International Journal of Evolutionary BiologyVolume 2013 (2013), Article ID 204240, 6 pageshttp://dx.doi.org/10.1155/2013/204240

Review Article

Pathogen-Driven Selection in the Human Genome

Rachele Cagliani and Manuela Sironi

Bioinformatics, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini (LC), Italy

Received 14 December 2012; Accepted 31 January 2013

Academic Editor: Stephane Boissinot

Copyright © 2013 Rachele Cagliani and Manuela Sironi. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Infectious diseases and epidemics have always accompanied and characterized human history, representing one of the main causes of death. Even today, despite progress in sanitation and medical research, infections are estimated to account for about 15% of deaths. The hypothesis whereby infectious diseases have been acting as a powerful selective pressure was formulated long ago, but it was not until the availability of large-scale genetic data and the development of novel methods to study molecular evolution that we could assess how pervasively infectious agents have shaped human genetic diversity. Indeed, recent evidences indicated that among the diverse environmental factors that acted as selective pressures during the evolution of our species, pathogen load had the strongest influence. Beside the textbook example of the major histocompatibility complex, selection signatures left by pathogen-exerted pressure can be identified at several human loci, including genes not directly involved in immune response. In the future, high-throughput technologies and the availability of genetic data from different populations are likely to provide novel insights into the evolutionary relationships between the human host and its pathogens. Hopefully, this will help identify the genetic determinants modulating the susceptibility to infectious diseases and will translate into new treatment strategies.

1. Infections: A Scourge throughout Human History

Infectious diseases and epidemics have always accompanied and characterized human history, representing one of the main causes of death. Even today, despite progress in sanitation and medical research, infectious diseases represented a major killer; data published by the World Health Organization (WHO 2008, http://www.who.int/en/) indicate that about 15% of deaths in the world's population are due to infectious and parasitic diseases, reaching about 41% in Africa. In the most recently published report (November 2012), the WHO estimated that in 2011 about 4.4 millions of children younger than 5 years died of infection.

Anatomically modern humans appeared in East Africa about 200,000 years ago, spread out from sub-Saharan Africa approximately 100,000 years ago, and subsequently colonized the rest of the world in a series of migratory events [1]. During this process, humans not only encountered a wide range of different environmental conditions, including diverse pathogen species, but also introduced changes in subsistence strategies that allowed the development of large, interconnected societies. Hunter/gatherer communities are thought to have suffered from infections with specific characteristics, that favor the maintenance of the agent in a small population. Wolfe and colleagues [2] identify these characteristics as (i) the presence of animal reservoirs; (ii) incomplete immunity, enabling previously infected subjects to remain in the pool of potential victims; (iii) a slow or chronic disease course, so that infected members can infect new victims over years. Thus, early humans possibly hosted a limited array of pathogenic species. However, the development of agriculture about 11,000 years ago led to a set of changes that favored the establishment of the most important epidemic diseases [2]. In particular, the domestication of animals and a sedentary lifestyle led to a steady increase in the exposure to zoonotic infections [3, 4]. Indeed, many of the most important pathogens in human history, such as smallpox and human morbillivirus (measles), evolved from diseases of domestic animals [3]. The presence of domestic herds is also thought to have increased human contact with vectors carrying malaria, yellow fever, dengue, trypanosomiasis, and filariasis.

With the development of urban centers, in about 3,000 BC, and increased communication between neighboring towns, human settlements became large enough to maintain diseases in an endemic form. This is the case, for example, for measles; for the longest part of its history, measles has been preserved by sequential outbreaks in rural villages, until the density of human populations was large enough to facilitate and support the presence of the infectious agent as an endemic pathogen [3]. The development of urban centers has also been accompanied by human expansion into new areas. The migration of Europeans in the New World during the fifteenth and sixteenth centuries is an example of the effect of population movement on pathogen transmission [5]. On the one hand, novel diseases, such as smallpox, measles, and typhus, were introduced in South and Central America, and the indigenous population, who had no or little natural resistance or immunity to these agents, were decimated: the population of Mexico was reduced from 20 millions to 3 millions between 1518 and 1568. On the other, shortly after Columbus's return from the New World, syphilis epidemics began to be recorded across Europe: although the issue is still debated, Treponema pallidum is thought to have been introduced to the Old World by crews returning from the Americas [6].

Human history has a rich record of epidemic and pandemic examples: from the plague of biblical times, through smallpox epidemics in Rome in the second and third centuries AD, to flu and bubonic plague epidemics. In relatively recent historical times, the 1918–1920 Spanish flu pandemic caused by far the highest mortality recorded in history: medical historians have estimated at least 20 million deaths [5].

Advances in medical science, the use of antibiotics, and vaccines, as well as improved hygienic conditions, have contributed to reduce the burden of infectious diseases and to eradicate some deadly pathogens (e.g., smallpox). Nonetheless, we have been witnessing the appearance and rapid spread of novel epidemics, first and foremost HIV/AIDS.

2. A Wide Spectrum of Selection Targets

Haldane, a pioneer in many fields of science, and in genetics in particular, was among the first to propose that, as infectious diseases had been a major threat to human populations, they had been acting as a powerful selective pressure and may be considered a major driver of evolution in our species [7]. A few years after this initial observation, he suggested that the high prevalence of thalassemia in the Mediterranean basin was the result of a selective pressure imposed by malaria [8]. We now know Haldane's hypotheses to be true, but it was not until the availability of large-scale genetic data and the development of novel methods to study molecular evolution that we could assess how strongly and pervasively infectious agents have shaped our genome(s). In fact, a recent genome-wide analysis has indicated that among the diverse environmental factors that most likely acted as selective pressures during the evolution of our species (climate, diet regimes, and infections), pathogen load had the strongest influence on the shaping of human genetic variability [9]. In their work, Fumagalli and coworkers [9] also indicated that the effect of distinct pathogens can at least in part be disentangled, although infectious agents were grouped into macrocategories (i.e., viruses, bacteria, helminths, and protozoa). Indeed, in his observations about thalassemia, Haldane chose a lucky rare example: the specific characteristics of Plasmodium infection and the strong selective pressure the parasite exerted allowed to draw a direct link between the infectious agent and specific loci showing very strong evidence of natural selection (e.g., DARC and G6PD [10, 11]). This has proved unfeasible for the large majority of human genes, whereby signatures of natural selection are described, but the underlying selective pressure (i.e., the specific pathogen) remains unknown. The case of thalassemia proposed by Haldane also points to another important aspect of pathogen-driven evolution: genes directly involved in immune response do not represent the only selection targets. Indeed, thalassemia is caused by inherited mutations of globin genes, which do not encode immune response effectors; nonetheless, HbS, the HBB allele responsible for sickle cell hemoglobin, is maintained by balancing selection at a frequency of about 10% in regions where Plasmodium is endemic because heterozygotes have a greatly reduced risk of developing severe malaria (reviewed in [12]). No direct involvement in immune response is also observed, for example, for glycophorins A and C (GYPC and GYPA), sialoglycoproteins abundantly expressed on the surface of red blood cells and exploited by Plasmodium falciparum for erythrocyte invasion [13, 14]. Both GYPC and GYPA have evolved adaptively in human populations, the underlying pressure being most likely accounted for by malaria [15–17]. Genetic variability at the GYPA and GYPC loci is responsible for the MNS and Gerbich blood group systems, respectively (Blood Group Antigen Gene Mutation Database (BGMUT) [18]). In humans, as many as 29 blood group systems have been described to date, and the molecular basis for most of them has been identified (Blood Group Antigen Gene Mutation Database (BGMUT) [18]). In the majority of cases, the genes specifying these systems encode a glycosyltransfrease or a glycosylated protein with an expression that is not limited to the erythrocyte. Here, again, Haldane had his say when he suggested that antigens constituted of glycoproteins account for a “surprising biochemical diversity by serological tests” and possibly play a role in resistance/predisposition to pathogen infection [19]. The ABO gene encodes a glycosyltransferase, and the ABO histoblood group was one of the first human polymorphisms identified. At the beginning of the twentieth century, the wide variability of A and B blood group frequencies across human populations had already been noticed [20]. Since then, we have learned that ABO polymorphisms have been maintained in human populations by the action of balancing selection, and that the null allele responsible for the O group has appeared at least three times during the evolution of our species [21, 22]. Indeed, a recent work indicated that ABO polymorphisms are transspecific (i.e., they are shared by descent among different primate species) and have been preserved by selection for millions of years, a very rare phenomenon outside the MHC (see the following) [23]. The expression of ABO histo-blood group antigens on the gastrointestinal mucosa and in bodily secretions (secretor phenotype) depends on the action of a fucosyltransferase encoded by FUT2 (Lewis blood group system); in different human populations distinct FUT2 polymorphisms make a portion of subjects “nonsecretors;” these variants have undergone distinct selective patterns in different geographic areas, ranging from long-standing balancing selection to recent selective sweeps, and suggest convergent evolution for the nonsecretor phenotype [24]. The evolutionary history of both ABO and FUT2 points to a long-lasting and widespread selective pressure: this is at least partially accounted for by infectious agents. Indeed, the susceptibility to a number of pathogens, including Plasmodium falciparum [25, 26], Norwalk virus [27], Campylobacter jejuni [28], Helicobacter pylori [29], and Vibrio cholerae [30], is modulated by ABO histoblood group and/or secretor status. In most cases, the different susceptibility to disease or to severe symptoms of disease is explained by the fact that ABO antigens are exploited as attachment sites by specific pathogen-encoded molecules, which, in turn, are subject to a selective pressure for increased ability to infect their host, as recently shown for the H. pylori babA gene, encoding the adhesin responsible for ABO antigen binding [31]. Indeed, their functioning as incidental pathogen receptors is thought to be the reason why other genes responsible for blood-histogroup phenotypes have been targeted by pathogen-driven selection in humans [9]. Aside from blood-group antigens, the exploitation of glycoconjugates, with specific preference for sialylated and fucosylated oligosaccharides, by pathogens seems to be common [32]. In line with this view, it has recently been shown that genes involved in the biosynthesis of glycan structures are preferential targets of virus-driven selective pressure [33]. In this respect, an interesting example is accounted for by the LARGE gene, encoding a glycosyltransferase that participates in the posttranslational modification of α-dystroglycan, a ubiquitous receptor for extracellular matrix proteins. Glycosylation by LARGE is critical for binding of arenaviruses of different phylogenetic origin, including Lassa fever virus (LFV) and lymphocytic choriomeningitis virus, to α-dystroglycan [34, 35]. LSV causes a deadly hemorrhagic fever and is endemic in West Africa. In a genome-wide screen for recent selective sweeps in humans, a major signal was detected at the LARGE locus in populations of African ancestry [36], and the same gene was described to be subject to virus-driven selection in another study [33]. Subsequent analyses indicated that the selection signal is confined to the two first introns of LARGE, suggesting that the selection target might be accounted for by one or more polymorphisms that regulate gene expression and consequently α-dystroglycan glycosylation and virus binding [37]. This interesting possibility remains to be experimentally verified.

3. Pathogen-Driven Selection at Immune Response Loci

Possibly, the best known example of natural selection in the human genome is accounted for by the major histocompatibility complex (MHC), located on the short arm of chromosome 6 in humans. As in most vertebrates, the human MHC comprises both class I and class II loci that encode molecules directly involved in the presentation of antigens to effector immune cells. The MHC represents the most polymorphic gene cluster in humans, and more than 2,700 alleles have been described for the most variable gene, HLAB (IMGT/HLA Database, European Bioinformatics Institute). KIR (killer-cell immunoglobulin-like receptors) genes, located in a cluster on chromosome 19q13.4, encode interactors of MHC class I molecules and are also highly polymorphic, with individual genes showing allelic variants and distinct haplotypes having a variable KIR gene number [38, 39].

A clear indication that the extreme variability at classes I and II HLA genes is determined by natural selection first came from the analysis of nucleotide substitution patterns; in the antigen-binding region, the rate of amino acid replacement substitutions is higher than that of synonymous substitutions, while the opposite occurs in gene regions not directly involved in antigen recognition [40, 41]. Indeed, several studies have now confirmed that the high level of diversity at MHC genes is the result of both balancing and directional selection [42–46], and HLA genes show trans-species polymorphisms and coalescent times that predate the split of the great ape lineages [47, 48]. The role of MHC molecules and their pattern of diversity clearly suggest adaptation to a wide range of pathogen species leading to amino acid diversification of the antigen binding groove. A formal demonstration that pathogens have represented the underlying selective pressure driving HLA class I molecular evolution came from an analysis of geographic diversity of HLAA, HLAB, and HLAC in human populations. Prugnolle and coworkers [49] analyzed 61 populations from different areas of the world and indicated that increased diversity at HLA class I genes (compared to the genome average) is observed in populations living in geographic regions where pathogen diversity is also high; the authors indicated that this effect is not merely explained by human demographic history, thus providing an elegant demonstration for a long-standing hypothesis. It is also worth mentioning that pathogen-driven selection on MHC genes has been proposed to influence mate choice in humans, at least in some populations [50]. The underlying idea is that the choice of an MHC-dissimilar mate, possibly through preferences based on body odour, would result in MHC-heterozygous offspring, who would be more resistant to pathogens. This hypothesis is still debated, as both contrasting and supporting evidences have been provided [50, 51].

Antigens loaded onto HLA class I molecules are generated from intracellular proteins by the antigen processing pathway, which contributes to shaping the antigenic repertoire displayed at the cell surface. The final step of antigen processing occurs in the endoplasmic reticulum where two aminopeptidases, encoded by ERAP1 and ERAP2, act in concert to trim peptides at their N-terminus [52]. Recent evidences have indicated that both genes have been targets of long-standing balancing selection in humans [53, 54]; as the aminopeptidases contribute to shape the antigenic repertoire displayed by HLA class I molecules, which, in turn, determines the ensuing response, it is tempting to speculate that the underlying selective pressure is represented by infectious agents. In line with this view, human cytomegalovirus (HCMV) encodes a microRNA (miR-US4-1) that specifically targets ERAP1, thus limiting the presentation of HCMV-derived peptides [55], whereas variants in ERAP2 have been associated with altered susceptibility to HIV-1 infection [54].

Clearly, natural selection exerted by infectious agents on the immune system is not confined to the MHC and to genes involved in antigen presentation and processing. A very nice example in this respect is represented by IFITM3 (interferon-induced transmembrane protein 3), a restriction factor for influenza A virus identified in a siRNA screen [56]. The gene has a central importance in protecting humans and mice from influenza, and a human synonymous variant in the gene affects the overall protein availability and the severity of infection [57]. Analysis of selection signatures in the gene indicated that it has been a targeted of recent positive selection in Africa [57]. Interestingly, IFITM3 seems to restrict other viral infections [56], suggesting that its evolutionary history has been driven by viral pathogens. This example, as well as those relative to the MHC and antigen presentation components, confirms that evolutionary analysis of candidate genes with a known role in immune response may reveal the traces of pathogen-driven selection. Nonetheless, the availability of large-scale data on human genetic diversity (e.g., the HapMap Project, the Human Genome Diversity Cell Line Panel, the 1000 Genomes Project, and others) has opened the possibility to screen the whole human genome for signatures of natural selection. Several analyses (e.g., [58–63]) exploited distinct approaches and invariably came up with the finding that genes involved in immune response are preferential selection targets. Specifically, natural selection was shown to target genes involved in both adaptive and innate immunity, and, following the MHC paradigm, the underlying selective pressure is likely to be accounted for by infectious agents. This hypothesis has been tested by authors that specifically modelled virus- and protozoa-driven selection and detected an overrepresentation of signals at immune response loci [17, 33]. Although valuable in their providing a comprehensive scenario, most of these studies relied on SNP genotype data and, as such, are not ideally suited to identify the specific variants targeted by selection. Resequencing efforts provide better information in this respect, as shown, for example, by an analysis of genetic diversity at NOD-like receptors (NLRs) in humans [64]; these genes encode cytoplasmic microbial sensors and can be divided into two subfamilies, NALP and NAIP, based on domain architecture. By extensive Sanger resequencing and population genetic analyses, Vasseur and coworkers [64] showed that NALP family members have evolved under stronger purifying selection compared to NAIPs, suggesting that the former plays a central nonredundant role, not necessarily limited to immune response. Also, the authors identified specific variants targeted by positive selection; a nice example is represented by the NLRP1 gene, which has recently been associated with susceptibility to congenital toxoplasmosis [65]: one haplotype carrying 7 nonsynonymous variants has increased in frequency worldwide as a result of positive selection; also, a more recent selective event affected the same gene in populations of European ancestry by targeting the Val1059Met polymorphism [64]. The authors detected natural selection signatures at the promoter region of CIITA, as well; the same variant targeted by selection represents a susceptibility allele for inflammatory diseases including rheumatoid arthritis, multiple sclerosis, and myocardial infarction [66]. Variants in NLRP1 have also been associated with the susceptibility to autoimmune diseases. Thus, these observations contribute novel evidences to a long-standing hypothesis, whereby, during the evolutionary history of humans, adaptation to infection has been traded off with increased susceptibility to autoimmune and inflammatory conditions. Observations supporting this view have increased in the last few years, and a recent genome-wide analysis of susceptibility to Crohn's disease, a chronic inflammatory disease of the digestive tract, indicated that some susceptibility alleles show signatures of balancing and directional selection, and that a significant overlap exists between Crohn's disease risk variants and those associated with mycobacterial disease (e.g., leprosy) [67].

4. Concluding Remarks

The ever-increasing availability of human genetic diversity data and the development of methods to study molecular evolution have provided support for a hypothesis formulated long ago, whereby infectious diseases have represented a major threat for human populations and, consequently, have contributed to shaping genetic diversity in our species. The development of high-throughput technologies, the availability of cell line panels from different human populations, and the progress in the fields of clinical immunology and epidemiology will provide novel insights into these issues. Thus, in the coming years we expect to witness further developments in our understanding of the molecular signatures associated with pathogen-driven selection, with special emphasis on the identification of the precise selection targets. Hopefully, these efforts will help us to gain insight into the genetic determinants modulating the susceptibility to infectious diseases that today afflict a large proportion of human subjects, and this knowledge will be translated into novel treatment strategies.

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