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Effects of pea aphid secondary endosymbionts on aphid resistance and development of the aphid parasitoid Aphidius ervi: a correlative study
Authors:Franklin N Nyabuga  Yannick Outreman  Jean‐Christophe Simon  David G Heckel  Wolfgang W Weisser
Institution:1. Institute of Ecology, Friedrich‐Schiller‐University, Dornburger Str. 159, 07743 Jena, Germany;2. UMR 1099 INRA‐Agrocampus Ouest‐Université Rennes 1 ‘Biologie des Organismes et des Populations appliquée à la Protection des Plantes’, 65, rue de Saint‐Brieuc CS 84215, 35042 Rennes Cedex, and BP 35327, 35653 Le Rheu Cedex, France;3. Max‐Planck‐Institute for Chemical Ecology, Department of Entomology, Hans‐Kn?ll‐Str. 8, 07745 Jena, Germany
Abstract:In order to reduce parasite‐induced mortality, hosts may be involved in mutualistic interactions in which the partner contributes to resistance against the parasite. The pea aphid, Acyrthosiphon pisum Harris (Hemiptera: Aphididae), harbours secondary bacterial endosymbionts, some of which have been reported to confer resistance against aphid parasitoids. Although this resistance often results in death of the developing parasitoid larvae, some parasitoid individuals succeed in developing into adults. Whether these individuals suffer from fitness reduction compared to parasitoids developing in pea aphid clones without symbionts has not been tested so far. Using 30 pea aphid clones that differed in their endosymbiont complement, we studied the effects of these endosymbionts on aphid resistance against the parasitoid Aphidius ervi Haliday (Hymenoptera: Braconidae: Aphidiinae), host–parasitoid physiological interactions, and fitness of emerging adult parasitoids. The number of symbiont species in an aphid clone was positively correlated with a number of resistance measurements but there were also clear symbiont‐specific effects on the host–parasitoid interaction. As in previous studies, pea aphid clones infected with Hamiltonella defensa Moran et al. showed resistance against the parasitoid. In addition, pea aphid clones infected with Regiella insecticola Moran et al. and co‐infections of H. defensaSpiroplasma, R. insecticolaSpiroplasma, and R. insecticolaH. defensa showed reduced levels of parasitism and mummification. Parasitoids emerging from symbiont‐infected aphid clones often had a longer developmental time and reduced mass. The number of teratocytes was generally lower when parasitoids oviposited in aphid clones with a symbiont complement. Interestingly, unparasitized aphids infected with Serratia symbiotica Moran et al. and R. insecticola had a higher fecundity than unparasitized aphids of uninfected pea aphid clones. We conclude that in addition to conferring resistance, pea aphid symbionts also negatively affect parasitoids that successfully hatch from aphid mummies. Because of the link between aphid resistance and the number of teratocytes, the mechanism underlying resistance by symbiont infection may involve interference with teratocyte development.
Keywords:secondary symbionts  facultative bacteria  parasitoid fitness  Acyrthosiphon pisum  Hymenoptera  Braconidae  Aphidiinae  Hemiptera  Aphididae
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