Evolution of virulence: coinfection and propagule production in spore-producing parasites

BACKGROUND: The evolution of within-host growth rates by parasites is expected to depend on a trade-off between propagule production and virulence. The presence of coinfections, however, is thought to alter this trade-off, and hence alter the evolutionarily stable strategy (ESS) for the parasite. Here I consider a model wherein the number of coinfections that are identical by descent can depend on the parasite's reproductive strategy. Transmission success was treated as being either a negative-linear or a negative-exponential function of the total number of propagules produced by all coinfections. RESULTS: Increasing the number of unrelated coinfections either selected for a decrease in reproductive output by the parasite (linear case), or had no effect on the ESS (exponential case). Nonetheless, the total number of propagules produced within each host increased in both cases. Increasing the relatedness among coinfections, however, selected for reductions in parasite reproduction in both cases. CONCLUSION: Unrelated coinfection may increase overall parasite virulence, but the result stems from adding more infections rather than to more aggressive growth by the individual infections. However, all else being equal, if the coinfections are more related than expected by chance alone, then the total reproductive output by all coinfections would be expected to be reduced, resulting in reduced virulence

Good vs complementary genes for parasite resistance and the evolution of mate choice

BACKGROUND: Female mate choice may be adaptive when males exhibit heritable genetic variation at loci encoding resistance to infectious disease. The Hamilton-Zuk hypothesis predicts that females should assess the genetic quality of males by monitoring traits that indicate health and vigor (condition-dependent choice, or CD). Alternatively, some females may employ a more direct method of screening and select mates based on the dissimilarity of alleles at the major histocompatibility loci (we refer to this as opposites-attract, or OA). Empirical studies suggest that both forms of mate choice exist, but little is known about the potential for natural selection to shape the two strategies in nature. RESULTS: We used computer simulation models to examine the evolutionary fates of the two forms of mate choice in populations at risk for infection by debilitating parasites. We found that populations exhibiting random mating (no mate choice) can be invaded and replaced completely by individuals practicing CD type mate choice. We also found that an allele encoding OA choice can increase when rare in randomly mating populations, but that it does not go to fixation under selection. A similar result was obtained when the OA strategy was introduced into populations practicing CD mate choice. As before, we found that the OA choice allele will increase when rare, and that it will not go to fixation under selection. The converse however was not true, as CD individuals gain no rare advantage when introduced into an OA population. CONCLUSIONS: Taken together, the results suggest that, when rare, OA is the best strategy for parasite evasion (of those considered here). The consequence of OA increasing in the population, however, is to reduce the parasite driven genotype oscillations and facilitate the breakdown of linkage disequilibrium at the disease-resistance loci. This leads to a neutrally stable situation in which different strategies have equal fitness, and suggests that multiple forms of mate choice may be expected to occur in populations at risk from infectious disease

Immune response to sympatric and allopatric parasites in a snail-trematode interaction

BACKGROUND: The outcome of parasite exposure depends on the (1) genetic specificity of the interaction, (2) induction of host defenses, and (3) parasite counter defenses. We studied both the genetic specificity for infection and the specificity for the host-defense response in a snail-trematode interaction (Potamopyrgus antipodarum-Microphallus sp.) by conducting a reciprocal cross-infection experiment between two populations of host and parasite. RESULTS: We found that infection was greater in sympatric host-parasite combinations. We also found that the host-defense response (hemocyte concentration) was induced by parasite exposure, but the response did not increase with increased parasite dose nor did it depend on parasite source, host source, or host-parasite combination. CONCLUSION: The results are consistent with a genetically specific host-parasite interaction, but inconsistent with a general arms-race type interaction where allocation to defense is the main determinant of host resistance

Disgust sensitivity is not associated with health in a rural Bangladeshi sample.

Disgust can be considered a psychological arm of the immune system that acts to prevent exposure to infectious agents. High disgust sensitivity is associated with greater behavioral avoidance of disease vectors and thus may reduce infection risk. A cross-sectional survey in rural Bangladesh provided no strong support for this hypothesis. In many species, the expression of pathogen- and predator-avoidance mechanisms is contingent on early life exposure to predators and pathogens. Using childhood health data collected in the 1990s, we examined if adults with more infectious diseases in childhood showed greater adult disgust sensitivity: no support for this association was found. Explanations for these null finding and possible directions for future research are discussed

Herbivore-mediated negative frequency-dependent selection underlies a trichome dimorphism in nature

Authors are grateful for funding provided by an NSF GRFP to J.K.G. (2015195769) and DEB‐1353970 to L.F.D.Negative frequency‐dependent selection (NFDS) has been shown to maintain polymorphism in a diverse array of traits. The action of NFDS has been confirmed through modeling, experimental approaches, and genetic analyses. In this study, we investigated NFDS in the wild using morph‐frequency changes spanning a 20‐year period from over 30 dimorphic populations of Datura wrightii. In these populations, plants either possess glandular (sticky) or non‐glandular (velvety) trichomes, and the ratio of these morphs varies substantially among populations. Our method provided evidence that NFDS, rather than drift or migration, is the primary force maintaining this dimorphism. Most populations that were initially dimorphic remained dimorphic, and the overall mean and variance in morph frequency did not change over time. Furthermore, morph‐frequency differences were not related to geographic distances. Together, these results indicate that neither directional selection, drift, or migration played a substantial role in determining morph frequencies. However, as predicted by negative frequency‐dependent selection, we found that the rare morph tended to increase in frequency, leading to a negative relationship between the change in the frequency of the sticky morph and its initial frequency. In addition, we found that morph‐frequency change over time was significantly correlated with the damage inflicted by two herbivores: Lema daturaphila and Tupiochoris notatus. The latter is a specialist on the sticky morph and damage by this herbivore was greatest when the sticky morph was common. The reverse was true for L. daturaphila, such that damage increased with the frequency of the velvety morph. These findings suggest that these herbivores contribute to balancing selection on the observed trichome dimorphism.Publisher PDFPeer reviewe

The cost of males in non-equilibrium populations

ABSTRACT Question: What is the cost of producing males in non-equilibrium sexual species? Background: Asexual reproduction is generally associated with non-equilibrium (r-selected) species, while sexual reproduction is generally associated with equilibrium (K-selected) species. Mathematical methods: The cost of males per reproductive time step was calculated as the ratio of the per-capita growth rate of an asexual population relative to the per-capita growth rate of a sexual population. Key assumptions: Sexual and asexual individuals are ecologically similar. Sexual females produce males, which do not contribute to the per-capita birth rate, whereas asexual females produce only female offspring. All else is equal. Conclusion: The cost of males per reproductive time step approaches two-fold in nonequilibrium populations where the birth rate is much greater than the death rate. In contrast, the cost of males per time step can be much less than two-fold in iteroparous populations at equilibrium. These results are consistent with the distribution of parthenogenesis in natural populations

Data from: Habitat heterogeneity, host population structure and parasite local adaptation

Reciprocal-transplant experiments have proven to be a powerful tool for detecting local adaptation (LA). More recently, reciprocal cross-inoculation experiments have been used to evaluate adaptation by parasites to their local host populations. These experiments are conceptually similar to reciprocal-transplant experiments, except that the "environment" (the host population) may have evolved in response to changes in the parasite population. Here, I use analytical tools and computer simulations to determine when parasites would be expected to be more infective to their local host populations than to allopatric host populations. The models assume that parasites have to genetically "match" their hosts in order to infect. I also assumed that different host clones were favored in different populations. When parasite virulence was low, clonal selection outweighed parasite-mediated selection, leading to low host diversity within populations and strong LA by parasites. At intermediate levels of virulence, parasite-mediated selection maintained high levels of host diversity within populations, which reduced or eliminated parasite LA. The loss of parasite LA was not associated with increased infectivity by parasites on allopatric hosts. Instead, the loss of LA was due to a reduction in infectivity of parasites on sympatric hosts. Finally, at high levels of parasite virulence, parasite-mediated selection lead to oscillatory host dynamics, and weak local adaption by parasites. Across all levels of virulence, the strength of parasite LA closely tracked the degree of host population structure (GST)

The cost of males in non-equilibrium populations

ABSTRACT Question: What is the cost of producing males in non-equilibrium sexual species? Background: Asexual reproduction is generally associated with non-equilibrium (r-selected) species, while sexual reproduction is generally associated with equilibrium (K-selected) species. Mathematical methods: The cost of males per reproductive time step was calculated as the ratio of the per-capita growth rate of an asexual population relative to the per-capita growth rate of a sexual population. Key assumptions: Sexual and asexual individuals are ecologically similar. Sexual females produce males, which do not contribute to the per-capita birth rate, whereas asexual females produce only female offspring. All else is equal. Conclusion: The cost of males per reproductive time step approaches two-fold in nonequilibrium populations where the birth rate is much greater than the death rate. In contrast, the cost of males per time step can be much less than two-fold in iteroparous populations at equilibrium. These results are consistent with the distribution of parthenogenesis in natural populations