- Open Access
Global genetic diversity of the Plasmodium vivax transmission-blocking vaccine candidate Pvs48/45
© Vallejo et al. 2016
- Received: 19 January 2016
- Accepted: 31 March 2016
- Published: 12 April 2016
Plasmodium vivax 48/45 protein is expressed on the surface of gametocytes/gametes and plays a key role in gamete fusion during fertilization. This protein was recently expressed in Escherichia coli host as a recombinant product that was highly immunogenic in mice and monkeys and induced antibodies with high transmission-blocking activity, suggesting its potential as a P. vivax transmission-blocking vaccine candidate. To determine sequence polymorphism of natural parasite isolates and its potential influence on the protein structure, all pvs48/45 sequences reported in databases from around the world as well as those from low-transmission settings of Latin America were compared.
Plasmodium vivax parasite isolates from malaria-endemic regions of Colombia, Brazil and Honduras (n = 60) were used to sequence the Pvs48/45 gene, and compared to those previously reported to GenBank and PlasmoDB (n = 222). Pvs48/45 gene haplotypes were analysed to determine the functional significance of genetic variation in protein structure and vaccine potential.
Nine non-synonymous substitutions (E35K, Y196H, H211N, K250N, D335Y, E353Q, A376T, K390T, K418R) and three synonymous substitutions (I73, T149, C156) that define seven different haplotypes were found among the 282 isolates from nine countries when compared with the Sal I reference sequence. Nucleotide diversity (π) was 0.00173 for worldwide samples (range 0.00033–0.00216), resulting in relatively high diversity in Myanmar and Colombia, and low diversity in Mexico, Peru and South Korea. The two most frequent substitutions (E353Q: 41.9 %, K250N: 39.5 %) were predicted to be located in antigenic regions without affecting putative B cell epitopes or the tertiary protein structure.
There is limited sequence polymorphism in pvs48/45 with noted geographical clustering among Asian and American isolates. The low genetic diversity of the protein does not influence the predicted antigenicity or protein structure and, therefore, supports its further development as transmission-blocking vaccine candidate.
- Latin American
- Korean Isolate
- Plasmodium Knowlesi
- Vivax Isolate
Malaria is an infectious parasitic disease caused by the genus Plasmodium which is transmitted by bites of infected Anopheles mosquitoes. Plasmodium falciparum and Plasmodium vivax are the two most common malaria parasites in humans, however differing in their clinical presentation and geographic distribution. Plasmodium falciparum causes the most severe symptoms and higher mortality, mainly among children under 5 years of age in Africa. Plasmodium vivax generally causes milder disease, is significantly less life-threatening  and is widely distributed in the Middle East, Asia, the Western Pacific, and Central and South America . Despite global efforts to control malaria transmission resulting in a significant decrease in global incidence during the last decade, it continues to challenge public health systems, particularly in tropical countries. Current global malaria control strategies will greatly benefit from the development of an effective vaccine that interrupts malaria transmission among individuals of endemic communities [3, 4].
Proteins expressed by parasite sexual stages, namely gametocytes/gametes, could induce effective immune responses in the human host that would prevent gamete fertilization and zygote formation when ingested by the mosquito during a blood meal .
Plasmodium Ps48/45 proteins are expressed by male and female gametocytes/gametes during the parasite maturation process, and are therefore classified as pre-fertilization antigens . These proteins belong to a family common to all Plasmodium species characterized by the presence of partially conserved domains containing six cysteine (Cys) amino acid residues that form one to three disulfide bridges, resulting in a specific tertiary structure [7, 8]. In P. falciparum, this protein (Pfs48/45) is expressed on the surface membrane of gametocytes  and is required for male fertility . In addition, Pfs48/45 is necessary for production of high antibody titers in individuals living in endemic areas [10, 11] that can reduce ookinete production and induce transmission-blocking activity [12–14]. It is currently considered a potential target for development as a transmission-blocking vaccine. As other proteins expressed on sexual forms, Pfs48/45 is rich in Cys residues, which has made it difficult to express as a recombinant product with proper conformation [5, 15]. Pvs48/45, the homologous protein in P. vivax, was recently expressed in Escherichia coli and its immunogenicity was assessed in mice and Aotus monkeys. These studies indicated high immunogenicity in both animal models and the elicited antibodies displayed significant and reproducible transmission-blocking activity in ex vivo P. vivax membrane-feeding assays (MFA) .
Genetic diversity could generate antigenic polymorphisms, which in turn could induce changes in critical epitopes and hamper vaccine efficacy. Successful development of an effective transmission-blocking vaccine is likely dependent on an assessment of the degree of genetic diversity in pvs48/45 among P. vivax parasite populations in malaria-endemic locations . Although available data indicate a limited Pvs48/45 genetic polymorphism on a regional scale [17, 18], knowledge of the sequence polymorphism on a broader scale and its potential impact on vaccine development is needed. Here, a total of 282 pvs48/45 sequences corresponding to parasites from eight countries from around the world were analysed for gene diversity to assess probable protein changes that could influence the immunogenicity and its vaccine potential.
Blood samples used in this study were obtained from studies approved by the Institutional Review Board (IRB) of the Malaria Vaccine and Drug Development Center (MVDC) under the codes CIV-01-042009, CIV 08-102010 and CIV 009. Samples from volunteers were not linked to the identity of the donor. Written informed consent was obtained from each volunteer at enrolment. All volunteers were adults over 18 years of age.
Origin of Plasmodium vivax samples
Origin of Latin American isolates used for pvs48/45 sequencing
Gracias a Dios
Valle del Cauca
Extraction and purification of parasite genomic DNA
Parasite genomic DNA was extracted from filter-paper blood spots using 10 % Chelex 100 (Biorad, USA) and from EDTA-blood samples using the salting-out method , and were identified with two-letter codes according to the country of origin as follows: Colombia (Co), Brazil (Br) and Honduras (Hn), followed by two numerical digits. Subsequently, DNA was purified using the PureLink Genomic DNA Mini Kit (Life Technologies, USA), according to the manufacturer’s instructions. DNA samples were tested by real-time quantitative PCR (qPCR) to confirm infection with P. vivax and rule out P. falciparum co-infection as previously described .
Amplification and sequencing of the Pvs48/45 gene in parasite samples from Latin America
Pvs48/45F (5′-GGAATAATTTCGACCACTC-3′) and Pvs 48/45R (5′- TCAGAAGTACAACAGGAG-3′) primers were designed to amplify the Pvs48/45 gene coding region (CDS annotation 1357 bp) from the pvs48/45 of Salvador I strain (PlasmoDB Id: PVX_083235). Amplification was performed in 25 μL reactions containing 2–4 μL genomic DNA, 500 nM of primers Pvs48/45F and Pvs48/45R, and 0.5 units of HotStar HiFidelity Polymerase (QIAGEN, Valencia, CA, USA). Thermal cycling conditions were as follows: initial denaturation for 5 min at 94 °C, followed by 39 cycles of: 94 °C for 30 s, 55 °C for 1 min, 72 °C for 2 min, and a final extension step at 72 °C for 10 min. Amplification products were analysed by gel electrophoresis in 1.2 % agarose gels and purified using the High Pure PCR product purification kit, according to the manufacturer’s recommendations (Roche Diagnostics, Mannheim, Germany). Purified PCR products were sequenced using the Big Dye Terminator Kit v3.1 (Applied Biosystems, Austin, TX, USA) in an ABI-PRISM Avant 3100 Automatic Genetic Analyzer (Applied Biosystems, Foster City, CA, USA) using primers Pvs48/45F and Pvs48/45R. Each purified product was sequenced in both directions by a minimum of two independent sequencing reactions until quality base calling value scores >20 (predictive sequencing error rate per base of 1.00 %) were obtained , as assessed with the Sequencing Analysis Software v.5.3 (Applied Biosystems).
Sequence assembling, alignment and statistical analysis
All sequences were assembled against the Sal I P. vivax pvs48/45 sequence reported in PlasmoDB (accession No. PVX_083235) using the reference assembler algorithm in Geneious 4.8.4  and corrections made by manual inspection. The primers sequences were removed before the analysis. Consensus sequences were aligned using the Geneious alignment algorithm and the alignment was used to calculate the number of segregating sites (S), singleton sites, singleton variable (SV) sites, parsimony informative (PI) sites, haplotype diversity (Hd), nucleotide diversity (π), and the average number of pair-wise nucleotide differences within the population (K), number of synonymous (dS) and non-synonymous (dN) substitutions with DnaSP 5.10 package using the Jukes-Cantor model. DNA polymorphism was analysed with a sliding window of 100 bases and a step of 25 bases for a haploid genome . To determine the influence of the geographical origin of the isolates on nucleotide diversity and DNA polymorphism, the same analysis discriminating between groups of samples from Brazil, Colombia and Honduras was performed. Output data were exported to Excel to plot overlapping π curves with standardized scales for the different groups. Numbers of synonymous (dS) and non-synonymous (dN) substitutions were compared by a two-tailed Z test (P < 0.05) using MEGA 6.06  using the Nei and Gojobori’s method  with the Jukes-Cantor correction and its standard deviation determined by 1000 boot-strap replications . Null hypothesis was dS = dN, thus indicating that the observed polymorphism was neutral.
Phylogenetic and epitope conservation analysis
Tajima’s D test and Fu and Li’s D and F tests using Plasmodium knowlesi pvs48/45 as an outgroup were performed on DNASP 5.10 to test for the neutral theory of evolution. Haplotypes reported in this study were compared to 132 pvs48/45 sequences reported in GenBank for South Korea , North Korea , India and Indonesia , and reference sequences from Brazil, India, Mauritania, and North Korea and Sal I, same as described above, for a total of 252 isolates. In silico translated DNA sequences were aligned to the Pfs48/45 3D7 amino acid sequence (PFD3D7_1346700) to ensure the localization of the single nucleotide polymorphisms (SNPs) in the Cys-rich domains (CRD) I, II, and III were epitopes I, II, III and V as previously reported . Phylogenetic analysis was performed with the 60 sequences reported in this study, and with the 49 sequences reported in GenBank.
Immune epitope mapping
In order to determine the presence of linear B cell epitopes in the Pvs48/45 protein sequence and the possible influence of the SNP in the predicted epitopes, an in silico analysis of the entire sequence was performed. Epitopes were predicted based on hydrophilicity, accessibility, polarity, flexibility estimation, combined with secondary structure analysis (Kolaskar-Tongaonkar antigenicity prediction methods) .
Molecular modelling of the 3D structure
Structural models of Pvs48/45 domains were built by using homology-based modelling. The known 3D structures of homologous proteins Pf12 from P. falciparum  and the immunodominant surface antigen from Toxoplasma gondii (Protein Data Bank IDs: 2YMO:A and 1KZQ:A) were used as templates. Sequence alignments were obtained by using a HHpred server , ClustalW program  and manual adjustment. Structural models were built using the HOMOLOGY module of Insight II program . Resulting structures were subjected to energy minimization using the procedure implemented in the Discovery sub-routine of Insight II.
Genetic polymorphism and amino acid changes
Pvs48/45 gene haplotypes
Amino acid changes found in the seven pvs48/45 haplotypes in Latin American isolates
Amino acid position
Global diversity of pvs48/45
Estimates of DNA sequence polymorphism and tests of neutrality for pvs48/45
Hd ± SD
π ± SD
0.221 ± 0.121
0.00033 ± 0.00033
0.445 ± 0.170
0.00123 ± 0.00094
0.841 ± 0.024
0.00188 ± 0.00073
0.218 ± 0.103
0.00034 ± 0.00046
0.526 ± 0.153
0.00058 ± 0.00062
0.610 ± 0.047
0.00168 ± 0.00087
0.889 ± 0.071
0.00216 ± 0.00110
0.484 ± 0.138
0.00116 ± 0.00101
0.611 ± 0.026
0.00053 ± 0.00004
0.0018 ± 0.042
0.00147 ± 0.00069
0.686 ± 0.00149
0.00173 ± 0.00149
Geographic distribution of vs48/45 haplotypes among LA isolates
The wild-type (Sal I-like) haplotype predominated among Brazilian (92 %), Peruvian (90 %), Mexican (87 %), and Honduran (71 %) isolates, however in Colombian isolates, it was the second-most frequent haplotype (24 %). Colombian isolates showed a major presence of haplotype I (52 %), which was less frequent in Honduran isolates (14 %), and not detected among Brazilian, Peruvian and Mexican samples. Haplotype VI, the most frequent in Myanmar and Thailand, was found only among Colombian isolates, whereas haplotype VII was only present in Colombia isolates. Colombia showed the greatest haplotype diversity (0.841 ± 0.024) with eight non-Sal I haplotypes circulating in the country.
Mapping of immune epitopes
Potential antigenic determinants for the Pvs48/45
# Antigenic region
SNPs location on 3D Pvs48/45 domain structure
This study showed a limited pvs48/45 genetic diversity in a total of 282 P. vivax isolates worldwide. Only 18 amino acid substitutions were found within the entire protein sequence of an estimated 450 amino acid residues. Plasmodium vivax sequences corresponded to isolates from nine distant countries in three continents. Two pvs48/45 haplotypes were found to be shared by Asian and LA parasites, with a strong geographical allele clustering. Recent studies on the diversity of pvs48/45 among P. vivax isolates circulating in the Korean peninsula, China and Thailand showed low levels of genetic diversity [17, 18, 21, 37]; likewise, Brazilian isolates showed almost no variation when compared to the Sal I reference strain (PVX_083235), originally from El Salvador.
Interestingly, Korean, Colombian and Honduran isolates displayed limited sequence polymorphism. Pvs48/45 nucleotide and amino acid substitutions in isolates from Korea were found at pre-CRD (E35K), CRD-2 (H211N and K250N) and CRD-3 (D335Y, A376T, I380T, K418R). Pvs48/45 was more conserved in the Korean populations where nucleotide diversity varied from 0.00053  to 0.00147 [17, 18], and the haplotypes V was unique for these populations. Plasmodium vivax was recently re-introduced into the peninsula of Korea with a rapid spread pattern, suggestive of a high genetic diversity . This could explain the greater pvs48/45 variability observed in Korean isolates as compared to isolates from Honduras and Mexico, and the almost absent variability among Brazilian isolates Despite the variability in the Korean isolates, globally, Pvs48/45 remains a highly conserved antigen compared to other transmission-blocking vaccine candidates.
Results are in agreement with previous observations that transmission-blocking vaccine candidate antigens Pvs25, Pvs28, Pvs48/45, and PvWARP showed limited sequence polymorphisms . More importantly, the limited polymorphism found here does not appear to affect the immunogenicity of predicted epitopes as only three of nine amino acid substitutions in isolates from Colombia and Honduras were located at CRD2 (H211N and K250N) and CRD3 (E353Q). No substitutions were observed in CRD1, in agreement with reports for Korean isolates and for P. falciparum in Kenyan, Thai, Indian, and Venezuelan isolates [39, 40]. However, further studies are required to confirm the role of these B cell epitopes and to identify T cell epitopes in defining the potential of Pvs48/45 as a transmission-blocking vaccine candidate.
Pvs48/45 Cys domains are important for proper conformation of immune epitopes [8, 45]. In Pfs48/45, four epitopes designated epitope V (CRD1), epitope IIb (CRD2), epitope III (CRD2), and epitope I (CRD3) have been described previously . The N-terminal CRD2 and CRD3 epitopes appear to be transmission-blocking targets as specific monoclonal antibodies to these regions have demonstrated an ability to prevent parasite fertilization, and consequently mosquito infection [12, 46].
Substitutions H211N and K250N are predicted to be located in loop regions , which could serve as potential vaccine targets. Interestingly, no amino acid substitutions were found in any of the Cys residues of Pvs48/45 in the present study, which are critical for proper presentation of the transmission-blocking epitopes . However, an amino acid substitution (E353Q) was found next to a Cys residue reported to be involved in a disulfide bond. The influence of this variation on the formation of the disulfide bridge is yet to be explored.
Although parasite antigen diversity has been explained in part by immune pressure on the parasite [41–43], it does not appear to apply to Pvs48/45 as the protein is highly immunogenic, and it is expressed during the entire gametocyte maturation process. For P. vivax sexual antigens the exposure to the immune system could be longer than in P. falciparum due to the early appearance of P. vivax gametocytes in circulation . However it does not appear to apply to Pvs48/45 as the protein is conserved and highly immunogenic under natural conditions.
Transmission-blocking vaccines have been considered a promising strategy/tool for malaria control/elimination. In P. vivax malaria it has been observed that gametocytogenesis occurs earlier than in P. falciparum and remains active even in asymptomatic carriers . Consequently, malaria transmission to mosquitoes is likely to be more efficient, and thus, transmission-blocking vaccines would have a greater impact .
There is limited sequence polymorphism in pvs48/45 with noted geographical clustering among Asian and American isolates. The low genetic diversity of the protein does not influence the predicted antigenicity or protein structure and, therefore, supports its further development as a transmission-blocking vaccine candidate with widespread global potential.
SH and MA conceived and designed the study; NM, AV and SH wrote the manuscript; NM and AT performed the laboratory work. AK performed structural modelling of Pvs48/45. ML and JA contributed reagents/materials/analytical tools. All authors critically revised the manuscript. All authors read and approved the final manuscript.
The authors thank the communities of the endemic areas of Brazil, Honduras and Colombia that participated in this study. Special thanks to Miguel Angel Hernandez for his technical assistance and Yoldy Benavides for statistical support. This work was supported by NIAID (Research Grant U19AI089702 and 1R01AI12123701) and Colciencias (Grant Contracts 360-2011, 685-2013 and 719-2013).
The authors declare that they have no competing interests.
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