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Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis

1. Facultative bacterial endosymbionts can protect their aphid hosts from natural enemies such as hymenopteran parasitoids. As such, they have the capability to modulate interactions between aphids, parasitoids and hyperparasitoids. However, the magnitude of these effects in natural aphid population...

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Autores principales: Ye, Zhengpei, Vollhardt, Ines M. G., Parth, Nadia, Rubbmark, Oskar, Traugott, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099228/
https://www.ncbi.nlm.nih.gov/pubmed/29928757
http://dx.doi.org/10.1111/1365-2656.12875
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author Ye, Zhengpei
Vollhardt, Ines M. G.
Parth, Nadia
Rubbmark, Oskar
Traugott, Michael
author_facet Ye, Zhengpei
Vollhardt, Ines M. G.
Parth, Nadia
Rubbmark, Oskar
Traugott, Michael
author_sort Ye, Zhengpei
collection PubMed
description 1. Facultative bacterial endosymbionts can protect their aphid hosts from natural enemies such as hymenopteran parasitoids. As such, they have the capability to modulate interactions between aphids, parasitoids and hyperparasitoids. However, the magnitude of these effects in natural aphid populations and their associated parasitoid communities is currently unknown. Moreover, environmental factors such as plant fertilization and landscape complexity are known to affect aphid–parasitoid interactions but it remains unclear how such environmental factors affect the interplay between aphids, parasitoids and endosymbionts. 2. Here, we tested whether facultative endosymbionts confer protection to parasitoids in natural populations of the English grain aphid, Sitobion avenae, and if this is affected by plant fertilization and landscape complexity. Furthermore, we examined whether the effects of facultative endosymbionts can cascade up to the hyperparasitoid level and increase primary‐hyperparasitoid food web specialization. 3. Living aphids and mummies were collected in fertilized and unfertilized plots within 13 wheat fields in Central Germany. We assessed the occurrence of primary parasitoid, hyperparasitoid and endosymbiont species in aphids and mummies using a newly established molecular approach. 4. Facultative endosymbiont infection rates were high across fields (~80%), independent of whether aphids were parasitized or unparasitized. Aphid mummies exhibited a significantly lower share of facultative endosymbiont infection (~38%). These findings suggest that facultative endosymbionts do not affect parasitoid oviposition behaviour, but decrease parasitoid survival in the host. Facultative endosymbiont infection rates were lower in mummies collected from fertilized compared to unfertilized plants, indicating that plant fertilization boosts the facultative endosymbiont protective effect. Furthermore, we found strong evidence for species‐specific and negative cascading effects of facultative endosymbionts on primary and hyperparasitoids, respectively. Facultative endosymbionts impacted parasitoid assemblages and increased the specialization of primary‐hyperparasitoid food webs: these effects were independent from and much stronger than other environmental factors. 5. The current findings strongly suggest that facultative endosymbionts act as a driving force in aphid–parasitoid–hyperparasitoid networks: they shape insect community composition at different trophic levels and modulate, directly and indirectly, the interactions between aphids, parasitoids and their environment.
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spelling pubmed-60992282018-08-23 Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis Ye, Zhengpei Vollhardt, Ines M. G. Parth, Nadia Rubbmark, Oskar Traugott, Michael J Anim Ecol Trophic Interactions 1. Facultative bacterial endosymbionts can protect their aphid hosts from natural enemies such as hymenopteran parasitoids. As such, they have the capability to modulate interactions between aphids, parasitoids and hyperparasitoids. However, the magnitude of these effects in natural aphid populations and their associated parasitoid communities is currently unknown. Moreover, environmental factors such as plant fertilization and landscape complexity are known to affect aphid–parasitoid interactions but it remains unclear how such environmental factors affect the interplay between aphids, parasitoids and endosymbionts. 2. Here, we tested whether facultative endosymbionts confer protection to parasitoids in natural populations of the English grain aphid, Sitobion avenae, and if this is affected by plant fertilization and landscape complexity. Furthermore, we examined whether the effects of facultative endosymbionts can cascade up to the hyperparasitoid level and increase primary‐hyperparasitoid food web specialization. 3. Living aphids and mummies were collected in fertilized and unfertilized plots within 13 wheat fields in Central Germany. We assessed the occurrence of primary parasitoid, hyperparasitoid and endosymbiont species in aphids and mummies using a newly established molecular approach. 4. Facultative endosymbiont infection rates were high across fields (~80%), independent of whether aphids were parasitized or unparasitized. Aphid mummies exhibited a significantly lower share of facultative endosymbiont infection (~38%). These findings suggest that facultative endosymbionts do not affect parasitoid oviposition behaviour, but decrease parasitoid survival in the host. Facultative endosymbiont infection rates were lower in mummies collected from fertilized compared to unfertilized plants, indicating that plant fertilization boosts the facultative endosymbiont protective effect. Furthermore, we found strong evidence for species‐specific and negative cascading effects of facultative endosymbionts on primary and hyperparasitoids, respectively. Facultative endosymbionts impacted parasitoid assemblages and increased the specialization of primary‐hyperparasitoid food webs: these effects were independent from and much stronger than other environmental factors. 5. The current findings strongly suggest that facultative endosymbionts act as a driving force in aphid–parasitoid–hyperparasitoid networks: they shape insect community composition at different trophic levels and modulate, directly and indirectly, the interactions between aphids, parasitoids and their environment. John Wiley and Sons Inc. 2018-07-16 2018-09 /pmc/articles/PMC6099228/ /pubmed/29928757 http://dx.doi.org/10.1111/1365-2656.12875 Text en © 2018 The Authors. Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Trophic Interactions
Ye, Zhengpei
Vollhardt, Ines M. G.
Parth, Nadia
Rubbmark, Oskar
Traugott, Michael
Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis
title Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis
title_full Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis
title_fullStr Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis
title_full_unstemmed Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis
title_short Facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: A correlative analysis
title_sort facultative bacterial endosymbionts shape parasitoid food webs in natural host populations: a correlative analysis
topic Trophic Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099228/
https://www.ncbi.nlm.nih.gov/pubmed/29928757
http://dx.doi.org/10.1111/1365-2656.12875
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