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Detecting ingested plant DNA in soil-living insect larvae

Although a significant proportion of plant tissue is located in roots and other below-ground parts of plants, little is known on the dietary choices of root-feeding insects. This is caused by a lack of adequate methodology which would allow tracking below-ground trophic interactions between insects...

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Detalles Bibliográficos
Autores principales: Staudacher, Karin, Wallinger, Corinna, Schallhart, Nikolaus, Traugott, Michael
Formato: Texto
Lenguaje:English
Publicado: Pergamon Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021716/
https://www.ncbi.nlm.nih.gov/pubmed/21317975
http://dx.doi.org/10.1016/j.soilbio.2010.10.022
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author Staudacher, Karin
Wallinger, Corinna
Schallhart, Nikolaus
Traugott, Michael
author_facet Staudacher, Karin
Wallinger, Corinna
Schallhart, Nikolaus
Traugott, Michael
author_sort Staudacher, Karin
collection PubMed
description Although a significant proportion of plant tissue is located in roots and other below-ground parts of plants, little is known on the dietary choices of root-feeding insects. This is caused by a lack of adequate methodology which would allow tracking below-ground trophic interactions between insects and plants. Here, we present a DNA-based approach to examine this relationship. Feeding experiments were established where either wheat (Triticum aestivum) or maize (Zea mays) was fed to Agriotes larvae (Coleoptera: Elateridae), allowing them to digest for up to 72 h. Due to the very small amount of plant tissue ingested (max = 6.76 mg), DNA extraction procedures and the sensitivity of polymerase chain reaction (PCR) had to be optimized. Whole-body DNA extracts of larvae were tested for the presence of both rbcL and trnL plastid DNA using universal primers. Moreover, based on cpDNA sequences encoding chloroplast tRNA for leucine (trnL), specific primers for maize and wheat were developed. With both, general and specific primers, plant DNA was detectable in the guts of Agriotes larvae for up to 72 h post-feeding, the maximum time of digestion in these experiments. No significant effect of time since feeding on plant DNA detection success was observed, except for the specific primers in maize-fed larvae. Here, plant DNA detection was negatively correlated with the duration of digestion. Both, meal size and initial mass of the individual larvae did not affect the rate of larvae testing positive for plant DNA. The outcomes of this study represent a first step towards a specific analysis of the dietary choices of soil-living herbivores to further increase our understanding of animal–plant feeding interactions in the soil.
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spelling pubmed-30217162011-02-11 Detecting ingested plant DNA in soil-living insect larvae Staudacher, Karin Wallinger, Corinna Schallhart, Nikolaus Traugott, Michael Soil Biol Biochem Article Although a significant proportion of plant tissue is located in roots and other below-ground parts of plants, little is known on the dietary choices of root-feeding insects. This is caused by a lack of adequate methodology which would allow tracking below-ground trophic interactions between insects and plants. Here, we present a DNA-based approach to examine this relationship. Feeding experiments were established where either wheat (Triticum aestivum) or maize (Zea mays) was fed to Agriotes larvae (Coleoptera: Elateridae), allowing them to digest for up to 72 h. Due to the very small amount of plant tissue ingested (max = 6.76 mg), DNA extraction procedures and the sensitivity of polymerase chain reaction (PCR) had to be optimized. Whole-body DNA extracts of larvae were tested for the presence of both rbcL and trnL plastid DNA using universal primers. Moreover, based on cpDNA sequences encoding chloroplast tRNA for leucine (trnL), specific primers for maize and wheat were developed. With both, general and specific primers, plant DNA was detectable in the guts of Agriotes larvae for up to 72 h post-feeding, the maximum time of digestion in these experiments. No significant effect of time since feeding on plant DNA detection success was observed, except for the specific primers in maize-fed larvae. Here, plant DNA detection was negatively correlated with the duration of digestion. Both, meal size and initial mass of the individual larvae did not affect the rate of larvae testing positive for plant DNA. The outcomes of this study represent a first step towards a specific analysis of the dietary choices of soil-living herbivores to further increase our understanding of animal–plant feeding interactions in the soil. Pergamon Press 2011-02 /pmc/articles/PMC3021716/ /pubmed/21317975 http://dx.doi.org/10.1016/j.soilbio.2010.10.022 Text en © 2011 Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Staudacher, Karin
Wallinger, Corinna
Schallhart, Nikolaus
Traugott, Michael
Detecting ingested plant DNA in soil-living insect larvae
title Detecting ingested plant DNA in soil-living insect larvae
title_full Detecting ingested plant DNA in soil-living insect larvae
title_fullStr Detecting ingested plant DNA in soil-living insect larvae
title_full_unstemmed Detecting ingested plant DNA in soil-living insect larvae
title_short Detecting ingested plant DNA in soil-living insect larvae
title_sort detecting ingested plant dna in soil-living insect larvae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021716/
https://www.ncbi.nlm.nih.gov/pubmed/21317975
http://dx.doi.org/10.1016/j.soilbio.2010.10.022
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