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Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle

BACKGROUND: Obligate bacterial symbionts alter the diets of host animals in numerous ways, but the ecological roles of facultative bacterial residents that colonize insect guts remain unclear. Carabid beetles are a common group of beneficial insects appreciated for their ability to consume insect pr...

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Autores principales: Lundgren, Jonathan G., Lehman, R. Michael
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877093/
https://www.ncbi.nlm.nih.gov/pubmed/20520762
http://dx.doi.org/10.1371/journal.pone.0010831
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author Lundgren, Jonathan G.
Lehman, R. Michael
author_facet Lundgren, Jonathan G.
Lehman, R. Michael
author_sort Lundgren, Jonathan G.
collection PubMed
description BACKGROUND: Obligate bacterial symbionts alter the diets of host animals in numerous ways, but the ecological roles of facultative bacterial residents that colonize insect guts remain unclear. Carabid beetles are a common group of beneficial insects appreciated for their ability to consume insect prey and seeds, but the contributions of microbes to diet diversification in this and similar groups of facultative granivores are largely unknown. METHODOLOGY AND PRINCIPAL FINDINGS: Using 16S rRNA gene clone libraries and terminal restriction fragment (tRF) length polymorphism analyses of these genes, we examined the bacterial communities within the guts of facultatively granivorous, adult Harpalus pensylvanicus (Carabidae), fed one of five dietary treatments: 1) an untreated Field population, 2) Seeds with antibiotics (seeds were from Chenopodium album), 3) Seeds without antibiotics, 4) Prey with antibiotics (prey were Acheta domesticus eggs), and 5) Prey without antibiotics. The number of seeds and prey consumed by each beetle were recorded following treatment. Harpalus pensylvanicus possessed a fairly simple gut community of approximately 3-4 bacterial operational taxonomic units (OTU) per beetle that were affiliated with the Gammaproteobacteria, Bacilli, Alphaproteobacteria, and Mollicutes. Bacterial communities of the host varied among the diet and antibiotic treatments. The field population and beetles fed seeds without antibiotics had the closest matching bacterial communities, and the communities in the beetles fed antibiotics were more closely related to each other than to those of the beetles that did not receive antibiotics. Antibiotics reduced and altered the bacterial communities found in the beetle guts. Moreover, beetles fed antibiotics ate fewer seeds, and those beetles that harbored the bacterium Enterococcus faecalis consumed more seeds on average than those lacking this symbiont. CONCLUSIONS/SIGNIFICANCE: We conclude that the relationships between the bacterium E. faecalis and this factultative granivore's ability to consume seeds merit further investigation, and that facultative associations with symbiotic bacteria have important implications for the nutritional ecology of their hosts.
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spelling pubmed-28770932010-06-02 Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle Lundgren, Jonathan G. Lehman, R. Michael PLoS One Research Article BACKGROUND: Obligate bacterial symbionts alter the diets of host animals in numerous ways, but the ecological roles of facultative bacterial residents that colonize insect guts remain unclear. Carabid beetles are a common group of beneficial insects appreciated for their ability to consume insect prey and seeds, but the contributions of microbes to diet diversification in this and similar groups of facultative granivores are largely unknown. METHODOLOGY AND PRINCIPAL FINDINGS: Using 16S rRNA gene clone libraries and terminal restriction fragment (tRF) length polymorphism analyses of these genes, we examined the bacterial communities within the guts of facultatively granivorous, adult Harpalus pensylvanicus (Carabidae), fed one of five dietary treatments: 1) an untreated Field population, 2) Seeds with antibiotics (seeds were from Chenopodium album), 3) Seeds without antibiotics, 4) Prey with antibiotics (prey were Acheta domesticus eggs), and 5) Prey without antibiotics. The number of seeds and prey consumed by each beetle were recorded following treatment. Harpalus pensylvanicus possessed a fairly simple gut community of approximately 3-4 bacterial operational taxonomic units (OTU) per beetle that were affiliated with the Gammaproteobacteria, Bacilli, Alphaproteobacteria, and Mollicutes. Bacterial communities of the host varied among the diet and antibiotic treatments. The field population and beetles fed seeds without antibiotics had the closest matching bacterial communities, and the communities in the beetles fed antibiotics were more closely related to each other than to those of the beetles that did not receive antibiotics. Antibiotics reduced and altered the bacterial communities found in the beetle guts. Moreover, beetles fed antibiotics ate fewer seeds, and those beetles that harbored the bacterium Enterococcus faecalis consumed more seeds on average than those lacking this symbiont. CONCLUSIONS/SIGNIFICANCE: We conclude that the relationships between the bacterium E. faecalis and this factultative granivore's ability to consume seeds merit further investigation, and that facultative associations with symbiotic bacteria have important implications for the nutritional ecology of their hosts. Public Library of Science 2010-05-26 /pmc/articles/PMC2877093/ /pubmed/20520762 http://dx.doi.org/10.1371/journal.pone.0010831 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Lundgren, Jonathan G.
Lehman, R. Michael
Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle
title Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle
title_full Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle
title_fullStr Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle
title_full_unstemmed Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle
title_short Bacterial Gut Symbionts Contribute to Seed Digestion in an Omnivorous Beetle
title_sort bacterial gut symbionts contribute to seed digestion in an omnivorous beetle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877093/
https://www.ncbi.nlm.nih.gov/pubmed/20520762
http://dx.doi.org/10.1371/journal.pone.0010831
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