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Dietary and developmental shifts in butterfly-associated bacterial communities

Bacterial communities associated with insects can substantially influence host ecology, evolution and behaviour. Host diet is a key factor that shapes bacterial communities, but the impact of dietary transitions across insect development is poorly understood. We analysed bacterial communities of 12...

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Detalles Bibliográficos
Autores principales: Phalnikar, Kruttika, Kunte, Krushnamegh, Agashe, Deepa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990769/
https://www.ncbi.nlm.nih.gov/pubmed/29892359
http://dx.doi.org/10.1098/rsos.171559
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author Phalnikar, Kruttika
Kunte, Krushnamegh
Agashe, Deepa
author_facet Phalnikar, Kruttika
Kunte, Krushnamegh
Agashe, Deepa
author_sort Phalnikar, Kruttika
collection PubMed
description Bacterial communities associated with insects can substantially influence host ecology, evolution and behaviour. Host diet is a key factor that shapes bacterial communities, but the impact of dietary transitions across insect development is poorly understood. We analysed bacterial communities of 12 butterfly species across different developmental stages, using amplicon sequencing of the 16S rRNA gene. Butterfly larvae typically consume leaves of a single host plant, whereas adults are more generalist nectar feeders. Thus, we expected bacterial communities to vary substantially across butterfly development. Surprisingly, only few species showed significant dietary and developmental transitions in bacterial communities, suggesting weak impacts of dietary transitions across butterfly development. On the other hand, bacterial communities were strongly influenced by butterfly species and family identity, potentially due to dietary and physiological variation across the host phylogeny. Larvae of most butterfly species largely mirrored bacterial community composition of their diets, suggesting passive acquisition rather than active selection. Overall, our results suggest that although butterflies harbour distinct microbiomes across taxonomic groups and dietary guilds, the dramatic dietary shifts that occur during development do not impose strong selection to maintain distinct bacterial communities across all butterfly hosts.
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spelling pubmed-59907692018-06-11 Dietary and developmental shifts in butterfly-associated bacterial communities Phalnikar, Kruttika Kunte, Krushnamegh Agashe, Deepa R Soc Open Sci Biology (Whole Organism) Bacterial communities associated with insects can substantially influence host ecology, evolution and behaviour. Host diet is a key factor that shapes bacterial communities, but the impact of dietary transitions across insect development is poorly understood. We analysed bacterial communities of 12 butterfly species across different developmental stages, using amplicon sequencing of the 16S rRNA gene. Butterfly larvae typically consume leaves of a single host plant, whereas adults are more generalist nectar feeders. Thus, we expected bacterial communities to vary substantially across butterfly development. Surprisingly, only few species showed significant dietary and developmental transitions in bacterial communities, suggesting weak impacts of dietary transitions across butterfly development. On the other hand, bacterial communities were strongly influenced by butterfly species and family identity, potentially due to dietary and physiological variation across the host phylogeny. Larvae of most butterfly species largely mirrored bacterial community composition of their diets, suggesting passive acquisition rather than active selection. Overall, our results suggest that although butterflies harbour distinct microbiomes across taxonomic groups and dietary guilds, the dramatic dietary shifts that occur during development do not impose strong selection to maintain distinct bacterial communities across all butterfly hosts. The Royal Society Publishing 2018-05-30 /pmc/articles/PMC5990769/ /pubmed/29892359 http://dx.doi.org/10.1098/rsos.171559 Text en © 2018 The Authors. http://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/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Phalnikar, Kruttika
Kunte, Krushnamegh
Agashe, Deepa
Dietary and developmental shifts in butterfly-associated bacterial communities
title Dietary and developmental shifts in butterfly-associated bacterial communities
title_full Dietary and developmental shifts in butterfly-associated bacterial communities
title_fullStr Dietary and developmental shifts in butterfly-associated bacterial communities
title_full_unstemmed Dietary and developmental shifts in butterfly-associated bacterial communities
title_short Dietary and developmental shifts in butterfly-associated bacterial communities
title_sort dietary and developmental shifts in butterfly-associated bacterial communities
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990769/
https://www.ncbi.nlm.nih.gov/pubmed/29892359
http://dx.doi.org/10.1098/rsos.171559
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