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Bacterial community composition of vermicompost-treated tomato rhizospheres

Vermicompost application has been shown to promote plant growth, alter the rhizosphere microbiome, and suppress plant pathogens. These beneficial properties are often attributed to the activity of vermicompost-associated microorganisms. However, little is known about the microbial shifts that occur...

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Autores principales: Munoz-Ucros, Juana, Panke-Buisse, Kevin, Robe, Jamison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7135065/
https://www.ncbi.nlm.nih.gov/pubmed/32251438
http://dx.doi.org/10.1371/journal.pone.0230577
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author Munoz-Ucros, Juana
Panke-Buisse, Kevin
Robe, Jamison
author_facet Munoz-Ucros, Juana
Panke-Buisse, Kevin
Robe, Jamison
author_sort Munoz-Ucros, Juana
collection PubMed
description Vermicompost application has been shown to promote plant growth, alter the rhizosphere microbiome, and suppress plant pathogens. These beneficial properties are often attributed to the activity of vermicompost-associated microorganisms. However, little is known about the microbial shifts that occur in the rhizosphere after vermicompost application. To better understand the impact of vermicompost treatments on the assembly of rhizosphere bacterial communities, 16S rDNA communities of vermicompost and rhizospheres of each peat- and soil-grown tomatoes were profiled after conventional fertigation, irrigation without additional nutrients, and addition of three different vermicompost-extracts. The full dataset consisted of 412 identified genera, of which 317 remained following stringent quality filtration. Tomato rhizosphere microbiome responses to treatments were complex and unique between peat and soil growth substrates. Direct colonization of vermicompost-origin taxa into rhizospheres was limited, with genera Photobacterium and Luteimonas colonizing peat rhizospheres, genera Truepera, Phenylobacterium, and Lysinibacillus colonizing soil rhizospheres, and genus Pelagibius appearing in both soil and peat rhizospheres. Further patterns of differential abundance and presence/absence between treatments highlight vermicompost-mediated effects on rhizosphere microbiome assembly as an interplay of rhizosphere medium, direct colonization of vermicompost-origin taxa and vermicompost-induced shifts in the rhizosphere microbial community. This exploratory analysis is intended to provide an initial look at 16S community composition of vermicompost and the effects of vermicompost treatment on the rhizosphere microbiome assembly to highlight interactions of potential merit for subsequent investigations.
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spelling pubmed-71350652020-04-09 Bacterial community composition of vermicompost-treated tomato rhizospheres Munoz-Ucros, Juana Panke-Buisse, Kevin Robe, Jamison PLoS One Research Article Vermicompost application has been shown to promote plant growth, alter the rhizosphere microbiome, and suppress plant pathogens. These beneficial properties are often attributed to the activity of vermicompost-associated microorganisms. However, little is known about the microbial shifts that occur in the rhizosphere after vermicompost application. To better understand the impact of vermicompost treatments on the assembly of rhizosphere bacterial communities, 16S rDNA communities of vermicompost and rhizospheres of each peat- and soil-grown tomatoes were profiled after conventional fertigation, irrigation without additional nutrients, and addition of three different vermicompost-extracts. The full dataset consisted of 412 identified genera, of which 317 remained following stringent quality filtration. Tomato rhizosphere microbiome responses to treatments were complex and unique between peat and soil growth substrates. Direct colonization of vermicompost-origin taxa into rhizospheres was limited, with genera Photobacterium and Luteimonas colonizing peat rhizospheres, genera Truepera, Phenylobacterium, and Lysinibacillus colonizing soil rhizospheres, and genus Pelagibius appearing in both soil and peat rhizospheres. Further patterns of differential abundance and presence/absence between treatments highlight vermicompost-mediated effects on rhizosphere microbiome assembly as an interplay of rhizosphere medium, direct colonization of vermicompost-origin taxa and vermicompost-induced shifts in the rhizosphere microbial community. This exploratory analysis is intended to provide an initial look at 16S community composition of vermicompost and the effects of vermicompost treatment on the rhizosphere microbiome assembly to highlight interactions of potential merit for subsequent investigations. Public Library of Science 2020-04-06 /pmc/articles/PMC7135065/ /pubmed/32251438 http://dx.doi.org/10.1371/journal.pone.0230577 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Munoz-Ucros, Juana
Panke-Buisse, Kevin
Robe, Jamison
Bacterial community composition of vermicompost-treated tomato rhizospheres
title Bacterial community composition of vermicompost-treated tomato rhizospheres
title_full Bacterial community composition of vermicompost-treated tomato rhizospheres
title_fullStr Bacterial community composition of vermicompost-treated tomato rhizospheres
title_full_unstemmed Bacterial community composition of vermicompost-treated tomato rhizospheres
title_short Bacterial community composition of vermicompost-treated tomato rhizospheres
title_sort bacterial community composition of vermicompost-treated tomato rhizospheres
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7135065/
https://www.ncbi.nlm.nih.gov/pubmed/32251438
http://dx.doi.org/10.1371/journal.pone.0230577
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