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Open Access Highly Accessed Research article

Phylogenomic analyses of malaria parasites and evolution of their exported proteins

Christian Pick1, Ingo Ebersberger2, Tobias Spielmann3, Iris Bruchhaus3 and Thorsten Burmester1*

Author Affiliations

1 Institute of Zoology and Zoological Museum, University of Hamburg, Martin-Luther-King-Platz 3, D-20146 Hamburg, Germany

2 Center of Integrative Bioinformatics Vienna, University of Vienna, Medical University of Vienna, University of Veterinary Medicine Vienna, Dr.-Bohrgasse 9, 1030 Vienna, Austria

3 Bernhard Nocht Institute for Tropical Medicine, Bernhard-Nocht-Str. 74, D-20359 Hamburg, Germany

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BMC Evolutionary Biology 2011, 11:167  doi:10.1186/1471-2148-11-167

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2148/11/167


Received:14 February 2011
Accepted:15 June 2011
Published:15 June 2011

© 2011 Pick et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Plasmodium falciparum is the most malignant agent of human malaria. It belongs to the taxon Laverania, which includes other ape-infecting Plasmodium species. The origin of the Laverania is still debated. P. falciparum exports pathogenicity-related proteins into the host cell using the Plasmodium export element (PEXEL). Predictions based on the presence of a PEXEL motif suggest that more than 300 proteins are exported by P. falciparum, while there are many fewer exported proteins in non-Laverania.

Results

A whole-genome approach was applied to resolve the phylogeny of eight Plasmodium species and four outgroup taxa. By using 218 orthologous proteins we received unanimous support for a sister group position of Laverania and avian malaria parasites. This observation was corroborated by the analyses of 28 exported proteins with orthologs present in all Plasmodium species. Most interestingly, several deviations from the P. falciparum PEXEL motif were found to be present in the orthologous sequences of non-Laverania.

Conclusion

Our phylogenomic analyses strongly support the hypotheses that the Laverania have been founded by a single Plasmodium species switching from birds to African great apes or vice versa. The deviations from the canonical PEXEL motif in orthologs may explain the comparably low number of exported proteins that have been predicted in non-Laverania.

Background

Malaria is one of the most common infectious diseases, putting about two billion humans at risk and resulting in about one million fatalities each year [1]. Malaria is caused by protozoan parasites of the genus Plasmodium (Haemosporidae; Apicomplexa). Species of this genus undergo a complex life cycle including an asexual proliferation phase in the erythrocytes of vertebrate hosts.

Although hundreds of Plasmodium species are currently known, only few infect humans. In moderate climate zones, human malaria infection is largely due to P. vivax, but the life-threatening form of this disease is almost exclusively caused by P. falciparum. About 60 years ago, the high pathogenicity of P. falciparum led to the proposal that this parasite may be a rather recent acquisition from a non-human host [2]. Since then, it has become evident that P. falciparum indeed is closely related to other Plasmodium species from African great apes [3,4]. Together they constitute the subgenus Laverania and several reciprocal host switches have occurred during the evolution of this group of malaria parasites [5-9].

The evolutionary ancestry of P. falciparum and the other Laverania is still a matter of debate. Until now, it has not been conclusively agreed on whether this subgenus is more closely related to other mammalian malaria parasites or whether it shares a common ancestry with bird-infecting Plasmodium species (reviewed in [10]). Most molecular phylogenetic studies of the genus Plasmodium are based on the analysis of single proteins such as cytochrome b oxidase, adenylosuccinate lyase, and caseinolytic protease C [10]. While these proteins contain sufficient phylogenetic information to resolve the relationships within the Laverania, multiple substitutions per site (homoplasy) limit their utility at a deeper phylogenetic level [10].

Upon invasion by P. falciparum, erythrocytes are subjected to an extensive remodeling process resulting in altered mechanical and adhesive properties [11]. Prominent examples include the formation of cytoadherence knobs at the erythrocyte membrane and the associated exposure of PfEMP1 (P. falciparum erythrocyte membrane protein) at the surface of the infected cell [12]. Plasmodium proteins involved in this remodeling process have to pass the parasitophorous vacuole membrane (PVM) on their way from the parasite into the erythrocyte; most of these proteins are characterized by a hydrophobic signal sequence for targeting the protein to the endoplasmic reticulum (ER) and a sequence motif (RxLxE/Q/D) either referred to as Plasmodium export element (PEXEL; [13]) or vacuolar transport signal [14].

The PEXEL motif is cleaved by the aspartyl protease plasmepsin V in the ER of the parasite [15-17] and the nascent protein is released into the parasitophorous vacuole. From there it is transported through the PVM into the host cell by the Plasmodium translocon of exported proteins (PTEX; [18]). Predictions based on the presence of the PEXEL suggest that more than 300 P. falciparum proteins are exported into the host cell [13,14,19,20]. Notably, PfEMP1s are structurally different, having an export element that precedes the signal sequence (R/KxL/V/MxE/D; cf. [13]). This export element appears to be necessary for export [13] but is not cleaved in vivo, and therefore might be functionally distinct [21].

The conservation of plasmepsin V and the components of PTEX throughout the genus Plasmodium indicates that the same protein export machinery is used by all Plasmodium species [16-18]. In addition, PEXEL sequences from P. falciparum proteins proved to be functional in rodent malaria parasites [13] and vice versa [22]. Thus, in principle, the screens to detect exported proteins in P. falciparum should be extendable to other Plasmodium species. However, surprisingly few proteins have been detected outside of the Laverania using the P. falciparum PEXEL motif, and it has been suggested that these species export substantially fewer proteins into the host cell than P. falciparum [13,14,19].

Non-Laverania, however, also induce elaborate morphological changes in their host cells and the low number of predicted exported proteins may argue for a prominent role of PEXEL-negative exported proteins (PNEPs; reviewed in [23]). An additional, thus far unexplored, explanation could be a slightly different consensus of the PEXEL motif in Plasmodium taxa other than Laverania that could hamper the prediction of these proteins. This would inevitably lead to an underestimation of the respective exportomes.

Here, we took advantage of the available genomic sequences from eight Plasmodium species and four other apicomplexan species. Orthologous proteins were identified and used (i) to reconstruct the phylogeny of these species, (ii) to obtain a set of exported P. falciparum proteins that are conserved throughout Plasmodium evolution, and (iii) to investigate the evolutionary plasticity of the corresponding Plasmodium export elements.

Methods

Source of sequence data

The genomic sequences of P. falciparum 3D7 [24], P. yoelii 17XNL [25], P. berghei Anka [26], P. chabaudi AS [26], P. knowlesi H [27], P. vivax Sal-1 [28], as well as P. reichenowi and P. gallinaceum (both unpublished data produced by the Wellcome Trust Sanger Institute; used with permission) were obtained from PlasmoDB v. 6.1 [29]; sequences of Toxoplasma gondii ME49 were obtained from ToxoDB v. 5.2 [30], sequences of Babesia bovis T2Bo from Integr8 [31], sequences of Cryptosporidium parvum Iowa from CryptoDB [32]; sequences of Theileria annulata Ankara [33] were downloaded from the Sanger Institute http://www.sanger.ac.uk/resources/downloads/protozoa/ webcite.

Collection of orthologs

The dataset of orthologous proteins for phylogeny reconstructions was compiled as described before [34]. In brief, InParanoid-TC was used with P. falciparum, P. vivax, P. knowlesi, P. yoelii, P. berghei, P. chabaudi, T. gondii, and B. bovis as primer taxa. For 921 proteins orthologs were present in all eight primer taxa. These 921 core orthologs served then as input for HaMStR to search for the corresponding proteins in P. reichenowi, P. gallinaceum, C. parvum, and T. annulata. Following search species - reference species pairs were used in the HaMStR search: P. reichenowi - P. falciparum, P. gallinaceum - P. falciparum, C. parvum - T. gondii, and T. annulata - B. bovis. HaMStR could extend 218 core orthologs with sequences from all four species such that each ortholog group consisted of twelve sequences. The amino acid sequences for each of the 218 core orthologs were aligned with MAFFT [35] using the options --maxiterate 1000 and --localpair. The 218 single alignments were concatenated to form a super-alignment with 192,102 aa positions. This super-alignment was processed twice: (i) positions for which less than half of the sequences were represented by an amino acid were removed, and (ii) Gblocks 0.91b [36] was applied using the following parameters: --minimum number of sequences for a conserved position was set to 7; --minimum number of sequences for a flanking position was set to 10; --maximum number of contiguous nonconserved positions was set to 4; --minimum length of a block was set to 10; and --allowed gap positions was set to none.

To obtain the collection of exported proteins that have functionally equivalent orthologs in the other Plasmodium species, the two most comprehensive predictions of exported P. falciparum proteins were used [19,20]. These predictions contain 396 and 422 proteins (not including the structurally distinct PfEMP1s), respectively; the combination of both resulted in a non-redundant set of 531 putatively exported proteins. Each protein was used as query for a tBLASTn search against the P. falciparum genome. Proteins, for which the E value of the best BLAST hit (not considering the hit against itself) was larger than 10-10, were considered to have no paralogs present in P. falciparum and were used for further analysis. For each paralog-free protein a reciprocal tBLASTn search was performed to identify candidate orthologs in the other Plasmodium species (E value cut-off: < 10-10). Proteins with a single ortholog present in each of the eight Plasmodium species were aligned with MAFFT [35] using the options --maxiterate 1000 and --localpair.

Phylogeny reconstruction

Maximum likelihood (ML) trees were reconstructed with RAxML v. 7.2.2 [37] using the WAG model [38] of amino acid sequence evolution with empirical amino acid frequencies (option F). Substitution rate heterogeneity was modeled using a gamma distribution, allowing for a fraction of invariant sites (option GAMMAI). Bayesian tree search was performed with PhyloBayes v. 3.2 [39] using the WAG model. Four MCMC chains were run for 10,000 cycles. Every 10th cycle was sampled and convergence of the chains was pair-wise checked with bpcomp allowing for a burn-in of 1,000 cycles. Increasing the burn-in or usage of other models of amino acid sequence evolution such as the CAT [40] or LG model [41] did not change the results (not shown).

Testing of alternative phylogenies

The small number of taxa in our study allows the evaluation of every possible tree topology. However, we reduced the number of tested trees by imposing the following constraints: monophyly of the genus Plasmodium; monophyly of B. bovis and T. annulata (Piroplasmida); monophyly of T. gondii and C. parvum (Eimeriorina); monophyly of P. yoelii and P. berghei; monophyly of P. falciparum and P. reichenowi; monophyly of P. vivax and P. knowlesi. Note that all seven constraints represent accepted evolutionary relationships (see references in Table 1) except the monophyly of T. gondii and C. parvum [42], and have been confirmed by our unrestricted heuristic tree searches. We computed the likelihood of the resulting 105 alternative tree topologies with TREE-PUZZLE v. 5.2.pl21.1 [43] using the WAG model of sequence evolution. Substitution rate heterogeneity was modeled with a gamma distribution assuming four rate categories and empirical amino acid frequencies. Hypothesis testing was performed using the routines provided by TREE-PUZZLE and by CONSEL [44].

Table 1. Molecular phylogenetic analyses attempting to resolve the relationships among malaria parasites.

Sequence analysis

Pairwise amino acid identities and similarities were calculated with GeneDoc v. 2.6 [45] using the Blosum 62 model. PEXEL sequences of the P. falciparum proteins were identified via a match to the published consensus sequences [13,14,19,20]. The putative PEXEL sequences of proteins from other Plasmodium species were extracted by aligning these proteins to their ortholog in P. falciparum; we then used the homologous amino acid positions to the P. falciparum PEXEL as candidate export elements in these species. PEXEL sequences from the individual proteins were aligned separately for each species by hand and the corresponding PEXEL motifs were generated with WebLogo [46]. Presence of hydrophobic signal sequences was assessed using SignalP v. 3.0 [47].

Results and Discussion

Evolutionary ancestry of P. falciparum and other Laverania

We extracted the genomic sequences of eight Plasmodium species (P. falciparum, P. reichenowi, P. vivax, P. knowlesi, P. gallinaceum, P. chabaudi, P. yoelii, and P. berghei) and four additional apicomplexan species (T. gondii, C. parvum, T. annulata, and B. bovis) from public databases. HaMStR, a Hidden Markov Model based tool [34], was used to identify 218 proteins with orthologs in all twelve species (Additional file 1). This number is similar to that used in a recent phylogenomic study of eight apicomplexan species, including two species from the genus Plasmodium [48].

Additional file 1. 218 P. falciparum proteins with orthologs present in P. reichenowi, P. vivax, P. knowlesi, P. gallinaceum, P. chabaudi, P. yoelii, and P. berghei, as well as the four outgroup taxa (T. gondii, C. parvum, T. annulata, and B. bovis).

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The single alignments of the 218 proteins were concatenated and positions for which less than half of the taxa were represented by an amino acid were removed. This resulted in a super-alignment with 135,360 aa positions (Additional file 2), which was used for initial maximum likelihood (ML) and Bayesian tree reconstructions. While tree topologies inferred from the ML analysis were identical with those obtained in later analyses (see below; Figure 1), MCMC chains did not converge on a single topology, indicating that the dataset includes conflicting phylogenetic information. Therefore, the 135,360 aa alignment was further processed using Gblocks [36]. This procedure has been demonstrated to improve phylogenetic analyses by reducing the impact of misaligned regions (due to very high sequence divergence) and homoplasy (due to sequence saturation) [49]. We obtained a final alignment comprising 49,521 aa positions and no missing data (Additional file 3). In Bayesian analysis, MCMC chains readily converged on the same topology (maxdiff: 0; meandiff: 0). In the resulting consensus tree all nodes received strong support and the same topology was obtained in ML analyses (Figure 1).

thumbnailFigure 1. Phylogenetic relationships of eight malaria parasites. Phylogenetic tree reconstructions were based on 218 proteins. The single alignments were concatenated to form a super-alignment and problematic alignment regions were subsequently removed with Gblocks. This procedure resulted in an alignment with 49,521 aa positions (no missing data), which was used for ML tree reconstruction and Bayesian tree search. T. gondii, C. parvum, T. annulata, and B. bovis were used as an outgroup to root the tree. Only the ML tree is displayed, but the topology of the Bayesian tree was identical. Numbers at the nodes denote bootstrap support values (left) and Bayesian posterior probabilities (right). The scale bar equals 0.05 expected substitutions per site. See also Additional files 1, 2 and 3.

Additional file 2. Alignment with 135,360 aa positions. Total amount of missing data was 10.2%; amount of missing data per species was 7.1% for T. gondii, 14.8% for C. parvum, 12.2% for T. annulata, 12.5% for B. bovis, 0.5%; for P. falciparum, 35.4% for P. reichenowi; 25.4% for P. gallinaceum, 0.7% for P. knowlesi, 0.6% for P. vivax, 0.8% for P. chabaudi, 4.0% for P. yoelii, and 14.2% for P. berghei.

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Additional file 3. Alignment with 49,521 aa positions. Total amount of missing data was none.

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The phylogenetic analyses show that the eight Plasmodium species form a monophyletic clade (100% bootstrap support and 1.00 Bayesian posterior probabilities). The malaria parasites from rodents (P. chabaudi, P. yoelii, and P. berghei) are clearly separated from those infecting birds and primates (100% bootstrap support and 1.00 Bayesian posterior probabilities). Notably, the Laverania (P. falciparum and P. reichenowi) do not group with the other primate-infecting malaria parasites, but form a well-supported clade with P. gallinaceum (99% bootstrap support and 1.00 Bayesian posterior probabilities).

ML as well as Bayesian methods return only the best tree and thus provide no information on other tree topologies with likelihoods that may not be significantly worse. To address this issue, 104 alternative tree topologies were tested by inferring their expected likelihood weights (ELW; [50]) and their probabilities in the approximately unbiased (AU) test [51]. All alternative tree topologies (including those with P. gallinaceum being the sister group of mammal Plasmodium species) were rejected with high confidence (Figure 2; Additional file 4). Thus, the position of P. gallinaceum as sister group to the Laverania receives unambiguous support from the data.

thumbnailFigure 2. Alternative relationships among major Plasmodium lineages resulting from different root placements. The results for the individual likelihood ratio tests are given below each tree. ELW, expected likelihood weights [50]; AU, approximately unbiased test [51]. T. gondii, C. parvum, T. annulata, and B. bovis were used as an outgroup. Note that only the results from analyses with rate heterogeneity are shown; results from analyses without rate heterogeneity were essentially the same. See also Additional file 4.

Additional file 4. Likelihood ratio tests for 104 different tree topologies (with and without rate heterogeneity), including their expected likelihood weights (ELW) and probabilities in the approximately unbiased (AU) test. User specified test trees, as well as TREE-PUZZLE and CONSEL output files are given.

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Until now, two other whole-genome approaches attempted to resolve the evolutionary relationships of the eight Plasmodium species. Dávalos and Perkins [52] based their analyses on a set of 104 proteins (~26,000 aa positions), recovering the same topology among Plasmodium species as displayed in Figure 1. However, no outgroup taxa were included to root the tree, and thus no information on the evolutionary ancestry of the Laverania could be provided. Silva et al. [53], on the other hand, based their analyses on a set of 29 proteins (~12,000 aa positions) and used two species from the genus Theileria to root the tree. While they proposed the monophyly of mammalian Plasmodium species, some of their results supported a grouping of P. gallinaceum and the Laverania.

Dávalos and Perkins [52] as well as Silva et al. [53] both used slow-evolving proteins for their phylogenetic inferences. To assess the effect of the evolutionary rate on our analysis, we partitioned the 218 proteins of our dataset. We first computed a ML tree for each protein individually. The length of this protein tree, i.e. the sum of its branch lengths, then served as an approximation for the evolutionary rate (Figure 3; see also Additional file 5). Subsequently, the proteins were categorized into three subsets according to their tree lengths. Dataset 1 comprised 65 slow-evolving proteins (tree lengths of less than two expected substitutions per site). Dataset 2 comprised 88 proteins evolving at an intermediate speed (tree lengths of two or more but less than four expected substitutions per site). Dataset 3 comprised the 66 fast-evolving proteins (tree length of four or more expected substitutions per site). For subsequent tree reconstruction, 65 proteins were randomly chosen from each partition such that the same number of proteins was used for each dataset. The individual alignments were concatenated, processed with Gblocks as described and used for ML tree reconstruction (Figure 4). All three datasets agree in placing P. gallinaceum as sister of the Laverania. The topology of the tree was thus identical with that inferred from the complete dataset (Figure 1). We conclude that our reconstruction of the Plasmodium phylogeny does not depend on the evolutionary rates of the proteins used for the phylogeny.

thumbnailFigure 3. Evolutionary rates of the 218 proteins used for phylogenetic inferences. The length of the individual protein trees, i.e. the sum of its branch lengths, served as an approximation for the evolutionary rate. Note that only the proteins of primer taxa (P. falciparum, P. vivax, P. knowlesi, P. yoelii, P. berghei, P. chabaudi, T. gondii, and B. bovis) were considered. See also Additional file 5.

thumbnailFigure 4. Phylogenetic relationships inferred using three subsets of proteins with varying evolutionary rates. The proteins used for the initial phylogenetic inference were categorized into three subsets each comprising 65 proteins: (A) Slow-evolving proteins (tree lengths of less than two expected substitutions per site); 13,670 aa of 50,332 aa (51%) were used for ML inference. (B) Proteins evolving at an intermediate speed (tree lengths of two or more but less than four expected substitutions per site); 14,967 aa of 27,063 aa (30%) were used for ML inference. (C) Fast-evolving-proteins (tree lengths of four or more expected substitutions per site); 12,021 aa of 96,774 aa (12%) were used for ML inference. T. gondii, C. parvum, T. annulata, and B. bovis were used to root the trees. Numbers at the nodes denote bootstrap support values; scale bars are equal to 0.05 expected substitutions per site.

Additional file 5. Sum of the expected substitutions per site for each of the 218 proteins used for phylogenetic inference. Note that only the proteins of primer taxa (P. falciparum, P. vivax, P. knowlesi, P. yoelii, P. berghei, P. chabaudi, T. gondii, and B. bovis) were considered.

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The bootstrap support for the clade consisting of P. gallinaceum and Laverania was maximal for the dataset comprising proteins evolving at an intermediate speed (98%) and minimal for the dataset comprising the fast-evolving proteins (76%). The branch leading to the clade consisting of P. gallinaceum and Laverania was short (~0.02 expected substitutions per site; cf. Figure 4). When using fast-evolving proteins, multiple substitutions in the dataset might confound the phylogenetic signal leading to artifacts due to long branch attraction [54]. On the other hand, using only slow-evolving proteins is likely to result in a dataset with a phylogenetic signal that is too weak to resolve this branch (see also Additional file 6). This may explain why proteins evolving with an intermediate rate provide the most robust tree.

Additional file 6. Split network analyses of Plasmodium phylogeny, as reconstructed from the 65 slow-evolving proteins in our dataset. The network was calculated with SplitsTree v. 4.11.3 [71], considering only splits with frequencies of at least 10%. Notably, a sister group position of P. gallinaceum to all mammalian Plasmodium species is not supported.

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The finding of a relationship between the Laverania and avian malaria parasites agrees with earlier studies by Waters et al. [55], Escalante and Ayala [56], and Kissinger et al. [57]. However, it contradicts more recent results by Perkins and Schall [58], Leclerc et al. [59], Roy and Irimia [60] and Martinsen et al. [61]. This discrepancy may be attributed to the limited phylogenetic information in the few proteins that were used in those studies [10]. While the selection of proteins may have some effect (see above), the number and choice of the outgroup taxa deserve particular attention (e.g., [62]). Alternative root placements lead to different conclusions about the order in which the individual Plasmodium species emerged (c.f. Figure 2). In many previous studies, only a single outgroup taxon was used (Table 1). Moreover, in some cases this outgroup was evolutionarily so distantly related that a meaningful placement of the root is unlikely (e.g., [63]). Most recent studies of Plasmodium phylogeny used selected species from the closely related genus Leucocytozoon as an outgroup (c.f. Table 1). However, the limited amount of sequence data available for this taxon - mainly a few mitochondrial genes - currently prevents its use in phylogenomic studies. Other haemosporidians (i.e., species from the genera Haemoproteus, Parahaemoproteus, and Hepatocystis) should not be considered as an outgroup since the genus Plasmodium has been shown to be paraphyletic with respect to these taxa (e.g., [61]). Alternative strategies for a reliable root placement employ the inclusion of multiple outgroup taxa to break the branch separating the ingroup from the outgroup, and the use of a comprehensive set of proteins [64]. Our trees include four apicomplexan species as an outgroup and are based on 218 orthologous proteins. We have obtained identical tree topologies by employing different tree reconstruction methods (ML and Bayesian inference) and different models of sequence evolution. Moreover, our findings remain unchanged when we use proteins with different evolutionary rates. Ultimately, likelihood ratio tests rejected all alternative tree topologies. Thus, we are confident that our root placement is robust and that P. gallinaceum and the Laverania indeed share a common ancestry.

An avian parasite as sister to the Laverania has significant implications: it suggests that a host switch from birds to African great apes or vice versa has occurred. Host switches have repeatedly taken place during the evolution of avian Plasmodium species [61]. Moreover, avian Plasmodium species are able to infect mammals under experimental conditions [65]. Both observations are congruent with an evolutionary scenario in which the laveranian lineage was established by a single Plasmodium species switching from birds to African great apes. Subsequent diversification of Laverania associated with multiple host switches within the apes eventually led to the emergence of P. falciparum in humans [5-9]. Note that this scenario also implies that the great diversity of malaria parasites infecting birds [61] may in fact derive from an early host switch by another mammalian Plasmodium species. At present, however, we cannot exclude the alternative scenario in which the avian Plasmodium lineage was established by a Plasmodium species from the laveranian lineage. Therefore, phylogenomic analyses considering additional Plasmodium species (and in particular those infecting birds and squamate reptiles) will be necessary to provide a more detailed picture of how the Laverania emerged.

Evolutionary plasticity of the Plasmodium export element

The availability of Plasmodium genome sequences together with the reliable reconstruction of their phylogenetic relationships provides a robust framework to investigate the evolutionary history of exported P. falciparum proteins. Here, we used 531 P. falciparum proteins that had been predicted to be exported into the host cell [19,20] to identify functionally equivalent orthologs in the other Plasmodium species. BLAST searches in the P. falciparum genome identified 102 proteins without any recognizable paralog (Additional file 7), whereas the other 429 proteins mainly belong to large gene families such as RIFINs (repetitive interspersed family) and STEVORs (subtelomeric variable open reading frames). These gene families have a complex evolutionary history and have undergone independent lineage-specific diversifications [19]. This indicates that even if homologs of these proteins exist in the other Plasmodium species, they do not necessarily share the same function. These proteins were therefore excluded from further analyses.

Additional file 7. 102 paralog-free P. falciparum proteins that are exported into the host cell and information on the presence or absence of orthologs in other Plamodium species.

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Subsequent BLAST searches for homologs of the 102 paralog-free proteins in the other Plasmodium species identified 33 proteins with a homolog present in each of the species (Table 2). Orthology between the members in the 33 groups of proteins was confirmed by inferring the corresponding sequence trees with a Bayesian approach as described in the Methods section (Figure 5; Additional file 7). Whereas in 27 cases this tree was congruent to the species tree, six sequence trees differed from the species tree in the position of the P. gallinaceum sequences. However, subsequent likelihood ratio tests revealed that superimposing the species tree did not lead to significantly worse likelihoods (Additional file 8). The pairwise similarities between the P. falciparum proteins and their orthologs in the other Plasmodium species are given in Table 2. The orthologs from P. reichenowi display the highest degree of similarity. This finding is expected given the sister group relationship of P. falciparum and P. reichenowi. Among the remaining six non-laveranian taxa the orthologs from P. gallinaceum are overall most similar to the P. falciparum proteins. This lends further support to our conclusion that the Laverania and P. gallinaceum share a common ancestry.

thumbnailFigure 5. Phylogenies of exported P. falciparum proteins and orthologs. Sequence trees were inferred using a Bayesian approach; Bayesian posterior probabilities are given at the nodes and scale bars are equal to 0.1 substitutions per site. Putative PEXEL sequences are given next to each species (shaded in grey). Presence of a preceding hydrophobic signal sequence is indicated by a black box; absence (due to missing or incorrectly annotated N-terminal sequence data) is indicated by a grey box. Note that only proteins with confirmed export in P. falciparum are shown. Abbreviations: Pfa, P. falciparum; Pre, P. reichenowi; Pga, P. gallinaceum; Pkn, P. knowlesi; Pvi, P. vivax; Pch, P. chabaudi; Pyo, P. yoelii; Pbe, P. berghei. See also Additional file 8.

Table 2. Exported P. falciparum proteins with one-to-one orthologs present in all Plasmodium species.

Additional file 8. Phylogeny of exported P. falciparum proteins with orthologs present in all Plasmodium species; corresponding amino acid alignments and information on the amount of missing data; P. falciparum PEXEL motifs and orthologous sequences of the other Plasmodium species.

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Both reciprocal best BLAST hit searches and phylogenetic tree reconstructions indicate that the proteins in the 33 groups are encoded by genes that remained single copy throughout evolution (one-to-one orthologs). Ample evidence exists that such one-to-one orthologs are functionally equivalent [66]. Therefore, we conclude that if the P. falciparum protein is exported, its orthologs in other Plasmodium species are exported as well and hence, that these proteins are suitable to assess the evolutionary plasticity of the PEXEL motif. Note that five of these 33 proteins have already been confirmed to be exported in P. falciparum using GFP-constructs ([20]; Table 2). However, five proteins appear not to be exported ([19,20]; Table 2); thus they were omitted from further analyses.

The amino acid alignments of the remaining 28 ortholog groups were used to identify the regions that correspond to the P. falciparum PEXEL in the sequences from the other species. Subsequently, the candidate PEXEL sequences from all proteins were extracted and aligned separately for each species (Additional file 8). From these alignments the individual PEXEL motifs were determined and compared to those of P. falciparum (Figure 6). The motifs were found to be largely similar across the different Plasmodium species. However, several deviations from the functionally important amino acids were observed; the amino acids at position 1 and 3 are crucial for an efficient cleavage by plasmepsin V, while the amino acid at position 5 affects the export rate of the nascent protein [67].

thumbnailFigure 6. Sequence logos representing the PEXEL motifs of eight Plasmodium species. Note that only the proteins presented in Table 2 were used to draw the individual PEXEL motifs. Phylogenetic relationships were drawn according to Figure 1. For details on how the PEXEL motif mediates protein export refer to the recent review by Goldberg and Cowman [21]. Abbreviations: Pfa, P. falciparum; Pre, P. reichenowi; Pga, P. gallinaceum; Pkn, P. knowlesi; Pvi, P. vivax; Pch, P. chabaudi; Pyo, P. yoelii, Pbe, P. berghei. See also Additional file 8.

The most prominent difference between the Plasmodium species was found for the positively charged amino acid at position 1 of the PEXEL motif. All 28 P. falciparum proteins harbor an arginine (R), whereas about 20% of the proteins from non-Laverania have a lysine (K) at this position. Three lines of evidence indicate that this alternate PEXEL is nevertheless functional: (i) lysine at position 1 of the PEXEL was found in orthologs of those P. falciparum proteins whose export into the host cell has been confirmed (Figure 5), and thus our observation is not restricted to proteins that might have been erroneously predicted as being exported; (ii) recent experimental evidence suggests that the typical cleavage at the leucine (L) at position 3 can occur in proteins containing lysine at position 1 (PFI1780w and MAL3P8.15; [70]); and (iii) a small number of proteins with a lysine at position 1 of the PEXEL have already been predicted to be exported using a Hidden Markov Model based prediction method (21 in P. falciparum, three or less in each of the other Plasmodium species; cf. [19]). Other deviations at position 1 that are less prominent include the presence of histidine (H) in the P. knowlesi and P. vivax orthologs of PFC0435w and of glutamine (Q) in the P. gallinaceum protein that is orthologous to PFA0210c (Figure 5). Both PFC0435w and PFA0210c belong to the confirmed set of exported proteins in P. falciparum [20] and therefore these PEXEL sequences are likely to be functional as well. Position 3, which almost invariably harbors a hydrophobic leucine (L), was also found almost invariable in the orthologs of the confirmed exported P. falciparum proteins. However, several orthologs of P. falciparum proteins that have not yet been confirmed to be exported have an isoleucine (I) at this position (Figure 6). Position 5, which is considered to be the least conserved position [13,14], was found to be even more variable in the group of confirmed exported P. falciparum proteins.

Even though it remains to be demonstrated that these orthologous proteins are cleaved and exported with the same efficiency, these observations suggest that the PEXEL motif is more variable than previously acknowledged. This provides a possible explanation for the small number of exported proteins predicted for some Plasmodium species. Taking this plasticity into account will be essential to arrive at a more comprehensive set of exported proteins for all Plasmodium species.

Conclusion

Our phylogenetic analyses of orthologs deduced from the Plasmodium genomes strongly suggests that the subgenus Laverania was established by a single host switch from birds to African great apes (or vice versa). However, sequences from additional bird-infecting Plasmodium species and the closely related Haemosporida are required to better understand the early evolution of the Laverania. Exported proteins, as identified by the PEXEL motif, play a major role in Plasmodium virulence and facilitate the parasite's survival in the host cell. Our results suggest that the number of exported proteins is higher in the non-laveranian Plasmodium species than previously assumed. Comprehensive knowledge of their diversity and evolution will help to unravel the emergence of the high pathogenicity of P. falciparum, and may allow the identification of novel targets for malaria therapy.

Authors' contributions

All authors conceived the study. CP and IE analyzed the data. All authors drafted the manuscript. All authors read and approved the final version of the manuscript.

Acknowledgements

The P. gallinaceum and P. reichenowi sequence data were produced by the parasite genomics group at the Wellcome Trust Sanger Institute and are available from http://www.sanger.ac.uk/resources/downloads/protozoa/. We thank Janus Borner for help with the software applications and Tina Koestler for helpful discussion. The studies were supported in part by the DFG priority program SPP 1174 Deep Metazoan Phylogeny [BU 956/8]. IE acknowledges support by a grant of the Wiener Wissenschafts-, Forschungs- und Technologie Fonds (WWTF) to Arndt von Haeseler, and from the DFG priority program SPP 1174 Deep Metazoan Phylogeny [HA 1628/9]. We thank two anonymous reviewers and the editor for their helpful comments, and Kathleen Rankin for correction of the language.

References

  1. World Health Organization: World malaria report 2009. Geneva; 2009.

  2. Boyd MF: Historical review. In In Malariology. Volume 2. Edited by Boyd, MF. Philadelphia: W.B. Saunders; 1949::3-25. OpenURL

  3. Escalante AA, Ayala FJ: Phylogeny of the malarial genus Plasmodium, derived from rRNA gene sequences.

    Proc Natl Acad Sci USA 1994, 9:11373-11377. OpenURL

  4. Ollomo B, Durand P, Prugnolle F, Douzery E, Arnathau C, Nkoghe D, Leroy E, Renaud F: A new malaria agent in African hominids.

    PLoS Pathog 2009, 5:e1000446. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  5. Rich SM, Leendertz FH, Xu G, LeBreton M, Djoko CF, Aminake MN, Takang EE, Diffo JL, Pike BL, Rosenthal BM, Formenty P, Boesch C, Ayala FJ, Wolfe ND: The origin of malignant malaria.

    Proc Natl Acad Sci USA 2009, 106:14902-14907. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  6. Duval L, Fourment M, Nerrienet E, Rousset D, Sadeuh SA, Goodman SM, Andriaholinirina NV, Randrianarivelojosia M, Paul RE, Robert V, Ayala FJ, Ariey F: African apes as reservoirs of Plasmodium falciparum and the origin and diversification of the Laverania subgenus.

    Proc Natl Acad Sci USA 2010, 107:10561-10566. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  7. Krief S, Escalante AA, Pacheco MA, Mugisha L, André C, Halbwax M, Fischer A, Krief JM, Kasenene JM, Crandfield M, Cornejo OE, Chavatte JM, Lin C, Letourneur F, Grüner AC, McCutchan TF, Rénia L, Snounou G: On the diversity of malaria parasites in African apes and the origin of Plasmodium falciparum from Bonobos.

    PLoS Pathog 2010, 6:e1000765. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  8. Liu W, Li Y, Learn GH, Rudicell RS, Robertson JD, Keele BF, Ndjango JB, Sanz CM, Morgan DB, Locatelli S, Gonder MK, Kranzusch PJ, Walsh PD, Delaporte E, Mpoudi-Ngole E, Georgiev AV, Muller MN, Shaw GM, Peeters M, Sharp PM, Rayner JC, Hahn BH: Origin of the human malaria parasite Plasmodium falciparum in gorillas.

    Nature 2010, 467:420-425. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  9. Prugnolle F, Durand P, Neel C, Ollomo B, Ayala FJ, Arnathau C, Etienne L, Mpoudi-Ngole E, Nkoghe D, Leroy E, Delaporte E, Peeters M, Renaud F: African great apes are natural hosts of multiple related malaria species, including Plasmodium falciparum.

    Proc Natl Acad Sci USA 2010, 107:1458-1463. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  10. Hagner SC, Misof B, Maier WA, Kampen H: Bayesian analysis of new and old malaria parasite DNA sequence data demonstrates the need for more phylogenetic signal to clarify the descent of Plasmodium falciparum.

    Parasitol Res 2007, 101:493-503. PubMed Abstract | Publisher Full Text OpenURL

  11. Maier AG, Rug M, O'Neill MT, Brown M, Chakravorty S, Szestak T, Chesson J, Wu Y, Hughes K, Coppel RL, Newbold C, Beeson JG, Craig A, Crabb BS, Cowman AF: Exported proteins required for virulence and rigidity of Plasmodium falciparum-infected human erythrocytes.

    Cell 2008, 134:48-61. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  12. Baruch DI, Pasloske BL, Singh HB, Bi X, Ma XC, Feldman M, Taraschi TF, Howard RJ: Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes.

    Cell 1995, 82:77-87. PubMed Abstract | Publisher Full Text OpenURL

  13. Marti M, Good RT, Rug M, Knuepfer E, Cowman AF: Targeting malaria virulence and remodeling proteins to the host erythrocyte.

    Science 2004, 306:1930-1933. PubMed Abstract | Publisher Full Text OpenURL

  14. Hiller NL, Bhattacharjee S, van Ooij C, Liolios K, Harrison T, Lopez-Estraño C, Haldar K: A host-targeting signal in virulence proteins reveals a secretome in malarial infection.

    Science 2004, 306:1934-1937. PubMed Abstract | Publisher Full Text OpenURL

  15. Chang HH, Falick AM, Carlton PM, Sedat JW, DeRisi JL, Marletta MA: N-terminal processing of proteins exported by malaria parasites.

    Mol Biochem Parasitol 2008, 160:107-115. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  16. Boddey JA, Hodder AN, Günther S, Gilson PR, Patsiouras H, Kapp EA, Pearce JA, de Koning-Ward TF, Simpson RJ, Crabb BS, Cowman AF: An aspartyl protease directs malaria effector proteins to the host cell.

    Nature 2010, 463:627-631. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  17. Russo I, Babbitt S, Muralidharan V, Butler T, Oksman A, Goldberg DE: Plasmepsin V licenses Plasmodium proteins for export into the host erythrocyte.

    Nature 2010, 463:632-636. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  18. de Koning-Ward TF, Gilson PR, Boddey JA, Rug M, Smith BJ, Papenfuss AT, Sanders PR, Lundie RJ, Maier AG, Cowman AF, Crabb BS: A newly discovered protein export machine in malaria parasites.

    Nature 2009, 459:945-949. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  19. Sargeant TJ, Marti M, Caler E, Carlton JM, Simpson K, Speed TP, Cowman AF: Lineage-specific expansion of proteins exported to erythrocytes in malaria parasites.

    Genome Biol 2006, 7:R12. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  20. van Ooij C, Tamez P, Bhattacharjee S, Hiller NL, Harrison T, Liolios K, Kooij T, Ramesar J, Balu B, Adams J, Waters AP, Janse CJ, Haldar K: The malaria secretome: from algorithms to essential function in blood stage infection.

    PLoS Pathog 2008, 4:e1000084. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  21. Goldberg DE, Cowman AF: Moving in and renovating: exporting proteins from Plasmodium into host erythrocytes.

    Nat Rev Microbiol 2010, 8:617-621. PubMed Abstract | Publisher Full Text OpenURL

  22. MacKenzie JJ, Gómez ND, Bhattacharjee S, Mann S, Haldar K: A Plasmodium falciparum host-targeting motif functions in export during blood stage infection of the rodent malarial parasite Plasmodium berghei.

    PLoS One 2008, 3:e2405. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  23. Spielmann T, Gilberger TW: Protein export in malaria parasites: do multiple export motifs add up to multiple export pathways?

    Trends Parasitol 2010, 26:6-10. PubMed Abstract | Publisher Full Text OpenURL

  24. Gardner MJ, Hall N, Fung E, White O, Berriman M, Hyman RW, Carlton JM, Pain A, Nelson KE, Bowman S, Paulsen IT, James K, Eisen JA, Rutherford K, Salzberg SL, Craig A, Kyes S, Chan MS, Nene V, Shallom SJ, Suh B, Peterson J, Angiuoli S, Pertea M, Allen J, Selengut J, Haft D, Mather MW, Vaidya AB, Martin DM, Fairlamb AH, Fraunholz MJ, Roos DS, Ralph SA, McFadden GI, Cummings LM, Subramanian GM, Mungall C, Venter JC, Carucci DJ, Hoffman SL, Newbold C, Davis RW, Fraser CM, Barrell B: Genome sequence of the human malaria parasite Plasmodium falciparum.

    Nature 2002, 419:498-511. PubMed Abstract | Publisher Full Text OpenURL

  25. Carlton JM, Angiuoli SV, Suh BB, Kooij TW, Pertea M, Silva JC, Ermolaeva MD, Allen JE, Selengut JD, Koo HL, Peterson JD, Pop M, Kosack DS, Shumway MF, Bidwell SL, Shallom SJ, van Aken SE, Riedmuller SB, Feldblyum TV, Cho JK, Quackenbush J, Sedegah M, Shoaibi A, Cummings LM, Florens L, Yates JR, Raine JD, Sinden RE, Harris MA, Cunningham DA, Preiser PR, Bergman LW, Vaidya AB, van Lin LH, Janse CJ, Waters AP, Smith HO, White OR, Salzberg SL, Venter JC, Fraser CM, Hoffman SL, Gardner MJ, Carucci DJ: Genome sequence and comparative analysis of the model rodent malaria parasite Plasmodium yoelii yoelii.

    Nature 2002, 419:512-519. PubMed Abstract | Publisher Full Text OpenURL

  26. Hall N, Karras M, Raine JD, Carlton JM, Kooij TW, Berriman M, Florens L, Janssen CS, Pain A, Christophides GK, James K, Rutherford K, Harris B, Harris D, Churcher C, Quail MA, Ormond D, Doggett J, Trueman HE, Mendoza J, Bidwell SL, Rajandream MA, Carucci DJ, Yates JR, Kafatos FC, Janse CJ, Barrell B, Turner CM, Waters AP, Sinden RE: A comprehensive survey of the Plasmodium life cycle by genomic, transcriptomic, and proteomic analyses.

    Science 2005, 307:82-86. PubMed Abstract | Publisher Full Text OpenURL

  27. Pain A, Böhme U, Berry AE, Mungall K, Finn RD, Jackson AP, Mourier T, Mistry J, Pasini EM, Aslett MA, Balasubrammaniam S, Borgwardt K, Brooks K, Carret C, Carver TJ, Cherevach I, Chillingworth T, Clark TG, Galinski MR, Hall N, Harper D, Harris D, Hauser H, Ivens A, Janssen CS, Keane T, Larke N, Lapp S, Marti M, Moule S, Meyer IM, Ormond D, Peters N, Sanders M, Sanders S, Sargeant TJ, Simmonds M, Smith F, Squares R, Thurston S, Tivey AR, Walker D, White B, Zuiderwijk E, Churcher C, Quail MA, Cowman AF, Turner CM, Rajandream MA, Kocken CH, Thomas AW, Newbold CI, Barrell BG, Berriman M: The genome of the simian and human malaria parasite Plasmodium knowlesi.

    Nature 2008, 455:799-803. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  28. Carlton JM, Adams JH, Silva JC, Bidwell SL, Lorenzi H, Caler E, Crabtree J, Angiuoli SV, Merino EF, Amedeo P, Cheng Q, Coulson RM, Crabb BS, Del Portillo HA, Essien K, Feldblyum TV, Fernandez-Becerra C, Gilson PR, Gueye AH, Guo X, Kang'a S, Kooij TW, Korsinczky M, Meyer EV, Nene V, Paulsen I, White O, Ralph SA, Ren Q, Sargeant TJ, Salzberg SL, Stoeckert CJ, Sullivan SA, Yamamoto MM, Hoffman SL, Wortman JR, Gardner MJ, Galinski MR, Barnwell JW, Fraser-Liggett CM: Comparative genomics of the neglected human malaria parasite Plasmodium vivax.

    Nature 2008, 455:757-763. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  29. Aurrecoechea C, Brestelli J, Brunk BP, Fischer S, Gajria B, Gao X, Gingle A, Grant G, Harb OS, Heiges M, Innamorato F, Iodice J, Kissinger JC, Kraemer ET, Li W, Miller JA, Nayak V, Pennington C, Pinney DF, Roos DS, Ross C, Srinivasamoorthy G, Stoeckert CJ Jr, Thibodeau R, Treatman C, Wang H: PlasmoDB: a functional genomic database for malaria parasites.

    Nucleic Acids Res 2009, 37:D539-543. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  30. Gajria B, Bahl A, Brestelli J, Dommer J, Fischer S, Gao X, Heiges M, Iodice J, Kissinger JC, Mackey AJ, Pinney DF, Roos DS, Stoeckert CJ Jr, Wang H, Brunk BP: ToxoDB: an integrated Toxoplasma gondii database resource.

    Nucleic Acids Res 2008, 36:D553-556. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  31. Kersey P, Bower L, Morris L, Horne A, Petryszak R, Kanz C, Kanapin A, Das U, Michoud K, Phan I, Gattiker A, Kulikova T, Faruque N, Duggan K, Mclaren P, Reimholz B, Duret L, Penel S, Reuter I, Apweiler R: Integr8 and Genome Reviews: integrated views of complete genomes and proteomes.

    Nucleic Acids Res 2005, 33:D297-302. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  32. Heiges M, Wang H, Robinson E, Aurrecoechea C, Gao X, Kaluskar N, Rhodes P, Wang S, He CZ, Su Y, Miller J, Kraemer E, Kissinger JC: CryptoDB: a Cryptosporidium bioinformatics resource update.

    Nucleic Acids Res 2006, 34:D419-422. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  33. Pain A, Renauld H, Berriman M, Murphy L, Yeats CA, Weir W, Kerhornou A, Aslett M, Bishop R, Bouchier C, Cochet M, Coulson RM, Cronin A, de Villiers EP, Fraser A, Fosker N, Gardner M, Goble A, Griffiths-Jones S, Harris DE, Katzer F, Larke N, Lord A, Maser P, McKellar S, Mooney P, Morton F, Nene V, O'Neil S, Price C, Quail MA, Rabbinowitsch E, Rawlings ND, Rutter S, Saunders D, Seeger K, Shah T, Squares R, Squares S, Tivey A, Walker AR, Woodward J, Dobbelaere DA, Langsley G, Rajandream MA, McKeever D, Shiels B, Tait A, Barrell B, Hall N: Genome of the host-cell transforming parasite Theileria annulata compared with T. parva.

    Science 2005, 309:131-133. PubMed Abstract | Publisher Full Text OpenURL

  34. Ebersberger I, Strauss S, von Haeseler A: HaMStR: profile hidden Markov model based search for orthologs in ESTs.

    BMC Evol Biol 2009, 9:157. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  35. Katoh K, Misawa K, Kuma K, Miyata T: MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform.

    Nucleic Acids Res 2002, 30:3059-3066. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  36. Castresana J: Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis.

    Mol Biol Evol 2000, 17:540-552. PubMed Abstract | Publisher Full Text OpenURL

  37. Stamatakis A: RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models.

    Bioinformatics 2006, 22:2688-2690. PubMed Abstract | Publisher Full Text OpenURL

  38. Whelan S, Goldman N: A general empirical model of protein evolution derived from multiple protein families using a maximum-likelihood approach.

    Mol Biol Evol 2001, 18:691-699. PubMed Abstract | Publisher Full Text OpenURL

  39. Lartillot N, Lepage T, Blanquart S: PhyloBayes 3: a Bayesian software package for phylogenetic reconstruction and molecular dating.

    Bioinformatics 2009, 25:2286-2288. PubMed Abstract | Publisher Full Text OpenURL

  40. Lartillot N, Philippe H: A Bayesian mixture model for across-site heterogeneities in the amino-acid replacement process.

    Mol Biol Evol 2004, 2:1095-1109. OpenURL

  41. Le SQ, Gascuel O: An improved general amino-acid replacement matrix.

    Mol Biol Evol 2008, 25:1307-1320. PubMed Abstract | Publisher Full Text OpenURL

  42. Templeton TJ, Enomoto S, Chen WJ, Huang CG, Lancto CA, Abrahamsen MS, Zhu G: A genome sequence survey for Ascogregarina taiwanensis supports evolutionary affiliation, but metabolic diversity between a gregarine and Cryptosporidium.

    Mol Biol Evol 2010, 27:235-248. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  43. Schmidt HA, Strimmer K, Vingron M, von Haeseler A: TREE-PUZZLE: maximum likelihood phylogenetic analysis using quartets and parallel computing.

    Bioinformatics 2002, 18:502-504. PubMed Abstract | Publisher Full Text OpenURL

  44. Shimodaira H, Hasegawa M: CONSEL: for assessing the confidence of phylogenetic tree selection.

    Bioinformatics 2001, 17:1246-1247. PubMed Abstract | Publisher Full Text OpenURL

  45. Nicholas KB, Nicholas HBJ, Deerfield DWI: GeneDoc: analysis and visualization of genetic variation.

    EMBnet NEWS 1997, 4:14. OpenURL

  46. Crooks GE, Hon G, Chandonia JM, Brenner SE: WebLogo: a sequence logo generator.

    Genome Res 2004, 14:1188-1190. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  47. Bendtsen JD, Nielsen H, von Heijne G, Brunak S: Improved prediction of signal peptides: SignalP 3.0.

    J Mol Biol 2004, 340:783-795. PubMed Abstract | Publisher Full Text OpenURL

  48. Kuo CH, Wares JP, Kissinger JC: The Apicomplexan whole-genome phylogeny: an analysis of incongruence among gene trees.

    Mol Biol Evol 2008, 25:2689-2698. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  49. Talavera G, Castresana J: Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments.

    Syst Biol 2007, 56:564-577. PubMed Abstract | Publisher Full Text OpenURL

  50. Strimmer K, Rambaut A: Inferring confidence sets of possibly misspecified gene trees.

    Proc Biol Sci 2002, 269:137-142. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  51. Shimodaira H: An approximately unbiased test of phylogenetic tree selection.

    Syst Biol 2002, 51:492-508. PubMed Abstract | Publisher Full Text OpenURL

  52. Dávalos LM, Perkins SL: Saturation and base composition bias explain phylogenomic conflict in Plasmodium.

    Genomics 2008, 91:433-442. PubMed Abstract | Publisher Full Text OpenURL

  53. Silva JC, Egan A, Friedman R, Munro JB, Carlton JM, Hughes AL: Genome sequences reveal divergence times of malaria parasite lineages.

    Parasitology 2010, 1:1-13. OpenURL

  54. Philippe H, Brinkmann H, Lavrov DV, Littlewood DT, Manuel M, Wörheide G, Baurain D: Resolving difficult phylogenetic questions: why more sequences are not enough.

    PLoS Biol 2011, 9:e1000602. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  55. Waters AP, Higgins DG, McCutchan TF: Plasmodium falciparum appears to have arisen as a result of lateral transfer between avian and human hosts.

    Proc Natl Acad Sci USA 1991, 88:3140-3144. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  56. Escalante AA, Ayala FJ: Evolutionary origin of Plasmodium and other Apicomplexa based on rRNA genes.

    Proc Natl Acad Sci USA 1995, 92:5793-5797. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  57. Kissinger JC, Souza PC, Soarest CO, Paul R, Wahl AM, Rathore D, McCutchan TF, Krettli AU: Molecular phylogenetic analysis of the avian malarial parasite Plasmodium (Novyella) juxtanucleare.

    J Parasitol 2002, 88:769-773. PubMed Abstract | Publisher Full Text OpenURL

  58. Perkins SL, Schall JJ: A molecular phylogeny of malarial parasites recovered from cytochrome b gene sequences.

    J Parasitol 2002, 88:972-978. PubMed Abstract | Publisher Full Text OpenURL

  59. Leclerc MC, Hugot JP, Durand P, Renaud F: Evolutionary relationships between 15 Plasmodium species from new and old world primates (including humans): an 18S rDNA cladistic analysis.

    Parasitology 2004, 129:677-684. PubMed Abstract | Publisher Full Text OpenURL

  60. Roy SW, Irimia M: Origins of human malaria: rare genomic changes and full mitochondrial genomes confirm the relationship of Plasmodium falciparum to other mammalian parasites but complicate the origins of Plasmodium vivax.

    Mol Biol Evol 2008, 25:1192-1198. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  61. Martinsen ES, Perkins SL, Schall JJ: A three-genome phylogeny of malaria parasites (Plasmodium and closely related genera): evolution of life-history traits and host switches.

    Mol Phylogenet Evol 2008, 47:261-273. PubMed Abstract | Publisher Full Text OpenURL

  62. Philippe H, Derelle R, Lopez P, Pick K, Borchiellini C, Boury-Esnault N, Vacelet J, Renard E, Houliston E, Quéinnec E, Da Silva C, Wincker P, Le Guyader H, Leys S, Jackson DJ, Schreiber F, Erpenbeck D, Morgenstern B, Wörheide G, Manuel M: Phylogenomics revives traditional views on deep animal relationships.

    Curr Biol 2009, 19:706-712. PubMed Abstract | Publisher Full Text OpenURL

  63. Delsuc F, Brinkmann H, Philippe H: Phylogenomics and the reconstruction of the tree of life.

    Nat Rev Genet 2005, 6:361-375. PubMed Abstract | Publisher Full Text OpenURL

  64. Graham SW, Olmstead RG, Barrett SC: Rooting phylogenetic trees with distant outgroups: a case study from the commelinoid monocots.

    Mol Biol Evol 2002, 19:1769-1781. PubMed Abstract | Publisher Full Text OpenURL

  65. McGhee B: The adaptation of the avian malaria parasite Plasmodium lophurae to a continuous existence in infant mice.

    J Infect Dis 1951, 88:86-97. PubMed Abstract | Publisher Full Text OpenURL

  66. Conant GC, Wolfe KH: Turning a hobby into a job: how duplicated genes find new functions.

    Nat Rev Genet 2008, 9:938-950. PubMed Abstract | Publisher Full Text OpenURL

  67. Boddey JA, Moritz RL, Simpson RJ, Cowman AF: Role of the Plasmodium export element in trafficking parasite proteins to the infected erythrocyte.

    Traffic 2009, 10:285-299. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  68. Qari SH, Shi YP, Pieniazek NJ, Collins WE, Lal AA: Phylogenetic relationship among the malaria parasites based on small subunit rRNA gene sequences: monophyletic nature of the human malaria parasite, Plasmodium falciparum.

    Mol Phylogenet Evol 1996, 6:157-165. PubMed Abstract | Publisher Full Text OpenURL

  69. Escalante AA, Freeland DE, Collins WE, Lal AA: The evolution of primate malaria parasites based on the gene encoding cytochrome b from the linear mitochondrial genome.

    Proc Natl Acad Sci USA 1998, 95:8124-8129. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  70. Rathore D, Wahl AM, Sullivan M, McCutchan TF: A phylogenetic comparison of gene trees constructed from plastid, mitochondrial and genomic DNA of Plasmodium species.

    Mol Biochem Parasitol 2001, 114:89-94. PubMed Abstract | Publisher Full Text OpenURL

  71. Huson DH: SplitsTree: analyzing and visualizing evolutionary data.

    Bioinformatics 1998, 14:68-73. PubMed Abstract | Publisher Full Text OpenURL