Cargando…

Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants

Beneficial root-associated microbes modify the physiological status of their host plants and affect direct and indirect plant defense against insect herbivores. While the effects of these microbes on direct plant defense against insect herbivores are well described, knowledge of the effect of the mi...

Descripción completa

Detalles Bibliográficos
Autores principales: Pangesti, Nurmi, Weldegergis, Berhane T., Langendorf, Benjamin, van Loon, Joop J. A., Dicke, Marcel, Pineda, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506461/
https://www.ncbi.nlm.nih.gov/pubmed/25783487
http://dx.doi.org/10.1007/s00442-015-3277-7
_version_ 1782381689637437440
author Pangesti, Nurmi
Weldegergis, Berhane T.
Langendorf, Benjamin
van Loon, Joop J. A.
Dicke, Marcel
Pineda, Ana
author_facet Pangesti, Nurmi
Weldegergis, Berhane T.
Langendorf, Benjamin
van Loon, Joop J. A.
Dicke, Marcel
Pineda, Ana
author_sort Pangesti, Nurmi
collection PubMed
description Beneficial root-associated microbes modify the physiological status of their host plants and affect direct and indirect plant defense against insect herbivores. While the effects of these microbes on direct plant defense against insect herbivores are well described, knowledge of the effect of the microbes on indirect plant defense against insect herbivores is still limited. In this study, we evaluate the role of the rhizobacterium Pseudomonas fluorescens WCS417r in indirect plant defense against the generalist leaf-chewing insect Mamestra brassicae through a combination of behavioral, chemical, and gene-transcriptional approaches. We show that rhizobacterial colonization of Arabidopsis thaliana roots results in an increased attraction of the parasitoid Microplitis mediator to caterpillar-infested plants. Volatile analysis revealed that rhizobacterial colonization suppressed the emission of the terpene (E)-α-bergamotene and the aromatics methyl salicylate and lilial in response to caterpillar feeding. Rhizobacterial colonization decreased the caterpillar-induced transcription of the terpene synthase genes TPS03 and TPS04. Rhizobacteria enhanced both the growth and the indirect defense of plants under caterpillar attack. This study shows that rhizobacteria have a high potential to enhance the biocontrol of leaf-chewing herbivores based on enhanced attraction of parasitoids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00442-015-3277-7) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4506461
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-45064612015-07-20 Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants Pangesti, Nurmi Weldegergis, Berhane T. Langendorf, Benjamin van Loon, Joop J. A. Dicke, Marcel Pineda, Ana Oecologia Plant-microbe-animal interactions - Original research Beneficial root-associated microbes modify the physiological status of their host plants and affect direct and indirect plant defense against insect herbivores. While the effects of these microbes on direct plant defense against insect herbivores are well described, knowledge of the effect of the microbes on indirect plant defense against insect herbivores is still limited. In this study, we evaluate the role of the rhizobacterium Pseudomonas fluorescens WCS417r in indirect plant defense against the generalist leaf-chewing insect Mamestra brassicae through a combination of behavioral, chemical, and gene-transcriptional approaches. We show that rhizobacterial colonization of Arabidopsis thaliana roots results in an increased attraction of the parasitoid Microplitis mediator to caterpillar-infested plants. Volatile analysis revealed that rhizobacterial colonization suppressed the emission of the terpene (E)-α-bergamotene and the aromatics methyl salicylate and lilial in response to caterpillar feeding. Rhizobacterial colonization decreased the caterpillar-induced transcription of the terpene synthase genes TPS03 and TPS04. Rhizobacteria enhanced both the growth and the indirect defense of plants under caterpillar attack. This study shows that rhizobacteria have a high potential to enhance the biocontrol of leaf-chewing herbivores based on enhanced attraction of parasitoids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00442-015-3277-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-03-19 2015 /pmc/articles/PMC4506461/ /pubmed/25783487 http://dx.doi.org/10.1007/s00442-015-3277-7 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Plant-microbe-animal interactions - Original research
Pangesti, Nurmi
Weldegergis, Berhane T.
Langendorf, Benjamin
van Loon, Joop J. A.
Dicke, Marcel
Pineda, Ana
Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
title Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
title_full Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
title_fullStr Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
title_full_unstemmed Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
title_short Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
title_sort rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plants
topic Plant-microbe-animal interactions - Original research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506461/
https://www.ncbi.nlm.nih.gov/pubmed/25783487
http://dx.doi.org/10.1007/s00442-015-3277-7
work_keys_str_mv AT pangestinurmi rhizobacterialcolonizationofrootsmodulatesplantvolatileemissionandenhancestheattractionofaparasitoidwasptohostinfestedplants
AT weldegergisberhanet rhizobacterialcolonizationofrootsmodulatesplantvolatileemissionandenhancestheattractionofaparasitoidwasptohostinfestedplants
AT langendorfbenjamin rhizobacterialcolonizationofrootsmodulatesplantvolatileemissionandenhancestheattractionofaparasitoidwasptohostinfestedplants
AT vanloonjoopja rhizobacterialcolonizationofrootsmodulatesplantvolatileemissionandenhancestheattractionofaparasitoidwasptohostinfestedplants
AT dickemarcel rhizobacterialcolonizationofrootsmodulatesplantvolatileemissionandenhancestheattractionofaparasitoidwasptohostinfestedplants
AT pinedaana rhizobacterialcolonizationofrootsmodulatesplantvolatileemissionandenhancestheattractionofaparasitoidwasptohostinfestedplants