HLA supertype variation across populations: new insights into the role of natural selection in the evolution of HLA-A and HLA-B polymorphisms
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- dos Santos Francisco, R., Buhler, S., Nunes, J.M. et al. Immunogenetics (2015) 67: 651. doi:10.1007/s00251-015-0875-9
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Supertypes are groups of human leukocyte antigen (HLA) alleles which bind overlapping sets of peptides due to sharing specific residues at the anchor positions—the B and F pockets—of the peptide-binding region (PBR). HLA alleles within the same supertype are expected to be functionally similar, while those from different supertypes are expected to be functionally distinct, presenting different sets of peptides. In this study, we applied the supertype classification to the HLA-A and HLA-B data of 55 worldwide populations in order to investigate the effect of natural selection on supertype rather than allelic variation at these loci. We compared the nucleotide diversity of the B and F pockets with that of the other PBR regions through a resampling procedure and compared the patterns of within-population heterozygosity (He) and between-population differentiation (GST) observed when using the supertype definition to those estimated when using randomized groups of alleles. At HLA-A, low levels of variation are observed at B and F pockets and randomized He and GST do not differ from the observed data. By contrast, HLA-B concentrates most of the differences between supertypes, the B pocket showing a particularly high level of variation. Moreover, at HLA-B, the reassignment of alleles into random groups does not reproduce the patterns of population differentiation observed with supertypes. We thus conclude that differently from HLA-A, for which supertype and allelic variation show similar patterns of nucleotide diversity within and between populations, HLA-B has likely evolved through specific adaptations of its B pocket to local pathogens.
KeywordsHLASupertypesHuman populationsNatural selectionPathogensAdaptation
The three classical human leukocyte antigen (HLA) class I genes, HLA-A, HLA-B, and HLA-C, are extremely polymorphic and exhibit thousands of alleles, most of them coding for different proteins (2112, 2789, and 1799 HLA-A, HLA-B, and HLA-C proteins currently defined, respectively) (Robinson et al. 2015). These molecules play a central role in the immune response by presenting processed peptides derived from proteins of the intracellular environment (including foreign ones derived from intracellular parasites such as viruses and some bacteria) to cytotoxic T lymphocytes and also functioning as ligands for the killer immunoglobulin-like receptor (KIR) of natural killer cells (Parham 2005).
Almost all of the HLA class I polymorphisms are clustered in exons 2 and 3, which code for the α1 and α2 extracellular domains of the HLA molecule. These domains form a groove-like structure known as the peptide-binding region (PBR) which engages the peptides (Saper et al. 1991). At the DNA level, the PBR codons exhibit striking features regarding their diversity, including a high heterozygosity (Parham et al. 1989; Lawlor et al. 1990; Hedrick et al. 1991) and high rates of non-synonymous substitutions (Hughes and Nei 1988; Takahata et al. 1992). These characteristics contrast with neutral expectations and support the hypothesis that balancing selection has maintained variation at these codons. The high levels of variation observed at the sites involved in peptide binding support a model of host-pathogen coevolution (Apanius et al. 1997), which states that the pathogenic microorganisms are the main evolutionary force shaping HLA variation (Borghans et al. 2004; Slade and McCallum 1992; Takahata and Nei 1990). Further supporting this hypothesis, several studies have demonstrated a positive correlation between the diversity level of some HLA genes and the richness of environmental pathogens (Prugnolle et al. 2005; Qutob et al. 2011; Sanchez-Mazas et al. 2012). These results corroborate the idea that the codons making up the PBR constitute the main targets of balancing selection within HLA genes. However, the analyses performed to date generally treat the PBR region as a homogeneous block, whereas it is in fact composed of six different pocket-like structures (A, B, C, D, E, and F). Each pocket accommodates one of the nine amino acid residues of the bound peptide (the first, second, third, sixth, seventh, and ninth, respectively) (Saper et al. 1991). Moreover, the binding affinity between a given HLA molecule and a specific peptide depends on the chemical properties of each PBR pocket (Saper et al. 1991).
The strongest interaction between HLA molecules and the bound peptides is accounted by the B and F pockets, which accommodate the second and ninth amino acid residues of the peptide, respectively (Saper et al. 1991). As the amino acids composing the B and F pockets play a central role in peptide recognition by the HLA molecules, Sidney et al. (1996) classified HLA alleles into supertypes, defined as groups of alleles sharing chemical properties at the B and F pockets. The logic behind the classification is that alleles within supertypes are expected to exhibit widely overlapping peptide repertoires, whereas alleles from different supertypes would more frequently bind non-overlapping sets of peptides. Supertypes were originally defined by sequencing endogenously bound ligands and searching for motifs shared by alleles that bind similar peptides and by analyzing the three-dimensional structure of the HLA molecules (Sette and Sidney 1999; Sidney et al. 1996, 2008). As a result, four supertypes were described for HLA-A (A1, A2, A3, and A24) and five for HLA-B (B7, B27, B44, B58, and B62), and they were originally assigned, respectively, to 31 HLA-A and 57 HLA-B alleles whose peptide-binding specificities were experimentally defined. These alleles were used to construct a reference panel for the B and F amino acid sequences. A set of 945 HLA-A and HLA-B alleles with unknown binding specificities were then checked for matches to the sequences of this panel (Sidney et al. 2008). Among these 945 previously unclassified alleles, 57 % presented a full match in both B and F pockets to alleles with known supertype status. Another 23.8 % presented partial matches with residues found in these pockets.
In line with the expectation that supertypes constitute a functionally relevant definition of HLA variation, several researchers have found that grouping alleles into supertypes is useful in disease association studies involving HLA loci (Alencar et al. 2013; Chakraborty et al. 2013; Cordery et al. 2012; Gilchuk et al. 2013; Karlsson et al. 2012, 2013; Kuniholm et al. 2013; Trachtenberg et al. 2003), allowing large numbers of rare alleles to be grouped according to a functional criterion, thus increasing the power of the studies. From an evolutionary point of view, natural selection is expected to leave a detectable signature on B and F pockets and, consequently, on the genotypes defined by examining HLA variation from the perspective of supertypes. For example, under the assumption that pathogen-driven selection shapes supertype frequencies, we expect genetic variation defined at the supertype level to show patterns of polymorphism and differentiation indicative of balancing selection to a greater degree than variation that is not related to supertype definition. The prediction that balancing selection on supertype variation would result in detectable genetic signatures was raised by Sette and Sidney (1999), who found that “supertype frequencies were high and fairly conserved among different ethnicities.” In addition, Naugler and Liwski (2008) argued that “natural selection should favor maximization of the heterozygosity of allele supertypes instead of the heterozygosity of individual alleles,” making explicit the hypothesis that supertypes, as defined by B and F pocket variations, constitute the level of variation that is the primary target of natural selection in HLA genes.
Both conservation of supertype frequencies between populations and increased heterozygosity at the supertype level are expected to generate a pattern of low-population differentiation when compared with those observed at the allelic level. Balancing selection at the supertype level would also enhance genetic variation at the B and F pockets compared with other regions of the PBR, increasing the chances of antigen recognition by the immune system. However, testing these hypotheses, i.e., comparing population differentiation and variability defined at the levels of HLA alleles and supertypes, respectively, represents a methodological challenge due to the difficulties in comparing measures of differentiation and heterozygosity for genetic variants that are defined by different attributes (alleles being defined by all variation in the coding region, by contrast with supertypes which are defined by a subset of codons). Indeed, because supertypes are sets of alleles, genetic variation defined at the allele level is nested within that defined at the supertype level. Therefore, heterozygosity at the supertype level is constrained to be lower or equal to that estimated at the allele level. Furthermore, because population genetic differentiation measured by statistics related to Wright’s FST is strongly determined by intrapopulation variability (Jost 2008), we expect higher levels of population differentiation at the supertype level simply because of the decreased number of supertype variants in comparison to alleles.
In the present study, our aim is to investigate whether the use of supertype instead of allele definitions at HLA-A and HLA-B loci reduces population differentiation and increases heterozygosity, as expected under a model of balancing selection acting on supertypes. For the reasons explained above, we control our analyses for the inherent differences in polymorphism between these two kinds of classification. Our approach consists in producing null distributions for population differentiation and heterozygosity by generating randomized sets of alleles (herein referred to as “random supertypes”) that match true supertype sampling properties (i.e., number of supertypes and number of alleles per supertype) without any biological criteria for pooling them together. We also analyze supertype variation at the nucleotide level by partitioning DNA sequences into segments corresponding to the different pockets within the PBR. Our hypothesis is that the B and F pockets, which are the major determinants of the peptide-binding specificities and used to define supertypes, constitute the main targets of balancing selection and thus retain higher levels of diversity compared to other PBR pockets.
Materials and methods
We used a database generated for the 13th International Histocompatibility Workshop (IHWS) (Mack et al. 2006) from which we excluded populations presenting (a) an allelic resolution lower than the first two sets of digits (now referred to as second field level of resolution), so as to only keep alleles differing at the protein level; (b) genotypic ambiguities; and (c) deviation from Hardy-Weinberg expectations. This filtering resulted in a dataset of 6435 and 6409 individuals typed for HLA-A and HLA-B, respectively, belonging to 55 different populations: seven sub-Saharan African (SSA), two North African (NAF), eight Southwest Asian (SWA), four European (EUR), 22 Southeast Asian (SEA), four Pacific islanders (PAC), four Australian aborigine (AUS), two North Asian (NEA), and two Native American (AME) populations (Supplementary Material Table 1-S). Almost half of these populations (24 out of 55) had demographic histories indicating that they were likely to have experienced severe founder effects (these populations were from Oceania, Taiwan, and the Americas). Because such reductions in diversity due to demographic effects can potentially mask signals of balancing selection, we carried out all the analyses with both the complete set of 55 populations and a reduced set of 30 populations (obtained by excluding those from Oceania, Taiwan, and the Americas).
We assigned all HLA-A and HLA-B alleles to their specific supertype as defined by the classification given in figures 1 (http://www.biomedcentral.com/1471-2172/9/1/figure/F1) and 2 (http://www.biomedcentral.com/1471-2172/9/1/figure/F2) from Sidney et al. (2008). The alleles not assigned to any supertype were treated in our analyses of population differentiation and molecular variation in two ways: (a) their allele-level definition was used and (b) they were pooled into groups of “non-classified alleles” (named NCA and NCB for HLA-A and HLA-B, respectively). We included A*29:01, A*29:02, A*29:03, A*30:01, A*30:08, and A*68:06 in the NCA group because of their ambiguous supertype allocation (Sidney et al. 2008), and all B*08 alleles were assigned to the NCB group because of their unique PBR structures, which make the peptide-binding profile unpredictable (Sidney et al. 2008).
Population genetic analyses
We tested the population samples for deviation from Hardy-Weinberg (HW) equilibrium using the Gene[rate] program which tests the null hypothesis of equilibrium on the basis of a log-likelihood ratio test on frequency estimates (both under HW and under a generalized non-HW model) (Nunes et al. 2014; Nunes 2014).
We wrote R scripts to estimate supertype frequencies by direct counting of alleles, generate summary statistics (number of alleles (k) and expected sample heterozygosity (He)), and estimate genetic differentiation between pairs of populations by using GST (Nei and Chesser 1983). Mantel tests (Mantel 1967) for assessing Pearson’s correlations between genetic distances obtained either from supertype or from allelic data were carried out using the ade4 R package (Dray and Dufour 2007), and all graphs and other statistical tests (e.g., Wilcoxon rank sum test) were also generated using R version 3.0.2 (Development Core Team 2011). In box plots, the boxes correspond to the interquartile range, the median is the thick line inside the box, and whiskers extend up to observations that are outside the box for less than 1.5 times the interquartile range. Dots are outliers to these limits. By using Arlequin 3.5 program (Excoffier and Lischer 2010), we performed a hierarchical analysis of molecular variance (AMOVA) for each supertype taken individually by pooling all others into a unique group of “non-classified alleles” for the calculations. In this way, we estimated the diversity among populations (FST), among populations within geographic regions (FSC), and among geographic regions (FCT) for each supertype.
Testing the molecular variation of the PBR pockets
Codon composition of the PBR pockets
Total size in base pairs (bp)
5, 7, 59, 63, 66, 99, 159, 163, 167, and 171
7, 9, 24, 25, 34, 45, 63, 66, 67, 70, and 99
C, D, and E
9, 70, 73, 74, 97, 99, 114, 147, 152, 155, 156, 159, and 160
77, 80, 81, 84, 116, 123, 143, 146, and 147
The B and F pockets were analyzed individually because of their central role in engaging peptides and in defining supertypes. As the C, D, and E pockets jointly make up the central region of the PBR and are shorter compared to other pockets, we pooled them for the present analysis. The A pocket was analyzed individually because of its position at one end of the PBR.
Total, within- and between-supertype π values were calculated in two ways: (a) by excluding the non-classified alleles and (b) by including the non-classified alleles as a single group. As the dataset is limited to alleles defined at second field level of resolution, no information about synonymous polymorphism is available. We addressed this problem by applying the same strategy as described by Buhler and Sanchez-Mazas (2011), which consisted in treating as missing data the nucleotide positions which were described as synonymous (Robinson et al. 2015). We excluded sites having more than 5 % missing data.
Testing genetic differentiation between populations based on supertypes
By fixing the number of alleles per supertype to that observed in the original dataset
Without any constraint on the number of alleles associated to a specific supertype
The randomizations were repeated 10,000 times, and p values were estimated empirically by determining the number of randomized datasets with GST values lower or He values higher than those observed for the true data.
Results and discussion
HLA-A and HLA-B supertype frequencies and their geographic distributions
Supertype differentiation indexes among populations (FST), among populations within geographic regions (FSC), and among geographic regions (FCT)
The HLA-B supertypes fall into two main categories regarding their frequency distributions. On the one hand, B7 and B44 exhibit a pattern resembling A2 and A3, with high average frequencies (Figs. 1a and 3) and relatively low levels of geographic structure (Table 2). Half of the populations present frequencies ranging from 18 to 31 % for B7 and from 21 to 32 % for B44, respectively (Figs. 1a and 3). Both B7 and B44 are observed in all populations (except B7 in the Yami; Figs. 1c and 3), with large numbers of alleles per population (Fig. 1b, c). By contrast, B58 and B62 exhibit very low frequencies, ranging from 0 to 5.8 % and from 2.9 to 18 % in half of the populations, respectively (Fig. 1a). Among the five HLA-B supertypes, B62 presents the highest level of population differentiation (FST = 11.38 %, p < 0.0001; Table 2), although with no clear geographic structure (FCT < FSC; Table 2). Such a geographic structure is only found for B58 (FCT of 5.6 %, almost twice as great as FSC; Table 2), which is observed in SSA populations at an average frequency of 33 % (from 23 to 60 %; Fig. 3), against 4.2 % in the other regions (Fig. 3) and no observation at all in many populations (18 out of 55; Fig. 3). The B27 supertype presents an intermediate pattern between B7/B44 and B58/B62. It exhibits relatively lower frequencies (from 7 to 19 % in half of the populations; Fig. 1a) and a higher level of population differentiation than B7 and B44 (FST = 7.5 %, p < 0.0001; Table 2) but no geographic structure (FCT very close to zero; Table 2). Contrasting with what is observed for the NCA, the non-classified alleles for HLA-B (NCB) are quite frequent, with frequencies ranging from 10 to 17 % in half of the populations (Fig. 1a). More than 75 % of populations present at least two different NCBs (Fig. 1b), and only two populations lack one of these alleles (Fig. 1c). The NCBs also exhibit a significant geographic structure, although not as strong as for NCA (Table 2).
In summary, based on the observed data, supertypes can be allocated into two main categories: on the one hand, A2, A3, B7, B27, and B44 fit the classical view that supertypes are evenly distributed (Figs. 1a, 2, and 3), poorly structured geographically (Table 2), and represented by a large number of alleles (Fig. 1b, c). On the other hand, A1, A24, B58, and B62 present a greater frequency variation among populations (Figs. 2 and 3 and Table 2), and in some cases significant geographic structure (i.e., for A1 and B58, both being very common in Africa), and are represented by a smaller number of alleles. Although the unclassified alleles have brought noise to the analysis, they should not be ignored. They are a consequence of the functional supertype classification, and they were kept to understand exactly how they influence the variations in HLA-A and HLA-B. As discussed above, the NCA consists of a small group of alleles, which reach high frequencies in island populations. On the other hand, NCB is a more heterogeneous group appearing in almost all populations.
Heterozygosity and interpopulation differentiation
Expected heterozygosity (He) of alleles and supertypes
Average allelic He
Average supertype He
Patterns of molecular variability for different PBR pockets of HLA-A and HLA-B
Our goal in this part of the study was to test the prediction that the B and F pockets of the PBR exhibit the highest levels of variation as a consequence of their crucial role in peptide binding, which is expected to result in a stronger effect of balancing selection.
The hypothesis that the pockets B and F are the main targets of balancing selection is thus partially supported for HLA-B, since pB presents by far the highest level of nucleotide diversity. Interestingly, van Deutekom and Kesmir (2015) recently showed that changes involving several of the B pocket’s amino acids had a profound impact on peptide-binding properties, which corroborates our interpretation. On the other hand, pF, which is not significantly different from pA at HLA-A, and from pCDE at HLA-B, does not present an increased value of πtotal which would be an evidence against balancing selection. It is important to note that these results were obtained independently from the classification of alleles into supertypes, since the determination of the pockets’ codons was taken from the classical study of Saper et al. (1991).
As pB presents the highest levels of variation at HLA-B and also accounts for most of the differences between HLA-B supertypes, we conclude that the variation between HLA-B supertypes accounts for most of the differences observed between HLA-B alleles. In other words, alleles classified within a same HLA-B supertype share more similarities than alleles assigned to different HLA-B supertypes. By contrast, most of the differences between HLA-A supertypes lie within pF, the pocket presenting the lowest πtotal values for this gene. Therefore, at this locus, the supertypes do not account for most of the variation between alleles (Fig. 6). In other words, HLA-A presents more variation within than between supertypes.
Simulation approach to test selection on supertypes
According to the definition of Sidney et al. (1996), alleles included within the same supertype have overlapping peptide-binding specificities. To test the effects of the supertype classification on expected heterozygosities (He) and pairwise differentiation (GST), we generated null distributions for these two statistics under the hypothesis that alleles within supertypes are a random collection, with no shared functional attributes. To this end, the assignment of alleles to supertypes was randomized by permuting the supertype labels attributed to each allele motif, as described in the “Materials and methods” section. As the same patterns were obtained using the two different simulation approaches (see “Materials and methods” section), we only present the results for the case without any constraint on the number of alleles associated to a specific supertype.
In summary, HLA-B supertypes are sets of alleles with B pocket resemblances, and these similarities can be interpreted directly in terms of peptide presentation profiles because HLA-B supertypes exhibit major differences regarding the chemical properties of pB. Thus, our results showing an increased differentiation at the level of HLA-B supertypes are consistent with an effect of natural selection resulting in local adaptation of populations to different pathogen environments. Through our simulations, the functional grouping of alleles reflected by the HLA-B supertypes is disrupted, creating randomized groups in the same way as described for HLA-A. The frequent allocation of common alleles into different randomized supertypes in the simulations thus provokes both an increase of He and a decrease of population differentiations (GST), when compared with the observed data (Figs. 7 and 8). In agreement with this interpretation, the inclusion of the Pacific, Australian, Taiwanese, and Native American populations reduces this effect because the patterns of variation at HLA-B for these populations resemble those observed at HLA-A, with a relatively low number of alleles belonging to different supertypes.
The supertype classification of HLA-A and HLA-B alleles has been widely used in medical research, with reports suggesting that supertype-level variation explains susceptibility or resistance to a series of pathogenic diseases (Alencar et al. 2013; Chakraborty et al. 2013; Cordery et al. 2012; Gilchuk et al. 2013; Karlsson et al. 2012, 2013; Kuniholm et al. 2013; Trachtenberg et al. 2003). This classification was proposed in the 1990s as an attempt to find, as described by Sette and Sidney (1999), “the common denominators and similarities hidden within this very large degree of polymorphism.” The same authors also stated that “the overall frequency of each of these supertypes is remarkably high and fairly conserved among very different ethnicities. Thus, there might be some advantage for human populations to present approximately five to ten main binding specificities and that each one of these is maintained at relatively high frequency.” According to our results, the variation among HLA-B supertypes does reflect the functional diversity at this locus and is thus in agreement with the above-mentioned hypothesis. Our results strongly indicate that the B pocket is likely to be the main target of natural selection at HLA-B, as it presents the highest levels of molecular variation and accounts for the main differences in the peptide presentation profiles for this gene. However, in contrast with classical expectations for loci evolving under balancing selection, our simulation results reveal that HLA-B supertype frequencies do not show a signature of balancing selection (i.e., we find lower He compared to those of randomly assigned groups of alleles), implying that each supertype is not maintained at relatively high frequencies in all populations. This result is supported by the geographically heterogeneous distributions of B58 and B62 (and, to a lesser extent, B27) frequencies among populations. Moreover, populations are more differentiated than expected for HLA-B supertypes (higher observed GST values than those obtained from randomly assigned groups of alleles). As most of the differences between HLA-B supertypes lie in the B pocket, this means that the differences in HLA-B supertype composition among populations can be interpreted in terms of peptide recognition. Thus, for HLA-B, our results support the idea that populations present more differences in peptide presentation profiles than expected, possibly due to local adaptations to pathogens.
By contrast, most of the differences between HLA-A alleles are not related with differences at the supertype level. This is supported by our simulation results showing that the randomly assigned groups of alleles often reproduce the observed patterns of variation and differentiation of HLA-A supertypes. Moreover, HLA-A alleles are more conserved at the sites involved in peptide binding, suggesting that they present a more conserved profile of peptides across populations, differing from what is observed for HLA-B. Of note, one possible caveat of inferring peptide binding through the supertype classification is that some peptides presented by HLA class I molecules are known to assume a looping conformation outside the peptide-binding groove. However, no matter how different conformations a peptide can adopt, the anchor amino acids located at the peptide ends remain the same, limited by the B and F pockets. In this way, this conformational variability exhibited by the peptides is also a consequence of the interaction between the peptide anchors and the B and F pockets and thus is not expected to change the results obtained here.
Our results suggest that the B pocket of the HLA-B molecules is the main target of natural selection, whereas no such signals could be retrieved for the other HLA-B pockets nor for the pockets of the HLA-A molecules in relation to the supertype classification. This conclusion matches the expectations that supertypes are the primary targets of selection for HLA-B but not for HLA-A. Following this idea, we could state that HLA-A supertypes are composed by alleles whose resemblances are not the consequence of a shared phylogenetic origin. A future extension of this work could be to explore whether the central pockets C, D, and E that have been shown to contain most of the variation at HLA-A could be used as an alternate functional classification for these alleles.
This work was supported by the Swiss National Science Foundation (SNSF) grant no. 31003A_144180 to ASM and São Paulo Research Foundation (FAPESP) 12/18010-0 and a CNPq productivity grant no. 308167/2012-0 to DM. RSF was supported by CNPq (grant no. 142130/2009-5) and CAPES (grant no. 12447/12-9). We also thank two anonymous reviewers for their useful comments.
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