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An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne

We have identified from the mutualistic grass endophyte Epichloë festucae a non-ribosomal peptide synthetase gene (sidN) encoding a siderophore synthetase. The enzymatic product of SidN is shown to be a novel extracellular siderophore designated as epichloënin A, related to ferrirubin from the ferri...

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Autores principales: Johnson, Linda J., Koulman, Albert, Christensen, Michael, Lane, Geoffrey A., Fraser, Karl, Forester, Natasha, Johnson, Richard D., Bryan, Gregory T., Rasmussen, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642064/
https://www.ncbi.nlm.nih.gov/pubmed/23658520
http://dx.doi.org/10.1371/journal.ppat.1003332
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author Johnson, Linda J.
Koulman, Albert
Christensen, Michael
Lane, Geoffrey A.
Fraser, Karl
Forester, Natasha
Johnson, Richard D.
Bryan, Gregory T.
Rasmussen, Susanne
author_facet Johnson, Linda J.
Koulman, Albert
Christensen, Michael
Lane, Geoffrey A.
Fraser, Karl
Forester, Natasha
Johnson, Richard D.
Bryan, Gregory T.
Rasmussen, Susanne
author_sort Johnson, Linda J.
collection PubMed
description We have identified from the mutualistic grass endophyte Epichloë festucae a non-ribosomal peptide synthetase gene (sidN) encoding a siderophore synthetase. The enzymatic product of SidN is shown to be a novel extracellular siderophore designated as epichloënin A, related to ferrirubin from the ferrichrome family. Targeted gene disruption of sidN eliminated biosynthesis of epichloënin A in vitro and in planta. During iron-depleted axenic growth, ΔsidN mutants accumulated the pathway intermediate N(5)-trans-anhydromevalonyl-N(5)-hydroxyornithine (trans-AMHO), displayed sensitivity to oxidative stress and showed deficiencies in both polarized hyphal growth and sporulation. Infection of Lolium perenne (perennial ryegrass) with ΔsidN mutants resulted in perturbations of the endophyte-grass symbioses. Deviations from the characteristic tightly regulated synchronous growth of the fungus with its plant partner were observed and infected plants were stunted. Analysis of these plants by light and transmission electron microscopy revealed abnormalities in the distribution and localization of ΔsidN mutant hyphae as well as deformities in hyphal ultrastructure. We hypothesize that lack of epichloënin A alters iron homeostasis of the symbiotum, changing it from mutually beneficial to antagonistic. Iron itself or epichloënin A may serve as an important molecular/cellular signal for controlling fungal growth and hence the symbiotic interaction.
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spelling pubmed-36420642013-05-08 An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne Johnson, Linda J. Koulman, Albert Christensen, Michael Lane, Geoffrey A. Fraser, Karl Forester, Natasha Johnson, Richard D. Bryan, Gregory T. Rasmussen, Susanne PLoS Pathog Research Article We have identified from the mutualistic grass endophyte Epichloë festucae a non-ribosomal peptide synthetase gene (sidN) encoding a siderophore synthetase. The enzymatic product of SidN is shown to be a novel extracellular siderophore designated as epichloënin A, related to ferrirubin from the ferrichrome family. Targeted gene disruption of sidN eliminated biosynthesis of epichloënin A in vitro and in planta. During iron-depleted axenic growth, ΔsidN mutants accumulated the pathway intermediate N(5)-trans-anhydromevalonyl-N(5)-hydroxyornithine (trans-AMHO), displayed sensitivity to oxidative stress and showed deficiencies in both polarized hyphal growth and sporulation. Infection of Lolium perenne (perennial ryegrass) with ΔsidN mutants resulted in perturbations of the endophyte-grass symbioses. Deviations from the characteristic tightly regulated synchronous growth of the fungus with its plant partner were observed and infected plants were stunted. Analysis of these plants by light and transmission electron microscopy revealed abnormalities in the distribution and localization of ΔsidN mutant hyphae as well as deformities in hyphal ultrastructure. We hypothesize that lack of epichloënin A alters iron homeostasis of the symbiotum, changing it from mutually beneficial to antagonistic. Iron itself or epichloënin A may serve as an important molecular/cellular signal for controlling fungal growth and hence the symbiotic interaction. Public Library of Science 2013-05-02 /pmc/articles/PMC3642064/ /pubmed/23658520 http://dx.doi.org/10.1371/journal.ppat.1003332 Text en © 2013 Johnson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Johnson, Linda J.
Koulman, Albert
Christensen, Michael
Lane, Geoffrey A.
Fraser, Karl
Forester, Natasha
Johnson, Richard D.
Bryan, Gregory T.
Rasmussen, Susanne
An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne
title An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne
title_full An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne
title_fullStr An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne
title_full_unstemmed An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne
title_short An Extracellular Siderophore Is Required to Maintain the Mutualistic Interaction of Epichloë festucae with Lolium perenne
title_sort extracellular siderophore is required to maintain the mutualistic interaction of epichloë festucae with lolium perenne
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642064/
https://www.ncbi.nlm.nih.gov/pubmed/23658520
http://dx.doi.org/10.1371/journal.ppat.1003332
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