Abstract:Ploidy-level variation is common and can drastically affect organismal fitness. We focus on the potential consequences of this variation for parasite resistance. First, we elucidate connections between ploidy variation and key factors determining resistance, including allelic diversity, gene expression and physiological condition. We then argue that systems featuring both natural and artificially manipulated ploidy variation should be used to evaluate whether ploidy level influences host -parasite interactions… Show more
“…5). A result similar to those from previous studies (King et al 2012), and in support of the invasion scenarios of M'Gonigle and Otto (2011). The results here being attributable to the proportion of I-S edges, and the general density of edges in the network.…”
Host-parasite co-evolution is a key component of the Red Queen Hypothesis (RQH). The RQH currently being one of the main hypotheses describing the evolution of sex and recombination. However, most analyses in this area have either ignored parasite transmission or included it either with mean field or simple frequency based models. Moreover models have rarely addressed the issue of male haploid species. We here use agent based models to qualify the interactions between host-and parasite-based transmission parameters and virulence comparing diploid with male-haploid species. We found diploid hosts to have a higher fitness under the inverse matching allele mode compared to male haplodiploid hosts which in turn have a higher fitness under the matching allele model . Selection for recombination was rare but whenever selection for recombination was evident (\6.6 %), the resulting recombination rates were both consistently higher and more frequent in male haploids.
“…5). A result similar to those from previous studies (King et al 2012), and in support of the invasion scenarios of M'Gonigle and Otto (2011). The results here being attributable to the proportion of I-S edges, and the general density of edges in the network.…”
Host-parasite co-evolution is a key component of the Red Queen Hypothesis (RQH). The RQH currently being one of the main hypotheses describing the evolution of sex and recombination. However, most analyses in this area have either ignored parasite transmission or included it either with mean field or simple frequency based models. Moreover models have rarely addressed the issue of male haploid species. We here use agent based models to qualify the interactions between host-and parasite-based transmission parameters and virulence comparing diploid with male-haploid species. We found diploid hosts to have a higher fitness under the inverse matching allele mode compared to male haplodiploid hosts which in turn have a higher fitness under the matching allele model . Selection for recombination was rare but whenever selection for recombination was evident (\6.6 %), the resulting recombination rates were both consistently higher and more frequent in male haploids.
“…A particular type of biotic interactions that has been associated with polyploidy is parasitism and parasite resistance [Nuismer and Otto, 2004;Osnas and Lively, 2006;M'Gonigle and Otto, 2011;King et al, 2012]. A role for polyploidy in immunity has been inferred in the context of (1) allelic and genetic diversity and (2) endopolyploidy (next paragraph).…”
Section: Polyploidy and Evolutionary Ecologymentioning
Polyploidy is rarer in animals than in plants. Why? Since Muller's observation in 1925, many hypotheses have been proposed and tested, but none were able to completely explain this intriguing fact. New genomic technologies enable the study of whole genomes to explain the constraints on or consequences of polyploidization, rather than focusing on specific genes or life history characteristics. Here, we review a selection of old and recent literature on polyploidy in animals, with emphasis on the consequences of polyploidization for gene expression patterns and genomic network interactions. We propose a conceptual model to contrast various scenarios for changes in genomic networks, which may serve as a framework to explain the different evolutionary dynamics of polyploidy in animals and plants. We also present new insights of genetic sex determination in animals and our emerging understanding of how animal sex determination systems may hamper or enable polyploidization, including some recent data on haplodiploids. We discuss the role of polyploidy in evolution and ecology, using a gene regulation perspective, and conclude with a synopsis regarding the effects of whole genome duplications on the balance of genomic networks. See also the sister articles focusing on plants by Ashman et al. and Madlung and Wendel in this themed issue.
“…Since ploidy-level variation can affect traits from gene expression to the rate of spread of beneficial mutations to immune function (reviewed in Otto and Whitton, 2000;Comai, 2005;Mable et al, 2011;King et al, 2012), it may be of relevance when considering the outcome of competition between sexual and asexual lineages that differ in ploidy.…”
Section: A Disadvantage Of Polyploidy?mentioning
confidence: 99%
“…This finding points to the importance of controlling for hybrid ancestry, which is very common in asexual polyploids, when evaluating the ecological consequences of polyploidy. Given the common co-occurrence of hybridization, polyploidy, and asexuality, it is perhaps not surprising that the extent to which polyploidy is likely to explain different distributions of sexual and asexual taxa is controversial and remains unclear (Mable, 2004;Lundmark and Saura, 2006;Vrijenhoek and Parker, 2009;Maniatsi et al, 2011;King et al, 2012).…”
Section: Consequences Of High P Content For Asexual Ecologymentioning
The predominance of sexual reproduction despite its costs indicates that sex provides substantial benefits, which are usually thought to derive from the direct genetic consequences of recombination and syngamy. While genetic benefits of sex are certainly important, sexual and asexual individuals, lineages, or populations may also differ in physiological and life history traits that could influence outcomes of competition between sexuals and asexuals across environmental gradients. Here, we address possible phenotypic costs of a very common correlate of asexuality, polyploidy. We suggest that polyploidy could confer resource costs related to the dietary phosphorus demands of nucleic acid production; such costs could facilitate the persistence of sex in situations where asexual taxa are of higher ploidy level and phosphorus availability limits important traits like growth and reproduction. We outline predictions regarding the distribution of diploid sexual and polyploid asexual taxa across biogeochemical gradients and provide suggestions for study systems and empirical approaches for testing elements of our hypothesis.
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