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Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet

Herbivores possess many counteradaptations to plant defenses, and a growing body of research describes the role of symbiotic gut bacteria in mediating herbivorous diets among insects. However, persistent bacterial symbioses have not been found in Lepidoptera, despite the fact that perhaps 99% of the...

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Autores principales: Whitaker, Melissa R. L., Salzman, Shayla, Sanders, Jon, Kaltenpoth, Martin, Pierce, Naomi E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129467/
https://www.ncbi.nlm.nih.gov/pubmed/27965647
http://dx.doi.org/10.3389/fmicb.2016.01920
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author Whitaker, Melissa R. L.
Salzman, Shayla
Sanders, Jon
Kaltenpoth, Martin
Pierce, Naomi E.
author_facet Whitaker, Melissa R. L.
Salzman, Shayla
Sanders, Jon
Kaltenpoth, Martin
Pierce, Naomi E.
author_sort Whitaker, Melissa R. L.
collection PubMed
description Herbivores possess many counteradaptations to plant defenses, and a growing body of research describes the role of symbiotic gut bacteria in mediating herbivorous diets among insects. However, persistent bacterial symbioses have not been found in Lepidoptera, despite the fact that perhaps 99% of the species in this order are herbivorous. We surveyed bacterial communities in the guts of larvae from 31 species of lycaenid butterflies whose caterpillars had diets ranging from obligate carnivory to strict herbivory. Contrary to our expectations, we found that the bacterial communities of carnivorous and herbivorous caterpillars do not differ in richness, diversity, or composition. Many of the observed bacterial genera are commonly found in soil and plant surfaces, and we detected known homopteran endosymbionts in the guts of homopterophagous species, suggesting that larvae acquire gut bacteria from their food and environment. These results indicate that lycaenid butterflies do not rely on specific bacterial symbioses to mediate their diverse diets, and provide further evidence of taxonomically depauperate bacterial communities among Lepidoptera.
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spelling pubmed-51294672016-12-13 Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet Whitaker, Melissa R. L. Salzman, Shayla Sanders, Jon Kaltenpoth, Martin Pierce, Naomi E. Front Microbiol Microbiology Herbivores possess many counteradaptations to plant defenses, and a growing body of research describes the role of symbiotic gut bacteria in mediating herbivorous diets among insects. However, persistent bacterial symbioses have not been found in Lepidoptera, despite the fact that perhaps 99% of the species in this order are herbivorous. We surveyed bacterial communities in the guts of larvae from 31 species of lycaenid butterflies whose caterpillars had diets ranging from obligate carnivory to strict herbivory. Contrary to our expectations, we found that the bacterial communities of carnivorous and herbivorous caterpillars do not differ in richness, diversity, or composition. Many of the observed bacterial genera are commonly found in soil and plant surfaces, and we detected known homopteran endosymbionts in the guts of homopterophagous species, suggesting that larvae acquire gut bacteria from their food and environment. These results indicate that lycaenid butterflies do not rely on specific bacterial symbioses to mediate their diverse diets, and provide further evidence of taxonomically depauperate bacterial communities among Lepidoptera. Frontiers Media S.A. 2016-11-30 /pmc/articles/PMC5129467/ /pubmed/27965647 http://dx.doi.org/10.3389/fmicb.2016.01920 Text en Copyright © 2016 Whitaker, Salzman, Sanders, Kaltenpoth and Pierce. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Whitaker, Melissa R. L.
Salzman, Shayla
Sanders, Jon
Kaltenpoth, Martin
Pierce, Naomi E.
Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet
title Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet
title_full Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet
title_fullStr Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet
title_full_unstemmed Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet
title_short Microbial Communities of Lycaenid Butterflies Do Not Correlate with Larval Diet
title_sort microbial communities of lycaenid butterflies do not correlate with larval diet
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129467/
https://www.ncbi.nlm.nih.gov/pubmed/27965647
http://dx.doi.org/10.3389/fmicb.2016.01920
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