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Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species

In the carnivorous plant genus Genlisea a unique lobster pot trapping mechanism supplements nutrition in nutrient-poor habitats. A wide spectrum of microbes frequently occurs in Genlisea's leaf-derived traps without clear relevance for Genlisea carnivory. We sequenced the metatranscriptomes of...

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Autores principales: Cao, Hieu X., Schmutzer, Thomas, Scholz, Uwe, Pecinka, Ales, Schubert, Ingo, Vu, Giang T. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500957/
https://www.ncbi.nlm.nih.gov/pubmed/26236284
http://dx.doi.org/10.3389/fmicb.2015.00526
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author Cao, Hieu X.
Schmutzer, Thomas
Scholz, Uwe
Pecinka, Ales
Schubert, Ingo
Vu, Giang T. H.
author_facet Cao, Hieu X.
Schmutzer, Thomas
Scholz, Uwe
Pecinka, Ales
Schubert, Ingo
Vu, Giang T. H.
author_sort Cao, Hieu X.
collection PubMed
description In the carnivorous plant genus Genlisea a unique lobster pot trapping mechanism supplements nutrition in nutrient-poor habitats. A wide spectrum of microbes frequently occurs in Genlisea's leaf-derived traps without clear relevance for Genlisea carnivory. We sequenced the metatranscriptomes of subterrestrial traps vs. the aerial chlorophyll-containing leaves of G. nigrocaulis and of G. hispidula. Ribosomal RNA assignment revealed soil-borne microbial diversity in Genlisea traps, with 92 genera of 19 phyla present in more than one sample. Microbes from 16 of these phyla including proteobacteria, green algae, amoebozoa, fungi, ciliates and metazoans, contributed additionally short-lived mRNA to the metatranscriptome. Furthermore, transcripts of 438 members of hydrolases (e.g., proteases, phosphatases, lipases), mainly resembling those of metazoans, ciliates and green algae, were found. Compared to aerial leaves, Genlisea traps displayed a transcriptional up-regulation of endogenous NADH oxidases generating reactive oxygen species as well as of acid phosphatases for prey digestion. A leaf-vs.-trap transcriptome comparison reflects that carnivory provides inorganic P- and different forms of N-compounds (ammonium, nitrate, amino acid, oligopeptides) and implies the need to protect trap cells against oxidative stress. The analysis elucidates a complex food web inside the Genlisea traps, and suggests ecological relationships between this plant genus and its entrapped microbiome.
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spelling pubmed-45009572015-07-31 Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species Cao, Hieu X. Schmutzer, Thomas Scholz, Uwe Pecinka, Ales Schubert, Ingo Vu, Giang T. H. Front Microbiol Plant Science In the carnivorous plant genus Genlisea a unique lobster pot trapping mechanism supplements nutrition in nutrient-poor habitats. A wide spectrum of microbes frequently occurs in Genlisea's leaf-derived traps without clear relevance for Genlisea carnivory. We sequenced the metatranscriptomes of subterrestrial traps vs. the aerial chlorophyll-containing leaves of G. nigrocaulis and of G. hispidula. Ribosomal RNA assignment revealed soil-borne microbial diversity in Genlisea traps, with 92 genera of 19 phyla present in more than one sample. Microbes from 16 of these phyla including proteobacteria, green algae, amoebozoa, fungi, ciliates and metazoans, contributed additionally short-lived mRNA to the metatranscriptome. Furthermore, transcripts of 438 members of hydrolases (e.g., proteases, phosphatases, lipases), mainly resembling those of metazoans, ciliates and green algae, were found. Compared to aerial leaves, Genlisea traps displayed a transcriptional up-regulation of endogenous NADH oxidases generating reactive oxygen species as well as of acid phosphatases for prey digestion. A leaf-vs.-trap transcriptome comparison reflects that carnivory provides inorganic P- and different forms of N-compounds (ammonium, nitrate, amino acid, oligopeptides) and implies the need to protect trap cells against oxidative stress. The analysis elucidates a complex food web inside the Genlisea traps, and suggests ecological relationships between this plant genus and its entrapped microbiome. Frontiers Media S.A. 2015-07-14 /pmc/articles/PMC4500957/ /pubmed/26236284 http://dx.doi.org/10.3389/fmicb.2015.00526 Text en Copyright © 2015 Cao, Schmutzer, Scholz, Pecinka, Schubert and Vu. 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 Plant Science
Cao, Hieu X.
Schmutzer, Thomas
Scholz, Uwe
Pecinka, Ales
Schubert, Ingo
Vu, Giang T. H.
Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species
title Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species
title_full Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species
title_fullStr Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species
title_full_unstemmed Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species
title_short Metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous Genlisea species
title_sort metatranscriptome analysis reveals host-microbiome interactions in traps of carnivorous genlisea species
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500957/
https://www.ncbi.nlm.nih.gov/pubmed/26236284
http://dx.doi.org/10.3389/fmicb.2015.00526
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