275 with asparagine (N) (ranging from 3 to 9 N) and at codon 859 with glutamic acid (E) (ranging from 2 to 3E). The CyRPA analysis was conducted in two fragments from the N and C-terminal ends. The N-terminal end fragment, codons 1 to 170, contained only one non-synonymous SNP, at codon 165 and found in only a single infection, while the C-terminal end though shorter in comparison contained three polymorphic sites.

Table 3 The number of samples from which capillary sequence data was obtained for each gene combination
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Table 4 The frequency of variants in the Rh5 complex genes identified by CS and WGS
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Genetic diversity in the Rh5 complex genes identified using whole genome sequencing data

Whole genome sequencing (WGS) SNP data for all the four genes were obtained from 68 independent samples from a previous drug trial (Additional File 4). A total of 55 SNPs were identified within the Rh5 gene complex: 10 in CyRPA, 14 in P113, 21 in Ripr and 10 in Rh5 as shown in Table 2. There was a total of eight synonymous polymorphisms, 1 in CyRPA, 5 in p113 and 2 in Ripr and forty-seven ns polymorphisms with CyRPA, p113, Rh5 and Ripr containing 9, 9, 10 and 19, respectively (Table 4). Seven of the eight synonymous SNPs (unique to the WGS data) were singletons except CyRPA codon 101 whose frequency was > 5%. Given that our WGS data only contained SNP data, we did not explore the repeat sequences identified by CS in the p113 gene.

Comparison of variants identified by CS and WGS with the global MalariaGEN data

In keeping with previous studies, the majority of variants in the Rh5 complex genes were rare, which meant that most were unique to each sequencing method, and very few SNPs were identified by both methods. In Rh5, CyRPA, p113 and Ripr we observed 5, 1, 4, and 8 SNPs, respectively, that were identified by both methods. The MalariaGEN global variation dataset was screened to explore whether SNPs were missed, perhaps due to methodological differences. This analysis established that all common variants identified in our analysis (MAF > 5%) for Rh5, P113 and Ripr were also found in the global MalariaGEN dataset, arguing against any systematic missing SNP identification issues. In addition, more than two thirds of the rare variant SNPs were identified in these samples had also been identified previously in the global MalariaGEN data, giving us confidence in the polymorphisms identified in this study using CS and WGS. Combining our data with global MalariaGEN data confirmed that the majority of variants in the genes encoding the Rh5 complex are rare mutations (Table 4).

Linkage disequilibrium analysis

The LD within and between genes was examined in SNPs with minor allele frequencies of > 5%. 6 SNPs and 4 SNPs were identified before and after Bonferroni correction, respectively. The 4 SNPs in LD after Bonferroni correction were within Rh5 and Ripr. In Rh5, LD was observed in codons 147 and 148, p < 0.0001 and in Ripr, LD was observed between codons 985 and 1003 p-value of < 0.01. Due to the high number of rare variant SNPs in CyRPA, none were included in the LD analysis.

Visualizing mutations on the protein complex structure

Mutations within known protein interacting regions were mapped onto published structures for the Rh5 protein complex. The structure of the CyRPA-Rh5 interaction has been published [21] and the Basigin structure was added to show its interaction with Rh5. The crystal structure of Ripr and P113 has not been solved and hence their polymorphic residues in these proteins could not be mapped. Rh5 interacts with BSG through an α-2, α-4 and a disulphide loop region [38]. This Rh5-basigin interacting region includes Rh5 codon 203, a SNP that was identified at a frequency of > 5% in both the CS and WGS. We mapped back the identified rare variants to the protein structures (Fig. 1), and only two SNPs in CyRPA (codon 292 identified by CS and codon 302 identified by both CS and WGS, both at MAF < 5%) were located within the CyRPA-Ripr interacting region [21]. The Ripr α- helix, Fig. 1, corresponding to amino acid residues 196 – 211, interacts with blade 6 of the CyRPA β-propeller, amino acids 281 to 311 [21]. All the SNPs identified by CS and WGS in Ripr fall outside the Ripr α- helix, where the structure has not been solved.

Fig. 1
figure 1

SNPs within protein–protein interacting regions of BSG, Rh5, CyRPA and Ripr. The interacting crystal structures of BSG (grey), Rh5 (yellow), CyRPA (green) and Ripr alpha helix (black) showing SNPs that fall within protein–protein interacting regions. In red, are the polymorphic residues identified in codon C203Y of Rh5 and codon D302E and F292V of CYPRA. Of the SNPs identified in the Rh5-CyRPA structure only the high frequency Rh5 codon 203 falls in the region that interacts with BSG. The singleton SNPs in codon F292V and D302E denoted by a hash#, lie within the region that interacts with Ripr. Apart from the short α-helical structure, the Ripr structure was not available on Protein Data Bank

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Discussion

The Rh5 complex is a relatively conserved set of proteins with few polymorphisms. They are not highly immunogenic, as previously shown [15, 23]. The negative population genetics summary statistics do not indicate balancing selection and show an excess of rare variants. This is consistent with an analysis of genomes from P. falciparum populations in Africa, which revealed that the majority of genes were associated with a negative Tajima’s D value. Therefore, suggesting there was a historical parasite population expansion in Africa [39,40,41]. The genes with a significant, negative population genetics summary statistics, indicate that these genes have a limited potential to retain mutations, in particular p113 and Ripr, which may be due to the parasite’s need to preserve their function. These proteins are involved in a critical step during the invasion of erythrocytes and this polymorphism data reinforces the fact that they are likely to make good vaccine candidates to inhibit invasion and prevent disease [42].

Sequence data was obtained using two different methods and resulted in the identification of more SNPs using whole genome sequencing (WGS) analysis than Capillary Sequencing (CS), but there are pros and cons to both approaches. In CS, each read is accompanied by a long (on average 500 bp) chromatogram, which makes it easy to assemble and align to a reference genome in order to manually identify variants, but the process as a whole is low-throughput. In WGS, millions of short reads are produced with each read being accompanied by a quality score. It is thus not feasible to manually check the quality of each nucleotide and quality score cut-offs are set in the bioinformatic pipelines to confidently call a nucleotide. This presents a challenge in identifying indels within repeat regions—because the assembly and alignment of these regions to reference genomes is based on short reads, confidence is often low in these regions, making it difficult to unambiguously determine the numbers of repeat nucleotides [43]. However, the ability of WGS to generate large numbers of reads and identify SNPs in mixed infections allows more robust identification of SNPs, and it is therefore more reliable in the detection of low frequency variants as compared to CS. The Global MalariaGEN dataset was used to confirm the SNPs identified by the two methods. A large majority (> 65%) of the SNPs described in these samples have also been described in other locations within the Global MalariaGEN data, providing confidence both the high frequency and rare SNPs detected. Furthermore, most SNPs that were only identified by one method were rare variants, making it not surprising that there were missed by the other method, as the two methods were applied to different sample sets. If a rare variant is only present in few infections, the chances of such infections being present in the samples used for both methods is significantly reduced. It is also important to note that the samples utilized in WGS and CS, were obtained in different time points, which are 2005–2007 and 2013, respectively. In addition, the parasites used in obtaining the whole genome sequence data underwent culture-adaptation prior to sequencing, therefore the quality of DNA is expected to be higher in culture adapted parasites due to less contamination by host DNA. Cultured P. falciparum parasites have been known to differ significantly from source populations due to adaptation to environments that exclude the host immune responses [44]. There are therefore multiple reasons that could explain why different SNPs were identified in the two different approaches.

The majority of the polymorphisms in this complex or merozoite invasion antigens were rare, which is in contrast to previous findings from surface exposed and abundant merozoite antigens such as apical membrane antigen 1 (AMA1) [45], merozoite surface protein 1 (MSP1) [45], MSP3 [46] and erythrocyte binding antigen-175 (EBA175) [47], which are under balancing selection and exhibit allele-specific immunity in vaccine trials. In a recent study of samples from Nigeria, only 5 non-synonymous SNPs were identified in Rh5: K62R, T81Q, P197S, C203Y and H240R [48], of which only the C203Y mutation was identified in our study, while codon 197 was described in the global MalariaGEN dataset, codons 62, 81 and 240 are potentially rare variant sites. Of note, the high frequency sites of codons 147 and 148 in this study were not identified in the Nigerian study. However these aforementioned sites were described alongside codons S197Y, C203Y and I410M as common variants occurring at a frequency above 10% globally [9]. However, the I410M mutation was a rare variant (< 5%) in our population. It appears that apart from a few high frequency sites that have been consistently identified in previous studies and in our study, most mutations in Rh5 are rare variants. Rh5 antibodies primarily inhibit parasite invasion by disrupting the Rh5-basigin interaction [38].

This study identified only one Rh5 mutation C203Y at the Rh5-Basigin interface. It has been shown that the Rh5 protein variant with the 203Y mutant binds to recombinant basigin with the same affinity as the Rh5 C203 wild type [49]. It is therefore likely that other rare Rh5 mutations that cluster around the basigin interface will prevent binding of monoclonal antibodies. Based on monoclonal antibody data [50], these SNPs fall within the region of a large number of mouse and human antibodies that have shown neutralising activity within codons 26–352, suggesting that the rare variants identified in this study will potentially have an effect on antibody binding epitopes [9, 11, 17]. A similar scenario is observed with CyRPA, where only 1 SNP (R339S) was identified from a sample of 12 geographically distinct laboratory isolates and 6 field isolates [22] and again this SNP was not identified in the Kilifi samples. An analysis of 80 Ripr sequences from Uganda, identified 16 SNPs of which two codons (190 and 259) were > 5% in frequency. This study only found 9 of the 16 Ugandan SNPs and the SNPs unique to the Ugandan population were all singletons [26]. Moreover, Ntege et al. [26] also showed, like this study, a negative and significant Tajima’s D index. These studies further indicate that these genes tend to contain rare variants. The common variants identified across all the study sites should be considered in future studies to determine if they influence the functionality of the multiple protein complex.

The low immunogenicity of Rh5 complex members in field studies [12, 15, 22] would suggest limited immune pressure on these antigens and thus a limited need for the parasite to acquire mutations to escape host immune responses. This could explain the limited high frequency polymorphisms and the excess of rare variants observed. Slightly higher responses have been observed for p113 in individuals in Kilifi, when compared to Rh5 [23]. Beside the role of p113 in invasion by binding to the Rh5 N-terminal region [18], p113 is also thought to be involved in translocation through association with the Plasmodium translocon of exported proteins (PTEX), which is known to be a mechanism of immune evasion [51]. Further investigation is required to understand the effect of P113 polymorphisms on translocation. While there is limited literature on natural immune responses to Ripr, we anticipate similar findings as seen with CyRPA and Rh5, given that Ripr is part of the same Rh5 protein complex. The Rh5 protein complex is hidden within the merozoite apical end during tight junction formation. It is, therefore, likely that these proteins are rarely exposed to the immune system and thus their immunogenicity in individuals living in malaria endemic regions is low. Their role in tight junction formation indicates an important function in merozoite invasion, which has been determined by an inability to genetically disrupt all of the 4 genes and by the protective immune responses generated by antigens like Rh5 and p113 [50].

Most of the observed SNPs were not in statistically significant LD with the exception of codons 147 and 148 for Rh5 and 985 and 1003 in CyRPA, which are 3 bp and 54 bp apart respectively. The limited LD is likely due to a combination of the fact that most of the SNPs are rare variants and therefore occur at a low frequency, and the limited sample size in this study. Rh5 codons, 147 and 148 are included in the protein structure [38] on the upstream of the alpha helix, while the structure of Ripr has not been fully resolved. Since they are high frequency SNPs, they may be involved in processes other than protein-proteins interactions, but these are yet to be determined. Only one high frequency SNP at Rh5 codon 203, identified by both CS and WGS, has been shown to be localized in the Rh5-basigin interface [38].

The development of new tools and adaptation of existing tools for use in malaria elimination and eradication remains a priority, and deeper understanding of polymorphism(s) in vaccine candidate genes is particularly important. This study highlights pros and cons to both CS and WGS approaches to identifying vaccine-relevant polymorphisms. The ideal molecular tool should be able to provide quality and high-throughput sequence reads capable of detecting low frequency variants including indels. One such approach would be amplicon deep sequencing, where longer fragment amplicons can be generated and sequenced using an NGS platform, focussing analysis on the regions of interest rather than the whole genome, but producing deeper and higher quality data than CS. Low frequency mutations should be assessed by functional assays to ascertain their biological and immunological relevance. One of the main obstacles in the development of effective vaccines for malaria is the occurrence of polymorphisms on candidate vaccine targets that result in strain-specific immunity. Among the members of the Rh5 complex, Rh5 is the most advanced in vaccine development. The identification of a limited number of high frequency polymorphisms on Rh5 shows promising prospects of Rh5 based vaccines in this region, but it is still possible that low frequency variants may lead to immune evasion—this needs to be systematically investigated.

Conclusion

One gene does not appear to conceal the other genes in the complex, by being more polymorphic and acting as a decoy to direct the immune pressure away from the rest of the genes in the complex. Thus, the limited polymorphisms are potentially a result of their hidden location in the apical end of the merozoite and their limited exposure to host immune responses. Due to the minimal acquisition of mutations, Rh5, CyRPA, Ripr and P113 proteins are potentially a good next-generation multi-antigen vaccine formulation.