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Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects

Endophytic insects provide the textbook examples of herbivores that manipulate their host plant’s physiology, putatively altering source/sink relationships by transferring cytokinins (CK) to create ‘green islands’ that increase the nutritional value of infested tissues. However, unambiguous demonstr...

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Autores principales: Brütting, Christoph, Crava, Cristina Maria, Schäfer, Martin, Schuman, Meredith C, Meldau, Stefan, Adam, Nora, Baldwin, Ian T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059766/
https://www.ncbi.nlm.nih.gov/pubmed/30014847
http://dx.doi.org/10.7554/eLife.36268
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author Brütting, Christoph
Crava, Cristina Maria
Schäfer, Martin
Schuman, Meredith C
Meldau, Stefan
Adam, Nora
Baldwin, Ian T
author_facet Brütting, Christoph
Crava, Cristina Maria
Schäfer, Martin
Schuman, Meredith C
Meldau, Stefan
Adam, Nora
Baldwin, Ian T
author_sort Brütting, Christoph
collection PubMed
description Endophytic insects provide the textbook examples of herbivores that manipulate their host plant’s physiology, putatively altering source/sink relationships by transferring cytokinins (CK) to create ‘green islands’ that increase the nutritional value of infested tissues. However, unambiguous demonstrations of CK transfer are lacking. Here we show that feeding by the free-living herbivore Tupiocoris notatus on Nicotiana attenuata is characterized by stable nutrient levels, increased CK levels and alterations in CK-related transcript levels in attacked leaves, in striking similarity to endophytic insects. Using (15)N-isotope labeling, we demonstrate that the CK N(6)-isopentenyladenine (IP) is transferred from insects to plants via their oral secretions. In the field, T. notatus preferentially attacks leaves with transgenically increased CK levels; plants with abrogated CK-perception are less tolerant of T. notatus feeding damage. We infer that this free-living insect uses CKs to manipulate source/sink relationships to increase food quality and minimize the fitness consequences of its feeding.
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spelling pubmed-60597662018-08-06 Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects Brütting, Christoph Crava, Cristina Maria Schäfer, Martin Schuman, Meredith C Meldau, Stefan Adam, Nora Baldwin, Ian T eLife Ecology Endophytic insects provide the textbook examples of herbivores that manipulate their host plant’s physiology, putatively altering source/sink relationships by transferring cytokinins (CK) to create ‘green islands’ that increase the nutritional value of infested tissues. However, unambiguous demonstrations of CK transfer are lacking. Here we show that feeding by the free-living herbivore Tupiocoris notatus on Nicotiana attenuata is characterized by stable nutrient levels, increased CK levels and alterations in CK-related transcript levels in attacked leaves, in striking similarity to endophytic insects. Using (15)N-isotope labeling, we demonstrate that the CK N(6)-isopentenyladenine (IP) is transferred from insects to plants via their oral secretions. In the field, T. notatus preferentially attacks leaves with transgenically increased CK levels; plants with abrogated CK-perception are less tolerant of T. notatus feeding damage. We infer that this free-living insect uses CKs to manipulate source/sink relationships to increase food quality and minimize the fitness consequences of its feeding. eLife Sciences Publications, Ltd 2018-07-17 /pmc/articles/PMC6059766/ /pubmed/30014847 http://dx.doi.org/10.7554/eLife.36268 Text en © 2018, Brütting et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Ecology
Brütting, Christoph
Crava, Cristina Maria
Schäfer, Martin
Schuman, Meredith C
Meldau, Stefan
Adam, Nora
Baldwin, Ian T
Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
title Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
title_full Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
title_fullStr Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
title_full_unstemmed Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
title_short Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
title_sort cytokinin transfer by a free-living mirid to nicotiana attenuata recapitulates a strategy of endophytic insects
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059766/
https://www.ncbi.nlm.nih.gov/pubmed/30014847
http://dx.doi.org/10.7554/eLife.36268
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