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Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria
The rhizosphere microbiome (rhizobiome) plays a critical role in plant health and development. However, the processes by which the constituent microbes interact to form and maintain a community are not well understood. To investigate these molecular processes, we examined pairwise interactions betwe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387576/ https://www.ncbi.nlm.nih.gov/pubmed/32793173 http://dx.doi.org/10.3389/fmicb.2020.01742 |
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author | Eng, Thomas Herbert, Robin A. Martinez, Uriel Wang, Brenda Chen, Joseph C. Brown, James B. Deutschbauer, Adam M. Bissell, Mina J. Mortimer, Jenny C. Mukhopadhyay, Aindrila |
author_facet | Eng, Thomas Herbert, Robin A. Martinez, Uriel Wang, Brenda Chen, Joseph C. Brown, James B. Deutschbauer, Adam M. Bissell, Mina J. Mortimer, Jenny C. Mukhopadhyay, Aindrila |
author_sort | Eng, Thomas |
collection | PubMed |
description | The rhizosphere microbiome (rhizobiome) plays a critical role in plant health and development. However, the processes by which the constituent microbes interact to form and maintain a community are not well understood. To investigate these molecular processes, we examined pairwise interactions between 11 different microbial isolates under select nutrient-rich and nutrient-limited conditions. We observed that when grown with media supplemented with 56 mM glucose, two microbial isolates were able to inhibit the growth of six other microbes. The interaction between microbes persisted even after the antagonistic microbe was removed, upon exposure to spent media. To probe the genetic basis for these antagonistic interactions, we used a barcoded transposon library in a proxy bacterium, Pseudomonas putida, to identify genes which showed enhanced sensitivity to the antagonistic factor(s) secreted by Acinetobacter sp. 02. Iron metabolism-related gene clusters in P. putida were implicated by this systems-level analysis. The supplementation of iron prevented the antagonistic interaction in the original microbial pair, supporting the hypothesis that iron limitation drives antagonistic microbial interactions between rhizobionts. We conclude that rhizobiome community composition is influenced by competition for limiting nutrients, with implications for growth and development of the plant. |
format | Online Article Text |
id | pubmed-7387576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73875762020-08-12 Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria Eng, Thomas Herbert, Robin A. Martinez, Uriel Wang, Brenda Chen, Joseph C. Brown, James B. Deutschbauer, Adam M. Bissell, Mina J. Mortimer, Jenny C. Mukhopadhyay, Aindrila Front Microbiol Microbiology The rhizosphere microbiome (rhizobiome) plays a critical role in plant health and development. However, the processes by which the constituent microbes interact to form and maintain a community are not well understood. To investigate these molecular processes, we examined pairwise interactions between 11 different microbial isolates under select nutrient-rich and nutrient-limited conditions. We observed that when grown with media supplemented with 56 mM glucose, two microbial isolates were able to inhibit the growth of six other microbes. The interaction between microbes persisted even after the antagonistic microbe was removed, upon exposure to spent media. To probe the genetic basis for these antagonistic interactions, we used a barcoded transposon library in a proxy bacterium, Pseudomonas putida, to identify genes which showed enhanced sensitivity to the antagonistic factor(s) secreted by Acinetobacter sp. 02. Iron metabolism-related gene clusters in P. putida were implicated by this systems-level analysis. The supplementation of iron prevented the antagonistic interaction in the original microbial pair, supporting the hypothesis that iron limitation drives antagonistic microbial interactions between rhizobionts. We conclude that rhizobiome community composition is influenced by competition for limiting nutrients, with implications for growth and development of the plant. Frontiers Media S.A. 2020-07-22 /pmc/articles/PMC7387576/ /pubmed/32793173 http://dx.doi.org/10.3389/fmicb.2020.01742 Text en Copyright © 2020 Eng, Herbert, Martinez, Wang, Chen, Brown, Deutschbauer, Bissell, Mortimer and Mukhopadhyay. 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) and the copyright owner(s) 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 | Microbiology Eng, Thomas Herbert, Robin A. Martinez, Uriel Wang, Brenda Chen, Joseph C. Brown, James B. Deutschbauer, Adam M. Bissell, Mina J. Mortimer, Jenny C. Mukhopadhyay, Aindrila Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria |
title | Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria |
title_full | Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria |
title_fullStr | Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria |
title_full_unstemmed | Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria |
title_short | Iron Supplementation Eliminates Antagonistic Interactions Between Root-Associated Bacteria |
title_sort | iron supplementation eliminates antagonistic interactions between root-associated bacteria |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387576/ https://www.ncbi.nlm.nih.gov/pubmed/32793173 http://dx.doi.org/10.3389/fmicb.2020.01742 |
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