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Genetic evidence for contribution of human dispersal to the genetic diversity of EBA-175 in Plasmodium falciparum

  • 1Email author,
  • 1, 2,
  • 3,
  • 4 and
  • 1, 2
Malaria Journal201514:293

https://doi.org/10.1186/s12936-015-0820-2

  • Received: 27 January 2015
  • Accepted: 21 May 2015
  • Published:

Abstract

Background

The 175-kDa erythrocyte binding antigen (EBA-175) of Plasmodium falciparum plays a crucial role in merozoite invasion into human erythrocytes. EBA-175 is believed to have been under diversifying selection; however, there have been no studies investigating the effect of dispersal of humans out of Africa on the genetic variation of EBA-175 in P. falciparum.

Methods

The PCR-direct sequencing was performed for a part of the eba-175 gene (regions II and III) using DNA samples obtained from Thai patients infected with P. falciparum. The divergence times for the P. falciparum eba-175 alleles were estimated assuming that P. falciparum/Plasmodium reichenowi divergence occurred 6 million years ago (MYA). To examine the possibility of diversifying selection, nonsynonymous and synonymous substitution rates for Plasmodium species were also estimated.

Results

A total of 32 eba-175 alleles were identified from 131 Thai P. falciparum isolates. Their estimated divergence time was 0.13–0.14 MYA, before the exodus of humans from Africa. A phylogenetic tree for a large sequence dataset of P. falciparum eba-175 alleles from across the world showed the presence of a basal Asian-specific cluster for all P. falciparum sequences. A markedly more nonsynonymous substitutions than synonymous substitutions in region II in P. falciparum was also detected, but not within Plasmodium species parasitizing African apes, suggesting that diversifying selection has acted specifically on P. falciparum eba-175.

Conclusions

Plasmodium falciparum eba-175 genetic diversity appeared to increase following the exodus of Asian ancestors from Africa. Diversifying selection may have played an important role in the diversification of eba-175 allelic lineages. The present results suggest that the dispersals of humans out of Africa influenced significantly the molecular evolution of P. falciparum EBA-175.

Keywords

  • Diversifying selection
  • EBA-175
  • Human evolution
  • Out-of-Africa
  • Plasmodium falciparum

Background

Approximately 200 Plasmodium species parasitize different vertebrate groups, including lizards, birds, and mammals [1]. Of them, five Plasmodium species, namely Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale (consisting of two subspecies, Plasmodium ovale curtisi and Plasmodium ovale wallikeri [2]), Plasmodium malariae, and Plasmodium knowlesi, can infect humans. In particular, P. falciparum causes the most severe form of malaria in humans; however, when compared with Plasmodium reichenowi found in chimpanzees (Pan troglodytes), P. falciparum appears to be phylogenetically distantly related to other human malaria parasites [1, 35].

The 175-kDa erythrocyte binding antigen (EBA-175) of P. falciparum binds with a sialic acid on human glycophorin A (GYPA); the interaction of these molecules is the part of a major pathway for malaria parasite invasion into erythrocytes. The primary structure of eba-175 gene is divided into seven regions, region I–VII [6]. Region II is a cysteine-rich region responsible for the interaction between EBA-175 and GYPA on the erythrocyte surface [7]. Previous studies have shown a significant excess of nonsynonymous substitutions over synonymous substitutions in this region in P. falciparum [811]; however, no studies have assessed to date the ratio of nonsynonymous to synonymous substitutions in other closely related Plasmodium species. Nonsynonymous substitution rates of host and pathogen are expected to increase synergistically as a consequence of the host-pathogen co-evolutionary arms race. When human and macaque genomes were compared, the gypa gene shows the highest number of nonsynonymous substitutions per nonsynonymous sites among 280 genes [10]. In addition, the rate of nonsynonymous substitutions in eba-175 gene is also the highest among 10 genes compared between P. falciparum and P. reichenowi [10]. Thus, the high level of genetic polymorphisms shown by eba-175 and gypa is likely to result from host–pathogen coevolution.

Amino acid substitutions in region II of eba-175 and gypa seem to have been enhanced by diversifying selection. However, it remains unclear how human evolution has influenced P. falciparum eba-175 genetic diversity. To elucidate this, in the present study, the regions II and III of eba-175 from a Thai P. falciparum population were examined. When compared with P. reichenowi eba-175 sequence, eba-175 alleles from this population can be traced back to approximately 130–140 thousand years ago. A further analysis for a large sequence dataset of P. falciparum eba-175 alleles from across the world revealed an Asian-specific basal cluster in a phylogenetic tree. In addition, an evolutionary analysis detected a significant excess of nonsynonymous substitutions over synonymous substitutions in the region II of eba-175 within the Thai P. falciparum population, but not within Plasmodium populations parasitizing African apes. Thus, the results from the present study suggest that human dispersal out of Africa contributed to the genetic diversification of P. falciparum eba-175.

Methods

Ethics statement

This study was approved by the Institutional Review Board of the Faculty of Tropical Medicine, Mahidol University, and the Research Ethics Committee of the School of Medicine, The University of Tokyo.

Subjects

Peripheral blood samples were obtained from 203 P. falciparum-infected patients from Thailand. In addition, a dataset of nucleotide sequences including isolates of human P. falciparum, gorilla (Gorilla gorilla) Plasmodium, chimpanzee Plasmodium, and P. reichenowi was built from data obtained from [12].

Experimental procedures for DNA sequencing of eba-175

Genomic DNA was extracted from pretreated peripheral blood samples from patients infected with P. falciparum using a QIAamp Blood Kit (Qiagen, Hilden, Germany). DNA fragments covering a part of the eba-175 coding sequence (regions II and III) of P. falciparum were amplified by PCR using the following sets of primers: EBA175-fragment1, 5′-ggaagaaatacttcatctaataacg-3′ (forward) and 5′-catcctttacttctggacacatcg-3′ (reverse), and EBA175-fragment2, 5′-gagactctgaaggttgaatgcaa-3′ (forward) and 5′-aggtgtattagacatatcttggtc-3′ (reverse). These primers were designed based on the eba-175 reference sequence from P. falciparum (GenBank accession no. X52524). PCR amplification was performed in a 13.0-µL reaction mixture containing 0.125 µL (0.125 µM) each of forward and reverse primers, 0.125 µL TAKARA LA Taq™ (5 units/µL), 1.25 µL 10× LA PCR™ Buffer II (Mg2+ free), 1.25 µL 25 mM MgCl2, 1.25 µL 2.5 mM dNTP mixture, 0.5 µL (5 ng) of genomic DNA template, and 8.375 µL dH2O using a GeneAmp® PCR System 9700 (Applied Biosystems, Foster City, CA, USA). The PCR cycling conditions for each primer pair were 60 s initial denaturation at 94°C, followed by 40 cycles of 30 s denaturation at 94°C, 30 s annealing at 56°C, and 150 s extension at 72°C, and a final step of 5 min extension at 72°C. The PCR products were subsequently sequenced using an ABI Prism 3100 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA). Primer sequences used for direct sequencing are available upon request. The isolates showing multiple superimposed electropherogram peaks at a single site following PCR-direct sequencing and a secondary peak greater than 30% of the predominant peak were considered to be mixed infections and excluded from further analyses. Low-quality sequences (i.e., high background noise or too weak signal) were also excluded. As a result, 131 sequences representing the single or most abundant sequence in each DNA sample were included in the analyses.

Data analyses

The nucleotide sequences obtained were aligned and translated into putative amino acid sequences using MEGA v.5.2 [13]. To examine the phylogenetic relations among 32 distinct eba-175 Thai P. falciparum alleles and two eba-175 P. reichenowi alleles (CBXM000000000 and AJ251848), a maximum likelihood (ML) tree was constructed based on the Hasegawa–Kishino–Yano model [14]. To obtain the ML tree, a nearest-neighbor-interchange (NNI) search was applied. In addition, a neighbor-joining (NJ) [15] tree was generated using 194 eba-175 partial region II sequences from P. falciparum worldwide and two P. reichenowi sequences (CBXM000000000 and AJ251848), based on the Nei–Gojobori (NG) model [16] and the Jukes–Cantor (JC) correction [17]. The construction of phylogenetic trees and estimation of best-fit substitution model for the ML tree were implemented in MEGA v.5.2 [13]. All the positions containing insertions/deletions were eliminated from the analyses (complete deletion option). Branch support values were computed by bootstrap analyses with 1,000 replications. A network of 194 P. falciparum and two P. reichenowi eba-175 alleles was also constructed based on synonymous substitutions using the neighbor-net method [18] in SplitsTree4 ver. 4.13.1 [19].

The time to the most recent common ancestor (tMRCA) of the eba-175 alleles from Thai falciparum was estimated from the linearized tree based on synonymous substitutions among the 32 distinct eba-175 alleles by using the MEGA v5.2 [13]. The neutral substitution rate was calculated assuming that P. falciparum and P. reichenowi diverged 6 million years ago (MYA) [5, 20]. In addition, the MCMCTree program in the PAML 4.8 package [21] was used to estimate tMRCA based on the amino acid sequences. The minimum and maximum age constraints on the root age (the divergence time between P. falciparum and P. reichenowi) were set to 5 and 7 MYA, respectively. The tMRCA estimation was based on a WAG model [22] for amino acid substitutions. In the MCMC process, sampling occurred every 100 generations for 10,000 generations and the first 50,000 generations were discarded as burn-in.

To detect the signatures of natural selection, the number of nonsynonymous substitutions per nonsynonymous site (d N) and synonymous substitutions per synonymous site (d S) for all the pairs formed by the 32 distinct Thai P. falciparum alleles, 16 from chimpanzee Plasmodium spp., 11 from gorilla Plasmodium spp., and four from P. reichenowi sequences were estimated using the NG model with the JC correction in MEGA v.5.2 [13]. Significant difference between d N and d S was assessed by Wilcoxon signed-rank test. For all the 131 Thai P. falciparum isolates, the numbers of nonsynonymous substitutions per nonsynonymous site (π N) and synonymous substitutions per synonymous site (π S) were also calculated in the same manner as d N and d S. In addition, the McDonald–Kreitman (MK) test [23] was performed for detecting natural selection signal using DnaSP v5 software [24]. Tajima’s D test [25] was performed for 131 Thai P. falciparum eba-175 sequences using DnaSP v5 software [24], where the test statistic was analytically calculated. A two-sided P value of less than 0.05 was considered statistically significant.

A Wu–Kabat plot was used to estimate the level of amino acid variability for the 32 distinct Thai P. falciparum eba-175 alleles [26]. The Wu–Kabat plot estimates the level of variability for each amino acid position in the sequence alignment, measured as the number of amino acids at each site divided by the maximum frequency of amino acid for all sites.

Results

Detection of eba-175 alleles

The nucleotide sequences of regions II and III of P. falciparum eba-175 were obtained by PCR-direct sequencing. The eba-175 region III showed highly divergent dimorphic segments, the F and C segments [termed Fseg (423 bp) and Cseg (342 bp)], as reported by Ware et al. [27]. A total of 32 distinct alleles [20 Fseg alleles (ca. 2,740 bp) and 12 Cseg alleles (ca. 2,660 bp)], defined by 30 polymorphic sites including insertions/deletions (site 744–749, and 2094), were detected from 131 P. falciparum isolates from Thailand [Fig. 1; Fseg alleles: F1_1F20 (Genbank accession numbers LC008232–LC008251) and Cseg alleles: C1C12 (Genbank accession numbers LC008252–LC008263)]. The nucleotide sequences of the 32 alleles were translated into 31 distinct amino acid sequences. Synonymous substitutions were found at only two sites in the allele sequences. On the other hand, nonsynonymous substitutions were found at 21 sites, not including an insertion/deletion site. The F and C segments were excluded from further analyses.
Fig. 1
Fig. 1

The 32 eba-175 alleles detected from 131 Thai patients infected with malaria. Dots indicate identity with allele C1 nucleotide sequence. Dashes indicate insertions/deletions. F and C segments are not shown.

Phylogenetic relations among eba-175 alleles

A ML tree was constructed based on the nucleotide sequences of 32 eba-175 alleles from Thai P. falciparum, and two eba-175 alleles from P. reichenowi (Fig. 2). In this ML tree, Fseg alleles formed a monophyletic clade with a relatively low bootstrap value (51%). A NJ tree was generated based on synonymous substitutions in region II to further analyze the phylogenetic relations among 194 P. falciparum eba-175 alleles, including a large sequence dataset from Genbank [12] (Fig. 3). In particular, in this NJ tree, some P. falciparum alleles isolated from Asia formed a single clade rooted in the most basal node from where all P. falciparum sequences diverged. All the alleles included in the Asian clade were characterized by a mutation in site 441, as shown in Fig. 1 (Asian-specific alleles contain cytosine nucleotide at site 441, where all other sequences contain a thymine). This Asian-specific cluster was also supported by the neighbor-net method (Additional file 1) and suggests that an ancestral allele in the cluster emerged in Asia and then rapidly spread across Asia after the out-of-Africa.
Fig. 2
Fig. 2

Maximum likelihood tree of eba-175 (2,304 bp) regions II and III from Thai Plasmodium falciparum. The distance based on nucleotide substitutions was calculated by the Hasegawa–Kishino–Yano model. Two P. reichenowi eba-175-like (Prei_eba-175) sequences were used as outgroups. Only bootstrap values larger than 50% are shown.

Fig. 3
Fig. 3

Neighbor-joining tree of eba-175 partial region II (1,692 bp) of P. falciparum across the world. The distance based on synonymous substitutions was calculated using the Nei–Gojobori method with Jukes–Cantor model. Two P. reichenowi eba-175-like sequences were used as outgroups. Only bootstrap values larger than 50% are shown.

Estimated divergence time

The d s values for regions II and III for all the pairs formed by the 32 distinct eba-175 alleles were calculated to estimate tMRCA of eba-175 alleles in the Thai population. The neutral mutation rate of the eba-175 gene was extrapolated from the calibration point derived from the divergence time of P. falciparum and P. reichenowi (6 MYA) [5, 20] by using the linearized tree of eba-175 alleles in the MEGA program [13]. Thus, the estimated neutral mutation rate was 1.0 × 10−8 per site per year. Accordingly, the estimated tMRCA for eba-175 was approximately 0.14 MYA. The number of synonymous substitutions observed in Thai P. falciparum isolates was small (maximum d S value = 2); consequently, MCMCTree was used to estimate the tMRCA of eba-175 alleles based on amino acid substitutions within region III. In this case, the estimated tMRCA was approximately 0.13 MYA (95% highest posterior density confidential interval = 0.07–0.23 MYA). Notably, these estimations rely on the assumption that P. falciparum and P. reichenowi diverged 6 MYA.

Diversifying selection on eba-175 region II

To search a signal of natural selection on region II of eba-175 in Thai P. falciparum, the d N and d S values for 32 long sequences (2,310 bp) were calculated (Table 1). A comparison of the two values revealed that the d N was significantly larger than d S (P value <2.2 × 10−16, Wilcoxon signed-rank test), suggesting that diversifying selection has influenced eba-175 diversification in human P. falciparum. In addition, this result was further supported by the comparison between π N and π S, including the allele frequencies of 131 Thai P. falciparum isolates (π N/π S = 2.62; P value <2.2 × 10−16, Wilcoxon signed-rank test). Subsequently, it was examined whether diversifying selection has also operated within other taxa, using sequence data from 16 and 11 Plasmodium spp. infecting chimpanzees and gorillas, respectively, and four P. reichenowi isolates (Table 1). Long sequence data from African apes Plasmodium isolates were unavailable; consequently, region II short sequences (390–396 bp) were used for this analysis. Similar to the results using long sequences, d N was significantly larger than d S in human P. falciparum (P value <2.2 × 10−16, Wilcoxon signed-rank test); on the other hand, d N was significantly smaller than d S in African apes Plasmodium (each P value <2.2 × 10−16, Wilcoxon signed-rank test for chimpanzee and gorilla Plasmodium isolates). No significant differences between d N and d S were detected for P. reichenowi (P value = 0.32, Wilcoxon signed-rank test). These results suggest that diversifying selection has only acted on eba-175 in human P. falciparum.
Table 1

Comparison of nonsynonymous (d N) and synonymous (d S substitution rates in Plasmodium eba-175 region II)

Species

N

Length (bp)

d N

d S

d N/d S

P value

Human Plasmodium falciparum isolates

32

2,310

0.005 ± 0.001

0.002 ± 0.001

2.98

<2.2 × 10−16

 

32

390

0.010 ± 0.004

0.000 ± 0.000

N/A

N/A

Chimpanzee Plasmodium isolates

16

396

0.089 ± 0.013

0.110 ± 0.026

0.81

<2.2 × 10−16

Gorilla Plasmodium isolates

11

396

0.169 ± 0.019

0.207 ± 0.037

0.82

<2.2 × 10−16

Plasmodium reichenowi

5

393

0.003 ± 0.002

0.005 ± 0.005

0.47

0.32

N/A not applicable.

The McDonald–Kreitman (MK) test [23] for sequences of eba-175 region II in 32 Thai P. falciparum alleles and one in P. reichenowi showed that the ratio of nonsynonymous to synonymous polymorphic sites within species (Pn/Ps = 19/1) was significantly higher than that of fixed sites between species (Dn/Ds = 116/48; P = 0.017, Fisher’s exact test). However, the MK test for Plasmodium isolates from African apes did not show significant differences between Pn/Ps and Dn/Ds (Pn/Ps = 59/23 and Dn/Ds = 14/6, P-value = 1.00 for 16 chimpanzee Plasmodium isolates and one P. reichenowi; Pn/Ps = 81/29 and Dn/Ds = 6/4, P = 0.46 for 11 gorilla Plasmodium isolates and one P. reichenowi). The results from the MK test suggest that either purifying selection or diversifying selection has acted on eba-175 in Thai P. falciparum population.

Tajima’s D test [25] was used to test for departure from selective neutrality in 131 eba-175 sequences of Thai P. falciparum. This test compares two population genetic parameters, one estimated from mean pairwise nucleotide differences and the other from the number of mutations. The results revealed a significant positive Tajima’s D value (Tajima’s D statistic = 3.01 and P value <0.01), suggesting the balancing selection on eba-175 in Thai P. falciparum. The possibility of a recent reduction in population size that provided the significant positive Tajima’s D statistic may be excluded, since both the d N/d S ratio test and the MK test also suggested the existence of positive diversifying selection.

To assess the relation between amino acid variability and the erythrocyte binding site, the level of amino acid variability at each site was examined using a Wu–Kabat plot (Additional file 2). The Wu–Kabat plot showed that the level of amino acid variability at some codon sites outside the sites of direct interaction between P. falciparum EBA-175 and human GYPA molecules [28] was higher than the variation level at their interaction sites. These variable sites may be located in regions recognized by human antibodies if the higher degree of variation is caused by diversifying selection favoring mutations to other amino acids.

Discussion

Modern humans are believed to have emerged in Africa approximately 0.2 MYA and subsequently dispersed and colonized other continents after their exodus from Africa (known as the “out-of-Africa event”) approximately 0.1 MYA, although the accuracy of these estimates remains a contentious issue [2932]. Here tMRCA for Thai P. falciparum eba-175 was examined, and our results, 0.14 MYA from synonymous substitutions and 0.13 MYA from amino acid substitutions, suggest that the tMRCA of Thai P. falciparum may predate the out-of-Africa event but after the emergence of modern humans. However, this estimation relies largely on the assumption that P. falciparum diverged from P. reichenowi 6 MYA [5, 20]. A recent phylogenetic analysis for Plasmodium infecting Homininae species suggested that Plasmodium infecting gorillas was transmitted to modern humans in recent times [33]. This possible recent evolutionary origin of human P. falciparum is incompatible with the present assumption of that P. falciparum/P. reichenowi divergence time is similar to that of humans/chimpanzees (i.e., ca. 6 MYA [3437]). However, regardless of the tMRCA estimate, ancestral human dispersal and recent increase in human population size, resulting in the increase in P. falciparum population size, are likely to have contributed to the eba-175 diversification of P. falciparum (i.e., the emergence of Asian-specific clade).

The comparison of d N/d S ratios of eba-175 region II sequences among Plasmodium species showed an excess of nonsynonymous substitutions over synonymous substitutions in human P. falciparum but not in Plasmodium spp. infecting African apes and P. reichenowi. The result suggests that diversifying selection has affected eba-175 region II in Thai P. falciparum, as previously reported [811]. The results on π N/π S ratios and MK test [23] also supported the diversifying selection hypothesis. On the other hand, the estimated d N/d S ratios and MK test [23] suggested that eba-175 genetic diversities in other Plasmodium relatives have not been affected by diversifying selection. Thus, the EBA-175 protein may be the target for the immune response against P. falciparum malaria only in humans.

In this study, the tMRCA was estimated under the assumption of no inter-allelic recombination. The presence of inter-allelic recombination may affect the estimation of tMRCA. Since the DnaSP program [24] suggested the existence of recombination among 32 eba-175 alleles (Minimum number of recombination events, Rm: 8), we investigated the possible recombinants by using the GENECONV program [38], and detected 21 possible recombinants. After the removal of 21 possible recombinants, we recalculated the tMRCA of the remaining 11 eba-175 alleles in Thai P. falciparum. The estimated tMRCA was approximately 0.12 MYA that was roughly equivalent to the tMRCA (0.14 MYA) estimated by using all of 32 alleles. In addition, the d N/d S ratio of 11 sequences not including recombinant sequences (2.46) was not largely different from that of 32 sequences (2.98). Thus, our results seem not to be affected by the presence of possible recombinants.

Conclusions

The genetic diversity in region II of P. falciparum eba-175 seems to have been increased after the exodus from Africa of ancestral modern humans. As a consequence of the human expansion followed by an increase in P. falciparum population size, diversifying selection may have efficiently maintained the nonsynonymous substitutions in region II of Thai P. falciparum eba-175. Human dispersal out of Africa would have had a major impact on molecular evolution of P. falciparum eba-175.

Declarations

Authors’ contributions

YY conducted the statistical analyses and wrote the manuscript. JP and HH collected blood samples. IN, JP, and HH extracted DNA from blood samples. IN carried out the experiments. YY, JP, and JO participated in the design of the study. JO was involved in the interpretation of the data and preparation of the manuscript. All authors have read and approved the final manuscript.

Acknowledgements

The authors deeply thank all the subjects for their participation in the study. This study was partly supported by KAKENHI (25650125) Grant-in-Aid for Challenging Exploratory Research and KAKENHI (26305015) Grant-in-Aid for Scientific Research (B), the Takeda Science Foundation, and KAKENHI (26-1601) Grant-in-Aid for JSPS Fellows.

Compliance with ethical guidelines

Competing interests The authors declare that they have no competing interests.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
(2)
Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
(3)
Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
(4)
Department of Social and Environmental Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

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