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An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris

BACKGROUND: Induced aboveground plant defenses against pathogens can have negative effects on belowground microbial symbionts. While a considerable number of studies have utilized chemical elicitors to experimentally induce such defenses, there is surprisingly little evidence that actual aboveground...

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Detalles Bibliográficos
Autores principales: Ballhorn, Daniel J, Younginger, Brett S, Kautz, Stefanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248430/
https://www.ncbi.nlm.nih.gov/pubmed/25429887
http://dx.doi.org/10.1186/s12870-014-0321-4
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author Ballhorn, Daniel J
Younginger, Brett S
Kautz, Stefanie
author_facet Ballhorn, Daniel J
Younginger, Brett S
Kautz, Stefanie
author_sort Ballhorn, Daniel J
collection PubMed
description BACKGROUND: Induced aboveground plant defenses against pathogens can have negative effects on belowground microbial symbionts. While a considerable number of studies have utilized chemical elicitors to experimentally induce such defenses, there is surprisingly little evidence that actual aboveground pathogens affect root-associated microbes. We report here that an aboveground fungal pathogen of common bean (Phaseolus vulgaris) induces a defense response that inhibits both the belowground formation of root nodules elicited by rhizobia and the colonization with arbuscular mycorrhizal fungi (AMF). RESULTS: Foliage of plants inoculated with either rhizobia or AMF was treated with both live Colletotrichum gloeosporioides—a generalist hemibiotrophic plant pathogen—and C. gloeosporioides fragments. Polyphenol oxidase (PPO), chitinase and β-1,3-glucanase activity in leaves and roots, as well as the number of rhizobia nodules and the extent of AMF colonization, were measured after pathogen treatments. Both the live pathogen and pathogen fragments significantly increased PPO, chitinase and β-1,3-glucanase activity in the leaves, but only PPO activity was increased in roots. The number of rhizobia nodules and the extent of AMF colonization was significantly reduced in treatment plants when compared to controls. CONCLUSION: We demonstrate that aboveground fungal pathogens can affect belowground mutualism with two very different types of microbial symbionts—rhizobia and AMF. Our results suggest that systemically induced PPO activity is functionally involved in this above-belowground interaction. We predict that the top-down effects we show here can drastically impact plant performance in soils with limited nutrients and water; abiotic stress conditions usually mitigated by microbial belowground mutualists. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0321-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-42484302014-12-02 An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris Ballhorn, Daniel J Younginger, Brett S Kautz, Stefanie BMC Plant Biol Research Article BACKGROUND: Induced aboveground plant defenses against pathogens can have negative effects on belowground microbial symbionts. While a considerable number of studies have utilized chemical elicitors to experimentally induce such defenses, there is surprisingly little evidence that actual aboveground pathogens affect root-associated microbes. We report here that an aboveground fungal pathogen of common bean (Phaseolus vulgaris) induces a defense response that inhibits both the belowground formation of root nodules elicited by rhizobia and the colonization with arbuscular mycorrhizal fungi (AMF). RESULTS: Foliage of plants inoculated with either rhizobia or AMF was treated with both live Colletotrichum gloeosporioides—a generalist hemibiotrophic plant pathogen—and C. gloeosporioides fragments. Polyphenol oxidase (PPO), chitinase and β-1,3-glucanase activity in leaves and roots, as well as the number of rhizobia nodules and the extent of AMF colonization, were measured after pathogen treatments. Both the live pathogen and pathogen fragments significantly increased PPO, chitinase and β-1,3-glucanase activity in the leaves, but only PPO activity was increased in roots. The number of rhizobia nodules and the extent of AMF colonization was significantly reduced in treatment plants when compared to controls. CONCLUSION: We demonstrate that aboveground fungal pathogens can affect belowground mutualism with two very different types of microbial symbionts—rhizobia and AMF. Our results suggest that systemically induced PPO activity is functionally involved in this above-belowground interaction. We predict that the top-down effects we show here can drastically impact plant performance in soils with limited nutrients and water; abiotic stress conditions usually mitigated by microbial belowground mutualists. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0321-4) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-28 /pmc/articles/PMC4248430/ /pubmed/25429887 http://dx.doi.org/10.1186/s12870-014-0321-4 Text en © Ballhorn et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ballhorn, Daniel J
Younginger, Brett S
Kautz, Stefanie
An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris
title An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris
title_full An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris
title_fullStr An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris
title_full_unstemmed An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris
title_short An aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in Phaseolus vulgaris
title_sort aboveground pathogen inhibits belowground rhizobia and arbuscular mycorrhizal fungi in phaseolus vulgaris
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248430/
https://www.ncbi.nlm.nih.gov/pubmed/25429887
http://dx.doi.org/10.1186/s12870-014-0321-4
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