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A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization
Soil-inhabiting fungal pathogens use chemical signals released by roots to direct hyphal growth towards the host plant. Whether other soil microorganisms exploit this capacity for their own benefit is currently unknown. Here we show that the endophytic rhizobacterium Rahnella aquatilis locates hypha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567819/ https://www.ncbi.nlm.nih.gov/pubmed/33067433 http://dx.doi.org/10.1038/s41467-020-18994-5 |
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author | Palmieri, Davide Vitale, Stefania Lima, Giuseppe Di Pietro, Antonio Turrà, David |
author_facet | Palmieri, Davide Vitale, Stefania Lima, Giuseppe Di Pietro, Antonio Turrà, David |
author_sort | Palmieri, Davide |
collection | PubMed |
description | Soil-inhabiting fungal pathogens use chemical signals released by roots to direct hyphal growth towards the host plant. Whether other soil microorganisms exploit this capacity for their own benefit is currently unknown. Here we show that the endophytic rhizobacterium Rahnella aquatilis locates hyphae of the root-infecting fungal pathogen Fusarium oxysporum through pH-mediated chemotaxis and uses them as highways to efficiently access and colonize plant roots. Secretion of gluconic acid (GlcA) by R. aquatilis in the rhizosphere leads to acidification and counteracts F. oxysporum-induced alkalinisation, a known virulence mechanism, thereby preventing fungal infection. Genetic abrogation or biochemical inhibition of GlcA-mediated acidification abolished biocontrol activity of R. aquatilis and restored fungal infection. These findings reveal a new way by which bacterial endophytes hijack hyphae of a fungal pathogen in the soil to gain preferential access to plant roots, thereby protecting the host from infection. |
format | Online Article Text |
id | pubmed-7567819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75678192020-10-19 A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization Palmieri, Davide Vitale, Stefania Lima, Giuseppe Di Pietro, Antonio Turrà, David Nat Commun Article Soil-inhabiting fungal pathogens use chemical signals released by roots to direct hyphal growth towards the host plant. Whether other soil microorganisms exploit this capacity for their own benefit is currently unknown. Here we show that the endophytic rhizobacterium Rahnella aquatilis locates hyphae of the root-infecting fungal pathogen Fusarium oxysporum through pH-mediated chemotaxis and uses them as highways to efficiently access and colonize plant roots. Secretion of gluconic acid (GlcA) by R. aquatilis in the rhizosphere leads to acidification and counteracts F. oxysporum-induced alkalinisation, a known virulence mechanism, thereby preventing fungal infection. Genetic abrogation or biochemical inhibition of GlcA-mediated acidification abolished biocontrol activity of R. aquatilis and restored fungal infection. These findings reveal a new way by which bacterial endophytes hijack hyphae of a fungal pathogen in the soil to gain preferential access to plant roots, thereby protecting the host from infection. Nature Publishing Group UK 2020-10-16 /pmc/articles/PMC7567819/ /pubmed/33067433 http://dx.doi.org/10.1038/s41467-020-18994-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Palmieri, Davide Vitale, Stefania Lima, Giuseppe Di Pietro, Antonio Turrà, David A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
title | A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
title_full | A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
title_fullStr | A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
title_full_unstemmed | A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
title_short | A bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
title_sort | bacterial endophyte exploits chemotropism of a fungal pathogen for plant colonization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567819/ https://www.ncbi.nlm.nih.gov/pubmed/33067433 http://dx.doi.org/10.1038/s41467-020-18994-5 |
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