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Gustatory polymorphism mediates a new adaptive courtship strategy
Human-imposed selection can lead to adaptive changes in sensory traits. However, rapid evolution of the sensory system can interfere with other behaviours, and animals must overcome such sensory conflicts. In response to intense selection by insecticide baits that contain glucose, German cockroaches...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050916/ https://www.ncbi.nlm.nih.gov/pubmed/36987637 http://dx.doi.org/10.1098/rspb.2022.2337 |
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author | Wada-Katsumata, Ayako Hatano, Eduardo Schal, Coby |
author_facet | Wada-Katsumata, Ayako Hatano, Eduardo Schal, Coby |
author_sort | Wada-Katsumata, Ayako |
collection | PubMed |
description | Human-imposed selection can lead to adaptive changes in sensory traits. However, rapid evolution of the sensory system can interfere with other behaviours, and animals must overcome such sensory conflicts. In response to intense selection by insecticide baits that contain glucose, German cockroaches evolved glucose-aversion (GA), which confers behavioural resistance against baits. During courtship the male offers the female a nuptial gift that contains maltose, which expediates copulation. However, the female's saliva rapidly hydrolyses maltose into glucose, which causes GA females to dismount the courting male, thus reducing their mating success. Comparative analysis revealed two adaptive traits in GA males. They produce more maltotriose, which is more resilient to salivary glucosidases, and they initiate copulation faster than wild-type males, before GA females interrupt their nuptial feeding and dismount the male. Recombinant lines of the two strains showed that the two emergent traits of GA males were not genetically associated with the GA trait. Results suggest that the two courtship traits emerged in response to the altered sexual behaviour of GA females and independently of the male's GA trait. Although rapid adaptive evolution generates sexual mismatches that lower fitness, compensatory behavioural evolution can correct these sensory discrepancies. |
format | Online Article Text |
id | pubmed-10050916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100509162023-03-30 Gustatory polymorphism mediates a new adaptive courtship strategy Wada-Katsumata, Ayako Hatano, Eduardo Schal, Coby Proc Biol Sci Behaviour Human-imposed selection can lead to adaptive changes in sensory traits. However, rapid evolution of the sensory system can interfere with other behaviours, and animals must overcome such sensory conflicts. In response to intense selection by insecticide baits that contain glucose, German cockroaches evolved glucose-aversion (GA), which confers behavioural resistance against baits. During courtship the male offers the female a nuptial gift that contains maltose, which expediates copulation. However, the female's saliva rapidly hydrolyses maltose into glucose, which causes GA females to dismount the courting male, thus reducing their mating success. Comparative analysis revealed two adaptive traits in GA males. They produce more maltotriose, which is more resilient to salivary glucosidases, and they initiate copulation faster than wild-type males, before GA females interrupt their nuptial feeding and dismount the male. Recombinant lines of the two strains showed that the two emergent traits of GA males were not genetically associated with the GA trait. Results suggest that the two courtship traits emerged in response to the altered sexual behaviour of GA females and independently of the male's GA trait. Although rapid adaptive evolution generates sexual mismatches that lower fitness, compensatory behavioural evolution can correct these sensory discrepancies. The Royal Society 2023-03-29 2023-03-29 /pmc/articles/PMC10050916/ /pubmed/36987637 http://dx.doi.org/10.1098/rspb.2022.2337 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Behaviour Wada-Katsumata, Ayako Hatano, Eduardo Schal, Coby Gustatory polymorphism mediates a new adaptive courtship strategy |
title | Gustatory polymorphism mediates a new adaptive courtship strategy |
title_full | Gustatory polymorphism mediates a new adaptive courtship strategy |
title_fullStr | Gustatory polymorphism mediates a new adaptive courtship strategy |
title_full_unstemmed | Gustatory polymorphism mediates a new adaptive courtship strategy |
title_short | Gustatory polymorphism mediates a new adaptive courtship strategy |
title_sort | gustatory polymorphism mediates a new adaptive courtship strategy |
topic | Behaviour |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050916/ https://www.ncbi.nlm.nih.gov/pubmed/36987637 http://dx.doi.org/10.1098/rspb.2022.2337 |
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