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Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes

BACKGROUND: Fungi are an attractive source of nutrients for predators. As part of their defense, some fungi are able to induce the production of anti-predator protein toxins in response to predation. A previous study on the interaction of the model mushroom Coprinopsis cinerea by the fungivorous nem...

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Autores principales: Tayyrov, Annageldi, Stanley, Claire E., Azevedo, Sophie, Künzler, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434838/
https://www.ncbi.nlm.nih.gov/pubmed/30909884
http://dx.doi.org/10.1186/s12864-019-5607-3
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author Tayyrov, Annageldi
Stanley, Claire E.
Azevedo, Sophie
Künzler, Markus
author_facet Tayyrov, Annageldi
Stanley, Claire E.
Azevedo, Sophie
Künzler, Markus
author_sort Tayyrov, Annageldi
collection PubMed
description BACKGROUND: Fungi are an attractive source of nutrients for predators. As part of their defense, some fungi are able to induce the production of anti-predator protein toxins in response to predation. A previous study on the interaction of the model mushroom Coprinopsis cinerea by the fungivorous nematode Aphelenchus avenae on agar plates has shown that the this fungal defense response is most pronounced in the part of the mycelium that is in direct contact with the nematode. Hence, we hypothesized that, for a comprehensive characterization of this defense response, an experimental setup that maximizes the zone of direct interaction between the fungal mycelium and the nematode, was needed. RESULTS: In this study, we conducted a transcriptome analysis of C. cinerea vegetative mycelium upon challenge with A. avenae using a tailor-made microfluidic device. The device was designed such that the interaction between the fungus and the nematode was confined to a specific area and that the mycelium could be retrieved from this area for analysis. We took samples from the confrontation area after different time periods and extracted and sequenced the poly(A)(+) RNA thereof. The identification of 1229 differentially expressed genes (DEGs) shows that this setup profoundly improved sensitivity over co-cultivation on agar plates where only 37 DEGs had been identified. The product of one of the most highly upregulated genes shows structural homology to bacterial pore-forming toxins, and revealed strong toxicity to various bacterivorous nematodes. In addition, bacteria associated with the fungivorous nematode A. avenae were profiled with 16S rRNA deep sequencing. Similar to the bacterivorous and plant-feeding nematodes, Proteobacteria and Bacteroidetes were the most dominant phyla in A. avenae. CONCLUSIONS: The use of a novel experimental setup for the investigation of the defense response of a fungal mycelium to predation by fungivorous nematodes resulted in the identification of a comprehensive set of DEGs and the discovery of a novel type of fungal defense protein against nematodes. The bacteria found to be associated with the fungivorous nematode are a possible explanation for the induction of some antibacterial defense proteins upon nematode challenge. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5607-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-64348382019-04-08 Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes Tayyrov, Annageldi Stanley, Claire E. Azevedo, Sophie Künzler, Markus BMC Genomics Research Article BACKGROUND: Fungi are an attractive source of nutrients for predators. As part of their defense, some fungi are able to induce the production of anti-predator protein toxins in response to predation. A previous study on the interaction of the model mushroom Coprinopsis cinerea by the fungivorous nematode Aphelenchus avenae on agar plates has shown that the this fungal defense response is most pronounced in the part of the mycelium that is in direct contact with the nematode. Hence, we hypothesized that, for a comprehensive characterization of this defense response, an experimental setup that maximizes the zone of direct interaction between the fungal mycelium and the nematode, was needed. RESULTS: In this study, we conducted a transcriptome analysis of C. cinerea vegetative mycelium upon challenge with A. avenae using a tailor-made microfluidic device. The device was designed such that the interaction between the fungus and the nematode was confined to a specific area and that the mycelium could be retrieved from this area for analysis. We took samples from the confrontation area after different time periods and extracted and sequenced the poly(A)(+) RNA thereof. The identification of 1229 differentially expressed genes (DEGs) shows that this setup profoundly improved sensitivity over co-cultivation on agar plates where only 37 DEGs had been identified. The product of one of the most highly upregulated genes shows structural homology to bacterial pore-forming toxins, and revealed strong toxicity to various bacterivorous nematodes. In addition, bacteria associated with the fungivorous nematode A. avenae were profiled with 16S rRNA deep sequencing. Similar to the bacterivorous and plant-feeding nematodes, Proteobacteria and Bacteroidetes were the most dominant phyla in A. avenae. CONCLUSIONS: The use of a novel experimental setup for the investigation of the defense response of a fungal mycelium to predation by fungivorous nematodes resulted in the identification of a comprehensive set of DEGs and the discovery of a novel type of fungal defense protein against nematodes. The bacteria found to be associated with the fungivorous nematode are a possible explanation for the induction of some antibacterial defense proteins upon nematode challenge. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5607-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-25 /pmc/articles/PMC6434838/ /pubmed/30909884 http://dx.doi.org/10.1186/s12864-019-5607-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tayyrov, Annageldi
Stanley, Claire E.
Azevedo, Sophie
Künzler, Markus
Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes
title Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes
title_full Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes
title_fullStr Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes
title_full_unstemmed Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes
title_short Combining microfluidics and RNA-sequencing to assess the inducible defensome of a mushroom against nematodes
title_sort combining microfluidics and rna-sequencing to assess the inducible defensome of a mushroom against nematodes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434838/
https://www.ncbi.nlm.nih.gov/pubmed/30909884
http://dx.doi.org/10.1186/s12864-019-5607-3
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