Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia

ABSTRACT Interactions between plant pathogens and root-associated microbes play an important role in determining disease outcomes. While several studies have suggested that steering these interactions may improve plant health, such approaches have remained challenging in practice. Because of low iro...

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Autores principales: Shaohua Gu, Tianjie Yang, Zhengying Shao, Tao Wang, Kehao Cao, Alexandre Jousset, Ville-Petri Friman, Cyrus Mallon, Xinlan Mei, Zhong Wei, Yangchun Xu, Qirong Shen, Thomas Pommier
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:9b3b42cabb78478ab165f4b890077d6d2021-12-02T19:47:39ZSiderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia10.1128/mSystems.00811-192379-5077https://doaj.org/article/9b3b42cabb78478ab165f4b890077d6d2020-06-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSystems.00811-19https://doaj.org/toc/2379-5077ABSTRACT Interactions between plant pathogens and root-associated microbes play an important role in determining disease outcomes. While several studies have suggested that steering these interactions may improve plant health, such approaches have remained challenging in practice. Because of low iron availability in most soils, competition for iron via secreted siderophore molecules might influence microbial interaction outcomes. Here, we tested if bacterial interactions mediated by iron-scavenging siderophores can be used to predict the disease suppressiveness of microbial consortia against soilborne Ralstonia solanacearum, a bacterial pathogen in the tomato rhizosphere. Iron availability significantly affected the interactions within inoculated consortia and between the consortia and the pathogen. We observed contrasting effects of siderophores and other nonsiderophore metabolites on the pathogen growth, while the siderophore effects were relatively much stronger. Specifically, disease incidence was reduced in vivo when the inoculated consortia produced siderophores that the pathogen could not use for its own growth. Employing siderophore-mediated interactions to engineer functionally robust microbial inoculants shows promise in protecting plants from soilborne pathogens. IMPORTANCE Soil-borne pathogens cause high losses in crop yields globally. The development of environmentally friendly approaches is urgently needed, but is often constrained by complex interactions between root-associated microbes and pathogens. Here, we demonstrate that the interactions within microbial consortia mediated by iron-scavenging siderophores play an important role in reducing pathogen infection and enhancing plant health. This study provides a promising and novel research direction for dealing with a wide range of microbial infections through iron exploitation, which is important for the colonization and infection of both plant and human hosts by pathogens.Shaohua GuTianjie YangZhengying ShaoTao WangKehao CaoAlexandre JoussetVille-Petri FrimanCyrus MallonXinlan MeiZhong WeiYangchun XuQirong ShenThomas PommierAmerican Society for MicrobiologyarticleSiderophoremicrobial interactionsplant healthplant pathogenssoil microbiologyMicrobiologyQR1-502ENmSystems, Vol 5, Iss 3 (2020)
institution DOAJ
collection DOAJ
language EN
topic Siderophore
microbial interactions
plant health
plant pathogens
soil microbiology
Microbiology
QR1-502
spellingShingle Siderophore
microbial interactions
plant health
plant pathogens
soil microbiology
Microbiology
QR1-502
Shaohua Gu
Tianjie Yang
Zhengying Shao
Tao Wang
Kehao Cao
Alexandre Jousset
Ville-Petri Friman
Cyrus Mallon
Xinlan Mei
Zhong Wei
Yangchun Xu
Qirong Shen
Thomas Pommier
Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia
description ABSTRACT Interactions between plant pathogens and root-associated microbes play an important role in determining disease outcomes. While several studies have suggested that steering these interactions may improve plant health, such approaches have remained challenging in practice. Because of low iron availability in most soils, competition for iron via secreted siderophore molecules might influence microbial interaction outcomes. Here, we tested if bacterial interactions mediated by iron-scavenging siderophores can be used to predict the disease suppressiveness of microbial consortia against soilborne Ralstonia solanacearum, a bacterial pathogen in the tomato rhizosphere. Iron availability significantly affected the interactions within inoculated consortia and between the consortia and the pathogen. We observed contrasting effects of siderophores and other nonsiderophore metabolites on the pathogen growth, while the siderophore effects were relatively much stronger. Specifically, disease incidence was reduced in vivo when the inoculated consortia produced siderophores that the pathogen could not use for its own growth. Employing siderophore-mediated interactions to engineer functionally robust microbial inoculants shows promise in protecting plants from soilborne pathogens. IMPORTANCE Soil-borne pathogens cause high losses in crop yields globally. The development of environmentally friendly approaches is urgently needed, but is often constrained by complex interactions between root-associated microbes and pathogens. Here, we demonstrate that the interactions within microbial consortia mediated by iron-scavenging siderophores play an important role in reducing pathogen infection and enhancing plant health. This study provides a promising and novel research direction for dealing with a wide range of microbial infections through iron exploitation, which is important for the colonization and infection of both plant and human hosts by pathogens.
format article
author Shaohua Gu
Tianjie Yang
Zhengying Shao
Tao Wang
Kehao Cao
Alexandre Jousset
Ville-Petri Friman
Cyrus Mallon
Xinlan Mei
Zhong Wei
Yangchun Xu
Qirong Shen
Thomas Pommier
author_facet Shaohua Gu
Tianjie Yang
Zhengying Shao
Tao Wang
Kehao Cao
Alexandre Jousset
Ville-Petri Friman
Cyrus Mallon
Xinlan Mei
Zhong Wei
Yangchun Xu
Qirong Shen
Thomas Pommier
author_sort Shaohua Gu
title Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia
title_short Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia
title_full Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia
title_fullStr Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia
title_full_unstemmed Siderophore-Mediated Interactions Determine the Disease Suppressiveness of Microbial Consortia
title_sort siderophore-mediated interactions determine the disease suppressiveness of microbial consortia
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/9b3b42cabb78478ab165f4b890077d6d
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