Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)

Herbivorous insects are often highly specialised, likely due to trade-offs in fitness on alternative host species. However, some pest insects are extremely adaptable and readily adopt novel hosts, sometimes causing rapid expansion of their host range as they spread from their original host and geogr...

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Main Authors: Thomas N. PRICE, Aoife LEONARD, Lesley T. LANCASTER
Format: Article
Language:English
Published: Institute of Entomology, Biology Centre, Czech Academy of Science 2017-05-01
Series:European Journal of Entomology
Subjects:
Online Access:https://www.eje.cz/artkey/eje-201701-0031_Warp-speed_adaptation_to_novel_hosts_after_300_generations_of_enforced_dietary_specialisation_in_the_seed_beetl.php
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author Thomas N. PRICE
Aoife LEONARD
Lesley T. LANCASTER
author_facet Thomas N. PRICE
Aoife LEONARD
Lesley T. LANCASTER
author_sort Thomas N. PRICE
collection DOAJ
description Herbivorous insects are often highly specialised, likely due to trade-offs in fitness on alternative host species. However, some pest insects are extremely adaptable and readily adopt novel hosts, sometimes causing rapid expansion of their host range as they spread from their original host and geographic origin. The genetic basis of this phenomenon is poorly understood, limiting our ability to predict or mitigate global insect pest outbreaks. We investigated the trajectory of early adaptation to novel hosts in a regionally-specialised global crop pest species (the cowpea seed beetle Callosobruchus maculatus). After experimentally-enforced dietary specialisation for nearly 300 generations, we measured changes in fitness over the first 5 generations of adaptation to 6 novel hosts. Of these, C. maculatus reproduced successfully on all but one, with reduced fitness observed on three hosts in the first generation. Loss of fitness was followed by very rapid, decelerating increases in fitness over the first 1-5 generations, resulting in comparable levels of population fitness to that observed on the original host after 5 generations. Heritability of fitness on novel hosts was high. Adaptation occurred primarily via changes in behavioural and phenological traits, and never via changes in offspring survival to adulthood, despite high heritability for this trait. These results suggest that C. maculatus possesses ample additive genetic variation for very rapid host shifts, despite a prolonged period of enforced specialization, and also suggest that some previously-inferred environmental maternal effects on host use may in part actually represent (rapidly) evolved changes. We highlight the need to examine in more detail the genetic architecture facilitating retention of high additive genetic variation for host shifts in extremely adaptable global crop pests.
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spelling doaj.art-e7de2b2c0ca5437e8f0d12fab1892ddb2022-12-21T19:06:37ZengInstitute of Entomology, Biology Centre, Czech Academy of ScienceEuropean Journal of Entomology1210-57591802-88292017-05-01114125726610.14411/eje.2017.031eje-201701-0031Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)Thomas N. PRICE0Aoife LEONARD1Lesley T. LANCASTER2Institute of Biological and Environmental Sciences, Zoology Building, University of Aberdeen, Aberdeen AB24 2TZ, UK; e-mails: t.price.12@aberdeen.ac.uk, r05al15@abdn.ac.uk, lesleylancaster@abdn.ac.ukInstitute of Biological and Environmental Sciences, Zoology Building, University of Aberdeen, Aberdeen AB24 2TZ, UK; e-mails: t.price.12@aberdeen.ac.uk, r05al15@abdn.ac.uk, lesleylancaster@abdn.ac.ukInstitute of Biological and Environmental Sciences, Zoology Building, University of Aberdeen, Aberdeen AB24 2TZ, UK; e-mails: t.price.12@aberdeen.ac.uk, r05al15@abdn.ac.uk, lesleylancaster@abdn.ac.ukHerbivorous insects are often highly specialised, likely due to trade-offs in fitness on alternative host species. However, some pest insects are extremely adaptable and readily adopt novel hosts, sometimes causing rapid expansion of their host range as they spread from their original host and geographic origin. The genetic basis of this phenomenon is poorly understood, limiting our ability to predict or mitigate global insect pest outbreaks. We investigated the trajectory of early adaptation to novel hosts in a regionally-specialised global crop pest species (the cowpea seed beetle Callosobruchus maculatus). After experimentally-enforced dietary specialisation for nearly 300 generations, we measured changes in fitness over the first 5 generations of adaptation to 6 novel hosts. Of these, C. maculatus reproduced successfully on all but one, with reduced fitness observed on three hosts in the first generation. Loss of fitness was followed by very rapid, decelerating increases in fitness over the first 1-5 generations, resulting in comparable levels of population fitness to that observed on the original host after 5 generations. Heritability of fitness on novel hosts was high. Adaptation occurred primarily via changes in behavioural and phenological traits, and never via changes in offspring survival to adulthood, despite high heritability for this trait. These results suggest that C. maculatus possesses ample additive genetic variation for very rapid host shifts, despite a prolonged period of enforced specialization, and also suggest that some previously-inferred environmental maternal effects on host use may in part actually represent (rapidly) evolved changes. We highlight the need to examine in more detail the genetic architecture facilitating retention of high additive genetic variation for host shifts in extremely adaptable global crop pests.https://www.eje.cz/artkey/eje-201701-0031_Warp-speed_adaptation_to_novel_hosts_after_300_generations_of_enforced_dietary_specialisation_in_the_seed_beetl.phpcoleopterachrysomelidaebruchinaecallosobruchus maculatusemerging crop pestshost shiftsgenetic variationadaptation trajectoryevolvabilityexperimental evolutionquasi-natural selectionheritability
spellingShingle Thomas N. PRICE
Aoife LEONARD
Lesley T. LANCASTER
Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
European Journal of Entomology
coleoptera
chrysomelidae
bruchinae
callosobruchus maculatus
emerging crop pests
host shifts
genetic variation
adaptation trajectory
evolvability
experimental evolution
quasi-natural selection
heritability
title Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
title_full Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
title_fullStr Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
title_full_unstemmed Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
title_short Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
title_sort warp speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle callosobruchus maculatus coleoptera chrysomelidae bruchinae
topic coleoptera
chrysomelidae
bruchinae
callosobruchus maculatus
emerging crop pests
host shifts
genetic variation
adaptation trajectory
evolvability
experimental evolution
quasi-natural selection
heritability
url https://www.eje.cz/artkey/eje-201701-0031_Warp-speed_adaptation_to_novel_hosts_after_300_generations_of_enforced_dietary_specialisation_in_the_seed_beetl.php
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AT aoifeleonard warpspeedadaptationtonovelhostsafter300generationsofenforceddietaryspecialisationintheseedbeetlecallosobruchusmaculatuscoleopterachrysomelidaebruchinae
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