Host–parasite coevolution


Host–parasite coevolution is a special case of coevolution, the reciprocal adaptive genetic change of a host and a parasite through reciprocal selective pressures.
It is characterized by reciprocal genetic change and thus changes in allele frequencies within populations. These are determined by three main types of selection dynamics: negative frequency-dependent selection when a rare allele has a selective advantage; overdominance caused by heterozygote advantage; and directional selective sweeps near an advantageous mutation.
Theories of host–parasite coevolution include the geographic mosaic theory, which assumes a selection mosaic, coevolutionary hotspots, and geographic mixing; the Red Queen hypothesis, which proposes that parasitism favours sexual reproduction in the host; and an evolutionary trade-off between transmission and virulence, since if the parasite kills its host too quickly, the parasite will not be able to reproduce.
Model systems include the nematode Caenorhabditis elegans with the bacterium Bacillus thuringiensis; the crustacean Daphnia and its numerous parasites; and Escherichia coli and the mammals whose intestines it inhabits.

Overview

and parasites exert reciprocal selective pressures on each other, which may lead to rapid reciprocal adaptation. For organisms with short generation times, host–parasite coevolution can be observed in comparatively small time periods, making it possible to study evolutionary change in real-time under both field and laboratory conditions. These interactions may thus serve as a counter-example to the common notion that evolution can only be detected across extended time.
The dynamics of these interactions are summarized in the Red Queen hypothesis, namely that both host and parasite have to change continuously to keep up with each other's adaptations.
Host–parasite coevolution is ubiquitous and of potential importance to all living organisms, including humans, domesticated animals and crops. Major diseases such as malaria, AIDS and influenza are caused by coevolving parasites. Better understanding of coevolutionary adaptations between parasite attack strategies and host immune systems may assist in the development of novel medications and vaccines.

Selection dynamics

Host–parasite coevolution is characterized by reciprocal genetic change and thus changes in allele frequencies within populations. These changes may be determined by three main types of selection dynamics.

Negative frequency dependent selection

An allele is subject to negative frequency dependent selection if a rare allelic variant has a selective advantage. For example, the parasite should adapt to the most common host genotype, because it can then infect a large number of hosts. In turn, a rare host genotype may then be favored by selection, its frequency will increase and eventually it becomes common. Subsequently, the parasite should adapt to the former infrequent genotype.
Coevolution determined by negative frequency dependent selection is rapid, potentially occurring across few generations. It maintains high genetic diversity by favoring uncommon alleles. This selection mode is expected for multicellular hosts, because adaptations can occur without the need for novel advantageous mutations, which are less likely to be frequent in these hosts because of relatively small population sizes and relatively long generation times.

Overdominant selection

occurs if the heterozygote phenotype has a fitness advantage over both homozygotes. One example is sickle cell anemia. It is due to a mutation in the hemoglobin gene leading to sickle shape formation of red blood cells, causing clotting in blood vessels, restricted blood flow, and reduced oxygen transport. At the same time, the mutation confers resistance to malaria, caused by Plasmodium parasites, which are passed off in red blood cells after transmission to humans by mosquitoes. Hence, homozygote and heterozygote genotypes for the sickle-cell disease allele show malaria resistance, while the homozygote suffers from severe disease phenotype. The alternative homozygote, which does not carry the sickle cell disease allele, is susceptible to infection by Plasmodium. As a consequence, the heterozygote genotype is selectively favored in areas with a high incidence of malaria.

Directional selection

If an allele provides a fitness benefit, its frequency will increase within a population – selection is directional or positive. Selective sweeps are one form of directional selection, where the increase in frequency will eventually lead to the fixation of the advantageous allele. The process is considered to be slower in comparison to negative frequency dependent selection. It may produce an "arms race", consisting of the repeated origin and fixation of new parasite virulence and host defence traits.
This mode of selection is likely to occur in interactions between unicellular organisms and viruses due to large population sizes, short generation times, often haploid genomes and horizontal gene transfer, which increase the probability of beneficial mutations arising and spreading through populations.

Theories

Geographic mosaic theory of coevolution

John N. Thompson's geographic mosaic theory of coevolution hypothesizes spatially divergent coevolutionary selection, producing genetic differentiation across populations. The model assumes three elements that jointly fuel coevolution:

1) a selection mosaic among populations
2) coevolutionary hotspots
3) geographic mixing of traits
Among plants,
Plantago lanceolata and its parasite the powdery mildew Podosphaera plantaginis have been intensively studied on the Aland islands in south-western Finland. P. plantaginis'' obtains nutrients from its host, a perennial herb, by sending feeding roots into the plant. There are more than 3000 host populations in this region, where both populations can evolve freely, in absence of human-imposed selection, in a heterogeneous landscape. Both partners can reproduce asexually or sexually. The system has spatially divergent coevolutionary dynamics across two metapopulations as predicted by the mosaic theory.

Red Queen hypothesis

The New Zealand freshwater snail Potamopyrgus antipodarum and its different trematode parasites represent a rather special model system. Populations of P. antipodarum consist of asexual clones and sexual individuals and therefore can be used to study the evolution and advantages of sexual reproduction. There is a high correlation between the presence of parasites and the frequency of sexual individuals within the different populations. This result is consistent with the Red Queen hypothesis that sexual reproduction is favoured during host–parasite coevolution. At the same time, the persistence of sex may also rely on other factors, for example Muller's ratchet and/or the avoidance of the accumulation of deleterious mutations.

Trade-off between transmission and virulence

Tribolium castaneum, the red flour beetle, is a host for the microsporidian Nosema whitei. This parasitoid kills its host for transmission, so the host's lifespan is important for the parasite's success. In turn, parasite fitness most likely depends on a trade-off between transmission and virulence. A higher virulence would increase the potential for the production of more offspring, but a higher spore load would affect the host's lifespan and therefore the transmission rate. This trade-off is supported by coevolutionary experiments, which revealed the decrease of virulence, a constant transmission potential and an increase in the host's lifespan over a period of time.
Further experiments demonstrated a higher recombination rate in the host during coevolutionary interactions, which may be selectively advantageous because it should increase diversity of host genotypes.
Resources are generally limited. Therefore, investment in one trait limits investment in other life-history traits. Moreover, genes are often pleiotropic, having multiple effects. Thus, a change in a pleiotropic immunity or virulence gene can automatically affect other traits. There is thus a trade-off between benefits and costs of the adaptive changes that may prevent the host population from becoming fully resistant or the parasite population from being highly pathogenic. The costs of gene pleiotropy have been investigated in coevolving Escherichia coli and bacteriophages. To inject their genetic material, phages need to bind to a specific bacterial cell surface receptor. The bacterium may prevent injection by altering the relevant binding site, e.g. in response to point mutations or deletion of the receptor. However, these receptors have important functions in bacterial metabolism. Their loss would thus decrease fitness. As a consequence, there is a trade-off between the advantages and disadvantages of a mutated receptor, leading to polymorphism at this locus.

Model systems for research

The nematode Caenorhabditis elegans and the bacterium Bacillus thuringiensis were only recently established as a model system for studying host–parasite coevolution. Laboratory evolution experiments provided evidence for many of the basic predictions of these coevolutionary interactions, including reciprocal genetic change, and increases in the rate of evolution and genetic diversity.

The crustacean
Daphnia and its numerous parasites have become one of the main model systems for studying coevolution.
The host can be asexual as well as sexual, so sexual reproduction can be stimulated in the laboratory. Decades of coevolution between
Daphnia magna and the bacterium Pasteuria ramosa have been reconstructed, reanimating resting stages of both species from laminated pond sediments and exposing hosts from each layer to parasites from the past, the same and the future layers. The study demonstrated that parasites were on average most infective with their contemporary hosts, consistent with negative frequency dependent selection.

Escherichia coli, a Gram-negative proteobacterium, is a common model in biological research, for which comprehensive data on various aspects of its life-history is available. It has been used extensively for evolution experiments, including those related to coevolution with phages. These studies revealed – among others – that coevolutionary adaptation may be influenced by pleiotropic effects of the involved genes. In particular, binding of the bacteriophage to E. coli surface receptor is the crucial step in the virus infection cycle. A mutation in the receptor's binding site may cause resistance. Such mutations often show pleiotropic effects and may cause a cost of resistance. In the presence of phages, such pleiotropy may lead to polymorphisms in the bacterial population and thus enhance biodiversity in the community.
Another model system consists of the plant- and animal-colonizing bacterium Pseudomonas and its bacteriophages. This system provided new insights into the dynamics of coevolutionary change. It demonstrated that coevolution may proceed via recurrent selective sweeps, favouring generalists for both antagonists. Furthermore, coevolution with phages may promote allopatric diversity, potentially enhancing biodiversity and possibly speciation. Host-parasite coevolution may also affect the underlying genetics, for example by favouring increased mutation rates in the host.
Tropical tree and liana interactions have also been the subject of study. Here lianas have been viewed as hyper-diverse generalist macro-parasites that affect host survival by parasitising on the host's structural support for access to canopy light, while usurping resources that would otherwise be available to their host. Host trees have widely varying levels of tolerance to infestation of their crowns by lianas.