Genotypic Variation and the Role of Defensive Endosymbionts in an All-Parthenogenetic Host-Parasitoid Interaction
Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Ly...
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Published in | Evolution Vol. 63; no. 6; pp. 1439 - 1450 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Malden, USA
Wiley/Blackwell
01.06.2009
Blackwell Publishing Inc Wiley-Blackwell Oxford University Press |
Subjects | |
Online Access | Get full text |
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Abstract | Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defense, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype-specificity in the H. defensa-free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoid genotypes differ in their ability to overcome H. defensa, resulting in an apparent host × parasitoid genotype interaction that may in fact be due to an underlying symbiont × parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa-bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixation and highlights the need to develop new models to understand the dynamics of endosymbiont-mediated coevolution. |
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AbstractList | Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid. Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defensa, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype-specificity in the H. defensa-free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoidgenotypes differ in their ability to overcome H. defensa, resulting in an apparent host × parasitoid genotype interaction that may in fact be due to an underlying symbiont × parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa-bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixationand highlights the need to develop new models to understand the dynamics of endosymbiont-mediated coevolution. Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defense, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype-specificity in the H. defensa-free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoid genotypes differ in their ability to overcome H. defensa, resulting in an apparent host × parasitoid genotype interaction that may in fact be due to an underlying symbiont × parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa-bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixation and highlights the need to develop new models to understand the dynamics of endosymbiont-mediated coevolution. Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defensa, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype-specificity in the H. defensa-free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoid genotypes differ in their ability to overcome H. defensa, resulting in an apparent host x parasitoid genotype interaction that may in fact be due to an underlying symbiont x parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa-bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixation and highlights the need to develop new models to understand the dynamics of endosymbiont-mediated coevolution. [PUBLICATION ABSTRACT] Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defense, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype-specificity in the H. defensa-free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoid genotypes differ in their ability to overcome H. defensa, resulting in an apparent host parasitoid genotype interaction that may in fact be due to an underlying symbiont parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa-bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixation and highlights the need to develop new models to understand the dynamics of endosymbiont-mediated coevolution. Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defensa, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype-specificity in the H. defensa-free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoid genotypes differ in their ability to overcome H. defensa, resulting in an apparent host x parasitoid genotype interaction that may in fact be due to an underlying symbiont x parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa-bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixation and highlights the need to develop new models to understand the dynamics of endosymbiont-mediated coevolution. Models of host–parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype‐specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge variation for susceptibility. This variation occurred at two levels. Clones harboring Hamiltonella defensa, a bacterial endosymbiont known to protect pea aphids against parasitoids, enjoyed greatly reduced susceptibility, yet clones without H. defensa also exhibited significant variation. Although there was no evidence for genotype‐specificity in the H. defensa‐free clones' interaction with parasitoids, we found such evidence in clones containing the bacterium. This suggests that parasitoid genotypes differ in their ability to overcome H. defensa, resulting in an apparent host × parasitoid genotype interaction that may in fact be due to an underlying symbiont × parasitoid genotype interaction. Aphid susceptibility to parasitoids correlated negatively with fecundity and rate of increase, due to H. defensa‐bearing clones being more fecund on average. Hence, possessing symbionts may also be favorable in the absence of parasitoids, which raises the question why H. defensa does not go to fixation and highlights the need to develop new models to understand the dynamics of endosymbiont‐mediated coevolution. |
Author | Castañeda, Luis E. Gouskov, Alexandre Vorburger, Christoph Sandrock, Christoph Ferrari, Julia |
Author_xml | – sequence: 1 givenname: Christoph surname: Vorburger fullname: Vorburger, Christoph email: chrisvor@zool.uzh.ch organization: E-mail – sequence: 2 givenname: Christoph surname: Sandrock fullname: Sandrock, Christoph email: christoph.sandrock@zool.uzh.ch organization: E-mail – sequence: 3 givenname: Alexandre surname: Gouskov fullname: Gouskov, Alexandre email: alexandre.gouskov@zool.uzh.ch organization: E-mail – sequence: 4 givenname: Luis E surname: Castañeda fullname: Castañeda, Luis E email: luiscastaneda@uach.cl organization: E-mail – sequence: 5 givenname: Julia surname: Ferrari fullname: Ferrari, Julia email: jf557@york.ac.uk organization: Present address: Department of Biology, University of York, York Y010 5YW, United Kingdom |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19228189$$D View this record in MEDLINE/PubMed |
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Snippet | Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if... Models of host–parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype‐specific or associated with costs, and if... |
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SubjectTerms | Animals Aphididae Aphids Aphids - microbiology Aphids - parasitology Aphids - physiology Aphis fabae Aphis fabae fabae Biological Evolution Cloning costs of resistance Endosymbionts Enterobacteriaceae - physiology Evolution Evolutionary biology Fecundity genetic correlations Genetic diversity Genetic Variation Genetics Genotype Genotype & phenotype Genotypes Hamiltonella defensa Host parasite relationships Host-Parasite Interactions - physiology Lysiphlebus Lysiphlebus fabarum Models, Genetic ORIGINAL ARTICLES Parasite hosts Parasites Parasitoids Parthenogenesis Peas Regiella insecticola Symbionts symbiosis Symbiosis - physiology trade-offs Wasps - physiology |
Title | Genotypic Variation and the Role of Defensive Endosymbionts in an All-Parthenogenetic Host-Parasitoid Interaction |
URI | http://www.bioone.org/doi/abs/10.1111/j.1558-5646.2009.00660.x https://api.istex.fr/ark:/67375/WNG-FPDP5DHT-T/fulltext.pdf https://www.jstor.org/stable/40306223 https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1558-5646.2009.00660.x https://www.ncbi.nlm.nih.gov/pubmed/19228189 https://www.proquest.com/docview/227059543/abstract/ https://search.proquest.com/docview/21140179 https://search.proquest.com/docview/67321338 |
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