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      Prior adaptation of parasitoids improves biological control of symbiont‐protected pests

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          Abstract

          There is increasing demand for sustainable pest management to reduce harmful effects of pesticides on the environment and human health. For pest aphids, biological control with parasitoid wasps provides a welcome alternative, particularly in greenhouses. However, aphids are frequently infected with the heritable bacterial endosymbiont Hamiltonella defensa, which increases resistance to parasitoids and thereby hampers biological control. Using the black bean aphid ( Aphis fabae) and its main parasitoid Lysiphlebus fabarum, we tested whether prior adaptation of parasitoids can improve the control of symbiont‐protected pests. We had parasitoid lines adapted to two different strains of H. defensa by experimental evolution, as well as parasitoids evolved on H. defensa‐free aphids. We compared their ability to control caged aphid populations comprising 60% unprotected and 40% H. defensa‐protected aphids, with both H. defensa strains present in the populations. Parasitoids that were not adapted to H. defensa had virtually no effect on aphid population dynamics compared to parasitoid‐free controls, but one of the adapted lines and a mixture of both adapted lines controlled aphids successfully, strongly benefitting plant growth. Selection by parasitoids altered aphid population composition in a very specific manner. Aphid populations became dominated by H. defensa‐protected aphids in the presence of parasitoids, and each adapted parasitoid line selected for the H. defensa strain it was not adapted to. This study shows, for the first time, that prior adaptation of parasitoids improves biological control of symbiont‐protected pests, but the high specificity of parasitoid counter‐resistance may represent a challenge for its implementation.

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          Facultative bacterial symbionts in aphids confer resistance to parasitic wasps.

          Symbiotic relationships between animals and microorganisms are common in nature, yet the factors controlling the abundance and distributions of symbionts are mostly unknown. Aphids have an obligate association with the bacterium Buchnera aphidicola (the primary symbiont) that has been shown to contribute directly to aphid fitness. In addition, aphids sometimes harbor other vertically transmitted bacteria (secondary symbionts), for which few benefits of infection have been previously documented. We carried out experiments to determine the consequences of these facultative symbioses in Acyrthosiphon pisum (the pea aphid) for vulnerability of the aphid host to a hymenopteran parasitoid, Aphidius ervi, a major natural enemy in field populations. Our results show that, in a controlled genetic background, infection confers resistance to parasitoid attack by causing high mortality of developing parasitoid larvae. Compared with uninfected controls, experimentally infected aphids were as likely to be attacked by ovipositing parasitoids but less likely to support parasitoid development. This strong interaction between a symbiotic bacterium and a host natural enemy provides a mechanism for the persistence and spread of symbiotic bacteria.
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            Persistent negative effects of pesticides on biodiversity and biological control potential on European farmland

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              Global Water Pollution and Human Health

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                Author and article information

                Contributors
                christoph.vorburger@eawag.ch
                Journal
                Evol Appl
                Evol Appl
                10.1111/(ISSN)1752-4571
                EVA
                Evolutionary Applications
                John Wiley and Sons Inc. (Hoboken )
                1752-4571
                06 March 2020
                September 2020
                : 13
                : 8 ( doiID: 10.1111/eva.v13.8 )
                : 1868-1876
                Affiliations
                [ 1 ] Aquatic Ecology Eawag Dübendorf Switzerland
                [ 2 ] Institute of Integrative Biology ETH Zürich Zürich Switzerland
                Author notes
                [*] [* ] Correspondence

                Christoph Vorburger, Aquatic Ecology, Eawag, Überlandstrasse 133, PO Box 611, 8600 Dübendorf, Switzerland.

                Email: christoph.vorburger@ 123456eawag.ch

                Author information
                https://orcid.org/0000-0002-3627-0841
                Article
                EVA12934
                10.1111/eva.12934
                7463345
                32908591
                654d3f70-ffd1-4209-8058-b416e16014f2
                © 2020 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd

                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.

                History
                : 20 December 2019
                : 02 February 2020
                : 04 February 2020
                Page count
                Figures: 3, Tables: 2, Pages: 9, Words: 7313
                Funding
                Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung , open-funder-registry 10.13039/501100001711;
                Award ID: 31003A_181969
                Award ID: CRSII3_154396
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                September 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.8 mode:remove_FC converted:02.09.2020

                Evolutionary Biology
                aphids,biological control,defensive symbiosis,parasitoid,resistance evolution
                Evolutionary Biology
                aphids, biological control, defensive symbiosis, parasitoid, resistance evolution

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